Spalding University School of Professional Psychology.
Cancer Treatment Centers of America Global, Inc.
Neuropsychology. 2021 Feb;35(2):220-231. doi: 10.1037/neu0000713.
The purpose of the study was to test the hypothesis that anticholinergic drug exposure is associated with cognitive decline in the Wisconsin Registry for Alzheimer's Prevention (WRAP) study. Secondary aims were to assess if the effects of anticholinergic drugs on different domains of cognitive functioning varied for the entire sample and by apolipoprotein ε4 status.
The WRAP study includes a sample of 1,573 subjects who self-reported medication use and were administered several cognitive tests four times over a decade. Partial correlations assessed relationships between reported days of definite anticholinergic drug exposure with changes in cognitive performance. Linear mixed models were conducted testing main effects for anticholinergic drug use and interaction effects between anticholinergic drug use, apolipoprotein ε4 status, and time on neuropsychological assessment performance.
Partial correlations indicated that days of anticholinergic drug exposure was associated with a decline in mental status for the entire sample (r = -.043, p = .011), and immediate verbal memory (r = -.066, p = .043), delayed verbal memory (r = -.077, p = .018), psychomotor speed (r = -.066, p = .043), and cognitive flexibility (r = -.067, p = .040) of apolipoprotein ε4 carriers only. The linear mixed-model results suggested that anticholinergic drug users had a greater decline than nonusers in delayed memory, psychomotor speed, and cognitive flexibility. Apolipoprotein ε4 carrier, anticholinergic drug users performed worse in delayed memory than nonusers and noncarrier, anticholinergic drug users.
Anticholinergic drug use may have deleterious effects on the cognitive functioning of subjects in populations at risk for dementia, especially among apolipoprotein ε4 carriers. (PsycInfo Database Record (c) 2021 APA, all rights reserved).
本研究旨在检验抗胆碱能药物暴露与威斯康星州阿尔茨海默病预防注册研究(WRAP)认知能力下降相关的假设。次要目的是评估抗胆碱能药物对整个样本和载脂蛋白 E4 状态不同认知功能域的影响是否存在差异。
WRAP 研究包括 1573 名自我报告用药情况的受试者,他们在十年内接受了多次认知测试。偏相关评估了报告的抗胆碱能药物暴露天数与认知表现变化之间的关系。线性混合模型用于测试抗胆碱能药物使用的主要影响以及抗胆碱能药物使用、载脂蛋白 E4 状态和神经心理评估表现之间的时间交互作用。
偏相关表明,抗胆碱能药物暴露天数与整个样本的精神状态下降(r=-.043,p=.011)以及即时言语记忆(r=-.066,p=.043)、延迟言语记忆(r=-.077,p=.018)、精神运动速度(r=-.066,p=.043)和认知灵活性(r=-.067,p=.040)呈负相关,仅载脂蛋白 E4 携带者。线性混合模型结果表明,抗胆碱能药物使用者比非使用者在延迟记忆、精神运动速度和认知灵活性方面下降更为明显。载脂蛋白 E4 携带者、抗胆碱能药物使用者在延迟记忆方面的表现比非使用者和非携带者、抗胆碱能药物使用者更差。
抗胆碱能药物的使用可能对痴呆风险人群的认知功能产生有害影响,尤其是在载脂蛋白 E4 携带者中。(PsycInfo 数据库记录(c)2021 APA,保留所有权利)。