دورية أكاديمية

Longitudinal evolution of motor and non-motor symptoms in early-stage multiple system atrophy: a 2-year prospective cohort study.

التفاصيل البيبلوغرافية
العنوان: Longitudinal evolution of motor and non-motor symptoms in early-stage multiple system atrophy: a 2-year prospective cohort study.
المؤلفون: Zhang, Lingyu, Hou, Yanbing, Cao, Bei, Wei, Qianqian, Ou, Ruwei, Liu, Kuncheng, Lin, Junyu, Yang, Tianmi, Xiao, Yi, Chen, Yongping, Song, Wei, Zhao, Bi, Shang, Huifang
المصدر: BMC Medicine; 11/17/2022, Vol. 20 Issue 1, p1-9, 9p
مصطلحات موضوعية: MULTIPLE system atrophy, GENERALIZED estimating equations, LONGITUDINAL method, COHORT analysis, CHINESE people, ESSENTIAL tremor
مستخلص: Background: The progression of motor and non-motor symptoms (NMS) and the sensitivity of each item of the Unified Multiple System Atrophy Rating Scale (UMSARS) to change remain unclear in Chinese patients with early-stage multiple system atrophy (MSA). We investigated the evolution of motor symptoms and NMS in early-stage MSA and the sensitivity of each item included in the UMSARS to change over a 2-year follow-up.Methods: Motor symptoms and NMS were recorded at baseline and at 1- and 2-year follow-ups based on the UMSARS and the NMS scale. Generalized estimating equation models were used. The sensitivity of an item included in the UMSARS to change was assessed by calculating a standardized effect using the mean annual change divided by the standard deviation of the change.Results: We enrolled 246 consecutive patients with MSA and 97 MSA completed the 2-year follow-up. The mean total UMSARS score increased by 11.90 and 22.54 points at the 1- and 2-year follow-ups, respectively. UMSARS-I items associated with motor functions were more sensitive to change and those associated with autonomic dysfunction showed less sensitivity to change. Items 4 (tremor at rest), 5 (action tremor), and 3 (ocular motor dysfunction) of the UMSARS-II were less sensitive to change. The prevalence and severity of NMS significantly increased over the 2-year follow-up.Conclusions: We observed significant progression in motor symptoms and NMS in patients with early-stage MSA. Our results provide useful information to support the revision of the UMSARS. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:17417015
DOI:10.1186/s12916-022-02645-1