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

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...

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Autores principales: Ballarini, Tommaso, Mueller, Karsten, Albrecht, Franziska, Růžička, Filip, Bezdicek, Ondrej, Růžička, Evžen, Roth, Jan, Vymazal, Josef, Jech, Robert, Schroeter, Matthias L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413309/
https://www.ncbi.nlm.nih.gov/pubmed/30558868
http://dx.doi.org/10.1016/j.nicl.2018.101636
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author Ballarini, Tommaso
Mueller, Karsten
Albrecht, Franziska
Růžička, Filip
Bezdicek, Ondrej
Růžička, Evžen
Roth, Jan
Vymazal, Josef
Jech, Robert
Schroeter, Matthias L.
author_facet Ballarini, Tommaso
Mueller, Karsten
Albrecht, Franziska
Růžička, Filip
Bezdicek, Ondrej
Růžička, Evžen
Roth, Jan
Vymazal, Josef
Jech, Robert
Schroeter, Matthias L.
author_sort Ballarini, Tommaso
collection PubMed
description 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.
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spelling pubmed-64133092019-03-21 Regional gray matter changes and age predict individual treatment response in Parkinson's disease Ballarini, Tommaso Mueller, Karsten Albrecht, Franziska Růžička, Filip Bezdicek, Ondrej Růžička, Evžen Roth, Jan Vymazal, Josef Jech, Robert Schroeter, Matthias L. Neuroimage Clin Article 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. Elsevier 2018-12-10 /pmc/articles/PMC6413309/ /pubmed/30558868 http://dx.doi.org/10.1016/j.nicl.2018.101636 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ballarini, Tommaso
Mueller, Karsten
Albrecht, Franziska
Růžička, Filip
Bezdicek, Ondrej
Růžička, Evžen
Roth, Jan
Vymazal, Josef
Jech, Robert
Schroeter, Matthias L.
Regional gray matter changes and age predict individual treatment response in Parkinson's disease
title Regional gray matter changes and age predict individual treatment response in Parkinson's disease
title_full Regional gray matter changes and age predict individual treatment response in Parkinson's disease
title_fullStr Regional gray matter changes and age predict individual treatment response in Parkinson's disease
title_full_unstemmed Regional gray matter changes and age predict individual treatment response in Parkinson's disease
title_short Regional gray matter changes and age predict individual treatment response in Parkinson's disease
title_sort regional gray matter changes and age predict individual treatment response in parkinson's disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413309/
https://www.ncbi.nlm.nih.gov/pubmed/30558868
http://dx.doi.org/10.1016/j.nicl.2018.101636
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