Progression of Parkinson's disease patients' subtypes based on cortical thinning: 4-year follow-up

dc.contributor.authorUribe, Carme
dc.contributor.authorSegura i Fàbregas, Bàrbara
dc.contributor.authorBaggio, Hugo César
dc.contributor.authorAbós, Alexandra
dc.contributor.authorGarcía Díaz, Anna I.
dc.contributor.authorCampabadal Delgado, Anna
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.accessioned2020-05-20T12:46:26Z
dc.date.available2020-05-20T12:46:26Z
dc.date.issued2019-05-11
dc.date.updated2020-05-20T12:46:26Z
dc.description.abstractBackground. Three cortical atrophy patterns were previously identified in non-demented Parkinson's disease patients using a data-driven approach based on cortical thickness data: i) parieto-temporal pattern of atrophy with worse cognitive performance (pattern 1), ii) occipital and frontal cortical atrophy with younger disease onset (pattern 2), and iii) non-detectable cortical atrophy (pattern 3). We aimed to investigate the evolution of these three patterns over time. Methods. Magnetic resonance imaging and neuropsychological assessment were obtained at baseline and follow-up (3.8±0.4 year apart) in a group of 45 Parkinson's disease patients and 22 healthy controls. FreeSurfer was used for cortical thickness analysis and global atrophy measures. Results. Temporo-parietal cortical thinning occurred in pattern 2, 3 and controls groups, and patients showed decline in processing speed (as measured by the Stroop Word-Color test, the Symbol Digits Modalities test and the Trail Making Test Part B) and in semantic fluency (animals). Pattern 3 patients showed more progressive cortical thinning in the left prefrontal cortex than controls and more right occipital thinning than pattern 2 patients over time. Pattern 1 patients had greater compromise in activities of the daily living and suffered higher attrition rate. Conclusion. The Parkinson's disease phenotypes identified using cluster analysis of cortical thickness data showed different progression over time. The presence of prefrontal thinning and younger disease onset at baseline was associated to less cortical degeneration, while non-atrophic patients progressed showing a temporo-parietal cortical thinning.
dc.format.extent33 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec690125
dc.identifier.issn1353-8020
dc.identifier.pmid31103485
dc.identifier.urihttps://hdl.handle.net/2445/161617
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.parkreldis.2019.05.012
dc.relation.ispartofParkinsonism & Related Disorders, 2019, vol. 64, p. 286-292
dc.relation.urihttps://doi.org/10.1016/j.parkreldis.2019.05.012
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationImatges per ressonància magnètica
dc.subject.classificationMalaltia de Parkinson
dc.subject.classificationEscorça cerebral
dc.subject.classificationEnvelliment cerebral
dc.subject.otherMagnetic resonance imaging
dc.subject.otherParkinson's disease
dc.subject.otherCerebral cortex
dc.subject.otherAging brain
dc.titleProgression of Parkinson's disease patients' subtypes based on cortical thinning: 4-year follow-up
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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