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dc.contributor.authorBrandkvist, Maria Charlotta
dc.contributor.authorBjørngaard, Johan Håkon
dc.contributor.authorØdegård, Rønnaug
dc.contributor.authorÅsvold, Bjørn Olav
dc.contributor.authorSmith, George Davey
dc.contributor.authorBrumpton, Ben Michael
dc.contributor.authorHveem, Kristian
dc.contributor.authorRichardson, Tom G.
dc.contributor.authorVie, Gunnhild Åberge
dc.date.accessioned2021-03-08T12:51:54Z
dc.date.available2021-03-08T12:51:54Z
dc.date.created2021-01-18T20:59:01Z
dc.date.issued2020
dc.identifier.issn0964-6906
dc.identifier.urihttps://hdl.handle.net/11250/2732186
dc.description.abstractFrom a life-course perspective, genetic and environmental factors driving childhood obesity may have a lasting inf luence on health later in life. However, how obesity trajectories vary throughout the life-course remains unknown. Recently, Richardson et al. created powerful early life and adult gene scores for body mass index (BMI) in a comprehensive attempt to Downloaded from https://academic.oup.com/hmg/article/29/24/3966/6020202 by guest on 05 March 2021 Human Molecular Genetics, 2020, Vol. 29, No. 24 3967 separate childhood and adult obesity. The childhood score was derived using questionnaire-based data administered to adults aged 40–69 regarding their relative body size at age 10, making it prone to recall and misclassification bias. We therefore attempted to validate the childhood and adult scores using measured BMI data in adolescence and adulthood among 66 963 individuals from the HUNT Study in Norway from 1963 to 2019. The predictive performance of the childhood score was better in adolescence and early adulthood, whereas the predictive performance of the adult score was better in adulthood. In the age group 12–15.9 years, the variance explained by the childhood polygenic risk score (PRS) was 6.7% versus 2.4% for the adult PRS. In the age group 24–29.9 years, the variance explained by the adult PRS was 3.9% versus 3.6% for the childhood PRS. Our findings support that genetic factors driving BMI differ at young age and in adulthood. Within the framework of multivariable Mendelian randomization, the validated childhood gene score can now be used to determine the consequence of childhood obesity on later disease.en_US
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.relation.urihttps://watermark.silverchair.com/ddaa256.pdf?token=AQECAHi208BE49Ooan9kkhW_Ercy7Dm3ZL_9Cf3qfKAc485ysgAAArIwggKuBgkqhkiG9w0BBwagggKfMIICmwIBADCCApQGCSqGSIb3DQEHATAeBglghkgBZQMEAS4wEQQMdEwGDOYM6pDtGH-J
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleSeparating the genetics of childhood and adult obesity: a validation study of genetic scores for body mass index in adolescence and adulthood in the HUNT Studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.journalHuman Molecular Geneticsen_US
dc.identifier.doi10.1093/hmg/ddaa256
dc.identifier.cristin1873720
dc.relation.projectNorges forskningsråd: 295989en_US
dc.relation.projectNorges forskningsråd: 250335en_US
dc.description.localcode© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
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