Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis
Low prosocial behavior in childhood has been consistently linked to later psychopathology, with evidence supporting the influence of both genetic and environmental factors on its development. Although neonatal DNA methylation (DNAm) has been found to prospectively associate with a range of psycholog...
| Authors: | , , , , , , , , , , , , , , , , , , , |
|---|---|
| Format: | article |
| Status: | Published version |
| Publication Date: | 2021 |
| Country: | España |
| Institution: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repository: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10230/49256 |
| Online Access: | http://hdl.handle.net/10230/49256 http://dx.doi.org/10.1002/ajmg.b.32862 |
| Access Level: | Open access |
| Keyword: | DNA methylation Cord blood Epigenome-wide association study Meta-analysis Prosocial behavior |
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Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis |
| title |
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis |
| spellingShingle |
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis Luo, Mannan DNA methylation Cord blood Epigenome-wide association study Meta-analysis Prosocial behavior |
| title_short |
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis |
| title_full |
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis |
| title_fullStr |
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis |
| title_full_unstemmed |
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis |
| title_sort |
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysis |
| dc.creator.none.fl_str_mv |
Luo, Mannan Meehan, Alan J. Walton, Esther Röder, Stefan Herberth, Gunda Zenclussen, Ana C. Cosín Tomàs, Marta Sunyer Deu, Jordi Mulder, Rosa H. Cortes Hidalgo, Andrea P. Bakermans-Kranenburg, Marian J. Felix, Janine Frédérique Relton, Caroline Suderman, Matthew Pappa, Irene Kok, Rianne Tiemeier, Henning van IJzendoorn, Marinus H. Barker, Edward D. Cecil, Charlotte A. M. |
| author |
Luo, Mannan |
| author_facet |
Luo, Mannan Meehan, Alan J. Walton, Esther Röder, Stefan Herberth, Gunda Zenclussen, Ana C. Cosín Tomàs, Marta Sunyer Deu, Jordi Mulder, Rosa H. Cortes Hidalgo, Andrea P. Bakermans-Kranenburg, Marian J. Felix, Janine Frédérique Relton, Caroline Suderman, Matthew Pappa, Irene Kok, Rianne Tiemeier, Henning van IJzendoorn, Marinus H. Barker, Edward D. Cecil, Charlotte A. M. |
| author_role |
author |
| author2 |
Meehan, Alan J. Walton, Esther Röder, Stefan Herberth, Gunda Zenclussen, Ana C. Cosín Tomàs, Marta Sunyer Deu, Jordi Mulder, Rosa H. Cortes Hidalgo, Andrea P. Bakermans-Kranenburg, Marian J. Felix, Janine Frédérique Relton, Caroline Suderman, Matthew Pappa, Irene Kok, Rianne Tiemeier, Henning van IJzendoorn, Marinus H. Barker, Edward D. Cecil, Charlotte A. M. |
| author2_role |
author author author author author author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
DNA methylation Cord blood Epigenome-wide association study Meta-analysis Prosocial behavior |
| topic |
DNA methylation Cord blood Epigenome-wide association study Meta-analysis Prosocial behavior |
| description |
Low prosocial behavior in childhood has been consistently linked to later psychopathology, with evidence supporting the influence of both genetic and environmental factors on its development. Although neonatal DNA methylation (DNAm) has been found to prospectively associate with a range of psychological traits in childhood, its potential role in prosocial development has yet to be investigated. This study investigated prospective associations between cord blood DNAm at birth and low prosocial behavior within and across four longitudinal birth cohorts from the Pregnancy And Childhood Epigenetics (PACE) Consortium. We examined (a) developmental trajectories of "chronic-low" versus "typical" prosocial behavior across childhood in a case-control design (N = 2,095), and (b) continuous "low prosocial" scores at comparable cross-cohort time-points (N = 2,121). Meta-analyses were performed to examine differentially methylated positions and regions. At the cohort-specific level, three CpGs were found to associate with chronic low prosocial behavior; however, none of these associations was replicated in another cohort. Meta-analysis revealed no epigenome-wide significant CpGs or regions. Overall, we found no evidence for associations between DNAm patterns at birth and low prosocial behavior across childhood. Findings highlight the importance of employing multi-cohort approaches to replicate epigenetic associations and reduce the risk of false positive discoveries. |
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2021 |
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2021 2021 2021 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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http://hdl.handle.net/10230/49256 http://dx.doi.org/10.1002/ajmg.b.32862 |
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http://hdl.handle.net/10230/49256 http://dx.doi.org/10.1002/ajmg.b.32862 |
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Inglés |
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Inglés |
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Am J Med Genet B Neuropsychiatr Genet. 2021;186(4):228-41 info:eu-repo/grantAgreement/EC/FP7/261357 info:eu-repo/grantAgreement/EC/FP7/308333 info:eu-repo/grantAgreement/EC/FP7/603794 info:eu-repo/grantAgreement/EC/H2020/634453 info:eu-repo/grantAgreement/EC/FP7/268479 info:eu-repo/grantAgreement/EC/H2020/669249 info:eu-repo/grantAgreement/EC/H2020/707404 info:eu-repo/grantAgreement/EC/H2020/848158 info:eu-repo/grantAgreement/ES/3PN/SAF2012-32991 |
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http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
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openAccess |
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Wiley |
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Wiley |
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reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Neonatal DNA methylation and childhood low prosocial behavior: An epigenome-wide association meta-analysisLuo, MannanMeehan, Alan J.Walton, EstherRöder, StefanHerberth, GundaZenclussen, Ana C.Cosín Tomàs, MartaSunyer Deu, JordiMulder, Rosa H.Cortes Hidalgo, Andrea P.Bakermans-Kranenburg, Marian J.Felix, Janine FrédériqueRelton, CarolineSuderman, MatthewPappa, IreneKok, RianneTiemeier, Henningvan IJzendoorn, Marinus H.Barker, Edward D.Cecil, Charlotte A. M.DNA methylationCord bloodEpigenome-wide association studyMeta-analysisProsocial behaviorLow prosocial behavior in childhood has been consistently linked to later psychopathology, with evidence supporting the influence of both genetic and environmental factors on its development. Although neonatal DNA methylation (DNAm) has been found to prospectively associate with a range of psychological traits in childhood, its potential role in prosocial development has yet to be investigated. This study investigated prospective associations between cord blood DNAm at birth and low prosocial behavior within and across four longitudinal birth cohorts from the Pregnancy And Childhood Epigenetics (PACE) Consortium. We examined (a) developmental trajectories of "chronic-low" versus "typical" prosocial behavior across childhood in a case-control design (N = 2,095), and (b) continuous "low prosocial" scores at comparable cross-cohort time-points (N = 2,121). Meta-analyses were performed to examine differentially methylated positions and regions. At the cohort-specific level, three CpGs were found to associate with chronic low prosocial behavior; however, none of these associations was replicated in another cohort. Meta-analysis revealed no epigenome-wide significant CpGs or regions. Overall, we found no evidence for associations between DNAm patterns at birth and low prosocial behavior across childhood. Findings highlight the importance of employing multi-cohort approaches to replicate epigenetic associations and reduce the risk of false positive discoveries.The epigenetic studies in INMA were mainly funded by grants from Instituto de Salud Carlos III (Red INMA G03/176, CB06/02/0041, CP18/00018), Spanish Ministry of Health (FIS-PI04/1436, FIS-PI08/1151 including FEDER funds, FIS-PI11/00610, FIS-FEDER-PI06/0867, FIS-FEDER-PI03-1615), Generalitat de Catalunya-CIRIT 1999SGR 00241, Fundació La marató de TV3 (090430), EU Commission (261357-MeDALL: Mechanisms of the Development of ALLergy), and European Research Council (268479-BREATHE: BRain dEvelopment and Air polluTion ultrafine particles in scHool childrEn). MCT is funded by a Juan de la Cierva—Formación Postdoctoral Contract awarded by Ministry of Science and Innovation (FJC2018-036335-I). The 4, 7, and 11 year follow-up visits was funded by grants from Instituto de Salud Carlos III (Red INMA G03/176; CB06/02/0041; PI041436; PI081151 incl. FEDER funds; PI12/01890 incl. FEDER funds; CP13/00054 incl. FEDER funds; PI15/00118 incl. FEDER funds; CP16/00128 incl. FEDER funds; PI16/00118 incl. FEDER funds; PI16/00261 incl. FEDER funds; PI18/00547 incl. FEDER funds), CIBERESP, Generalitat de Catalunya-CIRIT 1999SGR 00241, Generalitat de Catalunya-AGAUR (2009 SGR 501, 2014 SGR 822), Fundació La marató de TV3 (090430), Spanish Ministry of Economy and Competitiveness (SAF2012-32991 incl. FEDER funds), Agence Nationale de Securite Sanitaire de l'Alimentation de l'Environnement et du Travail (1262C0010; EST-2016 RF-21), EU Commission (261357, 308333, 603794 and 634453). We acknowledge support from the Spanish Ministry of Science and Innovation and State Research Agency through the “Centro de Excelencia Severo Ochoa 2019-2023” Program (CEX2018-000806-S), and support from the Generalitat de Catalunya through the CERCA Program.Wiley202120212021info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/49256http://dx.doi.org/10.1002/ajmg.b.32862reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésAm J Med Genet B Neuropsychiatr Genet. 2021;186(4):228-41info:eu-repo/grantAgreement/EC/FP7/261357info:eu-repo/grantAgreement/EC/FP7/308333info:eu-repo/grantAgreement/EC/FP7/603794info:eu-repo/grantAgreement/EC/H2020/634453info:eu-repo/grantAgreement/EC/FP7/268479info:eu-repo/grantAgreement/EC/H2020/669249info:eu-repo/grantAgreement/EC/H2020/707404info:eu-repo/grantAgreement/EC/H2020/848158info:eu-repo/grantAgreement/ES/3PN/SAF2012-32991© 2021 The Authors. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics published by Wiley Periodicals LLC. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.http://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:10230/492562026-05-29T05:05:01Z |
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15,81155 |