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Children's Health Volume 123 | Issue 6 | June 2015

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Environ Health Perspect; DOI:10.1289/ehp.1408417

In Utero and Childhood Polybrominated Diphenyl Ether Exposures and Body Mass at Age 7 Years: The CHAMACOS Study

Ayca Erkin-Cakmak,1 Kim G. Harley,1 Jonathan Chevrier,1,2 Asa Bradman,1 Katherine Kogut,1 Karen Huen,1 and Brenda Eskenazi1

Author Affiliations open
1Center for Environmental Research and Children’s Health (CERCH), School of Public Health, University of California, Berkeley, Berkeley, California, USA; 2Department of Epidemiology, Biostatistics and Occupational Health, McGill University Faculty of Medicine, Montréal, Québec, Canada

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  • Related EHP Article

    Erratum: “In Utero and Childhood Polybrominated Diphenyl Ether Exposures and Body Mass at Age 7 Years: The CHAMACOS Study”

    Ayca Erkin-Cakmak, Kim G. Harley, Jonathan Chevrier, Asa Bradman, Katherine Kogut, Karen Huen, and Brenda Eskenazi

    Background: Polybrominated diphenyl ethers (PBDEs) are lipophilic flame retardants that bioaccumulate in humans. Child serum PBDE concentrations in California are among the highest worldwide. PBDEs may be associated with obesity by disrupting endocrine systems.

    Objective: In this study, we examined whether pre- and postnatal exposure to the components of pentaBDE mixture was associated with childhood obesity in a population of Latino children participating in a longitudinal birth cohort study in the Salinas Valley, California.

    Methods: We measured PBDEs in serum collected from 224 mothers during pregnancy and their children at 7 years of age, and examined associations with body mass index (BMI) at age 7 years.

    Results: Maternal PBDE serum levels during pregnancy were associated with higher BMI z-scores in boys (BMI z-score βadjusted = 0.26; 95% CI: –0.19, 0.72) but lower scores in girls (BMI z-score βadjusted = –0.41; 95% CI: –0.87, –0.05) at 7 years of age (pinteraction = 0.04). In addition, child’s serum BDE-153 concentration (log10), but not other pentaBDE congeners, demonstrated inverse associations with BMI at age 7 years (BMI z-score βadjusted = –1.15; 95% CI: –1.53, –0.77), but there was no interaction by sex.

    Conclusions: We estimated sex-specific associations with maternal PBDE levels during pregnancy and BMI at 7 years of age, finding positive associations in boys and negative associations in girls. Children’s serum BDE-153 concentrations were inversely associated with BMI at 7 years with no difference by sex. Future studies should examine the longitudinal trends in obesity with PBDE exposure and changes in hormonal environment as children transition through puberty, as well as evaluate the potential for reverse causality.

  • Citation: Erkin-Cakmak A, Harley KG, Chevrier J, Bradman A, Kogut K, Huen K, Eskenazi B. 2015. In utero and childhood polybrominated diphenyl ether exposures and body mass at age 7 years: the CHAMACOS Study. Environ Health Perspect 123:636–642;

    Address correspondence to B. Eskenazi, Center for Environmental Research and Children’s Health (CERCH), School of Public Health, University of California, Berkeley, 1995 University Ave., Suite 265, Berkeley, CA 94720 USA. Telephone: (510) 642-3496. E-mail:

    We acknowledge the CHAMACOS (Center for the Health Assessment of Mothers and Children of Salinas) and the Centers for Disease Control and Prevention (CDC) staff, students, community partners, and participants and their families as well as N. Holland and her staff for assistance in specimen management. We gratefully acknowledge A. Sjödin and his laboratory staff at the CDC for the analysis of the PBDE blood concentrations.

    This study was made possible by research supported by grant numbers RD 83171001 and R82670901 from the U.S. Environmental Protection Agency (EPA); PO1 ES009605 and RO1ES015572 from the National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health; and RO1OH007400 from the National Institute for Occupational Safety and Health (NIOSH), CDC. Additional funding was provided by the University of California Institute for Mexico and the United States (UC MEXUS).

    The contents of this publication are solely the responsibility of the authors and do not necessarily represent the official position of the U.S. EPA, NIEHS, or NIOSH.

    The authors declare they have no actual or potential competing financial interests.

    Received: 13 March 2014
    Accepted: 24 February 2015
    Advance Publication: 27 February 2015
    Final Publication: 1 June 2015

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  • In Figure 1A, which represents the association between the difference in BMI z-score at age 7 and maternal serum PBDEs (ng/lipid), the line of the upper confidence interval of Σ4PBDE for girls incorrectly crossed the zero-line: The upper interval for girls is −0.05 and should appear below the zero-line. The corrected Figure 1 appears in this erratum.

    ehp.124-A68.g001Figure 1 – Point estimates and 95% CIs from (A) regression of maternal PBDE concentrations and anthropometric measurements at age 7 years, and (B) GEE model estimates of overall associations between 10-fold increases in maternal PBDE concentrations and repeated anthropometric measures (ages 2, 3.5, 5, and 7 years), with effect modification by sex, controlling for maternal age, education, prepregnancy BMI, years lived in the United States, gestational weight gain, poverty during pregnancy; and child gestational age, duration of breastfeeding, and fast food and soda consumption at age 7. pint, p-value for interaction.

    View larger image (TIF File)

    The authors regret this error.


Polybrominated diphenyl ethers (PBDEs) are flame retardants that have been used extensively in consumer products since the 1970s in three technical mixtures (penta-, octa-, and decabromo diphenyl ethers) (Besis and Samara 2012; Hale et al. 2003). PBDEs are lipophilic, accumulate in living organisms, and have an estimated half-life up to 12 years in humans (Geyer et al. 2004; Li et al. 2008; Wong et al. 2013). PBDE serum levels are about 20 times higher in the United States than Europe; Californians have the highest levels, likely due to state furniture flammability standards (Eskenazi et al. 2011; Sjödin et al. 2008; Zota et al. 2008). Although the pentaBDE mixture used in furniture, carpet padding, and infant products has been banned since 2004, pentaBDE congeners continue to be released from older furniture and are commonly found in house dust (Noyes et al. 2011).

PBDEs have been detected in cord blood, placental tissue, and breast milk and are transferred pre- and postnatally from women to their children (Herbstman et al. 2010; Wu et al. 2009). Young children’s hand-to-mouth behavior may contribute to additional exposures via oral and dermal contact with dust (Bradman et al. 2012; Lorber 2008).

Obesity is a growing public health problem worldwide (Booth et al. 2001; Lobstein 2004; Popkin and Doak 1998). Although obesity is primarily attributable to genetic predisposition, high calorie intake, and insufficient physical activity, exposure to endocrine-disrupting chemicals such as PBDEs may also play a role (Janesick and Blumberg 2011a; Legler and Brouwer 2003). Estrogen and androgen receptors in the brain and peripheral organs modulate programming of energy balance and distribution of body fat, and PBDEs are known to disrupt estrogen and androgen signaling (Legler et al. 2011). Although lower brominated PBDEs, including BDEs 28, 47, and 100, exhibit estrogenic activity, higher brominated compounds, such as BDE-153, show antiestrogenic properties (Meerts et al. 2001). PBDEs’ potential effect on obesity may also be caused by the disruption of thyroid hormone homeostasis, which regulates the basal metabolic rate and lipid metabolism. PBDE exposure is associated with reduced thyroxine (T4) in animal studies (Hallgren et al. 2001; Kuriyama et al. 2007; Zhou et al. 2002) and increased T4 or decreased thyroid-stimulating hormone (TSH) in human studies (Chevrier et al. 2010; Hagmar et al. 2001; Turyk et al. 2008). PBDEs may also have direct effects on lipid metabolism and adipogenesis (Hoppe and Carey 2007). In rodents exposed postnatally, pentaPBDEs cause an increase in in vitro isoproterenol-stimulated lipolysis and a decrease in insulin-stimulated glucose oxidation, but no effect on fat pad weight, adipocyte number, or adipocyte size (Hoppe and Carey 2007). PPARγ (peroxisome proliferator-activated receptor gamma) is the master regulator of adipocyte development, and activation of PPARγ can lead to adipogenesis and obesity. Although organotins (such as tributylin) and phthalates target PPARγ (Janesick and Blumberg 2011b), as of yet there is no evidence that PBDEs affect PPARγ activity.

In humans, results are conflicting as to whether postnatal PBDE exposure is related to childhood obesity (Lim et al. 2008; Turyk et al. 2010; Windham et al. 2010). However, no previous study has examined the effects of prenatal exposure. In the present study, we examined the association between pre- and postnatal exposure to pentaBDE congeners and measures of body mass in a population of California children participating in the Center for the Health Assessment of Mothers and Children of Salinas (CHAMACOS) study. Because of the purported effects of PBDEs on endocrine function, we also examined differences by child sex.


Participants and recruitment. Subjects in this study participated in CHAMACOS, a longitudinal birth cohort study investigating the effects of environmental exposures on the health of pregnant women and their children. Detailed methods are described elsewhere (Eskenazi et al. 2003, 2004). Briefly, pregnant women were enrolled between October 1999 and October 2000 from prenatal clinics serving low-income, Spanish-speaking residents in the Salinas Valley, California. Eligible women were at least 18 years of age, < 20 weeks gestation, qualified for low-income health insurance, spoke English or Spanish, and planned to deliver at a local hospital. Of 601 women initially enrolled, 531 were followed to the live birth of an infant. We excluded twins (n = 5), children not followed to 7 years of age (n = 172), and children whose mothers did not have adequate serum volumes for PBDE measurements (n = 55). We further excluded mother–child pairs who were missing PBDE measurements both during pregnancy and at child’s 7 years of age (n = 70), leaving a final sample size of 224. Compared with children in the cohort who were not followed, children included in the present analyses were more likely to be female and less likely to have low birth weight, with mothers who were older and breastfed longer (data not shown). They did not differ according to other sociodemographic characteristics listed in Table 1.

Table 1 - See HTML for full tableTable 1 – Prenatal and childhood blood PBDE concentrations (ng/g lipid) by demographic characteristics of the study population.

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Written informed consent was obtained from mothers, and children provided verbal assent at 7 years of age. Study activities were approved by the Institutional Review Board at the University of California, Berkeley, and the Centers for Disease Control and Prevention (CDC).

Procedure. Bilingual, bicultural study staff conducted structured interviews in English or Spanish twice during pregnancy (mean ± SD = 13.4 ± 5.2 and 25.7 ± 2.1 weeks of gestation), soon after delivery, and when children were 2, 3.5, 5, and 7 years of age. Child weight (kilograms) and height (centimeters) were measured at each follow-up visit. Weight was measured once using a digital scale (Tanita 1582; Tanita Corporation, Arlington Heights, IL). Barefoot standing height was measured in triplicate using a stadiometer (Seca 222; Seca, Chino, CA) and the measures were averaged. Starting at 5 years, waist circumference was measured in triplicate by placing a measuring tape around the abdomen at the level of the iliac crest, parallel to the floor and measures were averaged. Maternal prepregnancy body mass index (BMI) was calculated using the mothers’ self-reported prepregnancy weight and height measured by stadiometer.

PBDE exposure assessment. Blood samples were collected by venipuncture from mothers during pregnancy (26.7 ± 2.6 weeks gestation, n = 219) or at delivery (n = 60), and from children at the 7-year visit (7.1 ± 0.3 years, n = 272). Samples were immediately processed and stored at –80°C until shipment on dry ice to the CDC in Atlanta, Georgia, where they were analyzed for 10 PBDE congeners (BDEs 17, 28, 47, 66, 85, 99, 100, 153, 154, and 183) by gas chromatography–isotope dilution–high resolution mass spectrometry (Sjödin et al. 2004). The individual pentaBDE mixture congeners (BDEs 47, 99, 100, and 153) with detection frequencies ≥ 90% and the sum of these congeners were selected as the primary exposure. PBDE concentrations were adjusted for serum lipid levels and expressed on a serum lipid basis (nanograms per gram lipid). Total serum lipid concentrations were estimated based on triglycerides and total cholesterol measured using standard enzymatic methods (Roche Chemicals, Indianapolis, IN) (Phillips et al. 1989). The limits of detection (LODs) for BDE-47 ranged from 0.3 to 2.6 ng/g lipid for maternal samples, and 0.4 to 0.8 ng/g lipid for child samples. For all other congeners, LODs ranged between 0.2 and 0.7 ng/g lipid for maternal samples and 0.3 and 5.6 ng/g lipid for child samples. Laboratory blanks and spikes were included in each run.

Values below the LODs were assigned the machine-read value if a signal was detected and otherwise imputed at random based on a log-normal probability distribution whose parameters were determined using maximum likelihood estimation (Lubin et al. 2004).

Other laboratory analyses. The CDC also measured p,p´-dichl​orodipheny​ltrich​loroet​hane (DDT) and p,p´-dichlorodiphenyldichloroethylene (DDE) in maternal serum collected around the 26th week of gestation using gas chromatography–high resolution mass spectrometry (Eskenazi et al. 2006). TSH was measured by immunochemiluminometric assay (Quest Diagnostics’ Nichols Institute; San Juan Capistrano, CA) and free T4 using direct equilibrium dialysis followed by radioimmunoassay (Bayer ADVIA Centaur system; Siemens Healthcare Diagnostics, Deerfield, IL) (Nelson and Tomei 1988). Per the California Department of Health Services Neonatal Genetics Disease Screening Program, dried blood spots collected from newborns were analyzed for TSH using solid-phase, time-resolved sandwich fluoroimmunoassay (AutoDELPHIA system; PerkinElmer, Wellesley, MA).

Data analysis. We examined the distributions of PBDE concentrations and found them to be strongly right skewed; thus, they were log10 transformed to reduce the influence of outliers. We categorized PBDE concentration variables by quintiles to investigate nonmonotonic exposure–response relationships. We used Pearson correlations to assess the correlation between concentrations of the four PBDE congeners and between prenatal and child (at age 7 years) PBDE blood concentrations. Age- and sex-specific BMI z-scores and percentiles were computed using 2000 CDC growth charts (Kuczmarski et al. 2002). BMI < 85th percentile, between the 85th and 95th percentiles, and ≥ 95th percentile were defined as normal BMI, overweight, and obese, respectively.

We used multivariable regression to examine associations between maternal concentrations for each individual pentaBDE congener (BDEs 47, 99, 100, and 153) and for the sum of these four congeners (Σ4PBDE) and anthropometric measurements (BMI and waist circumference) of the children at each age (2, 3.5, 5 years). We also constructed separate models to examine associations between anthropometric measurements at 7 years and maternal as well as child PBDE concentrations at 7 years. Linear regression was used to examine the relationship of PBDE concentrations and continuous outcomes (BMI and waist circumference z-score), and logistic regression was used to examine categorical outcomes (BMI categories). Generalized estimating equation (GEE) models were used to examine the population average association between prenatal PBDE exposure and BMI z-score at ages 2, 3.5, 5, or 7 years (n = 224, average number of observations = 3.8), and (in separate models) waist circumference z-scores at ages 5 and 7 years (n = 224); standard errors and 95% confidence intervals (CIs) were estimated by using a robust (Huber–White) variance estimate.

Potential confounding variables were selected a priori based on the childhood obesity literature (Berkey et al. 2000; Ebbeling et al. 2002; Hernández et al. 1999; Levin and Govek 1998) and a directed acyclic graph (DAG) (see Supplemental Material, Figure S1). We considered the following as potential confounders: maternal age, education, prepregnancy BMI, years resided in the United States at enrollment, gestational weight gain, parity; family poverty status; and child sex, gestational age at delivery, duration of breastfeeding, and childhood dietary and physical activity characteristics (e.g., intake of soda, sweetened beverages, fast food, sweet and salty snacks, and time spent watching television and playing outside at 7 years). Based on the DAG, final models included the following covariates: maternal age, education, prepregnancy BMI, years resided in the United States, gestational weight gain, and poverty during pregnancy; and child gestational age at delivery, duration of breast feeding, and fast food and soda consumption at age 7 years.

We conducted a number of sensitivity analyses. Though lipid-adjusted log10 PBDE concentrations were the primary independent variable, we also considered wet-weight PBDE concentrations (wet-weight picograms per gram serum) adjusting for serum lipids (milligrams per deciliter) (Chevrier 2013). We also considered unlogged PBDE concentrations (nanograms per gram lipid). We also reran models of body mass of the children at 7 years controlling for both maternal and child PBDE concentrations in the same model. We also used categorical PBDE concentration variables (quintiles) to investigate nonmonotonic exposure–response relationships. Because maternal pregnancy PBDE serum concentrations have previously shown associations with TSH in CHAMACOS participants (Chevrier et al. 2010) and thyroid function is a determinant of obesity, we conducted sensitivity analyses to determine whether thyroid hormone could be a potential mediator (Cole and Hernán 2002). Specifically, we modeled associations of pregnancy PBDE with body mass at age 7 years adjusting separately for maternal TSH, maternal free T4, and neonatal TSH while controlling for confounders of the thyroid hormone–obesity relations (Cole and Hernán 2002). Although in our DAG we considered birth weight as potentially on the causal pathway (Harley et al. 2011) and that it might result in spurious findings if controlled for (Hernández-Díaz et al. 2006), we conducted sensitivity analysis controlling for birth weight. Because our study population has relatively high exposure to DDT and DDE (Bradman et al. 2005), we reran our main models controlling for DDT/E.

We adjusted for potential selection bias in the reduced sample by applying weights equal to inverse probability of being included in the final analysis. Weights were determined using a SuperLearner algorithm that minimizes cross-validated risks based on a loss function (van der Laan et al. 2007). Main effects and interactions were considered statistically significant at p < 0.05, and p < 0.10 based on two-tailed tests, respectively. All analyses were conducted with STATA version 12.1 (StataCorp, College Station, TX).


Participants’ characteristics. Table 1 presents demographic characteristics and maternal and child Σ4PBDE serum concentrations. At enrollment, mean (± SD) age of mothers was 25.7 ± 5.0 years. Before pregnancy, 64.3% of mothers were overweight or obese, and 54.5% gained more weight than recommended during pregnancy (American Congress of Obstetricians and Gynecologists 2013). The percent of the children who were obese increased from age 2 to 7 years [16.4% at age 2 (n = 207), 29.1% at age 3.5 (n = 203), 33.0% at age 5 (n = 209), 34.4% at age 7 (n = 221) were obese] (see Supplemental Material, Table S1). At age 7, 18.6% of children were overweight.

PBDE concentrations. The geometric means and 95% CIs for maternal and child Σ4PBDE concentrations were 25.35 (22.42, 28.65) and 83.03 (74.80, 92.17) ng/g lipid, respectively, with the largest contribution from BDE-47 (see Supplemental Material, Table S2). BDEs 47, 99, and 100 were highly correlated with each other and with Σ4PBDE (r > 0.90) in mothers and in children. BDE-153 was less strongly correlated with other congeners (0.72–0.89 in mothers and 0.65–0.76 in children) (see Supplemental Material, Table S3). As we previously reported, the correlation between maternal and child Σ4PBDE was 0.27 (p < 0.01) (Bradman et al. 2012).

Maternal PBDE concentrations and measures of child body mass. Maternal serum concentrations for each pentaBDE congener (BDEs 47, 99, 100, and 153) and for Σ4PBDE were not associated with any measures of the child’s body mass at age 7 years. Specifically, maternal serum Σ4PBDE concentration was not associated with the BMI z-score (βadjusted = –0.08; 95% CI: –0.41, 0.25), waist circumference z-score (βadjusted = –0.02; 95% CI: –2.45, 0.28), or the odds of being overweight at age 7 (ORadjusted = 0.82; 95% CI: 0.38, 1.79) (see Supplemental Material, Table S4). (Point estimates were reported in log10 scale.) However, we observed evidence of effect modification by sex for all four congeners and their sum (Figure 1A). Each 10-fold increase in maternal serum Σ4PBDE concentration was associated with a significant 0.41-unit decrease in BMI z-score in girls (95% CI: –0.87, –0.05) but with a nonsignificant increase in BMI z-score in boys (βadjusted = 0.26; 95% CI: –0.19, 0.72; pinteraction = 0.04). Waist circumference z-scores and obesity status models showed similar, significant effect modification by sex (see Supplemental Material, Table S5), though overweight status models did not (data not shown). Likewise, GEE models of associations with repeated measures of the outcomes from 2 to 7 years showed no overall association of maternal serum Σ4PBDE or individual penta-congener concentrations with BMI or waist circumference z-score (βadjusted = –0.02; 95% CI: –0.44, 0.39; βadjusted = –0.002; 95% CI: –0.29, 0.29 for Σ4PBDE, data not shown), but there was effect modification by sex for both outcomes (Figure 1B). Results for the above models did not change when controlling for child age 7 PBDE concentrations (data not shown). See Supplemental Material, Figure S2, for crude associations between maternal and child Σ4PBDE concentrations and BMI z-score, with regression lines for boys and girls at each age. Starting from age 2 years, an association between maternal BDE-153 exposure and BMI was observed with effect modification by child sex (see Supplemental Material, Table S6). At age 3.5 years, the relationship between maternal BDE-153 levels and BMI z-score was significantly negative in girls (βadjusted = –0.64; 95% CI: –1.23, –0.06) and significantly positive in boys (βadjusted = 0.99; 95% CI: 0.32, 1.66) (pinteraction < 0.01) (see Supplemental Material, Table S6).

Figure 1 - A) Two plots of point estimates with 95% CI for the difference in BMI z-score and waist circumference at age 7 (y-axes, respectively) according to maternal serum PBDE concentrations and child’s gender (x-axes). B) A) Two plots of point estimates with 95% CI for the difference in BMI z-score and waist circumference over all time points (y-axes, respectively) according to maternal serum PBDE concentrations and child’s gender (x-axes).Figure 1 – Point estimates and 95% CIs from (A) regression of maternal PBDE concentrations and anthropometric measurements at age 7 years, and (B) GEE model estimates of overall associations between 10-fold increases in maternal PBDE concentrations and repeated anthropometric measures (ages 2, 3.5, 5, and 7 years), with effect modification by sex, controlling for maternal age, education, prepregnancy BMI, years lived in the United States, gestational weight gain, poverty during pregnancy; and child gestational age, duration of breastfeeding, and fast food and soda consumption at age 7. pint, p-value for interaction.

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Child PBDE concentrations and measures of body mass. Table 2 shows the cross-sectional association of children’s age 7 serum Σ4PBDE concentrations and body mass measures. Child Σ4PBDE concentrations were associated with significantly lower in BMI (βadjusted = –0.44; 95% CI: –0.83, –0.06) and waist circumference z-scores (βadjusted = –0.35; 95% CI: –0.66, –0.04), and a significant decrease in odds of being overweight [adjusted odds ratio (ORadjusted) = 0.36 for each 10-fold increase in Σ4PBDE; 95% CI: 0.14, 0.94]. In particular, BDE-153 concentration was associated with significantly lower in BMI (βadjusted = –1.15; 95% CI: –1.53, –0.77) and waist circumference z-scores (βadjusted = –0.95; 95% CI: –1.26, –0.64). Figure 2 presents the relationship of BMI and waist circumference z-scores at age 7 with concurrent child BDE-153 concentrations (quintiles). We observed a monotonic decrease with increasing quartiles of exposure. We did not find evidence of effect modification by sex with Σ4PBDE or the individual penta-congeners in child sera (data not shown).

Table 2 - See HTML for full tableTable 2 – Unadjusted and adjusted associations between 10-fold increase in child serum concentrations of penta-PBDE (log10) and child body mass outcomes at age 7 years.

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Figure 2 - A) Estimated difference (95% CI) in BMI z-score (y-axis) according to child’s serum PBDE-153 concentration. B) Estimated difference (95% CI) in waist circumference (y-axis) according to child’s serum PBDE-153 concentration.Figure 2 – The point estimates and 95% CIs for each quintile (Q) of child BDE-153 (ranges were ≥ 6.19, 6.19–9.01, 9.01–13.25, 13.25–22.36, ≥ 22.36 ng/g lipid) for (A) BMI z-score and (B) waist circumference z-score controlling for maternal age, education, prepregnancy BMI, years lived in the United States, gestational weight gain, poverty during pregnancy; and child gestational age, duration of breast feeding, and fast food and soda consumption at age 7 years.

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Sensitivity analyses. Results for final models were qualitatively similar when we expressed PBDE concentrations on a serum volume basis controlling for serum lipid levels; when using unlogged PBDE concentrations (nanograms per gram lipid); when maternal and child PBDE concentrations were entered into the same model; and when we controlled for maternal TSH and free T4, neonatal TSH, child birth weight, and maternal DDT/E (data not shown). When we adjusted for potential selection bias in the reduced sample by applying weights equal to inverse probability of being included in the final analysis, our results did not change (data not shown).


In this study of 7-year-old Latino children in an agricultural California community, although we did not observe significant overall associations between maternal prenatal pentaBDE concentrations and measures of child’s body mass, we did demonstrate significant effect modifications by sex, with generally negative associations for girls but positive associations for boys. We also demonstrated that children’s serum PBDE concentrations at age 7 years, specifically BDE-153 concentration, were negatively associated with concurrent BMI z-score, waist circumference z-score, and being overweight for both sexes combined. Although we previously reported an association between maternal PBDE levels and child birth weight (Harley et al. 2011), controlling for birth weight did not alter our above findings, suggesting an association of PBDEs on child weight independent of birth weight.

To our knowledge, no previous studies in humans have examined prenatal PBDE exposure and child BMI. However, a single study in rats showed a modest increase (approximately 7%) in body weight in both sexes with perinatal pentaBDE exposure where the animals were treated by gavage with PBDEs that are commonly found in humans (i.e., BDEs 47, 99, 100, and 153) (Bondy et al. 2013). Previous human and animal studies of postnatal exposure have produced inconsistent results. Rodent studies of postnatal oral pentaBDE exposure have not shown associations with body weight (Ernest et al. 2012; Fowles et al. 1994; Stoker et al. 2004). In cross-sectional studies of human adults, one study reported a positive association between BMI and serum concentrations of BDEs 47, 99, and 100, but no relationship with BDE-153 (Turyk et al. 2010); and another study reported inverse associations with serum BDE-153 levels (as we observed here) but no association with other congeners (Lim et al. 2008). In a study of PBDEs and body mass in girls 6 to 9 years of age, Windham et al. (2010) reported that total child serum PBDE (sum of BDEs 28, 47, 99, 100, and 153), and BDEs 154 and 153 levels were significantly lower in overweight and obese girls relative to those with normal BMI).

The relationship between serum PBDE concentration and obesity is likely to be complex. We hypothesized that reverse causality, particularly for the higher lipophilic congeners, may explain, at least in part, the inverse relationship between child BDEs blood concentrations and body mass. Serum PBDE concentration is determined by the amount and route of exposure, homeostasis between tissues and extracellular fluids, and rates of metabolism and excretion (Staskal et al. 2006). Because each PBDE congener has different absorption rates from the gastrointestinal tract, lipophilicity, adipose tissue/serum concentration ratios, and elimination rates, individual serum congener measurements may not always reflect the level of external exposure or total body congener amount, and therefore may not be comparable (Bondy et al. 2011, 2013; Sanders et al. 2006; Staskal et al. 2006). For example, in our study population, the prevalence of obesity increased with age. As suggested previously for PBDEs and for other lipophilic compounds (Chevrier 2013), this weight gain might create an additional adipose tissue reservoir for storage of PBDEs, leading to diluted, and thus lower, concentrations in heavier individuals (Glynn et al. 2003). Thus, reverse causality may explain the inverse association of children’s serum BDE-153 concentration with children’s BMI z-score, waist circumference z-score, and overweight/obesity status, especially because BDE-153 is the most lipophilic, has the highest bioaccumulation capacity and adipose tissue/serum concentration ratio, and the lowest rate of metabolism and excretion (Bondy et al. 2011; Sanders et al. 2006; Staskal et al. 2006) compared with the other PBDEs measured. A cross-sectional study in adults that reported a negative association only between serum BDE-153 levels and BMI provides additional support (Lim et al. 2008).

In contrast, the observed relationships with in utero exposure cannot be readily explained by reverse causality. It has been proposed that in utero exposure to environmental chemicals can result in alteration of developmental programming of central endocrine regulatory systems, which in turn could result in higher or lower susceptibility to obesity later in life (Baillie-Hamilton 2002; Grün et al. 2006; Hanson and Gluckman 2008). Although we found little evidence to support a general “obesogenic” effect of in utero PBDE exposure, we found sex-specific differences—namely, positive associations between in utero PBDE exposure and childhood body mass in boys but an inverse relationship in girls. We previously reported in CHAMACOS that maternal urinary BPA concentrations were also negatively associated with BMI z-score of their daughters at 9 years of age (Harley et al. 2013). These findings remained unchanged when we controlled for maternal PBDE concentrations. PBDEs act on steroid receptors and may disrupt estrogen and androgen signaling in both sexes (Meerts et al. 2001; Stoker et al. 2005), but the sexually dimorphic nature of sex steroid milieu and distribution of their receptors in the central nervous system and adipose tissue may have contributed to the apparent sex-specific association with in utero PBDE exposure (Grün and Blumberg 2007). Although the exact pathophysiology has not been well described, sex-specific in utero effects of endocrine-disrupting compounds with weight have been reported by other studies (Karmaus et al. 2009; Petreas et al. 2011; Vilahur et al. 2013; Wolff et al. 2008).

This study has many strengths. The CHAMACOS study is a longitudinal birth cohort with PBDE concentrations measured in both maternal pregnancy and child serum and with multiple measures of child anthropometrics. Information on many potential confounders was available, and the population is relatively homogeneous with regard to race, socioeconomic status, and diet, which can reduce uncontrolled confounding. However, the results of this study may not be generalizable to the entire U.S. population due to the specific demographic makeup of the study population, the particularly high rates of childhood overweight and obesity in CHAMACOS (Ogden et al. 2012), and the relatively high child PBDE concentrations in California (Windham et al. 2010). One of the limitations of our study is the lack of detailed dietary information at each age of follow-up. Lack of measurement of hydroxyl metabolites of PBDEs, which are biologically active and may also disturb sex steroid receptor signaling, is another limitation. Although use of self-reported maternal prepregnancy weight is another weakness, this method was previously validated (Shin et al. 2014).


We evaluated potential obesogenic effects of in utero and postnatal exposure to PBDE in the CHAMACOS longitudinal birth cohort through 7 years of age. Our findings suggest that associations between in utero PBDE exposure and body weight at age 7 differ between boys and girls. Our analysis also shows an inverse association of child serum BDE-153, but not other pentaBDE congeners, with concurrent markers of body mass at age 7 years, though this may be attributable to reverse causality. Future studies should confirm this observed effect modification by sex and further examine whether the effect modification by sex observed in this study is modified by the changes in the hormonal environment through puberty. Finally, because PBDE flame retardants have been replaced by other potentially endocrine-disrupting chemicals, the obesogenic characteristics of these chemicals should also be investigated.


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