Duehring Jasmin A, Jacobs Diane M, Thomas Michael L, Dodge Hiroko H, Feldman Howard H, Edland Steven D
Division of Biostatistics, Herbert Wertheim School of Public Health and Human Longevity Science University of California San Diego La Jolla California USA.
Department of Neurosciences School of Medicine University of California San Diego La Jolla California USA.
Alzheimers Dement (N Y). 2025 Sep 9;11(3):e70154. doi: 10.1002/trc2.70154. eCollection 2025 Jul-Sep.
Practice effects (PEs) are a well-known potential confound in natural history studies of longitudinal cognitive decline in aging and early-stage Alzheimer's disease. The implication of PEs on Alzheimer's disease clinical trials is less well understood, although we have previously speculated that a "run-in" period of repeated cognitive assessments prior to randomization may improve the efficiency of clinical trials [Jacobs et al. 2017;3(4):531-535]. We have also described how the performance of composite outcome measures depends on parameters that may be influenced by PEs.
To investigate this, we used the cognitive battery within the National Alzheimer's Coordinating Center (NACC) Uniform Data Set to characterize the potential impact of PEs on clinical trial design and outcome measures. The analysis restricted to = 1094 amnestic mild cognitively impaired participants with 3 years of follow-up data. Linear mixed effects models estimate the magnitude of PEs observed in aMCI participants. Power calculations informed by the pattern of progression in the NACC sample were used to describe the net impact of PEs on trials with and without a run-in phase. Weighting parameters of optimal composite measures constructed from the NACC battery were also compared.
PEs were large, often exceeding the magnitude of annual rate of change observed in later assessments. Annualized rate of change, and therefore target treatment effect sufficient to achieve a specified percentage reduction in rate of decline, was larger after run-in. Sample size projections for the run-in design were a fraction of those required for trials without run-in. Weighting parameters that optimize composite outcome performance were also different for the two designs, underscoring the importance of considering design in the construction of composite outcomes.
Clinical trials randomizing after a run-in period measure treatment efficacy relative to decline unbiased by PEs, and require smaller sample size.
In the National Alzheimer's Coordinating Center (NACC), amnestic mild cognitive impairment (aMCI) cohort practice effects often exceed annualized rate of change.Run-in clinical trial designs can be used to extinguish practice effects.Rate of decline after run-in is faster and unbiased by practice effects.Run-in designs correctly target the most clinically relevant outcome signal.Practice effects also impact weighting of optimal composite measures.
在衰老和早期阿尔茨海默病纵向认知衰退的自然史研究中,练习效应(PEs)是一种众所周知的潜在混杂因素。尽管我们之前推测在随机分组前进行重复认知评估的“导入期”可能会提高临床试验的效率[雅各布斯等人,2017年;3(4):531 - 535],但PEs对阿尔茨海默病临床试验的影响尚不太清楚。我们还描述了复合结局指标的表现如何取决于可能受PEs影响的参数。
为了对此进行研究,我们使用了国家阿尔茨海默病协调中心(NACC)统一数据集中的认知测试组合,以描述PEs对临床试验设计和结局指标的潜在影响。分析仅限于1094名遗忘型轻度认知障碍参与者,他们有3年的随访数据。线性混合效应模型估计在遗忘型轻度认知障碍参与者中观察到的PEs大小。根据NACC样本中的进展模式进行的功效计算,用于描述PEs对有和没有导入期的试验的净影响。还比较了由NACC测试组合构建的最佳复合指标的加权参数。
PEs很大,常常超过后期评估中观察到的年变化率。导入期后的年化变化率以及因此足以实现特定下降率降低百分比的目标治疗效果更大。导入期设计的样本量预测是无导入期试验所需样本量的一小部分。两种设计中优化复合结局表现的加权参数也不同,这突出了在构建复合结局时考虑设计的重要性。
在导入期后进行随机分组的临床试验测量的是相对于不受PEs影响的衰退的治疗效果,并且需要较小的样本量。
在国家阿尔茨海默病协调中心(NACC),遗忘型轻度认知障碍(aMCI)队列的练习效应常常超过年化变化率。导入期临床试验设计可用于消除练习效应。导入期后的衰退速度更快且不受练习效应影响。导入期设计正确地针对了最具临床相关性的结局信号。练习效应也会影响最佳复合指标的加权。