Department of Epidemiology & Preventive Medicine, Monash University, ASPREE Co-ordinating Centre, Melbourne, Victoria, Australia.
Turner Institute for Brain and Mental Health, Monash University, Melbourne, VIC, Australia.
J Gen Intern Med. 2021 Jun;36(6):1629-1637. doi: 10.1007/s11606-020-06550-2. Epub 2021 Mar 22.
Anticholinergic medications may increase risk of dementia and stroke, but prospective studies in healthy older people are lacking.
Compare risk of incident dementia and stroke by anticholinergic burden among initially healthy older people.
Prospective cohort study.
Primary care (Australia and USA).
19,114 community-dwelling participants recruited for the ASPREE trial, aged 70+ years (65+ if US minorities) without major cardiovascular disease, dementia diagnosis, or Modified Mini-Mental State Examination score below 78/100.
Baseline anticholinergic exposure was calculated using the Anticholinergic Cognitive Burden (ACB) score. Dementia was adjudicated using Diagnostic and Statistical Manual of Mental Disorders volume IV criteria, and stroke using the World Health Organization definition.
At baseline, 15,000 participants (79%) had an ACB score of zero, 2930 (15%) a score of 1-2, and 1184 (6%) a score of ≥ 3 (indicating higher burden). After a median follow-up of 4.7 years and adjusting for baseline covariates, a baseline ACB score of ≥ 3 was associated with increased risk of ischemic stroke (adjusted HR 1.58, 95% CI 1.06, 2.35), or dementia (adjusted HR 1.36, 95% CI 1.01, 1.82), especially of mixed etiology (adjusted HR 1.53, 95% CI 1.06, 2.21). Results were similar for those exposed to moderate/highly anticholinergic medications.
Residual confounding and reverse causality are possible. Assessment of dose or duration was not possible.
High anticholinergic burden in initially healthy older people was associated with increased risk of incident dementia and ischemic stroke. A vascular effect may underlie this association. These findings highlight the importance of minimizing anticholinergic exposure in healthy older people.
抗胆碱能药物可能会增加痴呆和中风的风险,但缺乏针对健康老年人的前瞻性研究。
比较健康老年人中抗胆碱能药物负担与新发痴呆和中风风险的关系。
前瞻性队列研究。
初级保健(澳大利亚和美国)。
参加 ASPREE 试验的 19114 名社区居住的参与者,年龄在 70 岁以上(如果是美国少数民族,则为 65 岁以上),无重大心血管疾病、痴呆诊断或改良 Mini-Mental State 量表评分低于 78/100。
使用抗胆碱能认知负担 (ACB) 评分计算基线抗胆碱能暴露。使用精神障碍诊断和统计手册第四版标准确定痴呆,使用世界卫生组织定义确定中风。
基线时,15000 名参与者(79%)的 ACB 评分为 0,2930 名(15%)为 1-2,1184 名(6%)为≥3(表示负担较高)。中位随访 4.7 年后,调整基线协变量后,基线 ACB 评分≥3 与缺血性中风风险增加相关(调整后的 HR 1.58,95%CI 1.06,2.35),或痴呆(调整后的 HR 1.36,95%CI 1.01,1.82),尤其是混合病因(调整后的 HR 1.53,95%CI 1.06,2.21)。对于暴露于中度/高度抗胆碱能药物的人,结果相似。
可能存在残余混杂和反向因果关系。无法评估剂量或持续时间。
健康老年人中高抗胆碱能药物负担与新发痴呆和缺血性中风风险增加有关。血管效应可能是这种关联的基础。这些发现强调了在健康老年人中尽量减少抗胆碱能药物暴露的重要性。