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DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health

BACKGROUND: Prenatal smoking exposure has been associated with childhood attention-deficit/hyperactivity disorder (ADHD). However, the mechanism underlying this relationship remains unclear. We assessed whether DNA methylation differences may mediate the association between prenatal smoking exposure...

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Autores principales: Miyake, Kunio, Miyashita, Chihiro, Ikeda-Araki, Atsuko, Miura, Ryu, Itoh, Sachiko, Yamazaki, Keiko, Kobayashi, Sumitaka, Masuda, Hideyuki, Ooka, Tadao, Yamagata, Zentaro, Kishi, Reiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028116/
https://www.ncbi.nlm.nih.gov/pubmed/33827680
http://dx.doi.org/10.1186/s13148-021-01063-z
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author Miyake, Kunio
Miyashita, Chihiro
Ikeda-Araki, Atsuko
Miura, Ryu
Itoh, Sachiko
Yamazaki, Keiko
Kobayashi, Sumitaka
Masuda, Hideyuki
Ooka, Tadao
Yamagata, Zentaro
Kishi, Reiko
author_facet Miyake, Kunio
Miyashita, Chihiro
Ikeda-Araki, Atsuko
Miura, Ryu
Itoh, Sachiko
Yamazaki, Keiko
Kobayashi, Sumitaka
Masuda, Hideyuki
Ooka, Tadao
Yamagata, Zentaro
Kishi, Reiko
author_sort Miyake, Kunio
collection PubMed
description BACKGROUND: Prenatal smoking exposure has been associated with childhood attention-deficit/hyperactivity disorder (ADHD). However, the mechanism underlying this relationship remains unclear. We assessed whether DNA methylation differences may mediate the association between prenatal smoking exposure and ADHD symptoms at the age of 6 years. RESULTS: We selected 1150 mother–infant pairs from the Hokkaido Study on the Environment and Children’s Health. Mothers were categorized into three groups according to plasma cotinine levels at the third trimester: non-smokers (≤ 0.21 ng/mL), passive smokers (0.21–11.48 ng/mL), and active smokers (≥ 11.49 ng/mL). The children’s ADHD symptoms were determined by the ADHD-Rating Scale at the age of 6 years. Maternal active smoking during pregnancy was significantly associated with an increased risk of ADHD symptoms (odds ratio, 1.89; 95% confidence interval, 1.14–3.15) compared to non-smoking after adjusting for covariates. DNA methylation of the growth factor-independent 1 transcriptional repressor (GFI1) region, as determined by bisulfite next-generation sequencing of cord blood samples, mediated 48.4% of the total effect of the association between maternal active smoking during pregnancy and ADHD symptoms. DNA methylation patterns of other genes (aryl-hydrocarbon receptor repressor [AHRR], cytochrome P450 family 1 subfamily A member 1 [CYP1A1], estrogen receptor 1 [ESR1], and myosin IG [MYO1G]) regions did not exert a statistically significant mediation effect. CONCLUSIONS: Our findings demonstrated that DNA methylation of GFI1 mediated the association between maternal active smoking during pregnancy and ADHD symptoms at the age of 6 years. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01063-z.
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spelling pubmed-80281162021-04-08 DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health Miyake, Kunio Miyashita, Chihiro Ikeda-Araki, Atsuko Miura, Ryu Itoh, Sachiko Yamazaki, Keiko Kobayashi, Sumitaka Masuda, Hideyuki Ooka, Tadao Yamagata, Zentaro Kishi, Reiko Clin Epigenetics Research BACKGROUND: Prenatal smoking exposure has been associated with childhood attention-deficit/hyperactivity disorder (ADHD). However, the mechanism underlying this relationship remains unclear. We assessed whether DNA methylation differences may mediate the association between prenatal smoking exposure and ADHD symptoms at the age of 6 years. RESULTS: We selected 1150 mother–infant pairs from the Hokkaido Study on the Environment and Children’s Health. Mothers were categorized into three groups according to plasma cotinine levels at the third trimester: non-smokers (≤ 0.21 ng/mL), passive smokers (0.21–11.48 ng/mL), and active smokers (≥ 11.49 ng/mL). The children’s ADHD symptoms were determined by the ADHD-Rating Scale at the age of 6 years. Maternal active smoking during pregnancy was significantly associated with an increased risk of ADHD symptoms (odds ratio, 1.89; 95% confidence interval, 1.14–3.15) compared to non-smoking after adjusting for covariates. DNA methylation of the growth factor-independent 1 transcriptional repressor (GFI1) region, as determined by bisulfite next-generation sequencing of cord blood samples, mediated 48.4% of the total effect of the association between maternal active smoking during pregnancy and ADHD symptoms. DNA methylation patterns of other genes (aryl-hydrocarbon receptor repressor [AHRR], cytochrome P450 family 1 subfamily A member 1 [CYP1A1], estrogen receptor 1 [ESR1], and myosin IG [MYO1G]) regions did not exert a statistically significant mediation effect. CONCLUSIONS: Our findings demonstrated that DNA methylation of GFI1 mediated the association between maternal active smoking during pregnancy and ADHD symptoms at the age of 6 years. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01063-z. BioMed Central 2021-04-07 /pmc/articles/PMC8028116/ /pubmed/33827680 http://dx.doi.org/10.1186/s13148-021-01063-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Miyake, Kunio
Miyashita, Chihiro
Ikeda-Araki, Atsuko
Miura, Ryu
Itoh, Sachiko
Yamazaki, Keiko
Kobayashi, Sumitaka
Masuda, Hideyuki
Ooka, Tadao
Yamagata, Zentaro
Kishi, Reiko
DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health
title DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health
title_full DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health
title_fullStr DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health
title_full_unstemmed DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health
title_short DNA methylation of GFI1 as a mediator of the association between prenatal smoking exposure and ADHD symptoms at 6 years: the Hokkaido Study on Environment and Children’s Health
title_sort dna methylation of gfi1 as a mediator of the association between prenatal smoking exposure and adhd symptoms at 6 years: the hokkaido study on environment and children’s health
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028116/
https://www.ncbi.nlm.nih.gov/pubmed/33827680
http://dx.doi.org/10.1186/s13148-021-01063-z
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