Effect of prenatal bisphenol A exposure on early childhood body mass index through epigenetic influence on the insulin-like growth factor 2 receptor (IGF2R) gene.


Journal

Environment international
ISSN: 1873-6750
Titre abrégé: Environ Int
Pays: Netherlands
ID NLM: 7807270

Informations de publication

Date de publication:
10 2020
Historique:
received: 29 01 2020
revised: 22 06 2020
accepted: 23 06 2020
pubmed: 10 7 2020
medline: 12 1 2021
entrez: 10 7 2020
Statut: ppublish

Résumé

Epigenetic mechanisms have been suggested to play a role in the link between in utero exposure to bisphenol A (BPA) and pediatric obesity; however, there is little evidence regarding this mechanism in humans. We obtained data on obesity-associated CpG sites from a previous epigenome-wide association study, and then examined whether methylation at those CpG sites was influenced by prenatal BPA exposure. We then evaluated the relationship between CpG methylation status and body mass index (BMI) in a prospective children's cohort at ages 2, 4, 6, and 8 years. Methylation profiles of 59 children were longitudinally analyzed at ages 2 and 6 years using the Infinium Human Methylation BeadChip. A total of 594 CpG sites known to be BMI or obesity-associated sites were tested for an association with prenatal BPA levels, categorized into low and high exposure groups based on the 80th percentile of maternal BPA levels (2.68 μg/g creatinine), followed by an analysis of the association between DNA methylation and BMI from ages 2-8. There was a significant increase in the methylation levels of cg19196862 (IGF2R) in the high BPA group at age 2 years (p = 0.00030, false discovery rate corrected p < 0.10) but not at age 6. With one standard deviation increase of methylation at cg19196862 (IGF2R) at age 2 years, the linear mixed model analysis revealed that BMI during ages 2-8 years significantly increased by 0.49 (95% confidence interval; 0.08, 0.90) in girls, but not in boys. The indirect effect of prenatal BPA exposure on early childhood BMI through methylation at cg19196862 (IGF2R) at age 2 years was marginally significant. Prenatal exposure to BPA may influence differential methylation of IGF2R at age 2. This result indicates that a possible sensitive period of DNA methylation occurs earlier during development, which may affect BMI until later childhood in a sex-specific manner.

Identifiants

pubmed: 32645488
pii: S0160-4120(20)31884-5
doi: 10.1016/j.envint.2020.105929
pii:
doi:

Substances chimiques

Benzhydryl Compounds 0
IGF2R protein, human 0
Phenols 0
Receptor, IGF Type 2 0
Somatomedins 0
bisphenol A MLT3645I99

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105929

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

Yoon-Jung Choi (YJ)

Department of Preventive Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; Environmental Health Center, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

Young Ah Lee (YA)

Department of Pediatrics, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

Yun-Chul Hong (YC)

Department of Preventive Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; Environmental Health Center, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; Institute of Environmental Medicine, Seoul National University Medical Research Center, Seoul 03080, Republic of Korea.

Jinwoo Cho (J)

Institute of Environmental Medicine, Seoul National University Medical Research Center, Seoul 03080, Republic of Korea.

Kyung-Shin Lee (KS)

Department of Preventive Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; Environmental Health Center, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

Choong Ho Shin (CH)

Department of Pediatrics, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

Bung-Nyun Kim (BN)

Division of Children and Adolescent Psychiatry, Department of Psychiatry, Seoul National University Hospital, Seoul 03080, Republic of Korea.

Johanna Inhyang Kim (JI)

Department of Psychiatry, Hanyang University Medical Center, Seoul 04763, Republic of Korea.

Soo Jin Park (SJ)

Department of Surgery, Wonkwang University Sanbon Hospital, Gunpo 15865, Republic of Korea.

Hans Bisgaard (H)

COPSAC (Copenhagen Prospective Studies on Asthma in Childhood), Herlev and Gentofte Hospital, University of Copenhagen, 2820, Gentofte, Copenhagen, Denmark.

Klaus Bønnelykke (K)

COPSAC (Copenhagen Prospective Studies on Asthma in Childhood), Herlev and Gentofte Hospital, University of Copenhagen, 2820, Gentofte, Copenhagen, Denmark.

Youn-Hee Lim (YH)

Institute of Environmental Medicine, Seoul National University Medical Research Center, Seoul 03080, Republic of Korea; Section of Environmental Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen 1014, Denmark. Electronic address: younhee.lim@sund.ku.dk.

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Classifications MeSH