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神经退行性疾病中的运动徐缓:经病理证实病例的盲法视频分析。

Bradykinesia in Neurodegenerative Disorders: A Blinded Video Analysis of Pathology-Proven Cases.

机构信息

Gardner Family Center for Parkinson's Disease and Movement Disorders, Department of Neurology, University of Cincinnati, Cincinnati, Ohio, USA.

Department of Pathology, University of Cincinnati, Cincinnati, Ohio, USA.

出版信息

Mov Disord. 2023 Mar;38(3):496-501. doi: 10.1002/mds.29330. Epub 2023 Jan 27.

Abstract

BACKGROUND

Bradykinesia is a cardinal feature in parkinsonisms. No study has assessed the differential features of bradykinesia in patients with pathology-proven synucleinopathies and tauopathies.

OBJECTIVE

We examined whether bradykinesia features (speed, amplitude, rhythm, and sequence effect) may differ between pathology-proven synucleinopathies and tauopathies.

METHODS

Forty-two cases who underwent autopsy were included and divided into synucleinopathies (Parkinson's disease and dementia with Lewy bodies) and tauopathies (progressive supranuclear palsy). Two raters blinded to the diagnosis retrospectively scored the Movement Disorders Society-Unified Parkinson's Disease Rating Scale Part III and Modified Bradykinesia Rating Scale on standardized videotaped neurological examinations. Bradykinesia scores were compared using the Mann-Whitney test and logistic regression models to adjust for disease duration.

RESULTS

Demographic and clinical parameters were similar between synucleinopathies and tauopathies. There were no differences between speed, amplitude, rhythm, and sequence effect in synucleinopathies and tauopathies in unadjusted comparisons and adjusted models (all P > 0.05).

CONCLUSIONS

Clinical bradykinesia features do not distinguish the underlying neuropathology in neurodegenerative parkinsonisms. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

摘要

背景

运动迟缓是帕金森病的主要特征。目前尚无研究评估经病理证实的突触核蛋白病和tau 病患者运动迟缓的特征差异。

目的

我们研究了运动迟缓的特征(速度、幅度、节律和序列效应)是否可能在突触核蛋白病和 tau 病之间存在差异。

方法

共纳入 42 例接受尸检的患者,并分为突触核蛋白病(帕金森病和路易体痴呆)和 tau 病(进行性核上性麻痹)。两名对诊断不知情的评估者回顾性地对标准化录像神经检查的运动障碍协会统一帕金森病评定量表第 3 部分和改良运动迟缓评定量表进行评分。使用 Mann-Whitney 检验和逻辑回归模型比较运动迟缓评分,以调整疾病持续时间。

结果

突触核蛋白病和 tau 病之间的人口统计学和临床参数相似。在未调整的比较和调整模型中,突触核蛋白病和 tau 病的速度、幅度、节律和序列效应均无差异(均 P > 0.05)。

结论

临床运动迟缓特征不能区分神经退行性帕金森病中的潜在神经病理学。© 2023 作者。运动障碍由 Wiley 期刊有限责任公司代表国际帕金森和运动障碍协会出版。

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