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dc.date.accessioned2023-02-09T18:05:42Z
dc.date.available2023-02-09T18:05:42Z
dc.date.created2021-05-09T13:18:30Z
dc.date.issued2021
dc.identifier.citationRoe, James Michael Vidal-Piñeiro, Didac Sørensen, Øystein Brandmaier, Andreas M. Düzel, Sandra Gonzalez, Hector A. Kievit, Rogier A. Knights, Ethan Kühn, Simone Lindenberger, Ulman Mowinckel, Athanasia Monika Nyberg, Lars Park, Denise C. Pudas, Sara Rundle, Melissa M. Walhovd, Kristine B Fjell, Anders Martin Westerhausen, Rene . Asymmetric thinning of the cerebral cortex across the adult lifespan is accelerated in Alzheimer’s disease. Nature Communications. 2021, 12:721, 1-11
dc.identifier.urihttp://hdl.handle.net/10852/99846
dc.description.abstractAbstract Aging and Alzheimer’s disease (AD) are associated with progressive brain disorganization. Although structural asymmetry is an organizing feature of the cerebral cortex it is unknown whether continuous age- and AD-related cortical degradation alters cortical asymmetry. Here, in multiple longitudinal adult lifespan cohorts we show that higher-order cortical regions exhibiting pronounced asymmetry at age ~20 also show progressive asymmetry-loss across the adult lifespan. Hence, accelerated thinning of the (previously) thicker homotopic hemisphere is a feature of aging. This organizational principle showed high consistency across cohorts in the Lifebrain consortium, and both the topological patterns and temporal dynamics of asymmetry-loss were markedly similar across replicating samples. Asymmetry-change was further accelerated in AD. Results suggest a system-wide dedifferentiation of the adaptive asymmetric organization of heteromodal cortex in aging and AD.
dc.languageEN
dc.publisherNature Portfolio
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleAsymmetric thinning of the cerebral cortex across the adult lifespan is accelerated in Alzheimer’s disease
dc.title.alternativeENEngelskEnglishAsymmetric thinning of the cerebral cortex across the adult lifespan is accelerated in Alzheimer’s disease
dc.typeJournal article
dc.creator.authorRoe, James Michael
dc.creator.authorVidal-Piñeiro, Didac
dc.creator.authorSørensen, Øystein
dc.creator.authorBrandmaier, Andreas M.
dc.creator.authorDüzel, Sandra
dc.creator.authorGonzalez, Hector A.
dc.creator.authorKievit, Rogier A.
dc.creator.authorKnights, Ethan
dc.creator.authorKühn, Simone
dc.creator.authorLindenberger, Ulman
dc.creator.authorMowinckel, Athanasia Monika
dc.creator.authorNyberg, Lars
dc.creator.authorPark, Denise C.
dc.creator.authorPudas, Sara
dc.creator.authorRundle, Melissa M.
dc.creator.authorWalhovd, Kristine B
dc.creator.authorFjell, Anders Martin
dc.creator.authorWesterhausen, Rene
cristin.unitcode185,17,5,0
cristin.unitnamePsykologisk institutt
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1908977
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Nature Communications&rft.volume=12:721&rft.spage=1&rft.date=2021
dc.identifier.jtitleNature Communications
dc.identifier.volume12
dc.identifier.issue1
dc.identifier.doihttps://doi.org/10.1038/s41467-021-21057-y
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2041-1723
dc.type.versionPublishedVersion
cristin.articleid721
dc.relation.projectEC/H2020/732592
dc.relation.projectSIGMA2/NS9084S
dc.relation.projectSIGMA2/NS9737S
dc.relation.projectNFR/262453
dc.relation.projectNFR/249931
dc.relation.projectEU/283634
dc.relation.projectNFR/301395
dc.relation.projectEU/725025
dc.relation.projectEU/313440


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