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Brain age prediction using deep learning uncovers associated sequence variants

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dc.contributor Háskóli Íslands
dc.contributor University of Iceland
dc.contributor.author Jónsson, Benedikt Atli
dc.contributor.author Bjornsdottir, Gyda
dc.contributor.author Thorgeirsson, Thorgeir
dc.contributor.author Ellingsen, Lotta María
dc.contributor.author Walters, G. Bragi
dc.contributor.author Gudbjartsson, Daniel
dc.contributor.author Stefansson, Hreinn
dc.contributor.author Stefansson, Kari
dc.contributor.author Ulfarsson, Magnus
dc.date.accessioned 2020-02-10T11:04:46Z
dc.date.available 2020-02-10T11:04:46Z
dc.date.issued 2019-11-27
dc.identifier.citation Jonsson, B.A., Bjornsdottir, G., Thorgeirsson, T.E. et al. Brain age prediction using deep learning uncovers associated sequence variants. Nat Commun 10, 5409 (2019). https://doi.org/10.1038/s41467-019-13163-9
dc.identifier.issn 2041-1723
dc.identifier.uri https://hdl.handle.net/20.500.11815/1517
dc.description Publisher's version (útgefin grein).
dc.description.abstract Machine learning algorithms can be trained to estimate age from brain structural MRI. The difference between an individual’s predicted and chronological age, predicted age difference (PAD), is a phenotype of relevance to aging and brain disease. Here, we present a new deep learning approach to predict brain age from a T1-weighted MRI. The method was trained on a dataset of healthy Icelanders and tested on two datasets, IXI and UK Biobank, utilizing transfer learning to improve accuracy on new sites. A genome-wide association study (GWAS) of PAD in the UK Biobank data (discovery set: N= 12378 , replication set: N= 4456) yielded two sequence variants, rs1452628-T (β= − 0.08 , P= 1.15 × 10 − 9) and rs2435204-G (β= 0.102 , P= 9.73 × 1 0 − 12). The former is near KCNK2 and correlates with reduced sulcal width, whereas the latter correlates with reduced white matter surface area and tags a well-known inversion at 17q21.31 (H2).
dc.description.sponsorship This research has been conducted using the UK Biobank Resource under Application Number 24898. The research leading to these results has received support from the Innovative Medicines Initiative Joint Undertaking under grant agreements no. 115008 (NEWMEDS) and no. 115300 (EUAIMS), of which resources are composed of EFPIA in-kind contribution and financial contribution from the European Union’s Seventh Framework Programme (EU-FP7/2007-2013). The financial support from the European Commission to the NeuroPain project (FP7#HEALTH-2013-602891-2) is acknowledged. The authors are grateful to the participants, and we thank the research nurses and staff at the Recruitment centre (Þjónustumiðstöð rannsóknarverkefna).
dc.format.extent 5409
dc.language.iso en
dc.publisher Springer Science and Business Media LLC
dc.relation info:eu-repo/grantAgreement/EC/FP7/HEALTH-2013-602891-2
dc.relation.ispartofseries Nature Communications;10(1)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Heilinn
dc.subject Öldrun
dc.subject Erfðarannsóknir
dc.title Brain age prediction using deep learning uncovers associated sequence variants
dc.type info:eu-repo/semantics/article
dcterms.license Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/ licenses/by/4.0/.
dc.description.version Peer Reviewed
dc.identifier.journal Nature Communications
dc.identifier.doi 10.1038/s41467-019-13163-9


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