Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
J Gerontol A Biol Sci Med Sci. 2024 Mar 1;79(3). doi: 10.1093/gerona/glad260.
Apolipoprotein E (APOE)-ε4 allele is associated with cognitive decline; however, its potential to modify effects of vitamin D3 and omega-3s supplementation on later-life cognition is unclear. Our objectives were to estimate among the in-clinic subset of a randomized trial: (1) associations between APOE-ε4 and global and domain-specific cognitive change, with exploration of potential sex and race differences; and (2) modification by APOE-ε4 of effects of vitamin D3 and omega-3s supplementation on cognitive change.
From an ancillary study of depression prevention within a completed 2 × 2 factorial trial testing vitamin D3 (2 000 IU per day), omega-3s (1 g per day), and/or placebos, we included 743 older adults with baseline in-person neuropsychiatric assessments and APOE genotyping data. The primary outcome was change in global cognition (averaging z-scores of 9 tests) over 2 years. Secondarily, episodic memory and executive function/attention z-scores were examined. General linear models of response profiles with multiplicative interaction terms were constructed; stratified results were reported.
Mean age (standard deviation) was 67.1 (5.3) years; 50.6% were females; 24.9% were APOE-ε4 carriers. Compared to noncarriers, APOE-ε4 carriers had worse 2-year change in global cognition and episodic memory; differences were more apparent among females than males. There was no variation by race in APOE-ε4 associations with cognition. APOE-ε4 did not significantly modify effects of vitamin D3 or omega-3s, compared to placebo, on change in global cognition, episodic memory, or executive function/attention.
APOE-ε4 was associated with worse cognition but did not modify overall effects of vitamin D3 or omega-3 supplementation on cognition over 2 years.
载脂蛋白 E(APOE)-ε4 等位基因与认知能力下降有关;然而,其对维生素 D3 和 ω-3s 补充剂对晚年认知的影响的修饰作用尚不清楚。我们的目的是在一项随机试验的门诊亚组中估计:(1)APOE-ε4 与整体和特定领域认知变化之间的关联,并探索潜在的性别和种族差异;(2)APOE-ε4 对维生素 D3 和 ω-3s 补充剂对认知变化影响的修饰作用。
从一项已完成的 2×2 因子试验的抑郁症预防辅助研究中,我们纳入了 743 名基线进行了现场神经精神病学评估和 APOE 基因分型数据的老年人。主要结局是 2 年内整体认知的变化(平均 9 项测试的 z 分数)。其次,检查了情景记忆和执行功能/注意力 z 分数。构建了具有乘法交互项的响应曲线的一般线性模型;报告了分层结果。
平均年龄(标准差)为 67.1(5.3)岁;50.6%为女性;24.9%为 APOE-ε4 携带者。与非携带者相比,APOE-ε4 携带者的 2 年全球认知和情景记忆变化更差;女性之间的差异比男性更明显。APOE-ε4 与认知的种族差异无关。与安慰剂相比,APOE-ε4 对维生素 D3 或 ω-3s 的影响没有显著改变,对全球认知、情景记忆或执行功能/注意力的变化没有影响。
APOE-ε4 与认知能力下降有关,但在 2 年内,APOE-ε4 并未改变维生素 D3 或 ω-3s 补充剂对认知的总体影响。