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Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease

The longitudinal course of ICBs in patients with Parkinson’s disease (PwP) relative to controls has not been explored as of yet. The aim of this study is to determine the frequency, evolution and associated cognitive and clinical features of impulsive and compulsive behaviors (ICBs) over 4 years of...

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Autores principales: Erga, Aleksander H., Alves, Guido, Tysnes, Ole Bjørn, Pedersen, Kenn Freddy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954890/
https://www.ncbi.nlm.nih.gov/pubmed/31628533
http://dx.doi.org/10.1007/s00415-019-09584-7
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author Erga, Aleksander H.
Alves, Guido
Tysnes, Ole Bjørn
Pedersen, Kenn Freddy
author_facet Erga, Aleksander H.
Alves, Guido
Tysnes, Ole Bjørn
Pedersen, Kenn Freddy
author_sort Erga, Aleksander H.
collection PubMed
description The longitudinal course of ICBs in patients with Parkinson’s disease (PwP) relative to controls has not been explored as of yet. The aim of this study is to determine the frequency, evolution and associated cognitive and clinical features of impulsive and compulsive behaviors (ICBs) over 4 years of prospective follow-up in a population-based cohort with early Parkinson’s disease (PD). We recruited 124 cognitively intact participants with early PD and 156 matched controls from the Norwegian ParkWest study. ICBs were assessed using the self-report short form version of the Questionnaire for Impulsive–Compulsive Disorders in PD. Cognitive changes were examined in PwP with and without ICBs who completed the 4-year follow-up. Generalized linear mixed modelling and mixed linear regression were used to analyze clinical factors and cognitive changes associated with ICBs in PwP over time. ICBs were more common in PwP than controls at all visits, with an age-adjusted odds ratio (OR) varying between 2.5 (95% CI 1.1–5.6; p = 0.022) and 5.1 (95% CI 2.4–11.0; p < 0.001). The 4-year cumulative frequency of ICBs in PwP was 46.8% and 23.3% developed incident ICBs during the study period, but the presence of ICBs was non-persistent in nearly 30%. ICBs were independently associated with younger age (OR 0.95, 95% CI 0.91–0.99: p = 0.008) and use of dopamine agonist (OR 4.1, 95% CI 1.56–10.69). Cognitive changes over time did not differ between patients with and without ICBs. In conclusion, ICBs are common in PwP, but are often non-persistent and not associated with greater cognitive impairment over time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-019-09584-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-69548902020-01-23 Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease Erga, Aleksander H. Alves, Guido Tysnes, Ole Bjørn Pedersen, Kenn Freddy J Neurol Original Communication The longitudinal course of ICBs in patients with Parkinson’s disease (PwP) relative to controls has not been explored as of yet. The aim of this study is to determine the frequency, evolution and associated cognitive and clinical features of impulsive and compulsive behaviors (ICBs) over 4 years of prospective follow-up in a population-based cohort with early Parkinson’s disease (PD). We recruited 124 cognitively intact participants with early PD and 156 matched controls from the Norwegian ParkWest study. ICBs were assessed using the self-report short form version of the Questionnaire for Impulsive–Compulsive Disorders in PD. Cognitive changes were examined in PwP with and without ICBs who completed the 4-year follow-up. Generalized linear mixed modelling and mixed linear regression were used to analyze clinical factors and cognitive changes associated with ICBs in PwP over time. ICBs were more common in PwP than controls at all visits, with an age-adjusted odds ratio (OR) varying between 2.5 (95% CI 1.1–5.6; p = 0.022) and 5.1 (95% CI 2.4–11.0; p < 0.001). The 4-year cumulative frequency of ICBs in PwP was 46.8% and 23.3% developed incident ICBs during the study period, but the presence of ICBs was non-persistent in nearly 30%. ICBs were independently associated with younger age (OR 0.95, 95% CI 0.91–0.99: p = 0.008) and use of dopamine agonist (OR 4.1, 95% CI 1.56–10.69). Cognitive changes over time did not differ between patients with and without ICBs. In conclusion, ICBs are common in PwP, but are often non-persistent and not associated with greater cognitive impairment over time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-019-09584-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-10-18 2020 /pmc/articles/PMC6954890/ /pubmed/31628533 http://dx.doi.org/10.1007/s00415-019-09584-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Communication
Erga, Aleksander H.
Alves, Guido
Tysnes, Ole Bjørn
Pedersen, Kenn Freddy
Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease
title Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease
title_full Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease
title_fullStr Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease
title_full_unstemmed Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease
title_short Evolution of impulsive–compulsive behaviors and cognition in Parkinson’s disease
title_sort evolution of impulsive–compulsive behaviors and cognition in parkinson’s disease
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954890/
https://www.ncbi.nlm.nih.gov/pubmed/31628533
http://dx.doi.org/10.1007/s00415-019-09584-7
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