Benzodiazepine and Z-Drug Use and the Risk of Developing Dementia

被引:13
|
作者
Torres-Bondia, Francisco [1 ]
Dakterzada, Farida [2 ]
Galvan, Leonardo [3 ]
Buti, Miquel [4 ]
Besanson, Gaston [5 ,6 ]
Grill, Eric [5 ]
Buil, Roman [5 ,7 ]
de Batlle, Jordi [8 ,9 ,10 ]
Pinol-Ripoll, Gerard [2 ]
机构
[1] Arnau de Vilanova Univ Hosp, Pharm Dept, IRBLleida, Lleida, Spain
[2] Santa Maria Univ Hosp, Unitat Trastorns Cognitius Cognit Disorders Unit, IRBLleida, Lleida, Spain
[3] Serv Catala Salut Catalan Hlth Serv, Pharm Dept, Lleida, Spain
[4] Catalan Inst Hlth, Clin Evaluat Unit, Lleida, Spain
[5] Accenture Innovat Ctr, Barcelona, Spain
[6] Barcelona Grad Sch Econ, Barcelona, Spain
[7] Univ Oberta Catalunya, Barcelona, Spain
[8] Arnau de Vilanova Univ Hosp, Grp Translat Res Resp Med, Lleida, Spain
[9] Santa Maria Univ Hosp, IRBLleida, Lleida, Spain
[10] Biomed Res Networking Ctr Resp Dis, Madrid, Spain
来源
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY | 2022年 / 25卷 / 04期
关键词
Alzheimer's disease; benzodiazepine; dementia; cohort study; cognitive decline; Z-drug; DEVELOPING ALZHEIMERS-DISEASE; COGNITIVE DECLINE;
D O I
10.1093/ijnp/pyab073
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Benzodiazepines (BZDs) and Z-drugs (BZDRs) are among the most prescribed medications for anxiety and insomnia, especially among older adults. Our objective was to investigate the association between the use of BZDRs and the risk of dementia. Methods A community-based retrospective cohort study was conducted based on the data available from 2002 to 2015 in Catalan Health Service. This cohort included all BZDR users (N = 83 138) and nonusers (N = 84 652) older than 45 years. A minimum 5-year lag window and an adjustment for psychiatric problems were applied for the data analysis. Results The hazard ratio (HR) for the risk of incident dementia among BZDR users was 1.22 (95% CI = 1.15 to 1.31). This risk was not significant after adjusting the data confounding factors (HR = 1.01; 95% CI = 0.94 to 1.08). We observed a higher risk with short-to-intermediate half-life BZDs (HR = 1.11; 95% CI = 1.04 to 1.20) and Z-drugs (HR = 1.20; 95% CI = 1.07 to 1.33) than for intermediate-to-long half-life BZDs (HR = 1.01; 95% CI = 0.94 to 1.08). We demonstrated a higher risk of incident dementia (HR = 1.23; 95% CI = 1.07 to 1.41 and odds ratio = 1.38; 95% CI = 1.27 to 1.50, respectively) in patients who received 91 to 180 defined daily doses (DDDs) and >180 DDDs compared with patients who received <90 DDD. Regarding patient sex, the risk of dementia was higher in women than in men. Conclusion We found that the incidence of dementia was not higher among all BZDR users. Short half-life BZDs and Z-drugs increased the risk of dementia at the highest doses, especially in female patients, showing a dose-response relationship.
引用
收藏
页码:261 / 268
页数:8
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