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Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age

The aim of this study was to identify placental DNA methylation (DNAm) variations associated with adiposity at 3 years of age. We quantified placental DNAm using the Infinium MethylationEPIC BeadChips. We assessed associations between DNAm at single-CpGs and skinfold thickness using robust linear re...

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Autores principales: Gagné-Ouellet, Valérie, Breton, Edith, Thibeault, Kathrine, Fortin, Carol-Ann, Desgagné, Véronique, Girard Tremblay, Élise, Cardenas, Andres, Guérin, Renée, Perron, Patrice, Hivert, Marie-France, Bouchard, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582906/
https://www.ncbi.nlm.nih.gov/pubmed/33003475
http://dx.doi.org/10.3390/ijms21197201
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author Gagné-Ouellet, Valérie
Breton, Edith
Thibeault, Kathrine
Fortin, Carol-Ann
Desgagné, Véronique
Girard Tremblay, Élise
Cardenas, Andres
Guérin, Renée
Perron, Patrice
Hivert, Marie-France
Bouchard, Luigi
author_facet Gagné-Ouellet, Valérie
Breton, Edith
Thibeault, Kathrine
Fortin, Carol-Ann
Desgagné, Véronique
Girard Tremblay, Élise
Cardenas, Andres
Guérin, Renée
Perron, Patrice
Hivert, Marie-France
Bouchard, Luigi
author_sort Gagné-Ouellet, Valérie
collection PubMed
description The aim of this study was to identify placental DNA methylation (DNAm) variations associated with adiposity at 3 years of age. We quantified placental DNAm using the Infinium MethylationEPIC BeadChips. We assessed associations between DNAm at single-CpGs and skinfold thickness using robust linear regression models adjusted for gestational age, child’s sex, age at follow-up and cellular heterogeneity. We sought replication of DNAm association with child adiposity in an independent cohort. We quantified placental mRNA levels for annotated gene using qRT-PCR and tested for correlation with DNAm. Lower DNAm at cg22593959 and cg22436429 was associated with higher adiposity (β = −1.18, q = 0.002 and β = −0.82, q = 0.04). The cg22593959 is located in an intergenic region (chr7q31.3), whereas cg22436429 is within the TFAP2E gene (1p34.3). DNAm at cg22593959 and cg22436429 was correlated with mRNA levels at FAM3C (r(s) = −0.279, p = 0.005) and TFAP2E (r(s) = 0.216, p = 0.03). In an independent cohort, the association between placental DNAm at cg22593959 and childhood adiposity was of similar strength and direction (β = −3.8 ± 4.1, p = 0.36), yet non-significant. Four genomic regions were also associated with skinfold thickness within FMN1, MAGI2, SKAP2 and BMPR1B genes. We identified placental epigenetic variations associated with adiposity at 3 years of age suggesting that childhood fat accretion patterns might be established during fetal life.
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spelling pubmed-75829062020-10-28 Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age Gagné-Ouellet, Valérie Breton, Edith Thibeault, Kathrine Fortin, Carol-Ann Desgagné, Véronique Girard Tremblay, Élise Cardenas, Andres Guérin, Renée Perron, Patrice Hivert, Marie-France Bouchard, Luigi Int J Mol Sci Article The aim of this study was to identify placental DNA methylation (DNAm) variations associated with adiposity at 3 years of age. We quantified placental DNAm using the Infinium MethylationEPIC BeadChips. We assessed associations between DNAm at single-CpGs and skinfold thickness using robust linear regression models adjusted for gestational age, child’s sex, age at follow-up and cellular heterogeneity. We sought replication of DNAm association with child adiposity in an independent cohort. We quantified placental mRNA levels for annotated gene using qRT-PCR and tested for correlation with DNAm. Lower DNAm at cg22593959 and cg22436429 was associated with higher adiposity (β = −1.18, q = 0.002 and β = −0.82, q = 0.04). The cg22593959 is located in an intergenic region (chr7q31.3), whereas cg22436429 is within the TFAP2E gene (1p34.3). DNAm at cg22593959 and cg22436429 was correlated with mRNA levels at FAM3C (r(s) = −0.279, p = 0.005) and TFAP2E (r(s) = 0.216, p = 0.03). In an independent cohort, the association between placental DNAm at cg22593959 and childhood adiposity was of similar strength and direction (β = −3.8 ± 4.1, p = 0.36), yet non-significant. Four genomic regions were also associated with skinfold thickness within FMN1, MAGI2, SKAP2 and BMPR1B genes. We identified placental epigenetic variations associated with adiposity at 3 years of age suggesting that childhood fat accretion patterns might be established during fetal life. MDPI 2020-09-29 /pmc/articles/PMC7582906/ /pubmed/33003475 http://dx.doi.org/10.3390/ijms21197201 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gagné-Ouellet, Valérie
Breton, Edith
Thibeault, Kathrine
Fortin, Carol-Ann
Desgagné, Véronique
Girard Tremblay, Élise
Cardenas, Andres
Guérin, Renée
Perron, Patrice
Hivert, Marie-France
Bouchard, Luigi
Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age
title Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age
title_full Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age
title_fullStr Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age
title_full_unstemmed Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age
title_short Placental Epigenome-Wide Association Study Identified Loci Associated with Childhood Adiposity at 3 Years of Age
title_sort placental epigenome-wide association study identified loci associated with childhood adiposity at 3 years of age
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582906/
https://www.ncbi.nlm.nih.gov/pubmed/33003475
http://dx.doi.org/10.3390/ijms21197201
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