Deary Ian, Harris Sarah, Russ Tom, Cox Simon, Corley Janie
University of Edinburgh.
The University of Edinburgh.
Res Sq. 2025 May 7:rs.3.rs-6462650. doi: 10.21203/rs.3.rs-6462650/v1.
Variation in the gene for apolipoprotein E ( is one of the few variables that is associated with individual differences in age-related cognitive decline in humans. Therefore, it is important to understand the conditions that affect the strength of its effect. Here we examine how the effect size of variation (possession of one or more e4 alleles) on a test of general cognitive ability changes with age from 11 to 90 years. The data are from the Lothian Birth Cohorts of 1936 and 1921 who took the same cognitive test (the Moray House Test) at, respectively, 11, 70, 73, 79, and 11, 79, 87, 90. The standardised absolute effect of e4 on general cognitive ability was about zero at ages 11 (beta < 0.05) and 70 (beta ≤ 0.025) and increased linearly to beta = 0.30 (p < 0.001) at age 90. The effect sizes were minimally affected by adjusting for medical conditions (hypertension, diabetes, cardiovascular disease, stroke). However, the results were less robust to removing those participants who had developed dementia; effect sizes were reduced by about a third to a half, and were largely non-significant. The results suggest that the negative effect of e4 on cognitive functioning becomes greater with age; this urges more work to understand the mechanisms by which e4 status renders the older person's brain increasingly vulnerable to cognitive decline and dementia.
载脂蛋白E基因的变异是与人类年龄相关认知衰退的个体差异相关的少数变量之一。因此,了解影响其效应强度的条件很重要。在这里,我们研究了载脂蛋白E基因变异(拥有一个或多个ε4等位基因)对一般认知能力测试的效应大小如何随11岁至90岁的年龄变化。数据来自1936年和1921年的洛锡安出生队列,他们分别在11岁、70岁、73岁、79岁以及11岁、79岁、87岁、90岁时接受了相同的认知测试(莫雷豪斯测试)。ε4对一般认知能力的标准化绝对效应在11岁(β<0.05)和70岁(β≤0.025)时约为零,并在90岁时线性增加至β=0.30(p<0.001)。通过调整医疗状况(高血压、糖尿病、心血管疾病、中风),效应大小受到的影响最小。然而,去除那些已患痴呆症的参与者后,结果的稳健性较差;效应大小降低了约三分之一到一半,且大多无统计学意义。结果表明,ε4对认知功能的负面影响随年龄增长而增大;这促使人们开展更多工作来了解ε4状态使老年人的大脑越来越容易出现认知衰退和痴呆症的机制。