Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep35601
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dc.titleWhite matter microstructural characteristics in newly diagnosed Parkinson's disease: An unbiased whole-brain study
dc.contributor.authorWen M.-C.
dc.contributor.authorHeng H.S.E.
dc.contributor.authorNg S.Y.E.
dc.contributor.authorTan L.C.S.
dc.contributor.authorChan L.L.
dc.contributor.authorTan E.K.
dc.date.accessioned2018-11-26T04:03:44Z
dc.date.available2018-11-26T04:03:44Z
dc.date.issued2016
dc.identifier.citationWen M.-C., Heng H.S.E., Ng S.Y.E., Tan L.C.S., Chan L.L., Tan E.K. (2016). White matter microstructural characteristics in newly diagnosed Parkinson's disease: An unbiased whole-brain study. Scientific Reports 6 : 35601. ScholarBank@NUS Repository. https://doi.org/10.1038/srep35601
dc.identifier.issn20452322
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/148968
dc.description.abstractParkinson's disease (PD) is a debilitating neurodegenerative disorder. Findings on specific white matter (WM) alterations in PD have been inconsistent. We hypothesized that WM changes occur in early PD patients and unbiased whole-brain analysis may provide additional evidence of pathological WM changes in PD. In this study, we examined various indexes of WM microstructure in newly diagnosed PD patients at the whole-brain level. 64 PDs with Hoehn &Yahr stage 1 (HY1PDs), 87 PDs with Hoehn &Yahr stage 2 (HYPD2s), and 60 controls (HCs) were recruited. Tract-based spatial statistics (TBSS) and diffusion connectometry were used to identify changes of WM pathways associated with PD. There were no significant differences in axial diffusivity, but HY1PDs exhibited greater fractional anisotropy (FA) and decreased mean and radial diffusivities (MD and RD) in callosal, projection, and association fibres than HCs and HY2PDs. Motor severity was inversely correlated with FA, but positively correlated with MD and RD in PD patients. Connectometry analysis also revealed increased WM density in the aforementioned tracts in PD patients, compared with HCs. Our study reveals WM enhancement, suggesting neural compensations in early PD. Longitudinal follow-up studies are warranted to identify the trajectory of WM changes alongside the progression of PD. © 2016 The Author(s).
dc.publisherNature Publishing Group
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1038/srep35601
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page35601
dc.published.statepublished
dc.grant.idTCR12dec010
dc.grant.idSMF
dc.grant.fundingagencyNRF, National Research Foundation Singapore
dc.grant.fundingagencySingapore Millennium Foundation
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