School of Pharmacy, University of Eastern Finland, Kuopio, Finland.
Research Centre for Comparative Effectiveness and Patient Safety (RECEPS), University of Eastern Finland, Kuopio, Finland.
Acta Psychiatr Scand. 2018 Aug;138(2):91-100. doi: 10.1111/acps.12909. Epub 2018 May 31.
To assess the association between benzodiazepine and related drug (BZDR) use and risk of Alzheimer's disease (AD) with cumulative consumption and duration of use based models.
A nationwide nested case-control study of all Finnish community-dwelling persons who received clinically verified AD diagnosis in 2005-2011 (N = 70 719) and their matched controls (N = 282 862). AD diagnosis was based on DSM-IV and NINCDS-ADRDA criteria. BZDR purchases were extracted from the Prescription Register since 1995. The association between BZDR use and AD was assessed using conditional logistic regression with 5-year lag time between exposure and outcome.
Benzodiazepine and related drug use was associated with modestly increased risk of AD (adjusted OR 1.06, 95% CI 1.04-1.08). A dose-response relationship was observed with both cumulative consumption and duration. Adjustment for other psychotropics removed the cumulative dose-response relationship by attenuating the ORs in the highest dose category.
Benzodiazepine and related drug use in general was associated with modestly increased risk of AD. No major differences were observed between different subcategories of BZDRs (i.e. benzodiazepines, Z drugs, short-/medium-acting or long-acting BZDRs). As dose-response relationship abolished after adjustment for other psychotropics, it is possible that the association may partially be due to antidepressants and/or antipsychotics, or concomitant use of these medications.
评估苯二氮䓬类和相关药物(BZDR)使用与累积消费和使用时间模型的阿尔茨海默病(AD)风险之间的关联。
这是一项全国性的嵌套病例对照研究,研究对象为所有在 2005-2011 年期间在芬兰社区居住的人群,他们接受了临床确诊的 AD(N=70719),并与他们的匹配对照者(N=282862)进行了匹配。AD 的诊断基于 DSM-IV 和 NINCDS-ADRDA 标准。从 1995 年开始,从处方登记处提取 BZDR 购买记录。使用条件逻辑回归,在暴露和结果之间设置 5 年的滞后时间,评估 BZDR 使用与 AD 之间的关联。
苯二氮䓬类和相关药物的使用与 AD 的风险适度增加相关(调整后的 OR 1.06,95%CI 1.04-1.08)。观察到累积剂量与持续时间之间存在剂量-反应关系。通过削弱最高剂量类别中的 OR,调整其他精神药物后,消除了累积剂量-反应关系。
一般来说,苯二氮䓬类和相关药物的使用与 AD 的风险适度增加相关。在不同的 BZDR 亚类(即苯二氮䓬类、Z 药物、短/中效或长效 BZDR)之间没有观察到明显差异。由于在调整其他精神药物后,剂量-反应关系被消除,因此这种关联可能部分是由于抗抑郁药和/或抗精神病药,或这些药物的同时使用所致。