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Grantee Research Project Results

Final Report: Southern Center on Environmentally-Driven Disparities in Birth Outcomes

EPA Grant Number: R833293
Center: The Center for Study of Neurodevelopment and Improving Children's Health
Center Director: Murphy, Susan K.
Title: Southern Center on Environmentally-Driven Disparities in Birth Outcomes
Investigators: Miranda , Marie Lynn , Ashley-Koch, Allison , Auten, Richard , Foster, W. Michael , Gelfand, Alan , Gibson-Davis, Christina , Goodall, Jonathan , James, Sherman , Reiter, Jerome , Swamy, Geeta , Williams, Redford , Keating, Martha H. , Maxson, Pamela
Institution: Duke University
EPA Project Officer: Callan, Richard
Project Period: May 1, 2007 through April 30, 2012 (Extended to April 30, 2014)
Project Amount: $7,735,620
RFA: Centers for Children’s Environmental Health and Disease Prevention Research (2005) RFA Text |  Recipients Lists
Research Category: Children's Health , Human Health

Objective:

Center Overview
 
The central mission of the Southern Center on Environmentally-Driven Disparities in Birth Outcomes (SCEDDBO) was to determine how environmental, social and host factors jointly contribute to health disparities. Specific aims of the Center were:
  1. To develop and operate an interdisciplinary children’s health research center with a focus on understanding how biological, physiological, environmental and social aspects of vulnerability contribute to health disparities;
  2. To enhance research in children’s health at Duke by promoting research interactions among programs in biomedicine, pediatric and obstetric care, environmental health, and the social sciences and establishing an infrastructure to support and extend interdisciplinary research;
  3. To develop new methodologies for incorporating innovative statistical analysis into children’s environmental health research and policy practice, with a particular emphasis on spatial, genetic and proteomic analysis;
  4. To serve as a technical and educational resource to the local community, region, the nation, and to international agencies in the area of children’s health and health disparities; and
  5. To translate the results of the Center into direct interventions in clinical care and practice.
 
Administrative Core

The SCEDDBO was governed through an Administrative Core that includes an Executive Committee composed of the Director, the two Co-Directors, and the Project Manager; an Internal Steering Committee composed of members of the Executive Committee and the Directors of the Research Projects and the Facility and Community Outreach Cores, as well as a community member and the Director of the Durham County Health Department; and an External Advisory Committee composed of senior environmental health scientists, as well as community representatives, with expertise relevant to SCEDDBO, who provided informal consultation, as well as annual formal evaluation of Center research and outreach activities.

The specific aims of the Administrative Core are to:

a. Provide scientific direction and leadership;

b. Coordinate and foster interactions among research project and facility core investigators;

c. Provide administrative services for the Center;

d. Direct the Young Investigators program; and

e. Represent Duke’s SCEDDBO to the university, the community, the NIH, other Children’s Environmental Health Centers across the United States, and the policy and scientific community interested in children's environmental health more broadly.

In all activities, SCEDDBO emphasized the importance of diversity. The decision to focus on health disparities, the gender and racial diversity of Center leadership, the incorporation of natural, social and biomedical scientists, a commitment to community-based participatory research, and efforts to promote the careers of promising new investigators were all indicative of the importance that we place on fostering environments where all people can prosper.
 
 
Project A (C001): Mapping Disparities in Birth Outcomes
 
Project A utilized the conceptual framework of the “weathering hypothesis,” which posits that chronic and persistent stressors lead to accelerated biological aging of women, which in turn accounts for adverse birth outcomes among certain subpopulations. The central objective was to determine whether and to what extent joint exposures to socioeconomic and environmental stressors contribute to racial and ethnic health disparities in fetal growth restriction.
 
Using a geographically based nested study design moving from analysis of births for the entire State of North Carolina to six demographically and geographically distinct counties to a single health center, in addition to state-of-the-art Geographic Information Systems (GIS) applications with Bayesian spatial hierarchical modeling and other advanced spatial statistical approaches, the specific aims were to:
  1. Spatially link detailed birth record, fetal death certificate, socioeconomic, environmental, tax assessor, community-based and clinical obstetric data at highly resolved scales for the State of North Carolina from 1990 to 2003;
  2. Refine the concept of fetal growth restriction by (a) developing a joint distribution for birth weight and gestation using bivariate modeling for live births and fetal deaths—both separately and jointly, and (b) defining it in terms of fetal and infant mortality, rather than percentile cut points; and
  3. Determine whether and to what extent differential exposures to both environmental and social stressors help explain health disparities in fetal growth restriction among (a) African-American women compared to non-Hispanic white and Hispanic women, (b) Older African-American women compared to younger African-American women, (c) Hispanic women compared to non-Hispanic white and African-American women, and (d) foreign-born Hispanic women compared to U.S.-born Hispanic women.
This project evaluated a large number of factors in diverse populations, providing broad relevance for birth outcomes across time, space and demography. Identifying social and environmental factors contributing to fetal growth restriction helped improve our understanding of disease etiology and explain the racial disparity in disease incidence.
 
 
Project B (C002): Healthy Pregnancy, Healthy Baby: Studying Racial Disparities in Birth Outcomes
 
The central objective of the Healthy Pregnancy, Healthy Baby Study was to determine how the interaction of environmental, social and host factors contributes to disparities in birth outcomes between African-American and white women in the American South. There were four specific aims:
  1. Conduct a cohort study of pregnant women in Durham, NC designed to correlate birth weight, gestation, and birth weight x gestation with environmental, social and host factors;
  2. Develop community-level measures of environmental and social factors by inventorying neighborhood quality and the built environment in partnership with local community groups;
  3. Create a comprehensive data architecture, spatially resolved at the tax parcel level, of environmental, social and host factors affecting pregnant women by linking data from the cohort study and neighborhood assessments with additional environmental and socioeconomic data; and
  4. Determine whether and to what extent differential exposures explain health disparities in birth outcomes by applying innovative spatial and genetic statistical methods to:
  • Identify environmental, social and host factors that cluster to predict birth outcomes in the entire sample,
  • Determine whether these clusters are more or less present in African-American versus white populations and quantify the proportion of health disparities explained by differences in cluster frequency, and
  • Identify environmental, social and host factors that cluster to predict birth outcomes within the African-American and white subsamples and compare these clusters across racial groups.
 
Project C (C003): Perinatal Environmental Exposure Disparity and Neonatal Respiratory Health
  1. To determine whether maternal exposure to airborne particulates (PM) and/or ozone (1st hit) restricts fetal growth and/or postnatal growth, and impairs lung development/function in newborn mice;
  2. To determine whether PM and/or ozone exposure "reprograms" maternal inflammatory responses;
  3. To determine whether postnatal (2nd hit) ozone exposure further impairs postnatal somatic and lung development/function following maternal PM and/or ozone exposures;
  4. To determine whether genetic or developmental susceptibility to airway hyperreactivity exacerbates maternal and/or postnatal exposure effects on postnatal somatic and lung development/function.
 
Community Outreach and Translation Core (C004)
 
The central objective of the Community Outreach and Translation Core (COTC) was to create, implement and assess strategies to translate and apply the findings of SCEDDBO into relevant information for women of childbearing age, families, community groups, policy makers and health care professionals. The COTC conducted environmental health outreach and education directed at low-income and minority women and their children; enhanced the capacity of disadvantaged communities to understand threats posed by environmental contaminants; and provided a bridge between campus research, communities and policy makers. The specific aims of the COTC were to:
  1. Support the community-based neighborhood assessment being undertaken as part of Projects A and B;
  2. Partner with nursing programs at Duke-affiliated hospitals to develop and present curricula to nursing students on environmental exposures and maternal and child health outcomes;
  3. Develop culturally-appropriate advisory materials on environmental contaminants for low-income expectant or nursing mothers with low English proficiency;
  4. Deliver training to local health department personnel focused on environmental factors related to maternal health and pregnancy outcomes;
  5. Participate in regional, state and federal policy dialogues to provide decision makers with policy-relevant, science-based information concerning environmental exposures and health disparities related to maternal and child health and well-being; and
  6. Increase awareness of maternal health and health disparities by facilitating bidirectional exchanges between Center investigators, community members, public health advocacy groups, and policy makers.
 
Geographic Information System and Statistical Analysis Core (C005)
 
The overall objective of the GIS and Statistical Analysis (GISSA) Core was to support spatial and quantitative analysis needs of the Center research projects, as well as the COTC. Our specific aims included:
  1. Providing support for the development of environmental and social data layers needed to implement data analyses required for the research projects and the COTC;
  2. Providing statistical analysis, advice and consulting on the broad range of statistical issues that arise in conjunction with the research projects, with a particular emphasis on data reduction methods and modeling spatial and spatio-temporal data within a Bayesian framework; and
  3. Providing analysis for the unique needs of genetic data arising from the clinical and animal studies of the Center.
This support core facilitated the development of innovative quantitative methodology for children’s environmental health research associated with the projects and cores. Equally important, it enhanced substantive collaboration between statisticians and scientists involved in the research projects yielding improved analyses of research core data, as well as novel statistical modeling.

Summary/Accomplishments (Outputs/Outcomes):

Center Overview
 
SCEDDBO leveraged and promoted active partnerships among the Nicholas School of the Environment at Duke University, the School of Natural Resources and Environment at the University of Michigan (UM), the Duke University Medical Center, Trinity College of Arts and Sciences, and Duke’s Children's Environmental Health Initiative, as well as the Durham County Health Department (DCHD) and Lincoln Community Health Center (LCHC), Durham’s federally qualified health center. The Center brought together the expertise of obstetricians, pediatricians, genetic epidemiologists, spatial statisticians, environmental scientists, social epidemiologists, social psychologists, geographers and community organizations. SCEDDBO capitalized on substantial ongoing commitments by Duke University to foster strong interdisciplinary research programs in environmental health sciences.
 
During the project period, SCEDDBO was characterized by significant synergies across Center components. For example, our Community Assessment Project (CAP), conducted by the SCEDDBO COTC, assessed built environment variables for over 17,000 residential tax parcels in 2008 and for over 30,700 parcels in 2011, including the home addresses of over 65 percent of the 1,800 participants in Project B’s pregnancy cohort study and 4,279 women from the Project A data architecture (with the latter number increasing as additional years of birth record data become available). Findings from analyses of these datasets led to the decision to incorporate a nest deprivation model in our animal studies, which originally focused on air pollution exposures only. Over the course of the project period, we have published 80 papers resulting directly from the work of SCEDDBO.

Central to SCEDDBO’s mission to determine how environmental, social, and host factors (see Figure 1) jointly contribute to health disparities was the development of an underlying, multi-sourced, detailed data architecture. During the project period, we constructed a large-scale, spatially referenced data warehouse, linking birth record data to social and environmental exposures data. Among women in our sample population, exposure to air pollutants, including PM2.5 and PM10, is associated with poor pregnancy outcomes (Chang et al., 2012; Gray et al., 2010;Vinikoor-Imler et al., 2012). We have helped define meaningful exposure metrics for air pollution and how to incorporate uncertainty in personal exposure estimates derived from monitoring station measurements (Gray et al., 2011). To do so, we constructed a stochastic simulator to directly make predictions of individual level exposure that we related to birth weight (Berrocal et al., 2011). Additional work on air pollution identified windows of vulnerability for pregnant women (Chang et al., 2012; Gray et al., 2010). We re-conceptualized the analysis for binary pregnancy outcomes (e.g., preterm birth) as a time-to-event analysis, enabling us to examine air pollution in a time-varying setting, where exposure is conditional on the length of the entire pregnancy or the third trimester (Chang et al., 2010). To achieve improved estimates of air pollution exposure, we constructed spatial downscalers, fusing monitoring station data with computer model output to better assess environmental exposure at point level spatial resolution (Berrocal et al., 2010a; Berrocal et al., 2010b; Berrocal et al., 2011).

Figure 1
Figure 1. M.L. Miranda, P. Maxon, S. Edwards. 2009. "Environmental
contributors to disparities in pregnancy outcomes." Epidemiologic 
Reviews, 31:67-83. PMID: 19846592

Compared to non-Hispanic whites (NHW), non-Hispanic blacks (NHB) are more likely to live in neighborhoods characterized by poverty, elevated levels of environmental contaminants, and poor quality housing (Miranda et al., 2009). In related work on racial residential segregation (which is associated with higher environmental exposures), we observed a detrimental association between a spatial measure of neighborhood level racial residential segregation and pregnancy outcomes (Anthopolos et al., 2011). Racial residential segregation may impact health through the built environment. Using the Community Assessment Project data, we found that higher levels of housing damage, property disorder, tenure, and vacancy are associated with increased likelihood of preterm birth and low birth weight (Miranda, Messer, & Kroeger, 2012).

Statistical methods development has focused on outcome-exposure relationships. We emphasized joint modeling of related outcomes that can borrow strength from each other, such as birthweight and gestational age, which often helps with causal inference interpretation and illuminates subpopulations with differential risk for poor outcomes (Schwartz et al., 2010. See Figure 4). With binary outcomes (e.g., low birth weight and preterm birth) and normal outcomes, we have introduced additional borrowing of information with spatially correlated random effects (Neelon et al., 2012). Given the critical nature of health outcomes defined by distribution tails, such as low birth weight and preterm birth, in addition to the potential for differential covariate effects over the response distribution, we developed a new method to apply quantile regression in a spatial context (i.e., relaxing the assumption that observations in adjacent neighborhoods are independent). Applying this method, we observed differential effects of standard risk factors of birth weight, such as infant sex and birth order, along the birth weight response distribution.

Figure 4
FIgure 4. S. Schwartz, A. Gelfand, and M.L. Miranda. 2010. "Joint Baysian analysis of birthweight and censored gestational age using finite mixture
models." Statistics in Madicine 20; 20(16): 1710-1723.

We recruited and retained 1,800+ women from Duke University Medical Center and Lincoln Community Health Center for our Healthy Pregnancy, Healthy Baby Study. Data on maternal and neonatal medical indicators, psychosocial health, and environmental exposures were obtained. We genotyped the cohort for 412 Single Nucleotide Polymorphisms (SNPs) in 52 genes related to human environmental contaminant clearance, infection and inflammation, maternal stress response, and other potential drivers of health disparities. To better identify subpopulations among NHB women in our sample, we generated the Illumina African American Admixture Chip, based on 1,509 selected SNPs with disparate frequencies in the Yoruban (African) and European (Caucasian) HapMap samples. As an example, we found that race-specific allelic frequencies in the vitamin D receptor (VDR) gene suggest its potential as a gene involved in health disparities (Swamy et al., 2011).

We found that women who live in neighborhoods with higher levels of housing damage, vacancy, and renter-occupied units are more likely to have poor scores on measures of psychosocial health, compared to women with residence in neighborhoods with lower levels of these attributes (Messer et al., 2012). Linking individual psychosocial health to the built environment, we then sought to understand the pathway between psychosocial health and pregnancy. Poor psychosocial health is associated with the likelihood of engaging in health behaviors known to be harmful to pregnancy, like smoking (Maxson & Miranda, 2011; Maxson et al., 2012; Miranda, Edwards, & Myers, 2011; Zhu et al., 2012). Among women for whom we measured levels of polybrominated diphenyl ethers (PBDE) flame retardants, our data suggest that PBDEs may be affecting thyroid regulation throughout pregnancy (Stapleton et al., 2011). In companion work, we observed that maternal behaviors and the presence of electronics were associated with higher levels of PBDEs in maternal cord blood samples (Buttke et al., 2012).

Additionally, we have characterized mercury and lead levels among women in our sample: socioeconomic status is positively related to mercury levels controlling for fish consumption, and lead levels were more likely to stem from remobilization from historical rather than current exposures (Miranda, Edwards, & Maxson, 2011; Miranda, Edwards, Swamy, et al., 2010).

The Healthy Pregnancy, Healthy Baby Study has motivated innovative methods development in the areas of handling missing data and developing differential risk profiles. While the cohort study had a high retention rate (92%), scattered missingness across the many collected variables resulted in a limited number of complete cases. We developed a non-parametric approach for multiple imputation via chained equations that uses sequential regression trees as the conditional models – an approach that we demonstrate can result in more plausible imputations and hence more reliable inferences (Burgette & Reiter, 2010). A second missing data problem that we encountered stemmed from a change in the laboratories used to measure environmental contaminants in maternal blood (Burgette & Reiter, 2012b). To overcome the statistical challenges associated with not having any measurements on both scales, we developed a multiple imputation approach based on rank preservation.

The amount of detailed information in the Healthy Pregnancy, Healthy Baby Study led us to concentrate on ways to distill variables into meaningful summaries in order to construct risk profiles. For example, through Bayesian growth mixture modeling, we differentiated classes of pregnant women according to their mean arterial blood pressure curves and joint probabilities of adverse birth outcomes (Neelon et al., 2011). Such classes may be more clinically relevant than looking at individual risk factors one at a time. With a similar goal but in a quantile regression setting, we developed ways to reduce high dimensional predictor spaces and identify latent factors underlying clusters of observed variables (Burgette et al., 2011; Burgette & Reiter, 2012a; Zhu et al., 2012).

We used animal models to more precisely assess the contributions of joint and sequential perinatal and postnatal environmental stressors on health outcomes. We exposed pregnant mice to a standardized industrial PM by tracheal instillation throughout pregnancy, followed by intermittent ozone exposure to their offspring. Maternal PM treatment induced inflammatory responses in fetal compartments and augmented the effects of ozone on airway hyper-reactivity, a model system for human asthma (Auten et al., 2009). We chose ozone as a criterion air pollutant to model human asthma since childhood exposure has been strongly associated with the development of asthma, and for the strong potential of early life ozone exposure to have life-long health effects (Auten & Foster, 2011). In order to determine if traffic-related air pollutant exposure during pregnancy, already associated with the development of asthma and adverse pregnancy outcomes, could have similar "priming" effects in offspring exposed to ozone, we exposed pregnant mice to inhaled diesel exhaust or to instilled diesel particles. Exposure to diesel via the ambient, physiological route (and by instillation) also caused fetal inflammatory responses (↑fetal lung and placenta pro-inflammatory cytokines) and worsened the effects of ozone on postnatal airway hyperreactivity. Notably, the combined pre-natal exposure of maternal diesel inhalation and postnatal ozone exposure of offspring impaired lung development, while single exposures did not. Furthermore, the effects on airway hyperreactivity persisted to adulthood after ceasing ozone exposure for four weeks, a completely novel finding, consistent with our hypothesized schema of synergies between exposures across the life span (Auten et al., 2012).

Our prenatal air pollution exposure models provoked fetal inflammation (lung, placenta), known to be linked with other adverse health outcomes such as impaired neurological development, so we began a collaboration with Staci Bilbo, (and eventually made her Co-PI on Project C) to examine long-term effects of combined perinatal pollutant exposure and other stressors known to be prevalent in impoverished communities (maternal stress, obesity, exposure to indoor antigens). We secured additional support from the Duke Institute for Brain Sciences to support these preliminary studies. We have since determined that pre-natal diesel exposure in mice during pregnancy, when combined with a high-fat diet provided to adult offspring, produces activated brain microglia, increases anxiety behavior, and impairs cognition (Bolton et al., 2012).

The synergy among the research projects was facilitated by the GIS and Statistical Analysis (GISSA) Core. The GISSA Core allowed for data analysis of the very large amount of data through the use of high-end GIS applications in combination with Bayesian spatial hierarchical modeling and other advanced spatial statistical approaches, thus permitting multi-level analyses. Research Projects A and B both applied a Bayesian spatial hierarchical modeling approach to capture uncertainties in pregnancy outcomes and to elucidate the contributions of economic, sociocultural, and environmental stressors on health disparities in pregnancy outcomes.  State-of-the-art GIS methods allowed for sophisticated spatial statistical analyses at highly resolved spatial scales.  

The GISSA Core also provided the analysis of the biological response and genetic data generated in Research Projects B and C. The rich source of social, environmental, and host data in Project B, coupled with sophisticated statistical genetic approaches for identifying gene-gene and gene-environment interactions, provided the opportunity to make important discoveries of how these higher order interactions may be working together to promote or prevent adverse birth outcomes. By serving as a central clearinghouse for statistical analysis, the GISSA Core tracked outcomes in each project and used these discoveries to guide the analysis in each of the other projects. 

The COTC provided key support by developing community partnerships and leading the community outreach and translation effort. COTC materials have been disseminated widely throughout the community, and the COTC has met often with community groups and local agencies. In collaboration with the nursing programs at Duke and UNC Schools of Nursing, COTC designed and regularly delivered a comprehensive curriculum to nursing students on environmental exposures and maternal and child health outcomes. The COTC also developed a partnership with nutritionists in the NC Supplemental Nutrition Program for Women, Infants, and Children (WIC), developing advisory materials on mercury fish consumption for Latino families. In addition, the COTC partnered with the GISSA Core to offer no-cost GIS training to public health personnel. COTC also collaborated with a variety of regional, state, and federal advisory groups, SCEDDBO Director Marie Lynn Miranda served on the EPA's Children's Health Protections Advisory Committee (CHPAC).

Partnerships

A rich set of active relationships among community, campus, and organizational partners formed the basis for our center. First, we emphasized the connections among Duke, UNC, and U-M. Second, community partners and SCEDDBO investigators collaborated to improve environmental health in low-income areas throughout Durham County and across NC. These partnerships were and continue to be based on mutual interest in the effects of the environment on young children and pregnant women, as well as how environmental and social stressors interact to affect maternal and child health.

As a concrete example of our partnership approach, Durham Congregations, Associations, and Neighborhoods (Durham CAN) conducted a neighborhood audit that consisted of having volunteers take a block by block inventory of neighborhood problems, including broken or missing sidewalks, missing streetlights, roads in disrepair, litter, sewage and drainage problems, abandoned homes, and vacant/ overgrown lots. GISSA Core personnel converted the neighborhood audits into map-based visuals. Durham CAN used these maps in presentations to community groups, the Durham City Council, the Durham County Commissioners, and local government offices to negotiate improved conditions in target neighborhoods. In mapping the neighborhood audits for Durham CAN, we noted some clear problems with inter-coder reliability when comparing the audits across large sections of the city. We subsequently discussed joint work to improve the neighborhood audit. This collaborative effort formed the basis for the Community Assessment Project (see COTC).

During the project period, community partners and SCEDDBO investigators had multiple opportunities to explore mutual interests in designing projects that generate results that can be applied directly in the community. Our collective community-based experience convinced us that health disparities, particularly as they affect children, still represent the most important policy challenge in low income and minority communities. As we have jointly witnessed the disproportionate exposures to environmental contaminants, as well as the poor quality of the built environment and associated social stressors, we became convinced that real change in our communities requires an integrated understanding of environmental, social, and host factors.

 
Administrative Core

Website.  The Administrative Core provided material on SCEDDBO to the EPA for uploading to the EPA children’s centers website.  In addition, we updated our SCEDDBO website, linked off the website for the Children’s Environmental Health Initiative (cehi.snre.umich.edu).  We used our secure internal website that allowed for discussion boards, email communication, and document storage associated with the work of each of the SCEDDBO components.

Dissemination.  SCEDDBO work was disseminated in a multitude of ways over the seven years of the project. Highlights are presented here; each project summary has a relevant list of publications and presentations.

Dr. Miranda brought her perspective on geospatial analysis and its usefulness in assessing and analyzing public health issues via her participation in the US Centers for Disease Control and Prevention’s Geospatial Science and Healthy Communities Expert Panel, held in Atlanta, GA, in May 2008.

SCEDDBO offered a well-attended mini-symposium at the EPA in the Research Triangle Park in January 2009, designed to present EPA employees with a synopsis of the work that SCEDDBO does, emphasizing the environmental contributors to disparities in birth outcomes. Dr. Miranda represented the scientific mission of SCEDDBO as part of the USEPA’s BOSC review of the agency’s human health research program in January 2009.  Specifically, Dr. Miranda co-authored and presented with Ms. Devon Payne Sturgess (USEPA) a poster regarding Long Term Goal 3 entitled “Differential Vulnerability to Environmental Contaminants and Adverse Outcomes during Early Childhood.”  This poster was well-received and SCEDDBO was commented on very favorably by the BOSC review panel in its written report.

Dr. Miranda represented the scientific mission of SCEDDBO as part of the GEI Exposure Biology Program in August, 2009.  Specifically, Dr. Miranda presented a talk entitled “Combining Population Clinical, and Animal Models to Assess Exposure and Effects.”  Dr. Miranda also presented a talk at the USEPA’s “Strengthening Environmental Justice Research and Decision-Making” conference.  This talk was entitled, “Using GIS to Support EJ Results” and represented the broad work of the Children’s Environmental Health Initiative, including work done under the auspices of SCEDDBO. 

In addition, Dr. Miranda was the keynote speaker at our Nurses Conference, Environmental Considerations in Nursing Practice in May, 2010. She also spoke at the Environmental Health Summit in September, 2010.  SCEDDBO also co-sponsored a symposium “The Social Context of Environmental Exposures in Children” in March, 2011. Speakers from Harvard, the United States Environmental Protection Agency, the National Institute of Child Health and Human Development, and Duke University discussed the role of the social context of environmental exposures in children. The symposium was well attended and garnered much positive feedback.

In 2012, Dr. Miranda gave the plenary address at ISEE in Columbia, South Carolina. Her talk, “Of Mice, Maps, and Moms: Air quality impacts on human health,” discussed SCEDDBO’s geospatial work on air pollution and its effects on pregnancy outcomes. In July 2013, she presented the keynote address, “It takes a village: Integrated methods for addressing environmental health disparities,” at the NIEHS sponsored Environmental Health Disparities and Environmental Justice conference in RTP, North Carolina.

Identification of training opportunities.  The Administrative Core worked with all of the other SCEDDBO components to identify key training opportunities for investigators and other research staff.  Through this effort, we developed greater expertise in remotely sensed data, air pollution modeling, centering models of patient care, spatial statistics, and information science. These opportunities included both intensive short course and semester long coursework for several research staff, as well as travel to professional meetings for the graduate students and postdoctoral associates supported on the SCEDDBO grant. In addition, Dr. Alan Gelfand, Director of the GISSA Core, delivered a 2-day intensive short course on spatial statistics that was widely attended by SCEDDBO investigators and research staff. We also offered training workshops through our Community Outreach and Translation Core, with administrative support provided through the Administrative Core.

New Collaborations.  As part of our mission to both support the work of young investigators and advance the research mission of SCEDDBO, we began new collaborations with Dr. Staci Bilbo, Assistant Professor, Department of Psychology and Neuroscience, Duke University and Dr. Rebecca Fry, Associate Professor, Gillings Global School of Public Health, UNC. Our work with Dr. Bilbo focuses on new mouse models to explore the joint impact of environmental and social stressors on birth and developmental outcomes. Our work with Dr. Fry explores gene expression and epigenetic changes associated with in utero metals exposures, with a particular emphasis on cadmium.  In addition, we established a CDC-funded collaboration with Dr. Heather Stapleton, Associate Professor, Nicholas School of the Environment, Duke University. This study leveraged our ongoing clinical obstetrics project to assess in utero exposures to brominated flame retardants, as well as the relationship between brominated flame retardant body burden and maternal thyroid function. Multiple papers were published on this collective work (Bolton et al., 2013; Edwards et al., in press; Stapleton et al., 2011; Sanders et al., 2013; Buttke et al., 2013).

National Service. Duke hosted the Children’s Environmental Health Centers’ monthly conference calls for several years, 2007-2013. SCEDDBO investigators also helped organize the October 2010 and 2013 Children’s Centers conferences. In addition, Dr. Miranda served as a standing member of the Children’s Health Protection Advisory Committee. Dr. Miranda also served as a chartered member of the NIH’s Infectious Diseases, Reproductive Health, Asthma and Pulmonary Conditions (IRAP) Study Section. Multiple SCEDDBO investigators helped to review proposals for federal funding agencies, as well as review manuscripts for peer-reviewed journals.
 

Project A (C001): Mapping Disparities in Birth Outcomes

Central to SCEDDBO’s mission to determine how environmental, social and host factors (see Figure 1) jointly contribute to health disparities was the development of an underlying, multisourced, detailed data architecture. During the project period, we constructed a large-scale, spatially referenced data warehouse, linking birth record data to social and environmental exposures data. We have shown that among women in our sample population, exposure to air pollutants, including PM2.5 and PM10, and using proximity to roadways as a proxy variable, is associated with poor pregnancy outcomes, as measured by birth weight, preterm birth and maternal medical complications, controlling for maternal-level risk factors and neighborhood characteristics (Chang, et al., 2012; Gray, et al., 2010; Vinikoor-Imler, et al., 2012; Gray, et al., 2013; see Figure 2).
 
Figure 2
Figure 2. S. Gray, S.E. Edwards, and M.L. Miranda. 2013. "Race, socioeconomic status, and air pollution exposure in North Carolina." 
Environmental Research 126: 152-158. PMID: 23850144.
 
Our work has investigated how to define meaningful exposure metrics for air pollution in terms of the impact of geographic scale of aggregation and how to incorporate uncertainty in personal exposure estimates derived from monitoring station measurements (Gray, et al., 2011). To do so, we constructed a stochastic simulator to directly make predictions of individual-level exposure that we related to birth weight (Berrocal, et al., 2011). Additional work on air pollution has identified windows of vulnerability for expectant mothers (Chang, et al., 2012; Gray, et al., 2010). We reconceptualized the analysis for binary pregnancy outcomes like preterm birth as a time-to-event analysis instead of simple logistic regression, enabling us to examine air pollution in a time-varying setting, where exposure is conditional on the length of the entire pregnancy or the third trimester (Chang, et al., 2010; Chang, et al., 2012). With the goal of linking pregnancy outcomes to improved estimates of air pollution exposure, we have constructed spatial downscalers, which fuse monitoring station data with computer model output to better assess environmental exposure at point level spatial resolution (Berrocal, et al., 2010a; Berrocal, et al., 2010b; Berrocal, et al., 2011).
 
Compared to non-Hispanic whites (NHW), non-Hispanic blacks (NHB) are more likely to live in neighborhoods characterized by poverty, elevated levels of environmental contaminants, and poor quality housing (Miranda et al., 2009). In related work on racial residential segregation (which is associated with higher environmental exposures), we observed a detrimental association between a spatial measure of neighborhood level racial residential segregation and pregnancy outcomes (Anthopolos, et al., 2011; see Figure 3). Racial residential segregation may impact health through the built environment. Using the Community Assessment Project data, we found that higher levels of housing damage, property disorder, tenure and vacancy are associated with increased likelihood of preterm birth and low birth weight (Messer, et al., 2012). Linking these two lines of research, we then showed in a formal mediation framework that poor quality built environment accounts for approximately 35 percent of the total effect of racial residential segregation on preterm birth (Anthopolos, et al., 2014).
 
Figure 3
Figure 3.  R. Anthopolos, S.A. James, A.E. Gelfand, and M.L. Miranda. 2011. "A spacial measure of 
neighborhood-level racial isolation applied to low birthweight, preterm birth, and birthweight in North Carolina."
Spacial and Spacio Temporal Epidemiolgy 2(4): 235-246. PMID: 22748223.
 
In our statistical methods development, we focused on outcome-exposure relationships and emphasized joint modeling of related outcomes that can borrow strength from each other, such as birth weight and gestational age, which will often help with causal inference interpretation and illuminates subpopulations with differential risk for adverse joint birth outcomes (Schwartz, et al., 2010; see Figure 4.). For the case of binary outcomes (e.g., low birth weight and preterm birth) and normal outcomes, we have introduced additional borrowing of information at the contextual level with spatially correlated random effects (Neelon, et al., 2012; Neelon, Anthopolos and Miranda, 2014; Neelon, Gelfand and Miranda, 2014). Given the critical nature of health outcomes defined by distribution tails, such as low birth weight and preterm birth, in addition to the potential for differential covariate effects over the response distribution, we developed a new method to apply quantile regression in a spatial context (i.e., relaxing the assumption that observations in adjacent neighborhoods are independent). Applying this method, we observed differential effects of standard risk factors of birth weight, such as infant sex and birth order, along the birth weight response distribution (Lum and Gelfand, 2012).
 
Figure 4
Figure 4. S. Schwartz, A. Gelfand, and M.L. Miranda. 2010. "Joint Bayesian analysis of birthweight and 
censored gestational age using finite mixture models." Statistics in Medicine 20; 20(16): 1470 - 1723.
 
In addition, we have completed work on the impact of maternal age and birth order on birth weight (Swamy, et al., 2011), on modeling ordinal categorical data using Gaussian processes (Heaton, et al., 2011), the etiology of racial disparities in maternal hypertensive disorders (Miranda, et al., 2010), racial differences in seasonality patterns of poor pregnancy outcomes (Miranda, et al., 2011), the advantages of spatial analysis in environmental health research (Miranda and Edwards, 2011), the relationship between early childhood lead exposure and later school performance and exceptionality designations (Miranda, et al., 2007; Miranda, et al., 2009; Miranda, et al., 2010), on flexible Bayesian modeling techniques for functional and longitudinal data (Montagna S., et al, 2012), on joint spatial modeling of areal multivariate categorical data (Tassone, et al., 2010; see Figure 5), on optimal spatial designs for environmental health data (Xia, et al., Environmetrics, 2006), on the association between the built environment and child BMI (Miranda, et al., 2012), and on synthesizing categorical data sets from different sampling designs (Berrocal, et al., 2013).
 
Figure 5
Figure 5. E. Tassone, M.L. Miranda, and A. Gelfand. 2010. "Disaggreagted spacial modeling
for areal unit catagorical data." Journal of the Royal Statistical Society: Series C (Applied Statistics)
59, Part, pp. 175-190. PMID: PMC2999915.
 
Maternal Exposure to Air pollution. Over the project period, we have done much work on air pollution exposure and pregnancy outcomes. A continuing goal was the linking of the detailed birth record data to EPA PM10, PM2.5 and ozone monitoring data in order to study the impact of maternal exposure to air pollution on birth weight. To this end, in year 6 we were invited to write a review of air pollution effects on birth outcomes (Edwards, et al., forthcoming). We were especially focused on incorporating refined exposure metrics to most effectively characterize meaningful exposures, as well as to capture any windows of vulnerability. Significant progress was made on the relationship between birth outcomes and exposure to particulate matter and ozone separately, and the current focus is determining how to characterize joint exposure to both particulate matter and ozone. A manuscript on this work appeared in the Journal of Exposure Science and Environmental Epidemiology (Gray, et al., 2010). A critical issue in this work is addressing the misalignment between where monitoring stations are and where pregnant women live. Two approaches have been explored. One considers buffers of varying radii around monitoring sites to see how the exposure signal is affected by increasing distance from the site. The other attaches more uncertainty to the putative exposure as the distance from the monitoring site to the residence increases. Again, various exposure windows and metrics are considered. This work appeared in Statistics and Medicine (Gray, et al., 2011). Time-to-event investigation of the effect of particulate matter and birth outcomes appeared in Chang, et al. (2012a, 2012b).
 
As part of our larger efforts exploring the relationship of air pollution exposure and pregnancy outcomes, we sought to consider a relatively simple metric for assessing risk of exposure to air pollution, specifically traffic-related air pollution, which includes particulate matter and diesel exhaust, both of which were investigated within Project C. We utilized the statewide GIS layer of street-geocoded 2005–2007 births to calculate the proximity of each geocoded birth to the nearest primary and secondary roadway. While controlling for all standard covariates, we incorporated measures of air pollution exposure as dichotomous variables indicating residence within 500, 250, 150, 100, or 50 m of a primary or secondary roadway into models for birth weight, low birth weight (LBW), VLBW, preterm birth (PTB), VPTB, and any hypertensive disorder. Our findings indicate a significant dose-response relationship between proximity to a primary or secondary road and the adverse outcomes of PTB, VPTB and hypertension—for example, the probability of hypertension is increased by living within 500 m of a primary or secondary roadway, with this probability being even higher at 250 m, and still higher at each of 150, 100, and 50 m (Miranda, et al., 2013). In addition, much of our statistical development work, described below, used air pollution as the application.
 
Nulliparous Women. We explored the observed association between parity and risk of adverse birth outcomes (i.e., women having their first child are at increased risk of adverse outcomes compared to women who have already had at least one child). We linked births in the North Carolina Detailed Birth Record 1990–2007 with previous and subsequent births to the same mother using deterministic techniques that evaluated various combinations of maternal identifying variables to link births, including full name, maiden name, date and state of birth, parity, and date of last birth. We employed statistical and modeling-based analyses to estimate first birth outcome rate differences between nulliparas who did have a subsequent pregnancy versus those who did not. Among nulliparas that were not linked to a second birth, maternal-age-adjusted rates of multiple measures of adverse outcomes, including maternal medical complications, were almost all statistically higher compared to rates for linked women. This work suggests that the observed differences in rates of adverse outcomes between nulliparas and multiparas are partly attributable to higher risk women not having a subsequent pregnancy (either by choice or due to fecundity differences). (See Miranda, Edwards and Myers, 2011.)
 
Racial Residential Segregation. Our project on racial residential segregation enables quantification of racial exposure/isolation at finer spatial scales within SMSAs. Such a measure can be connected to measures of social and economic disadvantage at these scales to gain insight into how racial residential segregation has manifested itself across urban landscapes. In turn, this promises to reveal key insights into how to think about the spatial aspects of the social factors influencing health disparities. We are working to determine which facets of segregation best characterize the way community-level racial residential segregation acts to promote health disparities in birth outcomes. Although our initial efforts were statewide, we eventually decided that, given the significantly more detailed data available for Durham County, we would focus on this area to determine what variables are most important to characterizing racial residential segregation in terms of its health consequences (Anthopolos, et al., 2011; Anthopolos, et al., 2014; see Figure 6).
 
Figure 6
Figure 6. Spacial layout of racial isolation of blacks and poor quality built environment, census
block level, Community Assessment Project area, Durham, North Carolina.
 
Community Assessment Project/Built Environment. Built environment data was collected under the Community Assessment Project (described under COTC) and preliminary analysis focused on spatial layers capturing four primary attributes of the built environment—housing damage, property disorder, tenure and vacancy. Connection was made to pregnancy outcomes. Resultant work examining a biprobit regression model as well as marginal logistic regressions has appeared (Miranda, et al., 2012). Other work connecting the built environment with adverse birth outcomes appears in Miranda, Messer and Kroeger, 2012. Other manuscripts are described in Project B.
 
Seasonality. We have examined the relationship between seasonality and pregnancy outcomes. Our initial aspatial models indicated that the effect of season was most apparent among non-Hispanic white women (Miranda, Anthopolos and Edwards, 2011). We utilized spatial models to better understand what factors of season of conception or birth are influencing pregnancy outcomes.
 
Racial Disparities in Maternal Hypertensive Disorders. We analyzed data from North Carolina to determine how the pattern of maternal hypertensive disorders differs among non-Hispanic white, non-Hispanic black, and Hispanic women across the range of maternal ages. In addition we explored whether rates of poor birth outcomes, including low birth weight and preterm birth, among hypertensive women differed by race (Miranda, et al., 2010; Neelon, et al., 2011, Vinikoor-Imler, 2012).
 
Developmental Outcomes. Having linked the North Carolina statewide detailed birth record and educational record databases, we examined the impact of pregnancy-related events and exposures on neurodevelopmental outcomes in early childhood. Two manuscripts have been published. The first, published in JAMA Pediatrics (Gregory, et al., 2013), investigates whether induction and/or augmentation during labor may be associated with autism diagnosis in children in grades 3–8. In this work, we used logistic regression modeling for rare events data to first establish an association between labor induction/augmentation and autism diagnosis and then examine whether the association is robust to controlling for successive sets of potential confounders related to maternal demographics, maternal health conditions, and events of labor and delivery, as recorded in the detailed birth record. The second is in Pediatric and Perinatal Epidemiology, examining the joint effect of birth outcomes and maternal prenatal smoking on educational test scores in reading and math (Anthopolos, et al., 2013). This study finds that maternal prenatal smoking may interact with birth outcomes on reading and mathematics test scores, particularly among non-Hispanic white children. Additionally, improvements in birth outcomes, even within the clinically normal range, may be associated with improved academic performance.
 
Environmental Contributions to Disparities in Pregnancy Outcomes. We published an invited review article on social and environmental contributors to disparities in birth outcomes based on both national and North Carolina data, as a way of compiling the many literatures we have accessed throughout our work on Project A. The manuscript, published in Epidemiologic Reviews, reviews research on how environmental exposures affect pregnancy outcomes and how these exposures may be embedded within a context of significant social and host factor stress.
 
Statistical Methods Development. Our work was highly focused on statistical methods development, particularly in the areas of leveraging Bayesian hierarchical spatial modeling and developing multivariate modeling approaches to examining correlated outcomes.
 
Out of efforts to develop new spatial methodologies for addressing health disparities, we did additional methodological work on disaggregated spatial modeling for areal unit categorical data. This work used innovative statistical methodology that extends spatial disease mapping techniques to model subgroups within areal units using a spatially smoothed, multilevel loglinear model. This work appeared in the Journal of the Royal Statistical Society, Series C (Tassone, et al., 2010). An attractive feature of this methodology for public health applications is the possibility to elucidate health disparities across space, subgroups and space-subgroup interactions.
 
Another completed manuscript builds joint models for birthweight and gestational age using bivariate normal mixtures. Such joint modeling adjusts for maternal risk factors and provides mixture analysis of the residuals to help illuminate further subpopulations with differential risk for adverse joint birth outcomes. Modeling of the mixture components is done through gestational age and then birth weight given gestational age. Joint modeling eliminates potential causal inference concerns. A paper has appeared in Statistics in Medicine (Schwartz, et al., 2011). Follow-on work extended this effort to incorporate spatial structure, introducing spatial random effects in the regression modeling for both outcomes (Neelon, et al., 2012).
 
We also examined quantile regression methodology in explaining the effect of exposure on pregnancy outcomes. Rather than explaining mean birth weight as in customary regression models, we explained quantiles for birth weight. For instance, it would be of interest to explain the 10th percentile of birthweight since this is the threshold for declaring small for gestational age. Our work demonstrated that risk factors and environmental exposure affect different quantiles differently. (See Lum and Gelfand, 2012.)
 
In addition, we developed a flexible Bayesian spatial discrete-time survival model to estimate the effect of environmental exposure on the risk of preterm birth. We view gestational age as time-to-event data where each pregnancy enters the risk set at a prespecified time (e.g., the 32nd week). The pregnancy is then followed until either: (1) a birth occurs before the 37th week (preterm); or (2) it reaches the 37th week and a full-term birth is expected. As preliminary analysis, the methodology was applied to a dataset of geo-coded births in North Carolina from 2002. We estimated the risk of preterm birth associated with short-term exposure to fine particulate matter using air quality metrics derived from the EPA’s Statistically Fused Air Pollution Database. We also conducted a simulation study and compared the proposed approach to the standard case-control and time series design. (See Chang, et al., 2012; Chang, et al., 2013.)
 
Related work has studied the use of a PM2.5 exposure simulator to explain birthweight. In a published paper, a template is developed for using an environmental dose simulator to connect ambient exposure to personal exposure. Then, using various exposure metrics, calculated form these personal exposures, which are clinically plausible over the course of a pregnancy, linkage is built to adverse birth outcomes (Berrocal, et al., 2011).
 
Another component of our work focused on building spatial downscalers. Such modeling strategies enable the fusion of monitoring station data with computer model output to better assess environmental exposure at point level spatial resolution. Such downscalers can be dynamic, enabling the tracking of exposure through time. With improved estimation of local exposure, we can better examine the linkage between exposure and adverse birth outcomes. Three papers on this methodology have been published. The first, for the univariate case, appeared in the Journal of Agricultural, Biological and Environmental Statistics (Berrocal, et al., 2010). The second considers the bivariate problem, looking at downscaling two exposures (ozone and PM2.5), borrowing strength in the joint modeling (Berrocal, et al., 2010). The third focused on measurement error associated with downscaling. Such error is attributable both to misalignment between monitoring sites and model grids as well as to effects of neighboring grids on local monitoring site levels (Berrocal, et al., 2012).
 
Significant progress was made on the relationships between air pollution exposures, socioeconomic status, and birth outcomes. We extended our methodological work with spatial downscalers to conduct an applied analysis on racial and socioeconomic disparities in exposure to air pollution across the State of North Carolina (see Gray, et al., 2010). While previous studies of the environmental justice dimensions of air pollution limit analysis of populations living near air quality monitoring stations, we used space-time downscaling methods that we previously developed to output predictive surfaces of ozone (O3) and particulate matter < 2.5 μm in aerodynamic diameter (PM2.5) at the census-tract level covering all of North Carolina. This analysis sought to provide a better understanding of the environmental justice dimension of air pollution exposure across the entire North Carolina population. Moreover, in additional work (see Gray, et al., 2014), we linked the downscaled output to the detailed birth record in order to examine the joint effects of socioeconomic status and air pollution on birth outcomes, using the highly resolved estimated pollution exposures. The downscaled output allowed us to estimate the association between air pollution exposure and birth outcomes for times and locations where exposure data were otherwise unavailable.
 
We also continued building joint models in order to examine correlated outcomes. Joint modeling eliminates potential causal inference concerns (Schwartz, et al., 2010). In work under preparation, we examine the association between features of the built environment with the bivariate outcome of preterm birth and low birth weight (MacLehose, et al., in preparation). Additionally, we have developed multivariate spatial modeling to accommodate correlated continuous outcomes (Neelon, et al., 2014). This latter work incorporates correlation not only between jointly modeled outcomes but also among mothers living in nearby neighborhood units.
 
We furthered methodological work on expected performance accruing to synthesizing categorical datasets, with the objective of enhancing inference deals with a collection of datasets of varying sizes that are all relevant to a particular scientific question, but which include different subsets of the relevant variables, with some overlap (see Berrocal, et al., 2012). We synthesized cross-classified categorical datasets drawn from a common population where many of the sets are incomplete (i.e., one or more of the classification variables is unobserved), but at least one is completely observed. The method is expected to reduce uncertainty about the cell probabilities in the associated multiway contingency table.
 
We have synthesized our hypotheses concerning the adverse effects of racial residential segregation on the one hand, and poor quality built environment on poor birth outcomes on the other. Using advanced mediation models as the basis for our analytical approach, we examined whether poor quality built environment acts as a mediator in the relationship between racial residential segregation and preterm birth. This work developed a novel method to maintain an additive scale in estimating natural direct and indirect effects from nonlinear models (e.g., logistic regression). Additivity is required for interpreting the proportion of the total effect (i.e., the effect of the exposure, racial residential segregation, on the outcome) explained by the mediator (i.e., the poor quality built environment) in a causal framework. In addition, we developed a summary poor built environment index to avoid violating assumptions of no unmeasured confounding in the mediation model (Anthopolos, et al., 2014).
 
 
Project B (C002): Healthy Pregnancy, Healthy Baby: Studying Racial Disparities in Birth Outcomes
 
We successfully recruited 1889 women into our prospective cohort study, Healthy Pregnancy, Healthy Baby. Women were recruited from Duke University Medical Center (DUMC) and Lincoln Community Health Center. Demographic data indicate that we were highly successful recruiting women most at risk for adverse pregnancy outcomes, particularly low-income, low educational attainment, and non-Hispanic black women.
 
The following information was collected from participants in the Healthy Pregnancy, Healthy Baby Study:
  • Psychosocial measures: CES-D, perceived stress, self-efficacy, interpersonal support, paternal support, perceived racism, perceived community standing, pregnancy intention, John Henryism Active Coping Scale, NEO Five Factor Inventory of personality.
  • Environmental exposure survey measures: short survey on fish consumption, smoking pattern and exposure to secondhand smoke, and drinking water source.
  • Maternal and neonatal medical record abstraction: detailed prepregnancy medical and social history, antepartum complications, birth outcomes, and neonatal complications.
  • Blood samples for genetic and environmental analysis to assess candidate genes related to environmental contaminant (nicotine, cotinine, cadmium, lead, mercury, arsenic and manganese), metabolism, inflammation, vascular dysfunction and stress response.
  • Cord blood and placental samples are currently being stored for future genetic analysis and evaluation of activity at the maternal-fetal interface.
We were also highly successful in collection of participant-level data as well as biological samples, with greater than 90 percent attainment of maternal blood sample for genetic and environmental analyses. Collection of cord blood and placental samples, which began in June 2007, has also been successful with approximately 960 delivery samples collected.
 
All maternal data have been georeferenced (i.e., linked to the physical address of the mother) using GIS software. The Healthy Pregnancy/Healthy Baby Study also included two in-depth neighborhood assessments designed to capture both built environment and community-level social stressors and community resources. In order to increase the participant capture rate (first assessment: 40%), we expanded our second assessment area, successfully capturing approximately 70 percent of the participants. The cohort study and neighborhood assessment data are spatially linked to extensive environmental and demographic data at a highly resolved spatial scale.
 
We genotyped the cohort for 412 Single Nucleotide Polymorphisms (SNPs) in 52 genes related to human environmental contaminant clearance (heavy metals and environmental tobacco smoke), infection and inflammation (cytokines, chemokines, and bacterial pathogen recognition), maternal stress response (serotonin), and other pathways that have been implicated as potential drivers of health disparities (vascular responsivity). To better identify subpopulations among NHB women in our sample, we generated the Illumina African-American Admixture Chip, based on 1,509 selected SNPs with disparate frequencies in the Yoruban (African) and European (Caucasian) HapMap samples. For the purpose of addressing population stratification, we used clustering algorithms on the Illumina data to identify subpopulations within our NHB women and found that indeed some stratification does exist. Thus, we used the genome-wide percentage of European admixture as a continuous covariate in our candidate gene analyses.
 
Genetic Analysis
 
The Vitamin D receptor gene (VDR) has a wide variety of functions, including calcium homeostasis and modulating circulating levels. Subtle genetic variation has also been linked to adverse conditions including diabetes, cancer, renal disease and autoimmune disorders. In multivariable regression modeling, we found a significant association between the VDR variant (rs731236, a coding, synonymous SNP) and preterm birth (p = 0.04) for NHB women in our study population. The odds of having an infant born preterm were 2.9 times higher for women with the CC genotype at this marker compared with women with the TT genotype (p = 0.04) and were 3.8 times higher for women with the CC genotype compared with women with the CT genotype (p = 0.01). This same association did not hold true among the NHW women. Furthermore, in addition to 6 other SNPs within the VDR gene, rs731236 was also associated with infant birthweight among NHB but not NHW women (Swamy, et al., 2011)
 
The nitric oxide (NO) pathway is critical for managing oxidative damage in a variety of tissues. Reduced levels of endothelial nitric oxide synthase (NOS3) have been previously linked to preeclampsia, a maternal complication associated with preterm birth. But also pertinent to this project is that specific polymorphisms within the inducible nitric oxide synthase (NOS2A) gene have been associated with protection against malaria; thus, there may be population-specific selective forces leading to differential allele frequencies for the polymorphisms in these genes. For these reasons, we hypothesized that polymorphisms within the NOS genes may differentially affect risk for preterm birth among African-American mothers in our cohort. We examined 57 SNPs in the three nitric oxide synthase genes (NOS1, NOS2A and NOS3) for association with risk for preterm birth in our cohort. We identified 10 SNPs in NOS1, which were nominally associated with risk for preterm birth in our NHW subset of mothers. Only 1 SNP in NOS2A was nominally associated with preterm birth in our NHB subset of mothers. Thus, we did observe differential association with these genes and preterm birth as a function of maternal race. However, we were surprised that the effects that we observed were stronger for the NHW subset rather than the NHB subset.
 
We have also examined polymorphisms in the G-protein coupled receptor kinase 5 (GRK-5) gene. GRK-5 is associated with a pharmacogenomic interaction among African-Americans in the setting of cardiovascular disease and response to β-adrenergic receptor (βAR) blockade, which is standard therapy for cardiac failure and ischemia. Because of the association with cardiovascular disease, we hypothesized that GRK-5 genetic variation was associated with hypertensive disorders in pregnancy. We defined hypertensive disorders as chronic hypertension (CHTN = BP > 140/90 before 20 weeks), preeclampsia (BP > 140/90 and proteinuria), and CHTN + superimposed preeclampsia (CHTN with new onset or worsening proteinuria). Haplotype tagging single nucleotide polymorphisms (SNPs) were genotyped for GRK-5 via Taqman assays. Logistic regression was used to examine the relationship between maternal genotype and each hypertensive disorder among the NHB women, adjusting for age, education, insurance, tobacco use and prepregnancy BMI. CHTN was included as a covariate in the model for preeclampsia. In our NHB data set, 125 out of 587 participants (21%) were diagnosed with preeclampsia. Of the 17 SNPs examined, 3 were nominally associated with preeclampsia. For the most significant association with rs10886445 (global p = 0.0009), the odds of preeclampsia for NHB women with the CC genotype were 0.28 times that for NHB women with the TT genotype (CI: 0.1429, 0.552). For those NHB women with the CT genotype, the odds of developing preeclampsia were 0.33 times that for NHB women with the TT genotype (CI: 0.1682, 0.656). In addition, rs12416565 (global p = 0.003) and rs11198925 (global p = 0.02) were also nominally associated. For CHTN, only one marker (rs2420620, global p = 0.02) demonstrated nominal association. Similarly, for CHTN + preeclampsia, only one marker (rs10510055, global p = 0.02) demonstrated nominal association. Based on these results, we concluded that the GRK-5 gene may play a role in hypertensive disorders of pregnancy, particularly the development of preeclampsia.
 
In our NHB women, we have examined G*E between genes in the inflammatory pathway and ETS as they relate to infant birth weight and identified several nominal associations, the most significant being rs2069771 in the interleukin-2 gene with cadmium exposure (global p = 0.005) and rs9005 in the interleukin 1 receptor antagonist with cadmium exposure (global p = 0.006). In addition, also among the NHB women, we have identified G*E interactions between the n-acetyltransferase genes and cadmium exposure predicting maternal preeclampsia and infant outcomes. In particular, rs8190845 in NAT1 interacted with cadmium exposure to predict occurrence of preeclampsia in the mother (global p = 0.009). Additionally, rs17126345 , also in NAT1, interacted with cotinine exposure to predict the occurrence of preterm birth as defined as delivery prior to 37 weeks gestation (global p = 0.006).
 
The inflammatory response influences risk for adverse birth outcomes such as low birth weight. Variability in maternal inflammatory response may be exacerbated by exposure to air pollution during pregnancy. We examined how variation in maternal inflammatory genes interacts with air pollution to affect infant birth weight (BWT) in 673 NHB women participating in the Healthy Pregnancy, Healthy Baby Study. Maternal residential address at enrollment was georeferenced, and the distance to the nearest major roadway was calculated as a proxy for traffic-related air pollution exposure. One hundred five haplotype tagging SNPs were genotyped in 20 candidate genes on maternal DNA samples. Linear regression was used to examine the relationship between SNPs and infant BWT, adjusting for infant sex, maternal age, parity, education, insurance and smoking use. We also examined interactions between SNPs and roadway proximity. Consistent with previous reports, genetic variation in the inflammatory response provided evidence for main effects on infant BWT among NHB women in our study. We provide the first evidence that some of these genes interact with air pollution exposure to influence infant BWT.
 
Environmental Sampling
 
Using the maternal environmental blood samples collected on all participants in Project B, we characterized maternal exposures to toxics.
 
Lead. In addition to documenting the blood lead burdens among a cohort of pregnant women in Durham County, NC, we have been able to characterize current maternal exposures to lead by linking each participant to the tax parcel at which they resided during their pregnancy. We found that both year built and modeled lead exposure risk at participant’s residence during pregnancy were not predictive of maternal blood lead levels. Taken in combination with results showing that maternal blood levels increased with age, these findings indicate that maternal blood lead levels are much more likely the result of lead remobilization from historic exposures as opposed to contemporaneous exposures (Miranda, et al., 2010).
 
Mercury. Using self-reported fish consumption and maternal blood samples, we examined correlates of mercury levels during pregnancy. Higher income and education were associated with greater fish consumption, as well as higher levels of mercury when controlling for fish consumption (Miranda, Edwards, and Maxson, 2011). Our work with mercury led to our collaboration with WIC in North Carolina to craft culturally appropriate messages for Latina women who consume fish caught in North Carolina waters. This project is described under the COTC.
 
Cadmium. Cadmium is prevalent in the environment and understudied as a developmental toxicant. We conducted an analysis of maternal cadmium exposure and leukocyte DNA methylation patterns in 17 mother-newborn pairs. A methylated cytosine-guanine (CpG) island recovery assay was used to assess over 4.6 million sites spanning 16,421 CpG islands. Exposure to cadmium and cotinine was classified for each mother-newborn pair according to maternal blood levels. Comparative methylation analysis was performed to identify genes with differential methylation levels. DNA motifs that were overrepresented among the differentially methylated genes were identified. Subsets of genes were identified that showed altered DNA methylation levels in fetal DNA associated with exposure to cadmium (n = 61), cotinine (n = 366) or both (n = 30). In maternal DNA, subsets of cadmium-associated (n = 92) and cotinine-associated (n = 134) genes were identified. While the gene sets were largely distinct between mothers and newborns, functional similarities at the biological pathway level were identified, including transcriptional regulation and apoptosis. Furthermore, conserved DNA motifs with sequence similarity to specific transcription factor binding sites were identified within the CpG islands of the gene sets. This pilot investigation provides evidence for distinct patterns of DNA methylation alterations in fetal and maternal DNA associated with exposure to cadmium. The genes with differential methylation share common motifs at the sequence level suggesting that structural commonalities in DNA sequence may affect environmentally-related DNA methylation status (Sanders, et al., 2013). A paper describing risk factors for elevated levels of cadmium during pregnancy is forthcoming (Edwards, et al., forthcoming), and a paper linking cadmium levels with pregnancy outcome has been submitted (Johnson, et al., in submission).
 
Polybrominated Diphenyl Ether (PBDE). Our clinical obstetrics work led to a fruitful collaboration with Dr. Heather Stapleton, a leading expert in PBDE research. This work examined PBDE levels in pregnant women and the association with thyroid hormones (Stapleton, et al., 2011) and pregnancy outcomes (Miranda, et al., in submission). In Stapleton, et al., 2011, we found that BDEs 47, 99 and 100 were significantly and positively associated with free and total thyroxine levels and with total triiodothyronine levels above the normal range. The more recent work (by Miranda, et al.) shows that while certain maternal PBDE levels are negatively associated with infant head circumference, the relationship does not appear to be mediated by thyroid hormone levels.
 
Additional Projects
 
Residential mobility. With our access to the North Carolina Detailed Birth Record (DBR) in Project A, we have been able to link participants in Project B with their birth certificate data. Using maternal and infant identifying information, including name, place, and date of birth, we have been able to link 991 participants (99.9%) who completed the study and had a live birth by December 31, 2008 and 59 participants (76.6%) who were lost-to-follow-up but with an expected delivery date on or before December 31, 2008. This linkage allowed us to determine who is moving during pregnancy (by comparing the address at enrollment and the DBR address at delivery) and the nature of those moves, including the quality of the new location compared to the previous location (and thus changes in environment or exposure).
 
Proximity to Roadways. In parallel to the Project A work with road proximity metrics, we geocoded Project B participants to the tax parcel level and then calculated the distance to the nearest roadways. We extended the road proximity work in Project A by incorporating the rich set of variables available in Project B, including analysis looking at how psychosocial health and gene-by-environment interactions may influence the impact of traffic-related air pollution on birth outcomes (Miranda, et al., 2013).
 
Community Assessment Project/Built Environment. The Community Assessment Project assessed built environment variables at two times (2008 and 2011) for over 17,000 and 34,000 tax parcels, respectively, including the home addresses of over 70 percent of the participants in the Healthy Pregnancy, Healthy Baby Study. Seven scales (housing damage, property disorder, security measures, tenure, vacancy, violent crime and nuisances) have been constructed at five levels of geography (census block, primary adjacency neighborhood, census block group, census tract and city-defined neighborhoods). Analyses have assessed the relationship between the built environment and maternal psychosocial status (Messer, et al., 2012) and pregnancy outcomes (Miranda, et al., 2012).
 
Psychosocial Indicators. Analyses have been completed on psychosocial influences on birth outcomes. The relationships among pregnancy intention, psychosocial health and pregnancy outcomes have been examined, with a paper published (Maxson, et al., 2011). In addition, we have examined pregnancy intention, behavioral choice, and environmental exposures. The influences of psychosocial health and smoking status have been studied, with a resulting publication (Maxson, et al., 2012). In order to reduce the number of psychosocial variables, cluster analysis has been performed, resulting in three distinct clusters of women. Cluster analysis on the personality indices was also performed. A paper examining the relationship between the built environment as measured through the Community Assessment Project and women’s psychosocial health was published (Messer, et al., 2012). We will continue analysis with a focus on the relationships among psychosocial health, risk behaviors, chemical and nonchemical stressors, and pregnancy outcomes.
 
Maternal Medical Complications. Fetal health is not only individually determined, but is also influenced by maternal health and well-being. We continue our emphasis on maternal outcomes. In particular, we have focused on hypertensive disorders during pregnancy. We have identified factors that affect maternal blood pressure during pregnancy. In order to make use of all blood pressure readings collected across the pregnancy, we considered a variety of statistical approaches, including latent trajectory and sparse functional data models (Neelon, et al., 2011).
 
Statistical Methods Development. We developed new statistical methodologies designed to improve analysis of the Project B data, as well as to advance statistical analysis more broadly. A paper detailing statistical methodology developed in year 5 for accounting for mid-study changes in measurement scales won the Youden award for the best paper in interlaboratory testing methods this past year (Burgette and Reiter, 2012). These methods were needed because the Project B investigators switched laboratories for measuring blood levels of heavy metals midway through data collection in order to take advantage of finer measurement scales. Exploratory analysis indicated that the distributions of levels for several exposures were markedly different across the laboratories, so that analyses based on a simple concatenation of the two laboratories’ data would be biased. Using the second laboratory scale as the standard, so that effectively measurements before the laboratory switch are treated as missing, we developed general purpose methodology for imputing plausible values of the missing exposure measurements. The methods are based on assumptions about the relative ranks of measurements in the two scales, e.g., a measurement in the 10th percentile in one scale should be at the 10th percentile in the other scale. We implemented this methodology on the Project B data to provide the investigative team with improved data.
 
In addition, we developed and implemented methods for finding important predictors in quantile regression when there are a very large number of covariates. These methods adapted the lasso and elastic net penalties for quantile regression. We applied the methods on a mid-study sample of women to uncover a previously unreported interaction: women who smoke and who have high blood lead levels tend to have babies with lower birth weights (Burgette, et al., 2012).
 
We developed and implemented methods for using factor analysis models in the context of quantile regression. The investigative team believed that many of the predictors can be grouped into underlying factors. For example, the Project B data contain several variables that measure maternal stress, and arguably we should connect birth outcomes to the underlying factor of stress rather than its individual indicators. As another example, the data contain several imperfect indicators of smoking status, and we wanted to connect birth outcomes to the underyling factor of true smoking status. We implemented the model on a mid-study sample of women from Project B, and we found that the smoking factor was a strong predictor of low birth weight. An article on this research was accepted for publication in Biometrics (Burgette and Reiter, 2012).
 
We also developed a Bayesian growth mixture model to jointly examine the associations between longitudinal blood pressure measurements, PTB, and LBW. The model partitions women into distinct classes characterized by a mean arterial pressure (MAP) curve and joint probabilities of PTB and LBW. Each class contains a unique mixed effects model for MAP with class-specific regression coefficients and random effect covariances. To account for the high correlation between PTB and LBW, we introduced a bivariate probit model within each class to capture residual within-class dependence between PTB and LBW. The model permits the association between PTB and LBW to vary by class, so that for some classes, PTB and LBW may be positively correlated, while for others, they may be uncorrelated or negatively correlated. We also allowed maternal covariates to influence the class probabilities via a multinomial logit model. For posterior computation, we proposed an efficient Markov chain Monte Carlo algorithm that combines full-conditional Gibbs and Metropolis steps. We applied our model to a sample of 1027 women enrolled in the Healthy Pregnancy, Healthy Baby Study. A manuscript was published at Statistics in Medicine (Neelon, et al., 2011).
 
We developed new ways of handling missing data in large epidemiological studies in which interaction effects are suspected. The main approach is to adapt regression trees to perform multiple imputation. This approach was used to handle the missing data in Project B. This methodology has the potential to be utilized in a wide range of settings, including outside of epidemiological contexts. An article describing this work has been published in the American Journal of Epidemiology (Burgette, et al., 2010).
 
The team also examined approaches to performing Bayesian analysis after multiple imputation is used for missing data. This work was motivated by the use of the tree methodology for multiple imputation, because we are estimating Bayesian models with the completed datasets. This research was published in The American Statistician (Zhou, et al., 2010).
 
Finally, the team developed an approach for assessing sensitivity to unmeasured confounding when using principal stratification. This work was motivated by the presence of several intermediate variables in the prospective study of Project B, e.g., hypertension as an intermediate variable for gestation age. At this point, this work is at a theoretical stage; we have not yet applied it on Project B data. A manuscript on the theory has been published in Statistics in Medicine (Schwartz, et al., 2012).
 
Statistical Methods Development for Genetics. We also developed statistical methods for the genetic data. The first statistical innovation involving the genetic data is the adverse subpopulation regression (ASPR) for multivariate outcomes with high dimensional predictors. The ASPR is a two component latent class model, with the dominant component corresponding to (presumed) healthy individuals and the risk of falling in the minority component characterized via a logistic regression. The logistic regression model is designed to accommodate high-dimensional predictors, as occur in studies with a large number of gene by environment interactions, through use of a flexible nonparametric multiple shrinkage approach. The Gibbs sampler is developed for posterior computation. The method was evaluated with the Project B data and has been published in Statistics in Medicine (Zhu, et al., 2012).
 
The second innovation involving the genetic data was motivated by our analysis of the admixture data. The current genetic analysis tool that is most widely used (ANCESTRYMAP) is very limited in that it only allows consideration of qualitative, not quantitative, outcomes and does not allow for the incorporation of covariates. Thus, we have extended this method in our project (Zhu, et al., 2012).
 
One of the statistical innovations that we have been working on is the improvement of methodologies for admixture mapping. To that end, we developed a generalized admixture mapping (GLEAM) approach, a flexible and powerful regression method for both quantitative and qualitative traits, which is able to test for association between the trait and local ancestries in multiple loci simultaneously and adjust for covariates. The new method is based on the generalized linear model and utilizes a quadratic normal moment prior to incorporate admixture prior information. Through simulation, we demonstrated that GLEAM achieves lower type I error rate and higher power than existing methods both for qualitative traits and more significantly for quantitative traits. (See Zhu, et al., 2013.)
 
 
Project C (C003): Perinatal Environmental Exposure Disparity and Neonatal Respiratory Health
 
Significant progress was made in Project C. We determined that postnatal ozone (1 ppm x 3 hours/day, 3 days/week x 4 weeks) significantly impairs postnatal weight gain in C56BL/6 mice. Air pollutant exposure at a vulnerable window of postnatal development impairs growth. We also saw that postnatal ozone increases nebulized methacholine induced airway hyperreactivity (AHR) in C57BL/6 mice measured at 4 weeks but not 3 weeks. Ozone induced AHR is developmentally regulated.
 
We have that prenatal instillation of particulate matter (St. Louis particle, NIST#1648) twice weekly in time mated pregnant mice augments postnatal ozone-induced AHR in mice, measured at 4 weeks postnatal. Prenatal air pollutant exposure reprograms postnatal air pollutant responses that result in AHR (Auten, et al., Am J Resp Crit Care Med, 2009).
 
In studies in collaboration with M. Ian Gilmour, EPA , we exposed time-mated C56BL/6 pregnant mice to internal combustion engine diesel exhaust (0.5, 1, and 2 mg/m3 x 6 hours/day, 5 days/week, from gestation day 6–17) versus air control. Pups delivered to exposed dams were exposed postnatally to ozone as described above. Prenatal diesel exposure dose-dependently impaired lung compliance and pressure-volume loop hysteresis versus air or prenatal air postnatal ozone controls. There were parallel effects on nebulized methacholine challenge induced AHR. Prenatal ambient exposures to diesel particulates at doses relevant to human environmental exposure worsened postnatal ozone-induced lung function and AHR.
 
We published a manuscript that reported the effect of prenatal diesel particulate pulmonary exposure on postnatal ozone induced airway hyperreactivity (Auten, et al., Am J Resp Cell Mol Biol., 2012). The report showed dose-dependent effects of particulate matter inhalation on maternal inflammatory responses; synergistic effects of prenatal diesel exposure and postnatal ozone exposure on lung inflammatory cytokine responses, synergistic effects of prenatal diesel and postnatal ozone on postnatal airway hyperresponsiveness to inhaled methacholine challenge.
 
Because increasing evidence links nonchemical stressor effects on mothers and offspring to both AHR and cognitive development, we sought to determine if other stressors that would be typical coexposures in human experience would potentially exacerbate effects of air pollution exposure. In impoverished environments in the United States, this would include resource/housing deprivation and uncertainty, as well as poor diet. We therefore sought collaboration with investigators with expertise in behavioral/cognitive development and neuroinflammation, since that mechanism was likely common to the inflammatory mechanisms that underpin pollution effects on AHR.
 
We developed a mouse model of nest-restriction during pregnancy that had no effects on maternal licking and grooming in the first postnatal week, but which apparently unmasked adverse effects of diesel inhalation during pregnancy. Combined prenatal diesel aspiration and prenatal nest restriction of pregnant mice induced increased anxiety in offspring of both sexes and impaired cognition in male offspring. This sexually dimorphic response was parallel to changes in brain IL-1β and IL-10. Findings were reported in Environmental Health Perspectives (Bolton, et al., 2013). Only the combination of diesel inhalation and resource deprivation produced this finding. This suggests the importance of studying exposures in combination. However, our preliminary studies showed that these combined stressors did not affect AHR.
 
Because obesity is common to both childhood asthma and poverty, we conducted studies to determine if post-natal high fat diet could also worsen or unmask prenatal diesel effects on behavior and cognition. We exposed time-mated mice to spontaneous diesel exhaust in collaboration with Ian Gilmour. Offspring were randomly assigned to normal or high fat diet after weaning. The offspring that had combined prenatal exposure to inhaled diesel (dams) and post-natal high fat diet showed increased brain microglial activation, but only males demonstrated decreased spontaneous activity and increased anxiety behavior. Prenatal air pollution appeared to program offspring for increased susceptibility to diet-induced weight gain. These findings were reported in FASEB J (Bolton, et al., 2012).
 
 
Community Outreach and Translation Core (C004)
 
The Community Outreach and Translation Core (COTC) was an integral component of SCEDDBO, translating and disseminating research findings to the scientific and neighborhood communities. Over the project period, the COTC developed a wide and diverse network of collaborators among federal, state and local agencies; universities; and community groups. Activities with these diverse partners cover a broad spectrum of children’s environmental health issues, ranging from birth outcomes to lead poisoning prevention, environmental exposures, and obesity. Importantly, the COTC responded with detailed information to numerous requests from private citizens about a variety of environmental health concerns. Topics have ranged from lead and mercury exposure to electromagnetic fields, chloramines, and exposure to rubber crumblets. These requests were received through both the CEHI toll-free number and via the CEHI website.
 
We describe here four major contributions, which reflect Specific Aims 1-4, of the COTC during the project period. Specific Aims 5 and 6 were a part of the COTC’s daily mission. The end of the project has not lessened the commitment of the COTC to continue to serve the community. The COTC remains dedicated to fostering environments where all children can prosper.
 
Community Assessment Project. In Durham, there is continued citywide concern over quality of life issues, including neighborhood safety, housing quality and poverty. During the summer of 2008, a team of COTC-trained assessors conducted an on-foot, curb-side assessment of approximately 17,000 tax parcels in Durham, North Carolina, evaluating the built environment on 57 variables using handheld Global Positioning System (GPS) devices. The exercise was repeated again in the summer of 2011 over a larger geographic area that included roughly 30,700 tax parcels. Built environment data were combined with Durham crime data and tax assessor data. The two phases also captured 40% and 70%, respectively, of the physical addresses for participants in the Project B cohort, providing a detailed characterization of the local neighborhood environment for a significant subset of participants. In collaboration with the GISSA Core, CAP data were summarized into seven Neighborhood Health Indices. These indices have been linked to outcomes from Projects A and B. Our collaboration with community partners at all stages of the tool development, data collection and dissemination of results provides a model for engaging the community in an active research program. The COTC has disseminated the CAP results to multiple audiences (community members, public health professionals and government officials) through publication of a descriptive report, creation of Web-based resources, and in-person presentations. COTC personnel attended community meetings across the network of community-based organizations to discuss and display the results of the CAP and work with interested stakeholders on how to utilize the CAP results in their community development efforts. The COTC will continue to disseminate the CAP results to multiple audiences (community members, public health professionals and government officials) through publication of a descriptive report, creation of Web-based resources, and in-person presentations. The need extends past the project end date.
 
Building Capacity in Health Professionals. COTC investigators partnered with nursing programs to develop and present curricula to nursing students on environmental exposures and maternal and child health. A comprehensive project was designed to develop environmental health curricula for nursing students, nursing faculty, and practicing nurses. Supplemental funding from EPA’s Environmental Education Grant Program has enabled collaborations with the Ecology Center in Ann Arbor, MI to produce this curriculum. The resources developed during this project provide: (1) an organized synthesis of current information; (2) foundational knowledge for nursing school faculty; and (3) subject modules on environmental health concepts that can be incorporated into existing nursing curricula.
 
The COTC partnered with the GISSA Core to offer no-cost, hands-on training on environmental health issues, including the built environment, to public health professionals throughout North Carolina. Four all-day sessions were attended by 65 participants representing 18 NC counties, 18 different program areas of state government, 7 nonprofit organizations, and Durham city personnel. This course has broad ranging public health applications including policy guidance, community outreach and education, and program planning. The training was accredited for continuing education credits for Registered Sanitarians (the professional certification common to county health department personnel).
 
The COTC also partnered with the UNC School of Nursing and Healthcare without Harm to cosponsor an environmental health symposium for practicing nurses. The symposium, Environmental Considerations in Nursing Practice attracted nationally-recognized speakers and an audience of 60 practicing nurses. The event was also accredited for Continuing Nursing Education credits. COTC staff participated in all aspects of the planning and execution of this conference. SCEDDBO Director Marie Lynn Miranda presented the keynote address.
 
Culturally-Appropriate Advisory Materials on Environmental Contaminants. The COTC created and delivered culturally-appropriate methylmercury-contaminated fish consumption advisory information for low-income expectant or nursing mothers with low English proficiency. The COTC collaborated with the North Carolina WIC Program to design, test and deliver appropriate risk communication materials relating to North Carolina fish consumption advisories for methylmercury and federal advisories for a number of commercial fish species. The Latino population is at risk of methylmercury exposure from fish consumption, but may not be effectively reached through traditional fish advisory communication methods. Together with staff from the North Carolina Nutrition Services Branch (within the Department of Health and Human Services), we created an outreach model for communicating complicated environmental health information to pregnant or early postpartum Latina women. The intended audience was the nearly 17,000 Latina women who participate in WIC in North Carolina. Of all of the Latino babies born in North Carolina in 2005, 53 percent were born to mothers who participate in the WIC Program. In particular, we were interested in designing and testing culturally/linguistically appropriate messages and message delivery formats for fish consumption advisory information. The COTC established a number of dissemination efforts to distribute the mercury fish consumption fish advisory materials that were developed for Latino families (see Figure 8). Because the materials were distributed to families primarily by nutritionists in the WIC Program, considerable effort was expended to reach this audience. A series of webinars, accredited for continuing education credits for Registered Dieticians, were held for all WIC staff in North Carolina. The webinars were attended by 109 participants, representing 66 out of 88 (80%) of the WIC clinics in North Carolina. This work was adopted as part of the standard messaging from WIC counselors to WIC enrollees after the COTC personnel trained the counselors. This project also serves as a prototype for identifying best practices for communicating complex environmental health messages in culturally sensitive context.
 
Figure 8
Figure 8. Depiction of Tacle Box Sticker
 
Strong Partnerships. COTC staff collaborated with a variety of regional, state and federal advisory groups, including the American Lung Association Advisory Group, the Durham County Health Department Community Health Assessment Working Group, and the Obesity and Chronic Disease Committee of the Partnership for a Healthy Durham. In addition, SCEDDBO Director Marie Lynn Miranda was appointed to serve on EPA's CHPAC. The CHPAC is a federal advisory committee established in 1998 to provide independent advice to the EPA Administrator on regulations, research, and communications issues relevant to children's environmental health.
 
SCEDDBO investigators and the COTC PI, in particular, have established longstanding relationships with multiple community and organizational partners throughout North Carolina and nationally. These include the North Carolina Department of Environment and Natural Resources, Children’s Environmental Health Branch; the North Carolina Department of Health and Human Services, Occupational and Environmental Epidemiology Branch; the North Carolina Center for Geographic Information and Analysis; state and local health departments throughout North Carolina, as well as in other states (AR, CA, CO, IA, ID, IN, KS, LA, MA, ME, MI, MN, MS, MT, NC, NE, NH, NM, NY, PA, SC, SD, TX, UT, VT, WI); the Southeast Pediatric Environmental Health Specialty Unit; and a host of community-based organizations and public health advocacy groups. SCEDDBO investigators have also established connections with physicians, pharmacists, religious leaders, day care centers, and community centers. Furthermore, SCEDDBO investigators have developed relationships with agency officials from the Centers for Disease Control and Prevention (CDC), the United States Department of Housing and Urban Development (HUD), the National Institutes of Health (NIH), and EPA.
 
For all 7 years, COTC investigators mentored students from Duke University and the University of Michigan in the “Break the Cycle” project sponsored by EPA Region 4, Emory University, the Institute of Disadvantage and Disability, and the Southeast Pediatric Environmental Health Specialty Unit. The selected students presented environmental health data from SCEDDBO projects (Ouyang, 2011; Dadabhoy, et al., 2012; Modlin and Maxson, 2011; Gruber and Maxson, 2012; Henderson and Maxson, 2009; Koehrn and Keating, 2009; Martz et al., 2013; Henry et al., 2013). The conference was held in Atlanta, GA every spring. In May 2011, Dr. Pamela Maxson gave the keynote address at the conference (Maxson, 2012).
 
 
Geographic Information System and Statistical Analysis Core (C005)
 
Over the project period, the GISSA Core built and maintained a spatially and temporally linked data architecture for maternal and child health outcomes from the prenatal period to early childhood. The central objective was to track mothers and offspring in their residential environments at varying time slices. While capitalizing on the extensive data warehouse that we had assembled since the Center’s inception, we continued to integrate data layers into the architecture such as metrics from the EPA’s Air Quality System, National-Scale Air Toxics Assessment, fused air pollution data combining modeled and monitored data, and in-house constructed road proximity measures, in addition to the most recently available years of North Carolina statewide administrative data on births, educational outcomes, and blood lead levels. Based on linking methods described in previous reporting periods, the unique individual-level identifying record enables connections across multiple administrative databases on births, blood lead surveillance, deaths and educational outcomes. These datasets can each be examined separately and in various combinations according to the master linking file.
 
With the completion of participant recruitment in Project B in August 2011, GISSA staff focused on data quality control/quality assurance, along with finalizing the project analysis dataset and planning related studies with the participants. All of the participants have been integrated into a Geographic Information System with information on environmental exposures, factors of the built environment, and standard demographic data.
 
In addition to data acquisition, management and georeferencing, the GISSA Core provided innovative statistical support to each of the Projects. In Project A, the GISSA Core developed spatial models to better characterize associations between birth outcomes and environmental exposures, including air pollution and the built environment. In Project B, the GISSA Core supported multiple imputation efforts to construct finalized imputed datasets based on the full study population.
 
The GIS team street-geocoded all residential addresses in the 1990–2012 DBR data for the State of North Carolina, with the exception of 2010 births due to transitions in the birth record. Street geocoding, which allows us to link births to Census data resolved at the block level, have been completed for 80 percent of 1990–2009 birth records, with success rates increasing over time up to 82 percent by 1999. Success rates increased significantly as the years progressed, with 2000–2009 geocoded at 86 percent and 2011–2012 geocoded at 95 percent.
 
The DBR is compiled from questionnaires obtained at the time of birth certificate filing and includes elements essential to our proposed analyses. Available variables include, inter alia: maternal residence and state and country of birth; marital status; maternal and paternal race, Hispanic ethnicity and education; alcohol and tobacco use; plurality; parity; maternal complications; congenital anomalies; whether an infant death certificate was filed; and infant birth weight and gestational age. All 22 years of data have been integrated and standardized to facilitate data linkages and statistical analysis.
 
We developed methods for linking the North Carolina DBR data with other clinical and administrative datasets. These methods rely on the individually-identifying variables provided in the DBR, including full name and date of birth of both infant and mother. We first applied this methodology to link DBR data with participant data from Project B, matching participants who delivered between 2005 and 2009 to their corresponding record in the DBR. This linkage allowed us to examine how accurately the administrative dataset (DBR) captures key information, as well as undertake analysis of residential mobility during pregnancy. Using the 1990–2007 DBR, we linked births occurring to the same mother. This linkage allowed us to examine internatal spacing and birth outcomes across pregnancies, and by further combining this data with the DBR-linked Project B data, we were able to capture the participants' subsequent pregnancy outcomes. In addition, we used this method to link the DBR data with an administrative datasets of educational outcomes at the individual child level, which allowed us to examine how disparities in birth outcomes may have long-term implications for child development.
 
We expanded the environmental data layers available for use through the SCEDDBO data warehouse to include spatial data on road intensity, criteria air pollutants from the EPA’s AQS system, water quality, environmental releases documented in the Toxics Release Inventory, and housing quality.
 
We genotyped 1600 blood samples from pregnant women for 412 Single Nucleotide Polymorphisms (SNPs) in 52 genes, primarily involved in either metabolism of heavy metals or immune response. In addition, we generated the Illumina African-American Admixture Chip on 1016 NHB women.
 
The GISSA Core provided innovative statistical support to each of the Projects. For example, in Project A (references included under Project A), the GISSA Core provided statistical methods development to obtain unbiased estimates of the effect of air pollution exposure on birth outcomes (Chang, et al., 2012) and address measurement issues in aggregated estimates of ambient exposure to air pollution (Berrocal, et al., 2012; Gray, et al., 2011; Berrocal, et al., 2011). The GISSA Core marked a second publication on multiple imputation in Project B (references included under Project B). This work extended previously developed imputation methods (Burgette, et al., 2012) to handle inconsistent laboratory measurements (Burgette, et al., 2012).
 
In support of both Projects A and B, the GISSA Core developed quantile regression techniques to examine the effect of risk factors of interest at varying quantiles along the outcome distribution, rather than limiting analyses to mean effects. As a continuation of the Center’s work on joint outcome modeling (Lum and Gelfand, 2012; Burgette, et al., 2011; Burgette, et al., 2012), the GISSA Core also developed multivariate (Neelon, et al., 2011) modeling techniques to better understand individual and shared risk factors of related health outcomes, in addition to capturing geographic variation in disease risk through spatial methods.
 
Despite the project period ending, we will continue to develop and expand the geospatial data warehouse that supports analysis among various projects. The GIS team will continue to identify additional environmental layers to integrate into our data architecture. With the construction of the spatio-temporal data architecture, we will continue to conduct analyses that leverage the spatial and longitudinal nature of the data, focusing on the quantile and multivariate approaches already developed by our team. We will continue analyses on approximately 1,600 Project B participants with complete pregnancy data, genetic results and environmental results. Analyses will look at the joint impact of environmental, social and host factors on birth outcomes, especially as they differ by and within race. Identification of such coexposures could lead to development and implementation of strategies to prevent adverse birth outcomes, ultimately decreasing or eliminating the racial disparity.
 
Figure 7
Figure 7. Community Assessment Project Areas


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Journal Article Anthopolos R, James SA, Gelfand AE, Miranda ML. A spatial measure of neighborhood level racial isolation applied to low birthweight, preterm birth, and birthweight in North Carolina. Spatial and Spatio-temporal Epidemiology 2011;2(4):235-246. R833293 (2009)
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  • Journal Article Anthopolos R, Edwards SE, Miranda ML. Effects of maternal prenatal smoking and birth outcomes extending into the normal range on academic performance in fourth grade in North Carolina, USA. Paediatric and Perinatal Epidemiology 2013;27(6):564-574. R833293 (2012)
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  • Journal Article Anthopolos R, Kaufman JS, Messer LC, Miranda ML. Racial residential segregation and preterm birth: built environment as a mediator. Epidemiology 2014;25(3):397-405. R833293 (Final)
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  • Journal Article Auten RL, Potts EN, Mason SN, Fischer B, Huang Y, Foster WM. Maternal exposure to particulate matter increases postnatal ozone-induced airway hyperreactivity in juvenile mice. American Journal of Respiratory and Critical Care Medicine 2009;180(12):1218-1226. R833293 (Final)
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  • Journal Article Auten RL, Foster WM. Biochemical effects of ozone on asthma during postnatal development. Biochimica et Biophysica Acta 2011;1810(11):1114-1119. R833293 (2009)
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  • Journal Article Berrocal VJ, Gelfand AE, Holland DM. A bivariate space-time downscaler under space and time misalignment. Annals of Applied Statistics 2010;4(4):1942-1975. R833293 (2009)
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  • Journal Article Berrocal VJ, Gelfand AE, Holland DM. A spatio-temporal downscaler for output from numerical models. Journal of Agricultural, Biological, and Environmental Statistics 2010;15(2):176-197. R833293 (2009)
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  • Journal Article Berrocal VJ, Gelfand AE, Holland DM, Burke J, Miranda ML. On the use of a PM2.5 exposure simulator to explain birthweight. Environmetrics 2011;22(4):553-571. R833293 (2009)
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  • Journal Article Berrocal VJ, Gelfand AE, Holland DM. Space-time data fusion under error in computer model output: an application to modeling air quality. Biometrics 2012;68(3):837-848. R833293 (2011)
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  • Journal Article Berrocal VJ, Miranda ML, Gelfand AE, Bhattacharya S. Synthesizing categorical datasets to enhance inference. Statistical Methodology 2013;15:25-45. R833293 (2007)
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  • Journal Article Block ML, Elder A, Auten RL, Bilbo SD, Chen H, Chen J-C, Cory-Slechta DA, Costa D, Diaz-Sanchez D, Dorman DC, Gold DR, Gray K, Jeng HA, Kaufman JD, Kleinman MT, Kirshner A, Lawler C, Miller DS, Nadadur SS, Ritz B, Semmens EO, Tonelli LH, Veronesi B, Wright RO, Wright RJ. The outdoor air pollution and brain health workshop. NeuroToxicology 2012;33(5):972-984. R833293 (2011)
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  • Journal Article Bolton JL, Smith SH, Huff NC, Gilmour MI, Foster WM, Auten RL, Bilbo SD. Prenatal air pollution exposure induces neuroinflammation and predisposes offspring to weight gain in adulthood in a sex-specific manner. FASEB Journal 2012;26(11):4743-4754. R833293 (2011)
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  • Journal Article Bolton JL, Huff NC, Smith SH, Mason SN, Foster WM, Auten RL, Bilbo SD. Maternal stress and effects of prenatal air pollution on offspring mental health outcomes in mice. Environmental Health Perspectives 2013;121(9):1075-1082. R833293 (2012)
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  • Journal Article Bolton J, Auten R, Bilbo S. Prenatal air pollution exposure induces sexually dimorphic fetal programming of metabolic and neuroinflammatory outcomes in adult offspring. BRAIN BEHAVIOR AND IMMUNITY 2014;37:30-44. R833293 (Final)
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  • Journal Article Brown JS, Graham JA, Chen LC, Postlethwait EM, Ghio AJ, Foster WM, Gordon T. Panel discussion review: session four--assessing biological plausibility of epidemiological findings in air pollution research. Journal of Exposure Science and Environmental Epidemiology 2007;17(Suppl 2):S97-S105. R833293 (2007)
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  • Journal Article Burgette LF, Reiter JP. Multiple imputation for missing data via sequential regression trees. American Journal of Epidemiology 2010;172(9):1070-1076. R833293 (2008)
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  • Journal Article Burgette LF, Reiter JP, Miranda ML. Exploratory quantile regression with many covariates: an application to adverse birth outcomes. Epidemiology 2011;22(6):859-866. R833293 (2010)
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  • Journal Article Burgette LF, Reiter JP. Nonparametric Bayesian multiple imputation for missing data due to mid-study switching of measurement methods. Journal of the American Statistical Association 2012;107(498):439-449. R833293 (2010)
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  • Journal Article Burgette LF, Reiter JP. Modeling adverse birth outcomes via confirmatory factor quantile regression. Biometrics 2012;68(1):92-100. R833293 (2010)
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  • Journal Article Buttke DE, Wolkin A, Stapleton HM, Miranda ML. Associations between serum levels of polybrominated diphenyl ether (PBDE) flame retardants and environmental and behavioral factors in pregnant women. Journal of Exposure Science & Environmental Epidemiology 2013;23(2):176-182. R833293 (2011)
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  • Journal Article Chang HH, Reich BJ, Miranda ML. Chang et al. Respond to “Environmental exposures and preterm birth." American Journal of Epidemiology 2012;175(2):111-112. R833293 (2011)
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  • Journal Article Chang HH, Reich BJ, Miranda ML. Time-to-event analysis of fine particle air pollution and preterm birth: results from North Carolina, 2001-2005. American Journal of Epidemiology 2012;175(2):91-98. R833293 (2010)
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  • Journal Article Chang HH, Reich BJ, Miranda ML. A spatial time-to-event approach for estimating associations between air pollution and preterm birth. Journal of the Royal Statistical Society--Series C (Applied Statistics) 2013;62(2):167-179. R833293 (2011)
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  • Journal Article Dadabhoy FZ, Maxson PJ, Huff N, Auten RL. Perinatal exposure to air pollutants had adverse effects on behavioral outcomes in mice. International Journal on Disability and Human Development 2012;11(4):359-368. R833293 (Final)
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  • Journal Article Edwards SE, Strauss B, Miranda ML. Geocoding large population-level administrative datasets at highly resolved spatial scales. Transactions in GIS 2014;18(4):586-603. R833293 (Final)
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  • Journal Article Gray SC, Edwards SE, Miranda ML. Assessing exposure metrics for PM and birth weight models. Journal of Exposure Science and Environmental Epidemiology 2010;20(5):469-477. R833293 (2008)
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  • Journal Article Gray SC, Gelfand AE, Miranda ML. Hierarchical spatial modeling of uncertainty in air pollution and birth weight study. Statistics in Medicine 2011;30(17):2187-2198. R833293 (2010)
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  • Journal Article Gray SC, Edwards SE, Miranda ML. Race, socioeconomic status, and air pollution exposure in North Carolina. Environmental Research 2013;126:152-158. R833293 (2012)
    R833293 (Final)
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  • Journal Article Gray SC, Edwards SE, Schultz BD, Miranda ML. Assessing the impact of race, social factors and air pollution on birth outcomes: a population-based study. Environmental Health 2014;13(1):4. R833293 (2012)
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  • Abstract: Environmental Health-Abstract
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  • Journal Article Gregory SG, Anthopolos R, Osgood CE, Grotegut CA, Miranda ML. Association of autism with induced or augmented childbirth in North Carolina Birth Record (1990-1998) and Education Research (1997-2007) databases. JAMA Pediatrics 2013;167(10):959-966. R833293 (2012)
    R833293 (Final)
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  • Full-text: JAMA Pediatrics-Full Text HTML
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  • Journal Article Gruber A, Maxson P. Disparities in psychosocial health and the built environment during pregnancy. International Journal on Disability and Human Development 2012;11(4):377-385. R833293 (Final)
    R833293C004 (Final)
  • Abstract: De Gruyter-Abstract
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  • Journal Article Heaton MJ, Gray SC, Gelfand AE. Process modeling for contingency tables with ordered categories. Statistical Modelling 2012;12(3):211-228. R833293 (Final)
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  • Abstract: Statistical Modeling-Abstract
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  • Journal Article Henderson K, Maxson P. Obesity intervention strategies and the built environment in Durham, North Carolina. International Journal of Child and Adolescent Health 2009;2(3):Article 8. R833293 (Final)
    R833293C004 (Final)
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  • Journal Article Henry H, Anthopolos R, Maxson P. Traffic-related air pollution and pediatric asthma in Durham County, North Carolina. International Journal on Disability and Human Development 2013;12(4):467-471. R833293 (Final)
    R833293C004 (Final)
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  • Journal Article Kim JY, Burnett RT, Neas L, Thurston GD, Schwartz J, Tolbert PE, Brunekreef B, Goldberg MS, Romieu I. Panel discussion review: session two--interpretation of observed associations between multiple ambient air pollutants and health effects in epidemiologic analyses. Journal of Exposure Science and Environmental Epidemiology 2007;17(Suppl 2):S83-S89. R833293 (2008)
    R829213 (Final)
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  • Journal Article Koehrn KM, Keating MH. The regulation of agricultural pesticides in North Carolina: implications for migrant farm workers and their families. International Journal of Child and Adolescent Health 2009;2(3):Article 4. R833293 (Final)
    R833293C004 (Final)
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  • Journal Article Kroeger GL, Messer L, Edwards SE, Miranda ML. A novel tool for assessing and summarizing the built environment. International Journal of Health Geographics 2012;11:46 (13 pp.). R833293 (Final)
    R833293C004 (Final)
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  • Journal Article Lum K, Gelfand AE. Spatial quantile multiple regression using the asymmetric Laplace process. Bayesian Analysis 2012;7(2):235-258. R833293 (2011)
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  • Journal Article Martz M, Anthopolos R, Geller M, Maxson P. Pediatric obesity and food access in Durham, North Carolina. International Journal of Child Health and Human Development 2014;7(3). R833293 (Final)
    R833293C004 (Final)
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  • Journal Article Maxson PJ, Edwards SE, Ingram A, Miranda ML. Psychosocial differences between smokers and non-smokers during pregnancy. Addictive Behaviors 2012;37(2):153-159. R833293 (2011)
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  • Journal Article Maxson PJ. Together we can break the cycle. International Journal on Disability and Human Development 2012;11(4):307-314. R833293 (Final)
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  • Journal Article Maxson PJ, Edwards SE, Valentiner EM, Miranda ML. A multidimensional approach to characterizing psychosocial health during pregnancy. Maternal and Child Health Journal 2016;20(6):1103-1113. R833293 (Final)
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  • Journal Article Maxson P, Miranda ML. Pregnancy intention, demographic differences, and psychosocial health. Journal of Women's Health 2011;20(8):1215-1223. R833293 (2010)
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  • Journal Article Messer LC, Maxson P, Miranda ML. The urban built environment and associations with women's psychosocial health. Journal of Urban Health 2013;90(5):857-871. R833293 (2011)
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  • Journal Article Miranda ML, Keating MH, Edwards SE. Environmental justice implications of reduced reporting requirements for the Toxics Release Inventory Burden Reduction Rule. Environmental Science & Technology 2008;42(15):5407-5414. R833293 (Final)
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  • Journal Article Miranda ML, Maxson P, Edwards S. Environmental contributions to disparities in pregnancy outcomes. Epidemiologic Reviews 2009;31(1):67-83. R833293 (2008)
    R833293 (Final)
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  • Journal Article Miranda ML, Edwards SE, Swamy GK, Paul CJ, Neelon B. Blood lead levels among pregnant women: historical versus contemporaneous exposures. International Journal of Environmental Research and Public Health 2010;7(4):1508-1519. R833293 (2008)
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  • Journal Article Miranda ML, Swamy GK, Edwards S, Maxson P, Gelfand A, James S. Disparities in maternal hypertension and pregnancy outcomes: evidence from North Carolina, 1994-2003. Public Health Reports 2010;125(4):579-587. R833293 (2008)
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  • Journal Article Miranda ML, Maxson P, Kim D. Early childhood lead exposure and exceptionality designations for students. International Journal of Child Health and Human Development 2010;3(1):77-84. R833293 (2008)
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  • Abstract: International Journal of Child Health and Human Development-Abstract
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  • Journal Article Miranda ML, Edwards SE, Keating MH, Paul CJ. Making the environmental justice grade: the relative burden of air pollution exposure in the United States. International Journal of Environmental Research and Public Health 2011;8(6):1755-1771. R833293 (2011)
    R833293 (Final)
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  • Journal Article Miranda ML, Edwards S, Maxson PJ. Mercury levels in an urban pregnant population in Durham County, North Carolina. International Journal of Environmental Research in Public Health 2011;8(3):698-712. R833293 (2010)
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  • Journal Article Miranda ML, Edwards SE. Use of spatial analysis to support environmental health research and practice. North Carolina Medical Journal 2011;72(2):132-135. R833293 (2011)
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  • Journal Article Miranda ML, Edwards SE, Myers ER. Adverse birth outcomes among nulliparous vs. multiparous women. Public Health Reports 2011;126(6):797-805. R833293 (2010)
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  • Abstract: Public Health Reports-Abstract
  • Journal Article Miranda ML, Anthopolos R, Edwards SE. Seasonality of poor pregnancy outcomes in North Carolina. North Carolina Medical Journal 2011;72(6):447-453. R833293 (2010)
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  • Journal Article Miranda ML, Anthopolos R, Hastings D. A geospatial analysis of the effects of aviation gasoline on childhood blood lead levels. Environmental Health Perspectives 2011;119(10):1513-1516. R833293 (2011)
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  • Journal Article Miranda ML, Edwards SE, Anthopolos R, Dolinsky DH, Kemper AR. The built environment and childhood obesity in Durham, North Carolina. Clinical Pediatrics 2012;51(8):750-758. R833293 (2011)
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  • Journal Article Miranda ML, Messer LC, Kroeger GL. Associations between the quality of the residential built environment and pregnancy outcomes among women in North Carolina. Environmental Health Perspectives 2012;120(3):471-477. R833293 (2011)
    R833293 (Final)
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  • Journal Article Miranda ML, Edwards SE, Chang HH, Auten RL. Proximity to roadways and pregnancy outcomes. Journal of Exposure Science & Environmental Epidemiology 2013;23(1):32-38. R833293 (2011)
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  • Abstract: Nature-Abstract
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  • Journal Article Modlin E, Maxson P. Breaking the cycle of maternal depression: an initiative to improve children’s environmental health. International Journal of Child Health and Human Development 2010;3(4):405-411. R833293 (Final)
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  • Journal Article Montagna S, Tokdar ST, Neelon B, Dunson DB. Bayesian latent factor regression for functional and longitudinal data. Biometrics 2012;68(4):1064-1073. R833293 (2011)
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  • Journal Article Neelon B, Swamy GK, Burgette LF, Miranda ML. A Bayesian growth mixture model to examine maternal hypertension and birth outcomes. Statistics in Medicine 2011;30(22):2721-2735. R833293 (2010)
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  • Journal Article Neelon B, Anthopolos R, Miranda ML. A spatial bivariate probit model for correlated binary data with application to adverse birth outcomes. Statistical Methods in Medical Research 2014;23(2):119-133. R833293 (Final)
    R833293C001 (Final)
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  • Abstract: Sage Publications-Abstract
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  • Journal Article Neelon B, Gelfand AE, Miranda ML. A multivariate spatial mixture model for areal data: examining regional differences in standardized test scores. Journal of the Royal Statistical Societ--Series C (Applied Statistics) 2014;63(5):737-761. R833293 (Final)
    R833293C001 (Final)
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  • Other: University of Minnesota-Prepublication PDF
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  • Journal Article Ouyang R. The relationship between the built environment and birthweight. Reviews on Environmental Health 2011;26(3):181-186. R833293 (Final)
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  • Journal Article Sanders A, Smeester L, Rojas D, DeBussycher T, Wu M, Wright F, Zhou Y-H, Laine J, Rager J, Swamy G, Ashley-Koch A, Miranda ML, Fry R. Cadmium exposure and the epigenome: exposure-associated patterns of DNA methylation in leukocytes from mother-baby pairs. Epigenetics 2014;9(2):212-221. R833293 (Final)
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  • Journal Article Schwartz SL, Gelfand AE, Miranda ML. Joint Bayesian analysis of birthweight and censored gestational age using finite mixture models. Statistics in Medicine 2010;29(16):1710-1723. R833293 (2008)
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  • Journal Article Schwartz S, Li F, Reiter JP. Sensitivity analysis for unmeasured confounding in principal stratification settings with binary variables. Statistics in Medicine 2012;31(10):949-962. R833293 (2010)
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  • Journal Article Stapleton HM, Eagle S, Anthopolos R, Wolkin A, Miranda ML. Associations between polybrominated diphenyl ether (PBDE) flame retardants, phenolic metabolites, and thyroid hormones during pregnancy. Environmental Health Perspectives 2011;119(10):1454-1459. R833293 (2011)
    R833293 (Final)
    R833293C002 (2011)
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  • Journal Article Swamy GK, Garrett ME, Miranda ML, Ashley-Koch AE. Maternal vitamin D receptor genetic variation contributes to infant birthweight among black mothers. American Journal of Medical Genetics Part A 2011;155A(6):1264-1271. R833293 (2009)
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  • Journal Article Swamy GK, Edwards S, Gelfand A, James SA, Miranda ML. Maternal age, birth order, and race: differential effects on birthweight. Journal of Epidemiology and Community Health 2012;66(2):136-142. R833293 (2009)
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  • Journal Article Tassone EC, Miranda ML, Gelfand AE. Disaggregated spatial modelling for areal unit categorical data. Journal of the Royal Statistical Society--Series C (Applied Statistics) 2010;59(1):175-190. R833293 (2007)
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  • Journal Article Vinikoor-Imler LC, Gray SC, Edwards SE, Miranda ML. The effects of exposure to particulate matter and neighbourhood deprivation on gestational hypertension. Paediatric and Perinatal Epidemiology 2012;26(2):91-100. R833293 (2011)
    R833293 (Final)
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  • Journal Article Zhou X, Reiter JP. A note on Bayesian inference after multiple imputation. The American Statistician 2010;64(2):159-163. R833293 (2008)
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  • Journal Article Zhu B, Dunson DB, Ashley-Koch AE. Adverse subpopulation regression for multivariate outcomes with high-dimensional predictors. Statistics in Medicine 2012;31(29):4102-4113. R833293 (2011)
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  • Journal Article Zhu B, Ashley-Koch AE, Dunson DB. Generalized admixture mapping for complex traits. G3--Genes, Genomes, Genetics 2013;3(7):1165-1175. R833293 (2012)
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  • Journal Article Miranda ML, Anthopolos R, Wolkin A, Stapleton HM. Associations of birth outcomes with maternal polybrominated diphenyl ethers and thyroid hormones during pregnancy. Environment International 2015;85:244-253. R833293 (Final)
    R833293C002 (Final)
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  • Supplemental Keywords:

    Data fusion, meta analysis, disparities, spatial disaggregation, spatial interpolation, spatial modeling, racial residential segregation, built environment, birth outcomes, pregnancy, preterm birth, low birth weight, racial disparity, African American, environmental stressors, gene-environment interactions, psychosocial stressors, genes, single nucleotide polymorphisms, airway hyperreactivity, diesel exhaust particles, air pollution, lung function, epigenetic, innate immunity, Nqo1, neuroinflammation, maternal stress, risk communication, outreach, translation, participatory research, built environment, data fusion, meta analysis, disparities, spatial disaggregation, spatial interpolation, spatial modeling

    Progress and Final Reports:

    Original Abstract
  • 2007 Progress Report
  • 2008 Progress Report
  • 2009 Progress Report
  • 2010 Progress Report
  • 2011 Progress Report
  • 2012 Progress Report
  • Subprojects under this Center: (EPA does not fund or establish subprojects; EPA awards and manages the overall grant for this center).
    R833293C001 Research Project A: Mapping Disparities in Birth Outcomes
    R833293C002 Research Project B: Healthy Pregnancy, Healthy Baby: Studying Racial Disparities in Birth Outcomes
    R833293C003 Research Project C: Perinatal Environmental Exposure Disparity and Neonatal Respiratory Health
    R833293C004 Community Outreach and Translation Core
    R833293C005 Geographic Information System and Statistical Analysis Core

    Top of Page

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Conclusions drawn by the principal investigators have not been reviewed by the Agency.

    Project Research Results

    • 2012 Progress Report
    • 2011 Progress Report
    • 2010 Progress Report
    • 2009 Progress Report
    • 2008 Progress Report
    • 2007 Progress Report
    • Original Abstract
    163 publications for this center
    76 journal articles for this center

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