Patterns of cortical thinning in nondemented Parkinson's disease patients

dc.contributor.authorUribe, Carme
dc.contributor.authorSegura i Fàbregas, Bàrbara
dc.contributor.authorBaggio, Hugo César
dc.contributor.authorAbós, Alexandra
dc.contributor.authorMartí Domènech, Ma. Josep
dc.contributor.authorValldeoriola Serra, Francesc
dc.contributor.authorCompta, Yaroslau
dc.contributor.authorBargalló Alabart, Núria​
dc.contributor.authorJunqué i Plaja, Carme, 1955-
dc.date.accessioned2020-05-19T15:42:13Z
dc.date.available2020-05-19T15:42:13Z
dc.date.issued2016-05
dc.date.updated2020-05-19T15:42:13Z
dc.description.abstractBackground: Clinical variability in the Parkinson's disease phenotype suggests the existence of disease subtypes. We investigated whether distinct anatomical patterns of atrophy can be identified in Parkinson's disease using a hypothesis-free, datadriven approach based on cortical thickness data. Methods: T1-weighted 3-tesla MRI and a comprehensive neuropsychological assessment were performed in a sample of 88 nondemented Parkinson's disease patients and 31 healthy controls. We performed a hierarchical cluster analysis of imaging data using Ward's linkage method. A general linear model with cortical thickness data was used to compare clustering groups. Results: We observed 3 patterns of cortical thinning in patients when compared with healthy controls. Pattern 1 (n530, 34.09%) consisted of cortical atrophy in bilateral precentral gyrus, inferior and superior parietal lobules, cuneus, posterior cingulate, and parahippocampal gyrus. These patients showed worse cognitive performance when compared with controls and the other 2 patterns. Pattern 2 (n529, 32.95%) consisted of cortical atrophy involving occipital and frontal as well as superior parietal areas and included patients with younger age at onset. Finally, in pattern 3 (n529, 32.95%), there was no detectable cortical thinning. Patients in the 3 patterns did not differ in disease duration, motor severity, dopaminergic medication doses, or presence of mild cognitive impairment. Conclusions: Three cortical atrophy subtypes were identified in nondemented Parkinson's disease patients: (1) parieto-temporal pattern of atrophy with worse cognitive performance, (2) occipital and frontal cortical atrophy and younger disease onset, and (3) patients without detectable cortical atrophy. These findings may help identify prognosis markers in Parkinson's disease. VC 2016 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec662915
dc.identifier.issn0885-3185
dc.identifier.pmid27094093
dc.identifier.urihttps://hdl.handle.net/2445/161344
dc.language.isoeng
dc.publisherWiley
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1002/mds.26590
dc.relation.ispartofMovement Disorders, 2016, vol. 31, num. 5, p. 699-708
dc.relation.urihttps://doi.org/10.1002/mds.26590
dc.rightscc-by (c) International Parkinson and Movement Disorder Society, 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/es
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationMalaltia de Parkinson
dc.subject.classificationMalalties neurodegeneratives
dc.subject.classificationAnàlisi de conglomerats
dc.subject.otherParkinson's disease
dc.subject.otherNeurodegenerative Diseases
dc.subject.otherCluster analysis
dc.titlePatterns of cortical thinning in nondemented Parkinson's disease patients
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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