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dc.contributor.authorSillanpää, Elina
dc.contributor.authorOllikainen, Miina
dc.contributor.authorKaprio, Jaakko
dc.contributor.authorWang, Xiaoling
dc.contributor.authorLeskinen, Tuija
dc.contributor.authorKujala, Urho
dc.contributor.authorTörmäkangas, Timo
dc.date.accessioned2019-01-23T09:24:26Z
dc.date.available2019-01-23T09:24:26Z
dc.date.issued2019
dc.identifier.citationSillanpää, E., Ollikainen, M., Kaprio, J., Wang, X., Leskinen, T., Kujala, U., & Törmäkangas, T. (2019). Leisure-time physical activity and DNA methylation age : a twin study. <i>Clinical Epigenetics</i>, <i>11</i>(1), Article 12. <a href="https://doi.org/10.1186/s13148-019-0613-5" target="_blank">https://doi.org/10.1186/s13148-019-0613-5</a>
dc.identifier.otherCONVID_28880891
dc.identifier.otherTUTKAID_80429
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/62600
dc.description.abstractBackground: Epigenetic clocks may increase our understanding on human aging and how genetic and environmental factors regulate an individual aging process. One of the most promising clocks is Horvath’s DNA methylation (DNAm) age. Age acceleration, i.e., discrepancy between DNAm age and chronological age, tells us whether the person is biologically young or old compared to his/her chronological age. Several environmental and lifestyle factors have been shown to affect life span. We investigated genetic and environmental predictors of DNAm age in young and older monozygotic (MZ) and dizygotic (DZ) twins with a focus on leisure time physical activity. Results: Quantitative genetic modeling revealed that the relative contribution of non-shared environmental factors was larger among older compared with younger twin pairs [47% (95% CI 35, 63) vs. 26% (95% CI: 19, 35), p < 0.001]. Correspondingly, genetic variation accounted for less of the variance in older [53% (95% CI 37, 65)] compared with younger pairs [74% (95% CI 65, 82)]. We tested the hypothesis that leisure time physical activity is one of the non-shared environmental factors that affect epigenetic aging. A co-twin control analysis with older same-sex twin pairs (seven MZ and nine DZ pairs, mean age 60.4 years) who had persistent discordance in physical activity for 32 years according to reported/interviewed physical-activity data showed no differences among active and inactive co-twins, DNAm age being 60.7 vs. 61.8 years, respectively [between-group mean-difference: − 1.17 (95%CI − 3.43,1.10)]. Results from the younger cohort of twins supported findings that LTPA is not associated with DNAm age acceleration. Conclusions: In older subjects, a larger amount of variance in DNAm age acceleration was explained by non-shared environmental factors compared to young individuals. However, leisure time physical activity during adult years has at most a minor effect on DNAm age acceleration. This is consistent with recent findings that long-term leisure time physical activity in adulthood has little effect on mortality after controlling for genetic factors.fi
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.ispartofseriesClinical Epigenetics
dc.rightsCC BY 4.0
dc.subject.otherepigenetic clock
dc.subject.othermethylation
dc.subject.othertwin design
dc.subject.otherphysical activity
dc.titleLeisure-time physical activity and DNA methylation age : a twin study
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201901221273
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.oppiaineLiikuntalääketiedefi
dc.contributor.oppiaineGerontologia ja kansanterveysfi
dc.contributor.oppiaineGerontologian tutkimuskeskusfi
dc.contributor.oppiaineHyvinvoinnin tutkimuksen yhteisöfi
dc.contributor.oppiaineSports and Exercise Medicineen
dc.contributor.oppiaineGerontology and Public Healthen
dc.contributor.oppiaineGerontology Research Centeren
dc.contributor.oppiaineSchool of Wellbeingen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2019-01-22T16:15:05Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn1868-7075
dc.relation.numberinseries1
dc.relation.volume11
dc.type.versionpublishedVersion
dc.rights.copyright© The Author(s) 2019.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber286536
dc.subject.ysokvantitatiivinen genetiikka
dc.subject.ysofyysinen aktiivisuus
dc.subject.ysoepigenetiikka
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p12523
jyx.subject.urihttp://www.yso.fi/onto/yso/p23102
jyx.subject.urihttp://www.yso.fi/onto/yso/p24631
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1186/s13148-019-0613-5
dc.relation.funderSuomen Akatemiafi
dc.relation.funderResearch Council of Finlanden
jyx.fundingprogramTutkijatohtori, SAfi
jyx.fundingprogramPostdoctoral Researcher, AoFen
jyx.fundinginformationThis work was supported by the Academy of Finland [260001 to ES, 213506, 265240, 263278 to JK, 251316, 286536 to TT, and 297908 to MO], EC FP5 GenomEUtwin (JK), NIH NIH/NHLBI (grant HL104125), EC MC ITN Project EPITRAIN (JK & MO) project and the University of Helsinki Research Funds to MO, Sigrid Juselius Foundation to MO, Yrjö Jahnsson foundation (6868) and Juho Vainio foundation to ES. TWINACTIVE study was supported by the Finnish Ministry of Education and Culture (UMK), Academy of Finland (UMK), and Juho Vainio Foundation (UMK).
dc.type.okmA1


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