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

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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. / Choi, Yoon-Jung; Lee, Young Ah; Hong, Yun-Chul; Cho, Jinwoo; Lee, Kyung-Shin; Shin, Choong Ho; Kim, Bung-Nyun; Kim, Johanna Inhyang; Park, Soo Jin; Bisgaard, Hans; Bønnelykke, Klaus; Lim, Youn-Hee.

I: Environment International, Bind 143, 105929, 06.07.2020.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Choi, Y-J, Lee, YA, Hong, Y-C, Cho, J, Lee, K-S, Shin, CH, Kim, B-N, Kim, JI, Park, SJ, Bisgaard, H, Bønnelykke, K & Lim, Y-H 2020, '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', Environment International, bind 143, 105929. https://doi.org/10.1016/j.envint.2020.105929

APA

Choi, Y-J., Lee, Y. A., Hong, Y-C., Cho, J., Lee, K-S., Shin, C. H., Kim, B-N., Kim, J. I., Park, S. J., Bisgaard, H., Bønnelykke, K., & Lim, Y-H. (2020). 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. Environment International, 143, [105929]. https://doi.org/10.1016/j.envint.2020.105929

Vancouver

Choi Y-J, Lee YA, Hong Y-C, Cho J, Lee K-S, Shin CH o.a. 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. Environment International. 2020 jul. 6;143. 105929. https://doi.org/10.1016/j.envint.2020.105929

Author

Choi, Yoon-Jung ; Lee, Young Ah ; Hong, Yun-Chul ; Cho, Jinwoo ; Lee, Kyung-Shin ; Shin, Choong Ho ; Kim, Bung-Nyun ; Kim, Johanna Inhyang ; Park, Soo Jin ; Bisgaard, Hans ; Bønnelykke, Klaus ; Lim, Youn-Hee. / 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. I: Environment International. 2020 ; Bind 143.

Bibtex

@article{151f052bf8564da0bf794ac58e4ff1c7,
title = "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",
abstract = "OBJECTIVES: 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.METHODS: 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.RESULTS: 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.CONCLUSIONS: 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.",
author = "Yoon-Jung Choi and Lee, {Young Ah} and Yun-Chul Hong and Jinwoo Cho and Kyung-Shin Lee and Shin, {Choong Ho} and Bung-Nyun Kim and Kim, {Johanna Inhyang} and Park, {Soo Jin} and Hans Bisgaard and Klaus B{\o}nnelykke and Youn-Hee Lim",
note = "Copyright {\textcopyright} 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.",
year = "2020",
month = jul,
day = "6",
doi = "10.1016/j.envint.2020.105929",
language = "English",
volume = "143",
journal = "Environment international",
issn = "0160-4120",
publisher = "Pergamon Press",

}

RIS

TY - JOUR

T1 - 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

AU - Choi, Yoon-Jung

AU - Lee, Young Ah

AU - Hong, Yun-Chul

AU - Cho, Jinwoo

AU - Lee, Kyung-Shin

AU - Shin, Choong Ho

AU - Kim, Bung-Nyun

AU - Kim, Johanna Inhyang

AU - Park, Soo Jin

AU - Bisgaard, Hans

AU - Bønnelykke, Klaus

AU - Lim, Youn-Hee

N1 - Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.

PY - 2020/7/6

Y1 - 2020/7/6

N2 - OBJECTIVES: 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.METHODS: 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.RESULTS: 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.CONCLUSIONS: 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.

AB - OBJECTIVES: 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.METHODS: 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.RESULTS: 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.CONCLUSIONS: 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.

U2 - 10.1016/j.envint.2020.105929

DO - 10.1016/j.envint.2020.105929

M3 - Journal article

C2 - 32645488

VL - 143

JO - Environment international

JF - Environment international

SN - 0160-4120

M1 - 105929

ER -

ID: 244446477