Relations of clinical symptoms with dopamine transporter imaging in drug-naïve Parkinson's disease.


Journal

Clinical neurology and neurosurgery
ISSN: 1872-6968
Titre abrégé: Clin Neurol Neurosurg
Pays: Netherlands
ID NLM: 7502039

Informations de publication

Date de publication:
09 2020
Historique:
received: 02 05 2019
revised: 22 05 2020
accepted: 23 05 2020
pubmed: 28 6 2020
medline: 16 6 2021
entrez: 28 6 2020
Statut: ppublish

Résumé

The aim of the present study was to determine the relations of clinical symptoms with nigrostriatal neuron loss in drug-naïve patients with Parkinson's disease (PD). We examined the severity of motor symptoms and freezing of gait (FOG), falls and overactive bladder (OAB) in PD patients and their relations with striatal dopamine transporter (DAT) binding. Thirty-two untreated PD patients (14 men and 18 women with a mean age of 71.4 ± 7.2 years) were included in this study. Clinical assessments were performed by using Unified Parkinson's Disease Rating Scale (UPDRS) and overactive bladder symptom score (OABSS), and striatal dopamine transporter (DAT) binding was measured by The results showed that striatal DAT availability was significantly lower in the high UPDRS motor score group, high akinetic-rigid score group, FOG group, and OAB group than in the low UPDRS motor score group, low akinetic-rigid score group, non-FOG group, and non-OAB group. However, the results also showed that there was no significant difference in striatal DAT availability between the high tremor score group and low tremor score group or between the faller group and non-faller group. The severity of bradykinesia and axial symptoms and the existence of FOG and OAB in untreated PD patients are related to a decrease in striatal DAT availability. Severity of tremors and occurrence of falls are not related to a decrease in striatal DAT availability. The mechanisms underlying the clinical symptoms of PD involve not only dopaminergic pathways but also non-dopaminergic pathways.

Identifiants

pubmed: 32593043
pii: S0303-8467(20)30303-6
doi: 10.1016/j.clineuro.2020.105960
pii:
doi:

Substances chimiques

Dopamine Plasma Membrane Transport Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105960

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Yasunori Mito (Y)

Department of Neurology, Brain Science Center, Sapporo City General Hospital, Kita 11-nishi 13, Chuo Ku, Sapporo, Hokkaido 060-8604, Japan. Electronic address: yasunori.mito@doc.city.sapporo.jp.

Ichiro Yabe (I)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.

Hiroaki Yaguchi (H)

Department of Neurology, Brain Science Center, Sapporo City General Hospital, Kita 11-nishi 13, Chuo Ku, Sapporo, Hokkaido 060-8604, Japan.

Chika Sato (C)

Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.

Toshiki Takei (T)

Department of Diagnostic Radiology, Sapporo City General Hospital, Sapporo, Hokkaido, Japan.

Satoshi Terae (S)

Department of Diagnostic Radiology, Sapporo City General Hospital, Sapporo, Hokkaido, Japan.

Yasutaka Tajima (Y)

Department of Neurology, Brain Science Center, Sapporo City General Hospital, Kita 11-nishi 13, Chuo Ku, Sapporo, Hokkaido 060-8604, Japan.

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