分析帕金森病的“运动迟缓综合症”。

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY
Giulia Paparella,Martina De Riggi,Antonio Cannavacciuolo,Daniele Birreci,Davide Costa,Luca Angelini,Danilo Alunni Fegatelli,Alfonso Fasano,Alberto J Espay,Matteo Bologna
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引用次数: 0

摘要

运动迟缓是帕金森氏症的标志。我们最近提议将运动迟缓重新定义为一种复杂的运动异常,每一种都反映了不同的病理生理因素。目的分析帕金森病(PD)及健康老年人的“运动迟缓综合症”。方法对350例PD患者(未服药的192例,健康对照158例)进行手指叩击运动分析。129名患者的子样本也进行了药物测试。分组比较后进行无监督聚类。接受者工作特征(ROC)分析定义了最佳的运动截止点,以检测个体运动异常。然后,我们量化了每个受试者的患病率和这些特征的组合。利用贝叶斯定理,我们根据观察到的运动迟缓特征的组合来估计PD的概率。回归分析用于确定运动学改变的预测因子。结果与对照组相比,患者表现出速度和幅度降低、节奏和序列改变效应(p值均< 0.001)。聚类分析显示了大量的群体重叠。ROC分析显示,运动迟缓(运动缓慢)是区分PD最常见、最准确的特征,当合并其他运动异常(运动不足、心律失常、序列效应)时,其诊断能力会提高。正确识别PD的可能性随着观察到的异常数量的增加而增加,当所有特征都存在时,正确识别PD的可能性高达95%。左旋多巴改善了运动表现,但运动异常模式保持不变。结论详细的运动迟缓特征评估是区分PD个体与对照组的关键。诊断的准确性需要同时考虑多种运动异常,而不考虑具体的组合。推进我们对“运动迟缓综合症”的理解具有临床和病理生理意义。©2025作者。Wiley期刊有限责任公司代表国际帕金森和运动障碍学会出版的《运动障碍》。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analyzing the 'Bradykinesia Complex' in Parkinson's Disease.
BACKGROUND Bradykinesia is the hallmark sign of parkinsonism. We recently proposed redefining bradykinesia as a complex of motor abnormalities, each reflecting separate pathophysiological elements. OBJECTIVE To analyze the 'bradykinesia complex' in Parkinson's disease (PD) and healthy elderly individuals. METHODS We conducted a finger-tapping kinematic analysis in 350 individuals (192 PD patients OFF medication and 158 healthy controls). A subsample of 129 patients was also tested ON medication. Group comparisons were followed by unsupervised clustering. Receiver operating characteristic (ROC) analyses defined optimal kinematic cut-offs to detect individual motor abnormalities. We then quantified the prevalence and combinations of these features per subject. Using Bayes' theorem, we estimated the probability of PD based on the observed combination of bradykinesia features. Regression analyses served to identify predictors of kinematic alterations. RESULTS Patients exhibited reduced velocity and amplitude as well as altered rhythm and sequence effect compared with controls (all P-values < 0.001). Cluster analysis revealed substantial group overlap. ROC analyses showed that bradykinesia (movement slowness) was the most common and accurate feature for distinguishing PD, with its diagnostic power improving when combined with other motor abnormalities (hypokinesia, dysrhythmia, sequence effect). The likelihood of correctly identifying PD increased with the number of observed abnormalities, reaching up to 95% when all features were present. Levodopa improved motor performance, but the motor abnormality patterns remained unchanged. CONCLUSIONS The detailed bradykinesia features assessment was crucial for differentiating PD individuals from controls. Diagnostic accuracy requires considering multiple motor abnormalities together, irrespective of the specific combination. Advancing our understanding of the 'bradykinesia complex' has clinical and pathophysiological implications. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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来源期刊
Movement Disorders
Movement Disorders 医学-临床神经学
CiteScore
13.30
自引率
8.10%
发文量
371
审稿时长
12 months
期刊介绍: Movement Disorders publishes a variety of content types including Reviews, Viewpoints, Full Length Articles, Historical Reports, Brief Reports, and Letters. The journal considers original manuscripts on topics related to the diagnosis, therapeutics, pharmacology, biochemistry, physiology, etiology, genetics, and epidemiology of movement disorders. Appropriate topics include Parkinsonism, Chorea, Tremors, Dystonia, Myoclonus, Tics, Tardive Dyskinesia, Spasticity, and Ataxia.
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