Abreu Daisy, Ware Jennifer, Georgiou-Karistianis Nellie, Leavitt Blair R, Fitzer-Attas Cheryl J, Lobo Raquel, Fernandes Ana Raquel, Handley Olivia, Anderson Karen E, Stout Julie C, Sampaio Cristina
Associação para Investigação e Desenvolvimento da Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
CHDI Management/CHDI Foundation, Princeton, NJ, United States.
Front Neurol. 2021 Jul 15;12:595679. doi: 10.3389/fneur.2021.595679. eCollection 2021.
An understanding of the clinimetric properties of clinical assessments, including their constraints, is critical to sound clinical study and trial design. Utilizing data from Enroll-HD-a global, prospective HD observational study and clinical research platform-we examined several well-established HD clinical assessments across all stages of disease for evidence of instrument constraints, specifically floor/ceiling effects, to inform selection of appropriate instruments for use in future studies/trials and identify gaps in instrument utility over the life-course of the disease. Analyzing publicly available data from 6,614 HD gene-expansion carriers (HDGECs), we grouped participants into deciles based on baseline CAP score, which ranged from 26 to 229. We used descriptive statistics to characterize data distribution for 25 outcome measures (encompassing motor, function, cognition, and psychiatric/behavioral domains) in each CAP decile. A skewness statistic threshold of ±2 was defined to indicate floor/ceiling effects. We found evidence of floor/ceiling effects in the early premanifest stages of disease for most motor and function assessments (e.g., TMS, TFC) and select cognitive tasks (MMSE, Trail Making tests). Other cognitive assessments, and the HADS-SIS scales, performed well ubiquitously, with no evidence of floor/ceiling effects at any disease stage. Floor/ceiling effects were evident at every disease stage for certain assessments, including PBA-s measures. Ceiling effects were apparent for DCL from onset stages onwards, as expected. Developing instruments sensitive to subtle differences in performance at the earlier stages of the disease spectrum, particularly in motor and function domains, is warranted.
了解临床评估的测量学特性,包括其局限性,对于合理的临床研究和试验设计至关重要。利用来自全球前瞻性亨廷顿舞蹈病(HD)观察性研究和临床研究平台Enroll-HD的数据,我们在疾病的各个阶段对几种成熟的HD临床评估进行了检查,以寻找工具局限性的证据,特别是地板效应/天花板效应,为未来研究/试验中合适工具的选择提供依据,并确定疾病整个病程中工具效用的差距。通过分析6614名HD基因扩展携带者(HDGECs)的公开数据,我们根据基线CAP评分将参与者分为十分位数组,基线CAP评分范围为26至229。我们使用描述性统计来描述每个CAP十分位数组中25项结局指标(包括运动、功能、认知和精神/行为领域)的数据分布。定义了±2的偏度统计阈值来表示地板效应/天花板效应。我们发现,对于大多数运动和功能评估(如经颅磁刺激、定时起立-行走测试)以及某些认知任务(简易精神状态检查表、连线测试),在疾病的早期症状前期阶段存在地板效应/天花板效应的证据。其他认知评估以及医院焦虑抑郁量表-自我报告量表在各个阶段表现良好,在任何疾病阶段均无地板效应/天花板效应的证据。对于某些评估,包括PBA-s测量,在每个疾病阶段都存在地板效应/天花板效应。正如预期的那样,从发病阶段开始,DCL就明显存在天花板效应。有必要开发对疾病谱早期阶段表现的细微差异敏感的工具,特别是在运动和功能领域。