Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Int Psychogeriatr. 2024 Feb;36(2):142-148. doi: 10.1017/S1041610223000455. Epub 2023 May 26.
Older adults commonly take benzodiazepines (BZDs) that may have long-term adverse cognitive effects. We investigated whether BZD use was related to developing mild cognitive impairment (MCI) or dementia in cognitively normal older adults in the community.
SETTING/PARTICIPANTS: A population-based cohort ( = 1959) of adults aged 65 and over, recruited from communities of low socioeconomic status.
BZD use, Clinical Dementia Rating (CDR), anxiety symptoms, depression symptoms, sleep difficulties, and genotype.
We examined time from study entry to MCI (CDR = 0.5) and time from study entry to dementia (CDR ≥ 1) in participants who were cognitively normal at baseline (CDR = 0). We used survival analysis (Cox model), adjusted for age, sex, education, sleep, anxiety, and depression. For all the models, we included an interaction term between BZD use and .
Taking BZDs was significantly associated with higher risk of developing MCI, but not of developing dementia. The effect was not affected by genotype.
In a population-based sample of cognitively normal older adults, BZD use is associated with developing MCI, but not dementia. BZD use may be a potentially modifiable risk factor for MCI.
老年人通常会服用苯二氮䓬类药物(BZDs),这些药物可能会对认知产生长期的不良影响。我们研究了在认知正常的社区老年人中,BZD 的使用是否与轻度认知障碍(MCI)或痴呆的发展有关。
设置/参与者:一项基于人群的队列研究(n=1959),参与者为年龄在 65 岁及以上、来自社会经济地位较低社区的成年人。
BZD 使用情况、临床痴呆评定量表(CDR)、焦虑症状、抑郁症状、睡眠困难和 基因型。
我们在基线时认知正常(CDR=0)的参与者中,检查了从研究入组到 MCI(CDR=0.5)和从研究入组到痴呆(CDR≥1)的时间。我们使用生存分析(Cox 模型),调整了年龄、性别、教育程度、睡眠、焦虑和抑郁。对于所有模型,我们都包含了 BZD 使用和 基因型之间的交互项。
服用 BZDs 与发生 MCI 的风险显著增加相关,但与发生痴呆的风险无关。该效果不受 基因型的影响。
在认知正常的老年人群体中,BZD 的使用与 MCI 的发生有关,而与痴呆无关。BZD 的使用可能是 MCI 的一个潜在可改变的风险因素。