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dc.rights.licenseopenen_US
dc.contributor.authorBRIOLLAIS, Laurent
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorRUSTAND, Denis
dc.contributor.authorALLARD, Catherine
dc.contributor.authorWU, Yanyan
dc.contributor.authorXU, Jingxiong
dc.contributor.authorRAJAN, Samyukta Govinda
dc.contributor.authorHIVERT, Marie France
dc.contributor.authorDOYON, Myriam
dc.contributor.authorBOUCHARD, Luigi
dc.contributor.authorMCGOWAN, Patrick O.
dc.contributor.authorMATTHEWS, Steven
dc.contributor.authorLYE, Steven
dc.date.accessioned2022-01-19T09:30:57Z
dc.date.available2022-01-19T09:30:57Z
dc.date.issued2021-12-22
dc.identifier.issn1868-7075en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124434
dc.description.abstractEnBACKGROUND: The role of breastfeeding in modulating epigenetic factors has been suggested as a possible mechanism conferring its benefits on child development but it lacks evidence. Using extensive DNA methylation data from the ALSPAC child cohort, we characterized the genome-wide landscape of DNA methylation variations associated with the duration of exclusive breastfeeding and assessed whether these variations mediate the association between exclusive breastfeeding and BMI over different epochs of child growth. RESULTS: Exclusive breastfeeding elicits more substantial DNA methylation variations during infancy than at other periods of child growth. At the genome-wide level, 13 CpG sites in girls (miR-21, SNAPC3, ATP6V0A1, DHX15/PPARGC1A, LINC00398/ALOX5AP, FAM238C, NATP/NAT2, CUX1, TRAPPC9, OSBPL1A, ZNF185, FAM84A, PDPK1) and 2 CpG sites in boys (IL16 and NREP), mediate the association between exclusive breastfeeding and longitudinal BMI. We found enrichment of CpG sites located within miRNAs and key pathways (AMPK signaling pathway, insulin signaling pathway, endocytosis). Overall DNA methylation variation corresponding to 3 to 5 months of exclusive breastfeeding was associated with slower BMI growth the first 6 years of life compared to no breastfeeding and in a dose-response manner with exclusive breastfeeding duration. CONCLUSIONS: Our study confirmed the early postnatal period as a critical developmental period associated with substantial DNA methylation variations, which in turn could mitigate the development of overweight and obesity from infancy to early childhood. Since an accelerated growth during these developmental periods has been linked to the development of sustained obesity later in life, exclusive breastfeeding could have a major role in preventing the risks of overweight/obesity and children and adults through DNA methylation mechanisms occurring early in life.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enBreastfeeding
dc.subject.enDNA methylation
dc.subject.enMicroRNA
dc.subject.enBMI
dc.subject.enObesity
dc.subject.enMediation
dc.subject.enALSPAC
dc.subject.enChild cohort
dc.subject.enDOHaD
dc.title.enDNA methylation mediates the association between breastfeeding and early-life growth trajectories
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s13148-021-01209-zen_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed34937578en_US
bordeaux.journalClinical Epigeneticsen_US
bordeaux.page231en_US
bordeaux.volume13en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamBiostatisticsen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDWellcome Trusten_US
bordeaux.identifier.funderIDNational Institute of Child Health and Human Developmenten_US
bordeaux.identifier.funderIDNational Institutes of Healthen_US
bordeaux.identifier.funderIDAmerican Diabetes Associationen_US
bordeaux.identifier.funderIDFonds de Recherche du Québec - Santéen_US
bordeaux.identifier.funderIDDiabète Québecen_US
hal.identifierhal-03533953
hal.version1
hal.date.transferred2022-01-19T09:31:01Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Clinical%20Epigenetics&rft.date=2021-12-22&rft.volume=13&rft.issue=1&rft.spage=231&rft.epage=231&rft.eissn=1868-7075&rft.issn=1868-7075&rft.au=BRIOLLAIS,%20Laurent&RUSTAND,%20Denis&ALLARD,%20Catherine&WU,%20Yanyan&XU,%20Jingxiong&rft.genre=article


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