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用于ARSACS试验准备的临床结局评估选择 - 2年进展及对变化的反应 第1部分:疾病严重程度、吞咽、上肢功能和参与度

Selection of Clinical Outcome Assessments for Trial Readiness in ARSACS - 2-year Progression and Responsiveness to Change Part 1: Disease Severity, Swallowing, Upper Limb Function, and Participation.

作者信息

Lessard Isabelle, Hébert Luc J, Brais Bernard, Duchesne Elise, Rodrigue Xavier, Brisson Jean-Denis, Routhier François, Best Krista, Côté Isabelle, Gagnon Cynthia

机构信息

Centre ÉCOBES-Recherche Et Transfert, Cégep de Jonquière, Saguenay, Québec, Canada.

Groupe de Recherche Interdisciplinaire Sur Les Maladies Neuromusculaires (GRIMN), Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, Saguenay, Québec, Canada.

出版信息

Cerebellum. 2025 May 31;24(4):106. doi: 10.1007/s12311-025-01858-3.

DOI:10.1007/s12311-025-01858-3
PMID:40450178
Abstract

Progress has been made in developing new therapies for certain ataxias. To ensure clinical trial readiness and support the development of robust trial design, it is essential to know the disease progression rate and metrological properties of clinical outcome assessments (COAs), including their responsiveness to change. The objectives of this study were 1) to document over a trial-relevant time frame of two years the progression of disease severity, swallowing, upper limb function, and participation, and 2) to assess the responsiveness to change of related COAs in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), one of the most frequent recessive ataxias worldwide. Sixty participants from two neuromuscular clinics (Saguenay and Québec City, Canada) were included. The COAs were the Disease Severity Index for ARSACS (DSI-ARSACS), Scale for the Assessment and Rating of Ataxia (SARA), Swallowing Disturbance Questionnaire, grip and pinch strength, Standardized Finger-to-Nose test, TEMPA, Barthel Index, and Assessment of Life Habits questionnaire. Self-perception of previous-year progression of specific impairments was also documented using a global rating of change scale (GRS). A significant progression in the DSI-ARSACS (-1.5 points), SARA (+ 1.6 points), Barthel Index (-7.4 points), and grip (-2.3 kg) and pinch (-0.25 kg) strength was observed. Only a few COAs were able to specifically detect a difference in participants who reported worsening, with grip strength being the most sensitive COA to assess upper limb function. Since a high proportion of participants reported not having any impairments, the statistical power was limited for responsiveness analyses and further study would be needed.

摘要

在某些共济失调的新疗法开发方面已取得进展。为确保临床试验准备就绪并支持稳健试验设计的开展,了解疾病进展速度以及临床结局评估(COA)的计量特性至关重要,包括其对变化的反应性。本研究的目的是:1)在两年的试验相关时间范围内记录疾病严重程度、吞咽功能、上肢功能和参与度的进展情况;2)评估常染色体隐性遗传性夏勒沃魁北克痉挛性共济失调(ARSACS)患者(ARSACS是全球最常见的隐性共济失调之一)相关COA对变化的反应性。纳入了来自两家神经肌肉诊所(加拿大萨格奈和魁北克市)的60名参与者。所使用的COA包括ARSACS疾病严重程度指数(DSI - ARSACS)、共济失调评估与分级量表(SARA)、吞咽障碍问卷、握力和捏力、标准化指鼻试验、TEMPA、巴氏指数和生活习惯评估问卷。还使用整体变化评分量表(GRS)记录了对特定损伤前一年进展情况的自我认知。观察到DSI - ARSACS(-1.5分)、SARA(+1.6分)、巴氏指数(-7.4分)以及握力(-2.3千克)和捏力(-0.25千克)有显著进展。只有少数COA能够特异性地检测出报告病情恶化的参与者之间的差异,其中握力是评估上肢功能最敏感的COA。由于很大一部分参与者报告没有任何损伤,反应性分析的统计功效有限,需要进一步研究。

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本文引用的文献

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Toward a Better Understanding of Walking Speed in Ataxia of Charlevoix-Saguenay: a Factor Exploratory Study.探索性研究:更好地理解沙格奈-圣安娜小脑性共济失调的行走速度
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In Vitro Characterization of Motor Neurons and Purkinje Cells Differentiated from Induced Pluripotent Stem Cells Generated from Patients with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.从患有常染色体隐性遗传性沙勒沃伊 - 萨格奈痉挛性共济失调患者产生的诱导多能干细胞分化而来的运动神经元和浦肯野细胞的体外特性研究
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Multi-omic profiling reveals the ataxia protein sacsin is required for integrin trafficking and synaptic organization.多组学分析揭示共济失调蛋白 sacsin 对于整合素运输和突触组织是必需的。
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