Lessard Isabelle, Duchesne Elise, Hébert Luc J, Brais Bernard, Rodrigue Xavier, Routhier François, Best Krista, Brisson Jean-Denis, Thullier Florentin, Gaboury Sébastien, Côté Isabelle, Gagnon Cynthia
Centre ÉCOBES-Recherche Et Transfert, Cégep de Jonquière, Quebec, Canada.
Groupe de Recherche Interdisciplinaire Sur Les Maladies Neuromusculaires (GRIMN), Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, 2230 de L'Hôpital, Cp 1200, Jonquière, Quebec, G7X 7X2, Canada.
Cerebellum. 2025 May 7;24(4):95. doi: 10.1007/s12311-025-01849-4.
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is among the most prevalent types of recessive ataxia worldwide. Given the accelerated therapeutic advances for many ataxias, there is a need to improve trial readiness. This study aimed to document the progression of balance, lower limb coordination and mobility in adults with ARSACS according to their mobility stage (walker or not) over the trial-relevant time frame of two years, and responsiveness to change of related clinical outcome assessments (COAs). Sixty participants from two neuromuscular clinics (Saguenay and Québec City, Canada) were included. The COAs were the Lower Extremity Motor Coordination Test (LEMOCOT), Co-contraction index, 30-s Chair Stand test (30 s-CST), Timed Up & Go test (TUG), 10-Meter Walk Test (10mWT), Berg Balance Scale (BBS), and Activities-specific Balance Confidence-simplified (ABC-S) scale. Responsiveness was documented using an anchor-based method with self-perception of the progression of related COA outcomes in the previous year. A significant progression above the standard error of measurement was observed for the TUG (+ 7.8 s [24% compared with baseline]), 10mWT (-0.111 to-0.165 m/s [-17 to -20%]), BBS (-4.3 points [-24%]), and ABC-S (-4.3 points [-15%]), with some differences between mobility stages; participants using a walking aid or wheelchair showed greater progression. The TUG, 10mWT, and BBS were the most sensitive to change in COAs, detecting changes specifically in participants who reported getting worse. These results are pivotal for defining inclusion criteria and selecting COAs for future clinical trials.
常染色体隐性遗传性夏勒沃魁北克痉挛性共济失调(ARSACS)是全球最常见的隐性共济失调类型之一。鉴于许多共济失调疾病的治疗进展迅速,有必要提高试验准备水平。本研究旨在记录ARSACS成年患者在两年的试验相关时间范围内,根据其行动能力阶段(是否使用助行器),平衡、下肢协调性和行动能力的进展情况,以及相关临床结局评估(COA)对变化的反应性。纳入了来自加拿大魁北克省两家神经肌肉诊所(萨格奈和魁北克市)的60名参与者。COA包括下肢运动协调测试(LEMOCOT)、共同收缩指数、30秒椅子站立试验(30s - CST)、定时起立行走试验(TUG)、10米步行试验(10mWT)、伯格平衡量表(BBS)和特定活动平衡信心简化版(ABC - S)量表。使用基于锚定的方法记录反应性,该方法基于参与者对前一年相关COA结果进展的自我感知。在TUG(+7.8秒[与基线相比增加24%])、10mWT(-0.111至-0.165米/秒[-17%至-20%])、BBS(-4.3分[-24%])和ABC - S(-4.3分[-15%])方面观察到超过测量标准误差的显著进展,行动能力阶段之间存在一些差异;使用助行器或轮椅的参与者进展更大。TUG、10mWT和BBS对COA变化最敏感,能够特别检测出报告病情恶化的参与者的变化。这些结果对于确定未来临床试验的纳入标准和选择COA至关重要。