Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
Robarts Research Institute and the Department of Medical Biophysics, the University of Western Ontario, London, ON, Canada.
J Alzheimers Dis. 2020;74(3):747-757. doi: 10.3233/JAD-191097.
BACKGROUND/OBJECTIVE: Structural brain magnetic resonance imaging (MRI) is not mandatory in Alzheimer's disease (AD) research or clinical guidelines. We aimed to explore the use of structural brain MRI in AD/mild cognitive impairment (MCI) trials over the past 10 years and determine the frequency with which inclusion of standardized structural MRI acquisitions detects comorbid vascular and non-vascular pathologies.
We systematically searched ClinicalTrials.gov for AD clinical trials to determine their neuroimaging criteria and then used data from an AD/MCI cohort who underwent standardized MRI protocols, to determine type and incidence of clinically relevant comorbid pathologies.
Of 210 AD clinical trials, 105 (50%) included structural brain imaging in their eligibility criteria. Only 58 (27.6%) required MRI. 16,479 of 53,755 (30.7%) AD participants were in trials requiring MRI. In the observational AD/MCI cohort, 141 patients met clinical criteria; 22 (15.6%) had relevant MRI findings, of which 15 (10.6%) were exclusionary for the study.
In AD clinical trials over the last 10 years, over two-thirds of participants could have been enrolled without brain MRI and half without even a brain CT. In a study sample, relevant comorbid pathology was found in 15% of participants, despite careful screening. Standardized structural MRI should be incorporated into NIA-AA diagnostic guidelines (when available) and research frameworks routinely to reduce diagnostic heterogeneity.
背景/目的:结构性脑磁共振成像(MRI)在阿尔茨海默病(AD)研究或临床指南中并非强制性的。我们旨在探讨过去 10 年来 AD/轻度认知障碍(MCI)试验中结构性脑 MRI 的使用情况,并确定纳入标准化结构性 MRI 采集检测合并血管和非血管病变的频率。
我们系统地在 ClinicalTrials.gov 上搜索 AD 临床试验,以确定其神经影像学标准,然后使用接受标准化 MRI 方案的 AD/MCI 队列的数据,以确定临床上相关的合并病理类型和发生率。
在 210 项 AD 临床试验中,105 项(50%)在其纳入标准中包含结构性脑成像。只有 58 项(27.6%)需要 MRI。在需要 MRI 的试验中,53755 名 AD 参与者中有 16479 名(30.7%)。在观察性 AD/MCI 队列中,141 名患者符合临床标准;22 名(15.6%)有相关 MRI 发现,其中 15 名(10.6%)排除了该研究。
在过去 10 年的 AD 临床试验中,超过三分之二的参与者可以在没有脑 MRI 的情况下入组,甚至有一半的参与者可以在没有脑 CT 的情况下入组。在研究样本中,尽管进行了仔细的筛选,但仍有 15%的参与者存在相关的合并病理。标准化结构性 MRI 应纳入 NIA-AA 诊断指南(在可用时)和研究框架中,以减少诊断异质性。