White matter hyperintensities and risk of levodopa-induced dyskinesia in Parkinson's disease.


Journal

Annals of clinical and translational neurology
ISSN: 2328-9503
Titre abrégé: Ann Clin Transl Neurol
Pays: United States
ID NLM: 101623278

Informations de publication

Date de publication:
02 2020
Historique:
received: 09 11 2019
revised: 26 12 2019
accepted: 16 01 2020
pubmed: 8 2 2020
medline: 11 11 2021
entrez: 8 2 2020
Statut: ppublish

Résumé

To investigate whether the burden of white matter hyperintensities (WMHs) is associated with the risk of developing levodopa-induced dyskinesia (LID) in Parkinson's disease (PD). According to the Clinical Research Center for Dementia of South Korea WMH visual rating scale, 336 patients with drug-naïve early stage PD (follow-up >3 years) were divided into two groups of PD with minimal WMHs (PD-WMH-; n = 227) and moderate-to-severe WMHs (PD-WMH+; n = 109). The Cox regression model was used to estimate the hazard ratio for the development of LID in the PD-WMH + group compared with the PD-WMH- group, while adjusting for age at PD onset, sex, striatal dopamine depletion, and PD medication dose. Additionally, we assessed the effects of WMH burden rated by the Scheltens scale and regional WMH distribution on the development of LID. Patients in the PD-WMH + group were older and had more severe parkinsonian motor signs despite comparable striatal dopamine transporter availability than those in the PD-WMH- group. Patients in the PD-WMH + group had a higher risk of developing LID (hazard ratio, 2.66; P < 0.001) than those in the PD-WMH- group after adjustment for other confounding factors. A greater WMH burden was associated with earlier occurrence of LID (hazard ratio, 1.04; P = 0.001), although the effects of WMHs on LID development did not exhibit region-specific patterns. The present study demonstrates that the burden of WMHs is associated with occurrence of LID in patients with PD, suggesting comorbid WMHs as a risk factor for LID.

Identifiants

pubmed: 32032471
doi: 10.1002/acn3.50991
pmc: PMC7034502
doi:

Substances chimiques

Dopamine Agents 0
Levodopa 46627O600J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

229-238

Subventions

Organisme : National Research Foundation of Korea
Pays : International
Organisme : Ministry of Education
ID : NRF-2018R1D1A1B07048959
Pays : International
Organisme : Ministry of Science, ICT and Future Planning
ID : NRF-2019R1A2C2085462
Pays : International

Informations de copyright

© 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association.

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Auteurs

Seok Jong Chung (SJ)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Department of Neurology, Yongin Severance Hospital, Yonsei University Health System, Yongin, South Korea.

Han Soo Yoo (HS)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

Yang Hyun Lee (YH)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

Jin Ho Jung (JH)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

KyoungWon Baik (K)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

Byoung Seok Ye (BS)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

Young H Sohn (YH)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.

Phil Hyu Lee (PH)

Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.

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