School of Pharmacy, University of Washington, Seattle.
Group Health Research Institute, Seattle, Washington.
JAMA Intern Med. 2015 Mar;175(3):401-7. doi: 10.1001/jamainternmed.2014.7663.
Many medications have anticholinergic effects. In general, anticholinergic-induced cognitive impairment is considered reversible on discontinuation of anticholinergic therapy. However, a few studies suggest that anticholinergics may be associated with an increased risk for dementia.
To examine whether cumulative anticholinergic use is associated with a higher risk for incident dementia.
DESIGN, SETTING, AND PARTICIPANTS: Prospective population-based cohort study using data from the Adult Changes in Thought study in Group Health, an integrated health care delivery system in Seattle, Washington. We included 3434 participants 65 years or older with no dementia at study entry. Initial recruitment occurred from 1994 through 1996 and from 2000 through 2003. Beginning in 2004, continuous replacement for deaths occurred. All participants were followed up every 2 years. Data through September 30, 2012, were included in these analyses.
Computerized pharmacy dispensing data were used to ascertain cumulative anticholinergic exposure, which was defined as the total standardized daily doses (TSDDs) dispensed in the past 10 years. The most recent 12 months of use was excluded to avoid use related to prodromal symptoms. Cumulative exposure was updated as participants were followed up over time.
Incident dementia and Alzheimer disease using standard diagnostic criteria. Statistical analysis used Cox proportional hazards regression models adjusted for demographic characteristics, health behaviors, and health status, including comorbidities.
The most common anticholinergic classes used were tricyclic antidepressants, first-generation antihistamines, and bladder antimuscarinics. During a mean follow-up of 7.3 years, 797 participants (23.2%) developed dementia (637 of these [79.9%] developed Alzheimer disease). A 10-year cumulative dose-response relationship was observed for dementia and Alzheimer disease (test for trend, P < .001). For dementia, adjusted hazard ratios for cumulative anticholinergic use compared with nonuse were 0.92 (95% CI, 0.74-1.16) for TSDDs of 1 to 90; 1.19 (95% CI, 0.94-1.51) for TSDDs of 91 to 365; 1.23 (95% CI, 0.94-1.62) for TSDDs of 366 to 1095; and 1.54 (95% CI, 1.21-1.96) for TSDDs greater than 1095. A similar pattern of results was noted for Alzheimer disease. Results were robust in secondary, sensitivity, and post hoc analyses.
Higher cumulative anticholinergic use is associated with an increased risk for dementia. Efforts to increase awareness among health care professionals and older adults about this potential medication-related risk are important to minimize anticholinergic use over time.
许多药物具有抗胆碱能作用。一般来说,抗胆碱能引起的认知障碍被认为在停止抗胆碱能治疗后是可逆的。然而,一些研究表明,抗胆碱能药物可能与痴呆风险增加有关。
研究累积抗胆碱能药物的使用是否与更高的痴呆发病风险相关。
设计、地点和参与者:这是一项基于人群的前瞻性队列研究,使用了华盛顿州西雅图市团体健康成人思想变化研究中的数据。我们纳入了 3434 名年龄在 65 岁或以上、入组时无痴呆的参与者。最初的招募工作于 1994 年至 1996 年和 2000 年至 2003 年进行。从 2004 年开始,死亡的连续替换发生了。所有参与者每两年接受一次随访。这些分析纳入了截至 2012 年 9 月 30 日的数据。
使用计算机化的药房配药数据来确定累积抗胆碱能药物的暴露情况,这是通过过去 10 年中开出的总标准化日剂量(TSDDs)来定义的。最近的 12 个月的使用被排除在外,以避免与前驱症状有关的使用。随着参与者随时间的推移而被随访,累积暴露情况会不断更新。
采用标准诊断标准确定痴呆和阿尔茨海默病的发病情况。使用 Cox 比例风险回归模型进行统计分析,模型调整了人口统计学特征、健康行为和健康状况,包括合并症。
最常见的抗胆碱能药物类别是三环类抗抑郁药、第一代抗组胺药和膀胱抗毒蕈碱类药物。在平均 7.3 年的随访期间,797 名参与者(23.2%)患上了痴呆症(其中 637 名[79.9%]患有阿尔茨海默病)。痴呆症和阿尔茨海默病发病存在 10 年的累积剂量反应关系(趋势检验,P<0.001)。对于痴呆症,与非使用相比,累积抗胆碱能药物使用的调整后的危险比为 TSDDs 为 1 到 90 的 0.92(95%CI,0.74-1.16);TSDDS 为 91 到 365 的 1.19(95%CI,0.94-1.51);TSDDS 为 366 到 1095 的 1.23(95%CI,0.94-1.62);TSDDS 大于 1095 的 1.54(95%CI,1.21-1.96)。阿尔茨海默病也有类似的结果模式。在二次、敏感性和事后分析中,结果也是稳健的。
更高的累积抗胆碱能药物使用与痴呆风险增加相关。努力提高卫生保健专业人员和老年人对这种潜在药物相关风险的认识,对于随着时间的推移减少抗胆碱能药物的使用非常重要。