Please use this identifier to cite or link to this item: https://doi.org/10.1002/hbm.24928
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dc.titleLongitudinal trajectory of Amyloid-related hippocampal subfield atrophy in nondemented elderly
dc.contributor.authorZhang, L.
dc.contributor.authorMak, E.
dc.contributor.authorReilhac, A.
dc.contributor.authorShim, Hee Y.
dc.contributor.authorNg, K.K.
dc.contributor.authorOng, M.Q.W.
dc.contributor.authorJi, F.
dc.contributor.authorChong, E.J.Y.
dc.contributor.authorXu, X.
dc.contributor.authorWong, Z.X.
dc.contributor.authorStephenson, M.C.
dc.contributor.authorVenketasubramanian, N.
dc.contributor.authorTan, B.Y.
dc.contributor.authorO'Brien, J.T.
dc.contributor.authorZhou, J.H.
dc.contributor.authorChen, C.L.H.
dc.date.accessioned2021-08-10T10:02:14Z
dc.date.available2021-08-10T10:02:14Z
dc.date.issued2020
dc.identifier.citationZhang, L., Mak, E., Reilhac, A., Shim, Hee Y., Ng, K.K., Ong, M.Q.W., Ji, F., Chong, E.J.Y., Xu, X., Wong, Z.X., Stephenson, M.C., Venketasubramanian, N., Tan, B.Y., O'Brien, J.T., Zhou, J.H., Chen, C.L.H. (2020). Longitudinal trajectory of Amyloid-related hippocampal subfield atrophy in nondemented elderly. Human Brain Mapping 41 (8) : 2037-2047. ScholarBank@NUS Repository. https://doi.org/10.1002/hbm.24928
dc.identifier.issn10659471
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/196451
dc.description.abstractHippocampal atrophy and abnormal ?-Amyloid (A?) deposition are established markers of Alzheimer's disease (AD). Nonetheless, longitudinal trajectory of A?-associated hippocampal subfield atrophy prior to dementia remains unclear. We hypothesized that elevated A? correlated with longitudinal subfield atrophy selectively in no cognitive impairment (NCI), spreading to other subfields in mild cognitive impairment (MCI). We analyzed data from two independent longitudinal cohorts of nondemented elderly, including global PET-A? in AD-vulnerable cortical regions and longitudinal subfield volumes quantified with a novel auto-segmentation method (FreeSurfer v.6.0). Moreover, we investigated associations of A?-related progressive subfield atrophy with memory decline. Across both datasets, we found a converging pattern that higher A? correlated with faster CA1 volume decline in NCI. This pattern spread to other hippocampal subfields in MCI group, correlating with memory decline. Our results for the first time suggest a longitudinal focal-to-widespread trajectory of A?-associated hippocampal subfield atrophy over disease progression in nondemented elderly. © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc.
dc.publisherJohn Wiley and Sons Inc
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScopus OA2020
dc.subjecthippocampal subfield atrophy
dc.subjectlongitudinal atrophy trajectory
dc.subjectnondemented elderly
dc.subject?-Amyloid
dc.typeArticle
dc.contributor.departmentDEPT OF PHARMACOLOGY
dc.contributor.departmentDEAN'S OFFICE (MEDICINE)
dc.contributor.departmentDEPT OF MEDICINE
dc.description.doi10.1002/hbm.24928
dc.description.sourcetitleHuman Brain Mapping
dc.description.volume41
dc.description.issue8
dc.description.page2037-2047
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