PMID- 26493407 OWN - NLM STAT- MEDLINE DCOM- 20160927 LR - 20180408 IS - 1460-2350 (Electronic) IS - 0268-1161 (Linking) VI - 31 IP - 1 DP - 2016 Jan TI - Exposure of pregnant women to persistent organic pollutants and cord sex hormone levels. PG - 190-8 LID - 10.1093/humrep/dev260 [doi] AB - STUDY QUESTION: Is prenatal exposure to persistent organic pollutants (POPs) associated with variations of sex hormone levels in cord blood? SUMMARY ANSWER: Prenatal exposure to a number of POPs is associated with a disruption of hormone levels in cord blood, with sex specificities. WHAT IS KNOWN ALREADY: Epidemiological studies have reported disorders of reproductive health, in relation with POPs exposure during early life and the endocrine disruption properties of these chemicals have been suggested as possible mechanisms. STUDY DESIGN, SIZE, DURATION: A subset of 282 mother-child pairs was selected from the prospective population-based PELAGIE birth cohort (n = 3421, 2002-2006, Brittany, France). Pregnant women were recruited before 19 weeks of gestation and followed until delivery. PARTICIPANTS/MATERIALS, SETTING, METHODS: Sex hormone levels including sex hormone-binding globulin (SHBG), estradiol (E2), total testosterone (T), free testosterone (fT = T/SHBG) and the aromatase index (AI = T/E2) were measured in 282 cord blood samples. Anti-Mullerian hormone (AMH) was measured in male newborns only. Pesticide concentrations of alpha-endosulfan, beta-hexachlorocyclohexane (beta-HCH), gamma-HCH, dieldrin, pp'-dichlorodiphenyldichloroethylene (p,p'-DDE), hexachlorobenzene (HCB), heptachlor epoxide (HCE), as well as PCBs (congeners 153, 187 and the sum of anti-estrogenic PCBs 118, 138, and 170) and decabrominated diphenyl ether (BDE209) were also measured in cord blood. Associations between sex hormones and POPs exposure were explored using multiple linear regressions adjusted for potential confounders. MAIN RESULTS AND THE ROLE OF CHANCE: High PCB levels were associated with an increase of SHBG (P-trend < 0.01) and AMH (P-trend < 0.05) and a decrease of fT (P-trend < 0.05) and AI (P-trend < 0.01). High pesticide levels, particularly alpha-endosulfan and HCE, were associated with an increase of SHBG (P < 0.05) and E2 (P < 0.01) and a decrease of fT (P < 0.05) and AI (P < 0.01). Several of these associations were stronger, or specific, among male or female newborns. The associations were not altered in the sensitivity analyses. LIMITATIONS, REASONS FOR CAUTION: The study population was of relatively small sample size, and some compounds rarely detected in cord blood. The high level of correlation between POPs makes it difficult to identify the most contributing POPs. Hormone measurements were performed at birth (in cord blood) and may not adequately represent the infant endocrine system. Multiple statistical testing may have led to false-positive associations. WIDER IMPLICATIONS OF THE FINDINGS: Our results are in discordance with those reported in the only published study of the kind but in accordance with studies about prenatal exposure to other endocrine disruptors such as phthalates. These findings may help understanding the pathways involved in adverse reproductive outcomes associated with POPs exposure. STUDY FUNDING/COMPETING INTERESTS: The PELAGIE cohort is funded by Inserm, French Ministry of Health, French Ministry of Labor, InVS, ANR, ANSES, and French Ministry of Ecology. None of the authors has any competing interest to declare. CI - (c) The Author 2015. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oup.com. FAU - Warembourg, C AU - Warembourg C AD - Institut national de la sante et de la recherche medicale (Inserm), U1085, Institut de recherche en sante, environnement et travail (Irset), F-35043 Rennes, France Universite de Rennes 1, F-35043 Rennes, France charline.warembourg@gmail.com. FAU - Debost-Legrand, A AU - Debost-Legrand A AD - Institut national de la sante et de la recherche medicale (Inserm), U1085, Institut de recherche en sante, environnement et travail (Irset), F-35043 Rennes, France Centre Hospitalier Universitaire de Clermont-Ferrand, Service de Sante Publique, F-63000 Clermont-Ferrand, France Centre Hospitalier Universitaire de Clermont-Ferrand, EA 4681, PEPRADE, Universite d'Auvergne, F-63000 Clermont-Ferrand, France. FAU - Bonvallot, N AU - Bonvallot N AD - Institut national de la sante et de la recherche medicale (Inserm), U1085, Institut de recherche en sante, environnement et travail (Irset), F-35043 Rennes, France Ecole des hautes etudes en sante publique (EHESP), F-35043 Rennes, France. FAU - Massart, C AU - Massart C AD - Centre de Toxicologie du Quebec of the National Institute of Public Health, Quebec, Canada. FAU - Garlantezec, R AU - Garlantezec R AD - Institut national de la sante et de la recherche medicale (Inserm), U1085, Institut de recherche en sante, environnement et travail (Irset), F-35043 Rennes, France Ecole des hautes etudes en sante publique (EHESP), F-35043 Rennes, France. FAU - Monfort, C AU - Monfort C AD - Institut national de la sante et de la recherche medicale (Inserm), U1085, Institut de recherche en sante, environnement et travail (Irset), F-35043 Rennes, France Universite de Rennes 1, F-35043 Rennes, France. FAU - Gaudreau, E AU - Gaudreau E AD - Centre Hospitalier Universitaire de Rennes, Unite fonctionnelle d'hormonologie, Inserm U1414, Centre d'Investigation Clinique, F-35033 Rennes, France. FAU - Chevrier, C AU - Chevrier C AD - Institut national de la sante et de la recherche medicale (Inserm), U1085, Institut de recherche en sante, environnement et travail (Irset), F-35043 Rennes, France Universite de Rennes 1, F-35043 Rennes, France. FAU - Cordier, S AU - Cordier S AD - Institut national de la sante et de la recherche medicale (Inserm), U1085, Institut de recherche en sante, environnement et travail (Irset), F-35043 Rennes, France Universite de Rennes 1, F-35043 Rennes, France. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20151022 PL - England TA - Hum Reprod JT - Human reproduction (Oxford, England) JID - 8701199 RN - 0 (Biphenyl Compounds) RN - 0 (Endocrine Disruptors) RN - 0 (Gonadal Steroid Hormones) RN - 0 (Hydrocarbons, Chlorinated) SB - IM CIN - Hum Reprod. 2017 Jun 1;32(6):1363. PMID: 28453619 CIN - Hum Reprod. 2017 Jun 1;32(6):1360. PMID: 28453632 MH - Adult MH - Biphenyl Compounds/*adverse effects MH - Endocrine Disruptors/*adverse effects MH - Environmental Exposure/*adverse effects MH - Female MH - Fetal Blood/*metabolism MH - Follow-Up Studies MH - Gonadal Steroid Hormones/*blood MH - Humans MH - Hydrocarbons, Chlorinated/*adverse effects MH - Infant, Newborn MH - Male MH - Pregnancy MH - Sex Factors OTO - NOTNLM OT - cohort studies OT - endocrine disruptors OT - hormones OT - newborns OT - organochlorine compounds OT - polychlorinated biphenyls OT - steroids EDAT- 2015/10/24 06:00 MHDA- 2016/09/28 06:00 CRDT- 2015/10/24 06:00 PHST- 2015/02/12 00:00 [received] PHST- 2015/09/22 00:00 [accepted] PHST- 2015/10/24 06:00 [entrez] PHST- 2015/10/24 06:00 [pubmed] PHST- 2016/09/28 06:00 [medline] AID - dev260 [pii] AID - 10.1093/humrep/dev260 [doi] PST - ppublish SO - Hum Reprod. 2016 Jan;31(1):190-8. doi: 10.1093/humrep/dev260. Epub 2015 Oct 22.