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dc.contributor.authorMaglanoc, Luigi Angelo
dc.contributor.authorKaufmann, Tobias
dc.contributor.authorvan der Meer, Dennis
dc.contributor.authorMarquand, André F.
dc.contributor.authorWolfers, Thomas
dc.contributor.authorJonassen, Rune
dc.contributor.authorHilland, Eva
dc.contributor.authorAndreassen, Ole Andreas
dc.contributor.authorLandrø, Nils Inge
dc.contributor.authorWestlye, Lars Tjelta
dc.date.accessioned2019-12-03T09:55:16Z
dc.date.accessioned2019-12-06T10:09:30Z
dc.date.available2019-12-03T09:55:16Z
dc.date.available2019-12-06T10:09:30Z
dc.date.issued2019-10-18
dc.identifier.citationMaglanoc LA, Kaufmann T, van der Meer D, Marquand AF, Wolfers T, Jonassen R, Hilland E, Andreassen OA, Landrø NI, Westlye LT. Brain connectome mapping of complex human traits and their polygenic architecture using machine learning. Biological Psychiatry. 2019en
dc.identifier.issn0006-3223
dc.identifier.issn0006-3223
dc.identifier.issn1873-2402
dc.identifier.urihttps://hdl.handle.net/10642/7871
dc.description.abstractBackground: Mental disorders and individual characteristics such as intelligence and personality are complex traits sharing a largely unknown neuronal basis. Their genetic architectures are highly polygenic and overlapping, which is supported by heterogeneous phenotypic expression and substantial clinical overlap. Brain network analysis provides a non-invasive means of dissecting biological heterogeneity yet its sensitivity, specificity and validity in assessing individual characteristics relevant for brain function and mental health and their genetic underpinnings in clinical applications remains a challenge. Methods: In a machine learning approach, we predicted individual scores for educational attainment, fluid intelligence and dimensional measures of depression, anxiety and neuroticism using fMRI-based static and dynamic temporal synchronization between large-scale brain network nodes in 10,343 healthy individuals from the UK Biobank. In addition to age and sex to serve as our reference point, we also predicted individual polygenic scores for related phenotypes, and 13 different neuroticism traits and schizophrenia. Results: Beyond high accuracy for age and sex, supporting the biological sensitivity of the connectome-based features, permutation tests revealed above chance-level prediction accuracy for trait-level educational attainment and fluid intelligence. Educational attainment and fluid intelligence were mainly negatively associated with static brain connectivity in frontal and default mode networks, whereas age showed positive correlations with a more widespread pattern. In contrast, prediction accuracy was at chance level for depression, anxiety, neuroticism and polygenic scores across traits. Conclusion: These novel findings provide a benchmark for future studies linking the genetic architecture of individual and mental health traits with fMRI-based brain connectomics.en
dc.description.sponsorshipThe authors were funded by the Research Council of Norway (213837, 223723, 229129, 204966, 249795), the South-Eastern Norway Regional Health Authority (2014097, 2015073, 2016083, 2017112), the European Research Council under the European Union’s Horizon 2020 research and innovation program (ERC StG, Grant 802998), the Department of Psychology, University of Oslo and the KG Jebsen Stiftelsen.en
dc.language.isoenen
dc.publisherElsevieren
dc.relation.ispartofseriesBiological Psychiatry;Available online 29 October 2019
dc.relation.urihttps://doi.org/10.1016/j.biopsych.2019.10.011
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectfMRIen
dc.subjectFunctional connectivityen
dc.subjectHuman traitsen
dc.subjectPolygenic scoresen
dc.subjectMachine learningen
dc.subjectBrain networksen
dc.titleBrain connectome mapping of complex human traits and their polygenic architecture using machine learningen
dc.title.alternativeConnectome mapping of human traits and genetics
dc.typeJournal articleen
dc.typePeer revieweden
dc.date.updated2019-12-03T09:55:16Z
dc.description.versionacceptedVersionen
dc.identifier.doihttps://dx.doi.org/10.1016/j.biopsych.2019.10.011
dc.identifier.cristin1755555
dc.source.journalBiological Psychiatry
dc.relation.projectIDNotur/NorStore NS9114K
dc.relation.projectIDNotur/NorStore NS9666S


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© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0
license http://creativecommons.org/licenses/by-nc-nd/4.0/
Med mindre annet er angitt, så er denne innførselen lisensiert som © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/