Goh Kah L, Bhaskaran Krishnan, Minassian Caroline, Evans Stephen J W, Smeeth Liam, Douglas Ian J
KLG Drug Safety Ltd, Walnut House, 34 Rose Street, Wokingham, RG40 1XU, UK.
Br J Clin Pharmacol. 2015 Feb;79(2):337-50. doi: 10.1111/bcp.12511.
This was a cohort study to evaluate whether individuals exposed to angiotensin receptor blockers have a reduced risk of dementia compared with those exposed to angiotensin-converting enzyme inhibitors.
The study included new users of angiotensin receptor blockers or angiotensin-converting enzyme inhibitors (from 1995 to 2010) from UK primary care practices contributing to the Clinical Research Practice Datalink. The association between exposure to angiotensin receptor blockers and the risk of incident dementia was analysed using a Cox model, adjusting for age, sex, body mass index, diabetes, hypertension, heart failure, statin use, socioeconomic status, alcohol, smoking, number of consultations and calendar year.
A total of 426 089 persons were included in the primary analysis, with 45 541 persons exposed to angiotensin receptor blockers and the remainder to angiotensin-converting enzyme inhibitors. The total number of new diagnoses of dementia was 6517. There was weak evidence of a decreased risk of dementia with exposure to angiotensin receptor blockers, with follow-up beginning at 1 year after the start of treatment (adjusted hazard ratio 0.92, 95% confidence interval 0.85-1.00). An analysis restricted to the first 12 months after the index date showed a larger effect on dementia risk (adjusted hazard ratio 0.60, 95% confidence interval 0.50-0.72).
A small reduction in dementia risk was seen with angiotensin receptor blockers in comparison to angiotensin-converting enzyme inhibitors. However, the strongest association was seen in early follow-up, suggesting that the inverse association is unlikely to be causal, but instead reflects other important but unmeasured differences between angiotensin receptor blocker and angiotensin-converting enzyme inhibitor users.
本队列研究旨在评估与使用血管紧张素转换酶抑制剂的个体相比,使用血管紧张素受体阻滞剂的个体患痴呆症的风险是否降低。
该研究纳入了英国基层医疗实践中(1995年至2010年)使用血管紧张素受体阻滞剂或血管紧张素转换酶抑制剂的新用户,这些数据来自临床研究实践数据链。使用Cox模型分析血管紧张素受体阻滞剂暴露与新发痴呆症风险之间的关联,并对年龄、性别、体重指数、糖尿病、高血压、心力衰竭、他汀类药物使用、社会经济地位、饮酒、吸烟、就诊次数和日历年份进行调整。
初步分析共纳入426089人,其中45541人使用血管紧张素受体阻滞剂,其余使用血管紧张素转换酶抑制剂。痴呆症新诊断总数为6517例。有微弱证据表明,使用血管紧张素受体阻滞剂可降低痴呆症风险,随访从治疗开始后1年开始(调整后风险比0.92,95%置信区间0.85-1.00)。对索引日期后前12个月的分析显示,对痴呆症风险的影响更大(调整后风险比0.60,95%置信区间0.50-0.72)。
与血管紧张素转换酶抑制剂相比,血管紧张素受体阻滞剂可使痴呆症风险略有降低。然而,在早期随访中观察到最强的关联,这表明这种反向关联不太可能是因果关系,而更可能反映了血管紧张素受体阻滞剂使用者和血管紧张素转换酶抑制剂使用者之间其他重要但未测量的差异。