Research Division "Translational Genomics of Neurodegenerative Diseases," Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany.
German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Mov Disord. 2024 Jun;39(6):965-974. doi: 10.1002/mds.29788. Epub 2024 Mar 20.
Patient-focused outcomes present a central need for trial-readiness across all ataxias. The Activities of Daily Living part of the Friedreich Ataxia Rating Scale (FARS-ADL) captures functional impairment and longitudinal change but is only validated in Friedreich Ataxia.
Validation of FARS-ADL regarding disease severity and patient-meaningful impairment, and its sensitivity to change across genetic ataxias.
Real-world registry data of FARS-ADL in 298 ataxia patients across genotypes were analyzed, including (1) cross-correlation with FARS-stage, Scale for the Assessment and Rating of Ataxia (SARA), Patient-Reported Outcome Measure (PROM)-ataxia, and European Quality of Life 5 Dimensions visual analogue scale (EQ5D-VAS); (2) sensitivity to change within a trial-relevant 1-year median follow-up, anchored in Patient Global Impression of Change (PGI-C); and (3) general linear modeling of factors age, sex, and depression (nine-item Patient Health Questionnaire [PHQ-9]).
FARS-ADL correlated with overall disability (rho = 0.79), clinical disease severity (rho = 0.80), and patient-reported impairment (rho = 0.69, rho = -0.37), indicating comprehensive construct validity. Also at item level, and validated within genotype (SCA3, RFC1), FARS-ADL correlated with the corresponding SARA effector domains; and all items correlated to EQ5D-VAS quality of life. FARS-ADL was sensitive to change at a 1-year interval, progressing only in patients with worsening PGI-C. Minimal important change was 1.1. points based on intraindividual variability in patients with stable PGI-C. Depression was captured using FARS-ADL (+0.3 points/PHQ-9 count) and EQ5D-VAS, but not FARS-stage or SARA.
FARS-ADL reflects both disease severity and patient-meaningful impairment across genetic ataxias, with sensitivity to change in trial-relevant timescales in patients perceiving change. It thus presents a promising patient-focused outcome for upcoming ataxia trials. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
以患者为中心的结果是所有共济失调试验准备的核心需求。弗里德里希共济失调评定量表(FARS-ADL)的日常生活活动部分可捕捉功能障碍和纵向变化,但仅在弗里德里希共济失调中得到验证。
验证 FARS-ADL 与疾病严重程度和患者有意义的损害的相关性,以及其在遗传性共济失调中的变化敏感性。
对 298 名不同基因型共济失调患者的 FARS-ADL 真实世界登记数据进行分析,包括(1)与 FARS 分期、共济失调评定量表(SARA)、患者报告的结局测量(PROM-共济失调)和欧洲生活质量 5 维度视觉模拟量表(EQ5D-VAS)的交叉相关性;(2)在与试验相关的 1 年中位数随访内的变化敏感性,锚定在患者整体变化印象(PGI-C);(3)年龄、性别和抑郁(9 项患者健康问卷[PHQ-9])的一般线性建模。
FARS-ADL 与总体残疾(rho=0.79)、临床疾病严重程度(rho=0.80)和患者报告的损害(rho=0.69,rho=-0.37)相关,表明具有全面的结构效度。在项目水平上,在相应的 SCA3、RFC1 基因型中也得到了验证,FARS-ADL 与相应的 SARA 效应域相关;并且所有项目都与 EQ5D-VAS 生活质量相关。FARS-ADL 在 1 年间隔内具有变化敏感性,仅在 PGI-C 恶化的患者中进展。基于 PGI-C 稳定患者的个体内变异性,最小重要变化为 1.1 点。使用 FARS-ADL(+0.3 分/PHQ-9 计数)和 EQ5D-VAS 可以捕捉到抑郁,但不能用 FARS 分期或 SARA 捕捉到。
FARS-ADL 反映了遗传性共济失调中疾病严重程度和患者有意义的损害,在患者感知变化的试验相关时间尺度上具有变化敏感性。因此,它为即将到来的共济失调试验提供了一种有前途的以患者为中心的结局。