DNA methylation links prenatal smoking exposure to later life health outcomes in offspring
dc.contributor.author | Wiklund, Petri | |
dc.contributor.author | Karhunen, Ville | |
dc.contributor.author | Richmond, Rebecca C. | |
dc.contributor.author | Parmar, Priyanka | |
dc.contributor.author | Rodriguez, Alina | |
dc.contributor.author | De Silva, Maneka | |
dc.contributor.author | Wielscher, Matthias | |
dc.contributor.author | Rezwan, Faisal I. | |
dc.contributor.author | Richardson, Tom G. | |
dc.contributor.author | Veijola, Juha | |
dc.contributor.author | Herzig, Karl-Heinz | |
dc.contributor.author | Holloway, John W. | |
dc.contributor.author | Relton, Caroline L. | |
dc.contributor.author | Sebert, Sylvain | |
dc.contributor.author | Järvelin, Marjo-Riitta | |
dc.date.accessioned | 2019-07-25T05:40:29Z | |
dc.date.available | 2019-07-25T05:40:29Z | |
dc.date.issued | 2019 | |
dc.identifier.citation | Wiklund, P., Karhunen, V., Richmond, R. C., Parmar, P., Rodriguez, A., De Silva, M., Wielscher, M., Rezwan, F. I., Richardson, T. G., Veijola, J., Herzig, K.-H., Holloway, J. W., Relton, C. L., Sebert, S., & Järvelin, M.-R. (2019). DNA methylation links prenatal smoking exposure to later life health outcomes in offspring. <i>Clinical Epigenetics</i>, <i>11</i>, Article 97. <a href="https://doi.org/10.1186/s13148-019-0683-4" target="_blank">https://doi.org/10.1186/s13148-019-0683-4</a> | |
dc.identifier.other | CONVID_32133109 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/65110 | |
dc.description.abstract | Background: Maternal smoking during pregnancy is associated with adverse offspring health outcomes across their life course. We hypothesize that DNA methylation is a potential mediator of this relationship. Methods: We examined the association of prenatal maternal smoking with offspring blood DNA methylation in 2821 individuals (age 16 to 48 years) from five prospective birth cohort studies and perform Mendelian randomization and mediation analyses to assess whether methylation markers have causal effects on disease outcomes in the offspring. Results: We identify 69 differentially methylated CpGs in 36 genomic regions (P value < 1 × 10−7) associated with exposure to maternal smoking in adolescents and adults. Mendelian randomization analyses provided evidence for a causal role of four maternal smoking-related CpG sites on an increased risk of inflammatory bowel disease or schizophrenia. Further mediation analyses showed some evidence of cg25189904 in GNG12 gene mediating the effect of exposure to maternal smoking on schizophrenia-related outcomes. Conclusions: DNA methylation may represent a biological mechanism through which maternal smoking is associated with increased risk of psychiatric morbidity in the exposed offspring. | en |
dc.format.mimetype | application/pdf | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | Biomed Central | |
dc.relation.ispartofseries | Clinical Epigenetics | |
dc.rights | CC BY 4.0 | |
dc.subject.other | causality | |
dc.subject.other | DNA methylation | |
dc.subject.other | disease | |
dc.subject.other | life course | |
dc.subject.other | maternal smoking | |
dc.subject.other | mediation | |
dc.subject.other | persistence | |
dc.subject.other | pregnancy | |
dc.title | DNA methylation links prenatal smoking exposure to later life health outcomes in offspring | |
dc.type | research article | |
dc.identifier.urn | URN:NBN:fi:jyu-201907253673 | |
dc.contributor.laitos | Liikuntatieteellinen tiedekunta | fi |
dc.contributor.laitos | Faculty of Sport and Health Sciences | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.relation.issn | 1868-7075 | |
dc.relation.volume | 11 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © The Author(s) 2019 | |
dc.rights.accesslevel | openAccess | fi |
dc.type.publication | article | |
dc.subject.yso | kausaliteetti | |
dc.subject.yso | terveysvaikutukset | |
dc.subject.yso | DNA-metylaatio | |
dc.subject.yso | kohorttitutkimus | |
dc.subject.yso | raskaus | |
dc.subject.yso | tupakointi | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p333 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p15449 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p38350 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p25606 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p8749 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p10017 | |
dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
dc.relation.doi | 10.1186/s13148-019-0683-4 | |
jyx.fundinginformation | This project was supported by the Academy of Finland EGEA-project (285547), Biocenter, University of Oulu, Finland (75617), NHLBI grant 5R01HL087679-02 through the STAMPEED program (1RL1MH083268-01), ERDF European Regional Development Fund grant no. 539/2010 A31592, the EU H2020--PHC-2014 DynaHEALTH action (grant agreements no. 633595), EU H2020-HCO-2004 iHEALTH Action (grant agreement 643774), EU H2020-PHC-2014 ALEC Action (grant agreement no. 633212), EU H2020-SC1-2016-2017 LifeCycle Action (grant agreement no. 733206), EU H2020-MSCA-ITN-2016 CAPICE Action (grant agreement 721567) and MRC grant no. MR/M013138/1. | |
dc.type.okm | A1 |
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