Maternal Exposure to Ambient Levels of Benzene and Neural Tube Defects among Offspring: Texas, 1999–2004
[do action=”authors”]Philip J. Lupo1,2, Elaine Symanski1, D. Kim Waller1, Wenyaw Chan3, Peter H. Langlois4, Mark A. Canfield4, Laura E. Mitchell1,2[/do][do action=”affiliations”]1 Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, Texas, USA, 2 Human Genetics Center, and, 3 Division of Biostatistics, University of Texas School of Public Health, Houston, Texas, USA, 4 Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA[/do][do action=”citation-string”]Environ Health Perspect 119:397-402 (2011). http://dx.doi.org/10.1289/ehp.1002212 [online 05 October 2010] [/do]
Background: Previous studies have reported positive associations between maternal exposure to air pollutants and several adverse birth outcomes. However, there have been no studies assessing the association between environmental levels of hazardous air pollutants, such as benzene, and neural tube defects (NTDs), a common and serious group of congenital malformations.
Objective: Our goal was to conduct a case–control study assessing the association between ambient air levels of benzene, toluene, ethylbenzene, and xylene (BTEX) and the prevalence of NTDs among offspring.
Methods: The Texas Birth Defects Registry provided data on NTD cases (spina bifida and anencephaly) delivered between 1999 and 2004. The control group was a random sample of unaffected live births, frequency matched to cases on year of birth. Census tract–level estimates of annual BTEX levels were obtained from the U.S. Environmental Protection Agency 1999 Assessment System for Population Exposure Nationwide. Restricted cubic splines were used in mixed-effects logistic regression models to determine associations between each pollutant and NTD phenotype.
Results: Mothers living in census tracts with the highest benzene levels were more likely to have offspring with spina bifida than were women living in census tracts with the lowest levels (odds ratio = 2.30; 95% confidence interval, 1.22–4.33). No significant associations were observed between anencephaly and benzene or between any of the NTD phenotypes and toluene, ethylbenzene, or xylene.
Conclusion: In the first study to assess the relationship between environmental levels of BTEX and NTDs, we found an association between benzene and spina bifida. Our results contribute to the growing body of evidence regarding air pollutant exposure and adverse birth outcomes.
[/do][do action=”abstract”]Key words: air pollution, benzene, birth defects, BTEX, epidemiology, hazardous air pollutants, maternal exposure, neural tube defects[/do]
[do action=”notes-rule-above”]Address correspondence to E. Symanski, The University of Texas School of Public Health, 1200 Herman Pressler Dr., RAS 643, Houston, Texas 77030 USA. Telephone: (713) 500-9238. Fax: (713) 500-9264. E-mail: Elaine.Symanski@uth.tmc.edu[/do][do action=”notes”]This project was supported in part by the National Institute for Occupational Safety and Health (NIOSH)–funded Southwest Center for Occupational and Environmental Health Training grant T42OH008421 and the Centers for Disease Control and Prevention (CDC)–funded Texas Center for Birth Defects Research and Prevention through cooperative agreement U50/CCU613232.[/do][do action=”notes”]The authors declare they have no actual or potential competing financial interests.[/do][do action=”notes”]
We thank the staff and scientists at the Texas Birth Defects Epidemiology and Surveillance Branch who assisted in issues related to data collection and dissemination.
[/do][do action=”notes”] Received 25 March 2010; accepted 05 October 2010; online 05 October 2010.[/do]
Birth defects are the leading cause of infant mortality in the United States (Petrini et al. 2002), and more than 65% are of unknown origin (Bale et al. 2003). Neural tube defects (NTDs), one of the most common groups of birth defects, are complex malformations of the central nervous system that result from failure of neural tube closure (Christianson et al. 2006). Infants with NTDs experience both increased morbidity and mortality compared with their unaffected contemporaries (Mitchell et al. 2004; Wong and Paulozzi 2001). Although these defects are clinically significant, little is known about their etiology.
Hazardous air pollutants (HAPs), toxic substances commonly found in the air environment, are known or suspected to cause serious health effects [U.S. Environmental Protection Agency (EPA) 2007a]. HAPs are a heterogeneous group of pollutants that include organic solvents such as benzene, toluene, ethylbenzene, and xylene (BTEX) and are emitted from several sources. Human exposure to HAPs can result from inhalation, ingestion, and dermal absorption. Benzene is one of the most prevalent HAPs in urban areas (Mohamed et al. 2002) and is of particular interest because it has been associated with several adverse health outcomes including pediatric cancer and intrauterine growth restriction [International Agency for Research on Cancer (IARC) 1982, 1987; Slama et al. 2009; U.S. EPA 2007a; Whitworth et al. 2008; Yin et al. 1996].
Some studies have reported positive associations between maternal exposures to air pollutants other than HAPs (i.e., criteria pollutants) and birth defects, including ozone and certain cardiac defects (Gilboa et al. 2005; Ritz et al. 2002), ozone and oral clefts (Hwang and Jaakkola 2008), and particulate matter (PM) and nervous system defects (Rankin et al. 2009). Other studies have been inconclusive regarding the role of criteria pollutants on the prevalence of oral clefts (Hansen et al. 2009; Marshall et al. 2010) and congenital heart defects (Hansen et al. 2009; Strickland et al. 2009).
Occupational studies have demonstrated a positive association between maternal exposure to organic solvents (e.g., benzene) and birth defects, including NTDs (Brender et al. 2002; McMartin et al. 1998; Wennborg et al. 2005). Despite this association, no studies have assessed the effect of environmental levels of benzene or other HAPs on NTD prevalence. Therefore, we conducted a study to assess the association between maternal exposure to environmental levels of BTEX and the prevalence of NTDs in offspring. Benzene was the primary pollutant of interest because of its association with other adverse outcomes (IARC 1982; Whitworth et al. 2008). Toluene, ethylbenzene, and xylene were selected for investigation because of their association with benzene (Mohamed et al. 2002). This study was conducted in Texas, a state that ranks number one in the United States for benzene levels in ambient air and accounts for 48% of all benzene emissions in the nation (U.S. EPA 2007b).
Materials and Methods
Study population. Data on live births, stillbirths, and electively terminated fetuses with NTDs (spina bifida and anencephaly) delivered between 1 January 1999 and 31 December 2004 were obtained from the Texas Birth Defects Registry (n = 1,108) (Texas Department of State Health Services 2010). The registry is a population-based, active surveillance system that has monitored births, fetal deaths, and terminations throughout the state since 1999. We selected a stratified random sample of unaffected live births delivered in Texas between 1 January 1999 and 31 December 2004 as the control group, using a ratio of four controls to one case. Controls were frequency matched to cases by year of birth because of the decreasing birth prevalence of NTDs over time (Canfield et al. 2009a). This yielded a group of 4,132 controls. The study protocol was reviewed and approved by the institutional review boards of the Texas Department of State Health Services and the University of Texas Health Science Center at Houston.
Exposure assessment. Census tract–level estimates of ambient BTEX levels were obtained from the U.S. EPA 1999 Assessment System for Population Exposure Nationwide (ASPEN) (Rosenbaum et al. 1999; U.S. EPA 2006, 2008). The methods used for ASPEN have been described fully elsewhere (Rosenbaum et al. 1999; U.S. EPA 2006). Briefly, ASPEN is part of the National Air Toxic Assessment (Ozkaynak et al. 2008) and is based on the U.S. EPA Industrial Source Complex Long-Term Model. It takes into account emissions data, rate, location, and height of pollutant release; meteorological conditions; and the reactive decay, deposition, and transformation of pollutants. Ambient air levels of BTEX are reported as annual concentrations in micrograms per cubic meter (U.S. EPA 2006). Residential air levels of BTEX were estimated based on maternal address at delivery as reported on vital records for cases and controls. Addresses were geocoded and mapped to their respective census tracts by the Texas Department of State Health Services.
Potential confounders. Information on the following potential confounders was obtained or calculated from vital records data: sex of infant; year of birth; maternal race/ethnicity (non-Hispanic white, non-Hispanic black, Hispanic, or other); maternal birth place (United States, Mexico, or other); maternal age (< 20, 20–24, 25–29, 30–34, 35–39, or ≥ 40 years); maternal education (less than high school, high school, or more than high school); marital status (married or not married); parity (0, 1, 2, or ≥ 3); maternal smoking (no or yes); and season of conception (spring, summer, fall, or winter). Additionally, as the exposure assessment for BTEX was based on census tract–level estimates, we opted to include a census tract–level estimate of socioeconomic status (percentage below poverty level), which was obtained from the U.S. Census 2000 Summary File 3 (U.S. Census Bureau 2010). Percentage of census tract below poverty level was categorized into quartiles (low, medium-low, medium-high, and high poverty level) on the basis of the distribution among the controls.
Statistical analysis. Frequency distributions for categorical variables were determined for controls and the two NTD subgroups (spina bifida and anencephaly). Correlations between levels of BTEX were determined using Spearman’s rank correlation. We used mixed-effects logistic regression to assess associations between each HAP and NTD phenotype while accounting for the potential within-group correlation resulting from the use of a census tract–level exposure assignment (Szklo and Nieto 2007). There is strong evidence that risk factor profiles are different for spina bifida and anencephaly (Canfield et al. 2009b; Khoury et al. 1982; Lupo et al. 2010b; Mitchell 2005); therefore, analyses were conducted separately in these phenotypes.
Based on plots assessing the trend between benzene levels and NTD prevalence, the exposure–outcome relationship appeared nonlinear; therefore we opted to use restricted cubic splines. Specifically, restricted cubic splines were fit to logistic regression models assessing the association between each HAP and NTD phenotype. The output from these models indicated four knots (corresponding to specific ambient HAP levels) where the exposure–outcome relationship changed. These knots were then used to determine cut points for low (i.e., reference), low-medium, medium, medium-high, and high ambient air levels (Durrleman and Simon 1989) and used in the final models assessing the association between each HAP and NTD phenotype. Because the low (i.e., reference) exposure category represents approximately 5% of the total population, we also defined the reference group as the 10th, 15th, and 20th percentile of exposure for each HAP, based on the distribution among controls, to assess how sensitive the results were to the cut point chosen for the reference group.
Variables were incorporated as confounders in the final models if inclusion resulted in ≥ 10% change in the estimate of effect between the air pollutant and NTD phenotype. Year of birth was included in each multivariable model, because it was a matching factor between cases and controls (Szklo and Nieto 2007). Associations between each HAP and NTD phenotype were considered significant when p < 0.05. To formally examine nonlinearity in the exposure–outcome relationship, a likelihood ratio test was used, comparing a full model (i.e., with both linear and cubic spline terms) to a reduced model (i.e., with a linear term only) at a significance level of p < 0.05 (Durrleman and Simon 1989). All analyses were conducted using Intercooled Stata, version 10.1 (StataCorp LP, College Station, TX) or SAS version 9.2 (SAS Institute Inc., Cary, NC).
To minimize etiologic heterogeneity within the case group, cases with an associated chromosomal abnormality or other syndrome (n = 75) and those with a closed NTD (i.e., lipomyelomeningocele, n = 88) were excluded. Additionally, cases with missing geocoded maternal address were excluded (n = 109). After these exclusions, 533 spina bifida and 303 anencephaly cases were available for analysis. Of the 4,132 controls, 437 were excluded because of missing geocoded maternal address. The final control group consisted of 3,695 unaffected births for analysis. The proportion of case and control mothers missing address information was similar (11.5% and 10.5%, respectively), and differences between those with and without maternal address at delivery were minor (≤ 5%) on demographic factors (results not shown). Compared with controls, case mothers were more likely to be Hispanic, born in Mexico, young, and less educated (Table 1).
Scatterplots of benzene and each of the other HAPs (toluene, ethylbenzene, and xylene) are presented in Figure 1. Levels of BTEX were highly and significantly correlated (ρ^ ≥ 0.97, p < 0.001) (data not shown). Because of the high correlation between these compounds, statistical models including multiple pollutants were not assessed.
Results from the final models assessing the associations between BTEX and NTDs are presented in Table 2. After adjusting for year of birth, maternal race/ethnicity, education, census tract poverty level, and parity, mothers who lived in census tracts with the highest benzene levels were more likely to have offspring with spina bifida [odds ratio (OR) = 2.30; 95% confidence interval (CI), 1.22–4.33]. The degree of confounding from all covariates was modest; that is, adjusted ORs differed from crude ORs by no more than 15%. There were also positive associations with the low-medium (OR = 1.77; 95% CI, 1.04–3.00), medium (OR = 1.90; 95% CI, 1.11–3.24), and medium-high benzene exposure groups (OR = 1.40; 95% CI, 0.82–2.38). When the reference group was defined as less than or equal to the 10th, 15th, or 20th percentile of exposure, the association between maternal residence in a census tract with the highest benzene levels relative to the referent group and the prevalence of spina bifida remained, although it was attenuated (OR10th = 1.96; 95% CI, 1.17–3.28; OR15th = 1.59; 95% CI, 1.00–2.54; and OR20th = 1.57; 95% CI, 1.00–2.46).
Based on the likelihood ratio test between the adjusted model with cubic splines and the model without the spline terms, there was a significant nonlinear relationship between maternal benzene exposure and spina bifida prevalence (p = 0.03). To further illustrate the nonlinear trend between benzene and NTDs, the estimated logits (and 95% confidence bands) were plotted against increasing benzene levels (Figure 2). For spina bifida, the logit appears to steadily increase when benzene levels are ≥ 3 μg/m3 and becomes statistically significant after benzene levels are approximately > 5 μg/m3 (Figure 2A), whereas no such trend was seen with anencephaly (Figure 2B).
We found a significant association between the prevalence of spina bifida in offspring and maternal exposure to ambient levels of benzene as estimated from the 1999 U.S. EPA ASPEN model (U.S. EPA 2006). The association was greatest for those in the highest exposure group. Positive associations between benzene and spina bifida were also observed in lower exposure categories; however, there was no monotonic dose–response relationship. Our finding that the risk of having a spina bifida-affected infant more than doubled for mothers living in census tracts with estimated benzene levels of ≥ 3 μg/m3 is in keeping with a report classifying individuals living in areas with benzene levels > 3.4 μg/m3 as being at the greatest risk for adverse health effects (Sexton et al. 2007). There were also associations with toluene, ethylbenzene, and xylene and between BTEX and anencephaly; however, these associations were not statistically significant.
The association between benzene levels and spina bifida appears to be nonlinear. This is supported by studies reporting nonlinear associations between personal exposure to benzene and various biomarkers (i.e., urinary metabolites and albumin adducts) of exposure using data collected on occupationally and environmentally exposed individuals, whereby exposure-metabolite curves became steeper at higher exposure levels (Kim et al. 2006; Lin et al. 2007).
Despite the strong correlations between the BTEX compounds, a significant association with spina bifida was seen only with benzene. Scatterplots of benzene and each of the other HAPs (toluene, ethylbenzene, and xylene) indicate that the correlations between pollutants are not as great at higher levels (Figure 1). In addition, we found lower correlations between benzene and the other pollutants (toluene, ethylbenzene, and xylene) when we restricted the analyses to census tracts with the highest benzene levels (n = 119) (ρ^ = 0.62, 0.71, and 0.77, respectively).
Benzene is known to cross the placenta and has been found in cord blood at levels equal to or higher than maternal blood [Agency for Toxic Substances and Disease Registry (ATSDR) 2007]. Moreover, benzene can lead to genetic toxicity by covalently binding to DNA and forming DNA adducts, which, if not repaired, disrupt the microenvironment of the cell, leading to inhibition of important enzymes, cell death, and alteration of other cells (ATSDR 2007; Kim et al. 2006; Lan et al. 2004). If this occurs during the critical window of development, the complex cellular processes involved in neurulation (e.g., folate metabolism, cell proliferation, cellular adhesion, and vascular development) may be disturbed, resulting in NTDs.
Oxidative stress could also play a role in the teratogenic effect of benzene. Reactive oxygen species (ROS) formed after benzene exposure lead to DNA strand breakage and fragmentation leading to cell mutation (Hansen 2006; Xia et al. 2004). The importance of oxidative stress as a mechanism of teratogenesis is suggested by several animal studies (Fantel 1996). Treatment of pregnant rabbits and mice with ROS inhibitors diminished the effect of teratogens and reduced the amount of DNA oxidation (Liu and Wells 1995; Parman et al. 1999; Wells et al. 1997). One study conducted in rats demonstrated that increased embryonic oxidation resulted in failure of neural tube closure (Morriss and New 1979).
Positive associations between maternal occupational exposures to organic solvents and congenital malformations have been reported. One study assessing maternal occupational exposure to benzene reported an OR of 5.3 (95% CI, 1.4–21.1) for neural crest malformations (including NTDs) (Wennborg et al. 2005). In addition, among Mexican Americans, mothers occupationally exposed to solvents were 2.5 times as likely (95% CI, 1.3–4.7) to have NTD-affected pregnancies than control mothers (Brender et al. 2002). In a meta-analysis of five studies (not including the two previously discussed), mothers who were occupationally exposed to organic solvents had 1.6 times greater odds (95% CI, 1.2–2.3) of having an infant with a birth defect (including NTDs) (McMartin et al. 1998).
A potential limitation of this study is related to the exposure assessment, which relied on modeled predictions of ambient air levels of BTEX (i.e., the ASPEN model) and may have resulted in misclassification. Personal exposure is a function of outdoor and indoor pollutant levels, as well as individual behavior (i.e., time spent outdoors vs. indoors) (Lee et al. 2004). However, it has been shown that for benzene, the ASPEN model is a good surrogate for exposure measures based on personal monitoring (Payne-Sturges et al. 2004). The fact that ASPEN data were available only for 1999 and not for the entire study period is an additional potential limitation. This may be a suitable surrogate for other years, because the sources of HAPs (e.g., emissions from roadways and industrial facilities) were unlikely to change during the study period (Grant et al. 2007; Sexton et al. 2007; Whitworth et al. 2008). Additionally, information on maternal periconceptional use of folic acid and/or multivitamins (a potential confounder) was not available. However, this population represents pregnancies conceived after mandatory folic acid fortification (January 1998), and a recent study found little evidence of an association between NTDs and maternal folic acid intake or multivitamin use since fortification (Mosley et al. 2009). Finally, exposure misclassification due to use of maternal address at time of delivery is also a potential source of bias in this study. Because NTDs develop within the first 4 weeks after conception, address at delivery may be different than address during the critical window of exposure (Selevan et al. 2000). However, our own analyses using cases and controls from Texas included in the National Birth Defects Prevention Study, with complete residential information during pregnancy, suggest there was no significant change in benzene exposure assignment when using address at delivery versus address at conception (Lupo et al. 2010a).
Strengths of this study include the use of a population-based birth defects registry that employs an active surveillance system to ascertain cases throughout the state of Texas. This should limit the potential for selection bias. Furthermore, the Texas Birth Defects Registry includes information on pregnancy terminations, reducing any potential bias due to the exclusion of these cases. An additional strength was the use of a relatively small (census tract–level) measure of exposure. Using larger geographic units to estimate exposure (e.g., counties) may not capture the spatial variability of benzene (Pratt et al. 2004). Furthermore, separate analyses were conducted for spina bifida and anencephaly, as opposed to combining the groups into a single phenotype. This is important, as the effects of some exposures appear to be heterogeneous across the subtypes of NTDs (Lupo et al. 2010b; Mitchell 2005).
This study provides the first assessment of the relationship between maternal exposure to ambient levels of BTEX and the prevalence of NTDs in offspring. Our analyses suggest that maternal exposure to ambient levels of benzene is associated with the prevalence of spina bifida among offspring. We believe that future investigations of air pollutants and NTDs should include additional measures of exposure (e.g., air pollutant monitoring and biomarker data) and additional covariate information (e.g., genotypes and nutrient status).
- ATSDR (Agency for Toxic Substances and Disease Registry). 2007. Toxicological Profile of Benzene. Available: http://www.atsdr.cdc.gov/toxprofiles/tp3.pdf [accessed 19 July 2010]
- Bale JR, Stoll BJ, Lucas AO. 2003. Reducing Birth Defects: Meeting the Challenge in the Developing World.; Washington, DC:National Academies Press.
- Brender J, Suarez L, Hendricks K, Baetz RA, Larsen R. 2002. Parental occupation and neural tube defect-affected pregnancies among Mexican Americans. J Occup Environ Med 44(7):650–656.
- Canfield MA, Marengo L, Ramadhani TA, Suarez L, Brender JD, Scheuerle A. 2009. . The prevalence and predictors of anencephaly and spina bifida in Texas. Paediatr Perinat Epidemiol 23(1):41–50.
- Canfield MA, Ramadhani TA, Shaw GM, Carmichael SL, Waller DK, Mosley BS, et al. 2009. . Anencephaly and spina bifida among Hispanics: maternal, sociodemographic, and acculturation factors in the National Birth Defects Prevention Study. Birth Defects Res A Clin Mol Teratol 85(7):637–646.
- Christianson A, Howson CP, Modell B. 2006. Global Report on Birth Defects. White Plains, NY:March of Dimes.
- Durrleman S, Simon R.. 1989. Flexible regression models with cubic splines. Stat Med 8(5):551–561.
- Fantel AG. 1996. Reactive oxygen species in developmental toxicity: review and hypothesis. Teratology 53(3):196–217.
- Gilboa SM, Mendola P, Olshan AF, Langlois PH, Savitz DA, Loomis D, et al. 2005. Relation between ambient air quality and selected birth defects, seven county study, Texas, 1997–2000. Am J Epidemiol 162(3):238–252.
- Grant RL, Leopold V, McCant D, Honeycutt M. 2007. Spatial and temporal trend evaluation of ambient concentrations of 1,3-butadiene and chloroprene in Texas. Chem Biol Interact 166(1–3):44–51.
- Hansen CA, Barnett AG, Jalaludin BB, Morgan GG. 2009. Ambient air pollution and birth defects in Brisbane, Australia. PLoS One 4(4):e5408.doi:10.1371/journal.pone.0005408 [Online 30 April 2009]
- Hansen JM. 2006. Oxidative stress as a mechanism of teratogenesis. Birth Defects Res C Embryo Today 78(4):293–307.
- Hwang BF, Jaakkola JJ. 2008. Ozone and other air pollutants and the risk of oral clefts. Environ Health Perspect 116:1411–1415.
- IARC (International Agency for Research on Cancer) 1982. Some Industrial Chemicals and Dyestuffs. IARC Monogr Eval Carcinog Risks Hum 29..
- IARC (International Agency for Research on Cancer) 1987. Overall Evaluations of Carcinogenicity: An Updating of IARC Monographs Volumes 1 to 42. IARC Monogr Eval Carcinog Risks Hum Suppl 7..
- Khoury MJ, Erickson JD, James LM. 1982. Etiologic heterogeneity of neural tube defects. II. Clues from family studies. Am J Hum Genet 34(6):980–987.
- Kim S, Vermeulen R, Waidyanatha S, Johnson BA, Lan Q, Smith MT, et al. 2006. Modeling human metabolism of benzene following occupational and environmental exposures. Cancer Epidemiol Biomarkers Prev 15(11):2246–2252.
- Lan Q, Zhang L, Li G, Vermeulen R, Weinberg RS, Dosemeci M, et al. 2004. Hematotoxicity in workers exposed to low levels of benzene. Science 306(5702):1774–1776.
- Lee K, Parkhurst WJ, Xue J, Ozkaynak AH, Neuberg D, Spengler JD. 2004. Outdoor/indoor/personal ozone exposures of children in Nashville, Tennessee. J Air Waste Manag Assoc 54(3):352–359.
- Lin YS, Vermeulen R, Tsai CH, Waidyanatha S, Lan Q, Rothman N, et al. 2007. Albumin adducts of electrophilic benzene metabolites in benzene-exposed and control workers. Environ Health Perspect 115:28–34.
- Liu L, Wells PG. 1995. DNA oxidation as a potential molecular mechanism mediating drug-induced birth defects: phenytoin and structurally related teratogens initiate the formation of 8-hydroxy-2’-deoxyguanosine in vitro and in vivo in murine maternal hepatic and embryonic tissues. Free Radic Biol Med 19(5):639–648.
- Lupo PJ, Symanski E, Chan W, Mitchell LE, Waller DK, Canfield MA, et al. 2010. . Differences in exposure assignment between conception and delivery: the impact of maternal mobility. Paediatr Perinat Epidemiol 24(2):200–208.
- Lupo PJ, Symanski E, Waller DK, Chan W, Canfield MA, Langlois PH, et al. 2010. . Polytomous logistic regression as a tool for exploring heterogeneity across birth defect subtypes: an example using anencephaly and spina bifida. Birth Defects Res A Clin Mol Teratol 88(8):701–705.
- Marshall EG, Harris G, Wartenberg D. 2010. Oral cleft defects and maternal exposure to ambient air pollutants in New Jersey. Birth Defects Res A Clin Mol Teratol 88(4):205–215.
- McMartin KI, Chu M, Kopecky E, Einarson TR, Koren G. 1998. Pregnancy outcome following maternal organic solvent exposure: a meta-analysis of epidemiologic studies. Am J Ind Med 34(3):288–292.
- Mitchell LE. 2005. Epidemiology of neural tube defects. Am J Med Genet C Semin Med Genet 135(1):88–94.
- Mitchell LE, Adzick NS, Melchionne J, Pasquariello PS, Sutton LN, Whitehead AS. 2004. Spina bifida. Lancet 364(9448):1885–1895.
- Mohamed MF, Kang D, Aneja VP. 2002. Volatile organic compounds in some urban locations in United States. Chemosphere 47(8):863–882.
- Morriss GM, New DA. 1979. Effect of oxygen concentration on morphogenesis of cranial neural folds and neural crest in cultured rat embryos. J Embryol Exp Morphol 54:17–35.
- Mosley BS, Cleves MA, Siega-Riz AM, Shaw GM, Canfield MA, Waller DK, et al. 2009. Neural tube defects and maternal folate intake among pregnancies conceived after folic acid fortification in the United States. Am J Epidemiol 169(1):9–17.
- Ozkaynak H, Palma T, Touma JS, Thurman J. 2008. Modeling population exposures to outdoor sources of hazardous air pollutants. J Expo Sci Environ Epidemiol 18(1):45–58.
- Parman T, Wiley MJ, Wells PG. 1999. Free radical-mediated oxidative DNA damage in the mechanism of thalidomide teratogenicity. Nat Med 5(5):582–585.
- Payne-Sturges DC, Burke TA, Breysse P, Diener-West M, Buckley TJ. 2004. Personal exposure meets risk assessment: a comparison of measured and modeled exposures and risks in an urban community. Environ Health Perspect 112:589–598.
- Petrini J, Damus K, Russell R, Poschman K, Davidoff MJ, Mattison D. 2002. Contribution of birth defects to infant mortality in the United States. Teratology 66: suppl 1S3–S6.
- Pratt GC, Wu CY, Bock D, Adgate JL, Ramachandran G, Stock TH, et al. 2004. Comparing air dispersion model predictions with measured concentrations of VOCs in urban communities. Environ Sci Technol 38(7):1949–1959.
- Rankin J, Chadwick T, Natarajan M, Howel D, Pearce MS, Pless-Mulloli T. 2009. Maternal exposure to ambient air pollutants and risk of congenital anomalies. Environ Res 109(2):181–187.
- Ritz B, Yu F, Fruin S, Chapa G, Shaw GM, Harris JA. 2002. Ambient air pollution and risk of birth defects in Southern California. Am J Epidemiol 155(1):17–25.
- Rosenbaum AS, Axelrad DA, Woodruff TJ, Wei YH, Ligocki MP, Cohen JP. 1999. National estimates of outdoor air toxics concentrations. J Air Waste Manag Assoc 49(10):1138–1152.
- Selevan SG, Kimmel CA, Mendola P. 2000. Identifying critical windows of exposure for children’s health. Environ Health Perspect 108: suppl 3451–455.
- Sexton K, Linder SH, Marko D, Bethel H, Lupo PJ. 2007. Comparative assessment of air pollution-related health risks in Houston. Environ Health Perspect 115:1388–1393.
- Slama R, Thiebaugeorges O, Goua V, Aussel L, Sacco P, Bohet A, et al. 2009. Maternal personal exposure to airborne benzene and intrauterine growth. Environ Health Perspect 117:1313–1321.
- Strickland MJ, Klein M, Correa A, Reller MD, Mahle WT, Riehle-Colarusso TJ, et al. 2009. Ambient air pollution and cardiovascular malformations in Atlanta, Georgia, 1986–2003. Am J Epidemiol 169(8):1004–1014.
- Szklo M, Nieto FJ. 2007. Stratification and adjustment: multivariate analysis in epidemiology. In: Epidemiology: Beyond the Basics. Boston:Jones & Bartlett Learning. pp. 227–295.
- Texas Department of State Health Services 2010. Texas Birth Defects Epidemiology & Surveillance. Available: http://www.dshs.state.tx.us/birthdefects/ [accessed 28 January 2011]
- U.S. Census Bureau 2010. U.S. Census Bureau Data Sets. Available: http://factfinder.census.gov/servlet/DatasetMainPageServlet [accessed 28 January 2011]
- U.S. EPA (U.S. Environmental Protection Agency) 2006. The ASPEN Model. Available: http://www.epa.gov/ttn/atw/nata/aspen.html [accessed 19 July 2010]
- U.S. EPA (U.S. Environmental Protection Agency) 2007a. About Air Toxics. Available: http://www.epa.gov/ttn/atw/allabout.html [accessed 5 September 2009]
- U.S. EPA (U.S. Environmental Protection Agency) 2007b. Access the Air Quality System Data Mart. Available: http://www.epa.gov/ttn/airs/aqsdatamart/access.htm [accessed 11 September 2009]
- U.S. EPA (U.S. Environmental Protection Agency) 2008. 1999 National-Scale Air Toxics Assessment: 1999 Data Tables. Available: http://www.epa.gov/ttn/atw/nata1999/tables.html [accessed 22 January 2008]
- Wells PG, Kim PM, Laposa RR, Nicol CJ, Parman T, Winn LM. 1997. Oxidative damage in chemical teratogenesis. Mutat Res 396(1–2):65–78.
- Wennborg H, Magnusson LL, Bonde JP, Olsen J. 2005. Congenital malformations related to maternal exposure to specific agents in biomedical research laboratories. J Occup Environ Med 47(1):11–19.
- Whitworth KW, Symanski E, Coker AL. 2008. Childhood lymphohematopoietic cancer incidence and hazardous air pollutants in southeast Texas, 1995–2004. Environ Health Perspect 116:1576–1580.
- Wong LY, Paulozzi LJ. 2001. Survival of infants with spina bifida: a population study, 1979–94. Paediatr Perinat Epidemiol 15(4):374–378.
- Xia T, Korge P, Weiss JN, Li N, Venkatesen MI, Sioutas C, et al. 2004. Quinones and aromatic chemical compounds in particulate matter induce mitochondrial dysfunction: implications for ultrafine particle toxicity. Environ Health Perspect 112:1347–1358.
- Yin SN, Hayes RB, Linet MS, Li GL, Dosemeci M, Travis LB, et al. 1996. An expanded cohort study of cancer among benzene-exposed workers in China. Benzene Study Group. Environ Health Perspect 104: suppl 61339–1341.
Come visit EHP Editor-in-Chief Sally Darney at the 29th Annual Scientific Conference of the International Society of Environmental Epidemiology, to be held in Sydney, Australia, 24–28 September 2017. She looks forward to talking with EHP authors, reviewers, and editors. Contact Sally directly to make an appointment with her.
EHP is pleased to announce that “Maternal and Cord Blood Manganese Concentrations and Early Childhood Neurodevelopment among Residents near a Mining-Impacted Superfund Site,” published in EHP on 28 June 2017, has been selected by the Children’s Environmental Health Network (CEHN) as its August 2017 Article of the Month. (more…)