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抗胆碱能药物暴露与痴呆风险:有适度证据表明存在关联,但不能证明因果关系。

Anticholinergic Drug Exposure and the Risk of Dementia: There Is Modest Evidence for an Association but Not for Causality.

机构信息

Department of Psychopharmacology, National Institute of Mental Health and Neurosciences, Bangalore, India.

出版信息

J Clin Psychiatry. 2019 Aug 6;80(4):19f13000. doi: 10.4088/JCP.19f13000.

Abstract

Many observational studies published during the past 15 years have found an association between anticholinergic drug exposure and the risk of incident dementia. Animal data suggest plausible causal mechanisms for this finding. The results of a recent, large, and well-conducted study on the subject were widely disseminated by the lay and scientific media. This study addressed protopathic bias by examining anticholinergic drug exposure in time windows 1-11, 3-13, and 5-20 years before the identification of dementia. In brief, the study found that, pooling anticholinergic drug exposure across 11 drug categories, exposure in smallest to largest cumulative dosing groups was significantly associated with incident dementia risk, with an apparently dose-dependent relationship in unadjusted as well as adjusted analyses in all time windows prior to dementia identification. Whereas these findings appear compelling, there are at least 4 elephants in the room. First, only 3 of 11 anticholinergic drug categories were consistently associated with an increased risk of dementia; this suggests that anticholinergic activity may be an irrelevant common denominator. Second, for 2 of these 3 categories (antidepressant and antipsychotic drugs), confounding by indication seemed a distinct possibility. Third, in many analyses it seemed that exposure for as little as the equivalent of 1-90 days sufficed to increase the risk of dementia at a time interval of up to 20 years later; a causal mechanism here would need to have strong neurotoxic effects to result in the widespread brain changes that characterize dementia. Finally, the associations were almost uniformly stronger for vascular dementia than for Alzheimer's disease, making the identification of a causal mechanism even more challenging. Deprescribing anticholinergics to reduce state-dependent cognitive impairment, or to reduce the risk of delirium in vulnerable demographic and medical populations, is reasonable. Deprescribing anticholinergics to reduce the risk of future dementia is presently unwarranted.

摘要

过去 15 年来,许多观察性研究发现抗胆碱能药物暴露与痴呆症发病风险之间存在关联。动物研究数据为这一发现提供了合理的因果机制。最近一项关于这一主题的大型、精心设计的研究的结果被大众和科学界广泛传播。该研究通过在痴呆症确诊前 1-11 年、3-13 年和 5-20 年的时间窗口内检查抗胆碱能药物暴露,解决了先驱偏倚问题。简而言之,该研究发现,将 11 类抗胆碱能药物的暴露情况汇总后,在最小至最大累积剂量组中,暴露与痴呆症发病风险显著相关,在痴呆症确诊前所有时间窗口的未调整和调整分析中,均显示出明显的剂量依赖性关系。虽然这些发现似乎令人信服,但至少有 4 个明显的问题。首先,只有 11 种抗胆碱能药物类别中的 3 种与痴呆症风险增加始终相关;这表明抗胆碱能活性可能是一个无关的共同因素。其次,对于这 3 个类别中的 2 个(抗抑郁药和抗精神病药),指示性混杂似乎是一种明显的可能性。第三,在许多分析中,似乎只需暴露相当于 1-90 天的时间,就足以在长达 20 年的时间间隔后增加痴呆症的风险;在此情况下,因果机制需要具有强烈的神经毒性作用,才能导致广泛的大脑变化,从而导致痴呆症。最后,血管性痴呆症的相关性几乎普遍强于阿尔茨海默病,这使得确定因果机制更加具有挑战性。为了减轻与状态相关的认知障碍,或降低脆弱的人群和医疗人群发生谵妄的风险,减少抗胆碱能药物的使用是合理的。但是,目前减少抗胆碱能药物的使用以降低未来痴呆症的风险是没有依据的。

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