Department of Neurology, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Department of Psychology and Latin American Latino Studies Institute, Fordham University, The Bronx, New York, USA.
Alzheimers Dement. 2022 Apr;18(4):810-823. doi: 10.1002/alz.12433. Epub 2021 Sep 30.
To generalize safety and efficacy findings, it is essential that diverse populations are well represented in Alzheimer's disease (AD) drug trials. In this review, we aimed to investigate participant diversity in disease-modifying AD trials over time, and the frequencies of participant eligibility criteria.
A systematic review was performed using Medline, Embase, the Cochrane Library, and Clinicaltrials.gov, identifying 2247 records.
In the 101 included AD trials, participants were predominantly White (median percentage: 94.7%, interquartile range: 81.0-96.7%); and this percentage showed no significant increase or decrease over time (2001-2019). Eligibility criteria such as exclusion of persons with psychiatric illness (78.2%), cardiovascular disease (71.3%) and cerebrovascular disease (68.3%), obligated caregiver attendance (80.2%), and specific Mini-Mental State Examination scores (90.1%; no significant increase/decrease over time) may have led to a disproportionate exclusion of ethnoracially diverse individuals.
Ethnoracially diverse participants continue to be underrepresented in AD clinical trials. Several recommendations are provided to broaden eligibility criteria.
为了推广安全性和疗效发现,阿尔茨海默病(AD)药物试验必须充分代表不同人群。在本综述中,我们旨在调查 AD 试验中随时间推移的参与者多样性,以及参与者资格标准的出现频率。
使用 Medline、Embase、Cochrane 图书馆和 Clinicaltrials.gov 进行系统综述,确定了 2247 份记录。
在 101 项纳入的 AD 试验中,参与者主要为白人(中位数百分比:94.7%,四分位距:81.0-96.7%);而且这一比例随时间推移没有显著增加或减少(2001-2019)。排除有精神病史(78.2%)、心血管疾病(71.3%)和脑血管疾病(68.3%)、需要照顾者陪同(80.2%)以及特定的简易精神状态检查评分(90.1%;随时间推移没有显著增加/减少)等资格标准可能导致种族和民族多样化的个体被不成比例地排除在外。
种族和民族多样化的参与者在 AD 临床试验中继续代表性不足。提出了一些扩大资格标准的建议。