Regional gray matter changes and age predict individual treatment response in Parkinson's disease.


Journal

NeuroImage. Clinical
ISSN: 2213-1582
Titre abrégé: Neuroimage Clin
Pays: Netherlands
ID NLM: 101597070

Informations de publication

Date de publication:
2019
Historique:
received: 14 05 2018
revised: 30 08 2018
accepted: 09 12 2018
pubmed: 19 12 2018
medline: 18 12 2019
entrez: 19 12 2018
Statut: ppublish

Résumé

We aimed at testing the potential of biomarkers in predicting individual patient response to dopaminergic therapy for Parkinson's disease. Treatment efficacy was assessed in 30 Parkinson's disease patients as motor symptoms improvement from unmedicated to medicated state as assessed by the Unified Parkinson's Disease Rating Scale score III. Patients were stratified into weak and strong responders according to the individual treatment response. A multiple regression was implemented to test the prediction accuracy of age, disease duration and treatment dose and length. Univariate voxel-based morphometry was applied to investigate differences between the two groups on age-corrected T1-weighted magnetic resonance images. Multivariate support vector machine classification was used to predict individual treatment response based on neuroimaging data. Among clinical data, increasing age predicted a weaker treatment response. Additionally, weak responders presented greater brain atrophy in the left temporoparietal operculum. Support vector machine classification revealed that gray matter density in this brain region, including additionally the supplementary and primary motor areas and the cerebellum, was able to differentiate weak and strong responders with 74% accuracy. Remarkably, age and regional gray matter density of the left temporoparietal operculum predicted both and independently treatment response as shown in a combined regression analysis. In conclusion, both increasing age and reduced gray matter density are valid and independent predictors of dopaminergic therapy response in Parkinson's disease.

Identifiants

pubmed: 30558868
pii: S2213-1582(18)30384-X
doi: 10.1016/j.nicl.2018.101636
pmc: PMC6413309
pii:
doi:

Substances chimiques

Antiparkinson Agents 0
Levodopa 46627O600J

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101636

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Tommaso Ballarini (T)

Max-Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

Karsten Mueller (K)

Max-Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

Franziska Albrecht (F)

Max-Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

Filip Růžička (F)

Department of Neurology, Charles University, First Faculty of Medicine, Prague, Czech Republic; Department of Radiology, Na Homolce Hospital, Prague, Czech Republic.

Ondrej Bezdicek (O)

Department of Neurology, Charles University, First Faculty of Medicine, Prague, Czech Republic.

Evžen Růžička (E)

Department of Neurology, Charles University, First Faculty of Medicine, Prague, Czech Republic.

Jan Roth (J)

Department of Neurology, Charles University, First Faculty of Medicine, Prague, Czech Republic.

Josef Vymazal (J)

Department of Radiology, Na Homolce Hospital, Prague, Czech Republic.

Robert Jech (R)

Department of Neurology, Charles University, First Faculty of Medicine, Prague, Czech Republic; Department of Radiology, Na Homolce Hospital, Prague, Czech Republic.

Matthias L Schroeter (ML)

Max-Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany; Clinic for Cognitive Neurology, University Clinic, Leipzig, Germany; FTLD Consortium, Germany. Electronic address: schroet@cbs.mpg.de.

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