Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
University of Glasgow, Glasgow, UK.
Cochrane Database Syst Rev. 2021 May 5;5(5):CD013540. doi: 10.1002/14651858.CD013540.pub2.
BACKGROUND: Medications with anticholinergic properties are commonly prescribed to older adults. The cumulative anticholinergic effect of all the medications a person takes is referred to as the 'anticholinergic burden' because of its potential to cause adverse effects. It is possible that high anticholinergic burden may be a risk factor for development of cognitive decline or dementia. There are various scales available to measure anticholinergic burden but agreement between them is often poor. OBJECTIVES: To assess whether anticholinergic burden, as defined at the level of each individual scale, is a prognostic factor for future cognitive decline or dementia in cognitively unimpaired older adults. SEARCH METHODS: We searched the following databases from inception to 24 March 2021: MEDLINE (OvidSP), Embase (OvidSP), PsycINFO (OvidSP), CINAHL (EBSCOhost), and ISI Web of Science Core Collection (ISI Web of Science). SELECTION CRITERIA: We included prospective and retrospective longitudinal cohort and case-control observational studies with a minimum of one year' follow-up that examined the association between an anticholinergic burden measurement scale and future cognitive decline or dementia in cognitively unimpaired older adults. DATA COLLECTION AND ANALYSIS: Two review authors independently assessed studies for inclusion, and undertook data extraction, assessment of risk of bias, and GRADE assessment. We extracted odds ratios (OR) and hazard ratios, with 95% confidence intervals (CI), and linear data on the association between anticholinergic burden and cognitive decline or dementia. We intended to pool each metric separately; however, only OR-based data were suitable for pooling via a random-effects meta-analysis. We initially established adjusted and unadjusted pooled rates for each available anticholinergic scale; then, as an exploratory analysis, established pooled rates on the prespecified association across scales. We examined variability based on severity of anticholinergic burden. MAIN RESULTS: We identified 25 studies that met our inclusion criteria (968,428 older adults). Twenty studies were conducted in the community care setting, two in primary care clinics, and three in secondary care settings. Eight studies (320,906 participants) provided suitable data for meta-analysis. The Anticholinergic Cognitive Burden scale (ACB scale) was the only scale with sufficient data for 'scale-based' meta-analysis. Unadjusted ORs suggested an increased risk for cognitive decline or dementia in older adults with an anticholinergic burden (OR 1.47, 95% CI 1.09 to 1.96) and adjusted ORs similarly suggested an increased risk for anticholinergic burden, defined according to the ACB scale (OR 2.63, 95% CI 1.09 to 6.29). Exploratory analysis combining adjusted ORs across available scales supported these results (OR 2.16, 95% CI 1.38 to 3.38), and there was evidence of variability in risk based on severity of anticholinergic burden (ACB scale 1: OR 2.18, 95% CI 1.11 to 4.29; ACB scale 2: OR 2.71, 95% CI 2.01 to 3.56; ACB scale 3: OR 3.27, 95% CI 1.41 to 7.61); however, overall GRADE evaluation of certainty of the evidence was low. AUTHORS' CONCLUSIONS: There is low-certainty evidence that older adults without cognitive impairment who take medications with anticholinergic effects may be at increased risk of cognitive decline or dementia.
背景:具有抗胆碱能特性的药物通常开给老年人。一个人服用的所有药物的累积抗胆碱能效应被称为“抗胆碱能负担”,因为它有可能引起不良反应。高抗胆碱能负担可能是认知能力下降或痴呆发展的一个风险因素。有各种量表可用于衡量抗胆碱能负担,但它们之间的一致性往往很差。
目的:评估个体量表定义的抗胆碱能负担是否是认知正常的老年人未来认知能力下降或痴呆的预后因素。
检索方法:我们从成立到 2021 年 3 月 24 日检索了以下数据库:MEDLINE(OvidSP)、Embase(OvidSP)、PsycINFO(OvidSP)、CINAHL(EBSCOhost)和 ISI Web of Science 核心合集(ISI Web of Science)。
选择标准:我们纳入了前瞻性和回顾性纵向队列研究和病例对照观察研究,随访时间至少为一年,研究了认知正常的老年人中抗胆碱能负担测量量表与未来认知能力下降或痴呆之间的关系。
数据收集和分析:两名综述作者独立评估了纳入研究,并进行了数据提取、偏倚风险评估和 GRADE 评估。我们提取了比值比(OR)和风险比,以及 95%置信区间(CI),以及抗胆碱能负担与认知能力下降或痴呆之间的线性关联数据。我们打算分别对每个指标进行汇总;然而,只有基于 OR 的数据适合通过随机效应荟萃分析进行汇总。我们最初为每个可用的抗胆碱能量表建立了调整和未调整的汇总率;然后,作为探索性分析,根据各量表建立了汇总的关联率。我们根据抗胆碱能负担的严重程度检查了变异性。
主要结果:我们确定了 25 项符合我们纳入标准的研究(968428 名老年人)。20 项研究在社区护理环境中进行,2 项在初级保健诊所进行,3 项在二级保健环境中进行。八项研究(320906 名参与者)提供了适合荟萃分析的数据。只有抗胆碱能认知负担量表(ACB 量表)有足够的数据进行“基于量表”的荟萃分析。未调整的 OR 表明,抗胆碱能负担的老年人认知能力下降或痴呆的风险增加(OR 1.47,95%CI 1.09 至 1.96),根据 ACB 量表调整后的 OR 也同样表明抗胆碱能负担的风险增加(OR 2.63,95%CI 1.09 至 6.29)。对可用量表的调整后 OR 进行的探索性分析支持了这些结果(OR 2.16,95%CI 1.38 至 3.38),并且根据抗胆碱能负担的严重程度存在风险变化的证据(ACB 量表 1:OR 2.18,95%CI 1.11 至 4.29;ACB 量表 2:OR 2.71,95%CI 2.01 至 3.56;ACB 量表 3:OR 3.27,95%CI 1.41 至 7.61);然而,总体而言,证据的确定性评价为低水平。
作者结论:有低确定性证据表明,没有认知障碍的服用具有抗胆碱能作用的药物的老年人可能有更高的认知能力下降或痴呆风险。
Cochrane Database Syst Rev. 2021-5-5
Cochrane Database Syst Rev. 2022-8-22
Cochrane Database Syst Rev. 2022-2-1
Cochrane Database Syst Rev. 2021-11-8
Cochrane Database Syst Rev. 2021-2-22
Dement Neuropsychol. 2025-8-22
Basic Clin Pharmacol Toxicol. 2025-10
Front Public Health. 2025-7-17
Afr J Prim Health Care Fam Med. 2025-3-31
Aust J Rural Health. 2025-4
Front Med (Lausanne). 2025-2-12
Pharmacoepidemiol Drug Saf. 2020-12
Eur J Clin Pharmacol. 2021-2