Associations of Anti-Hypertensive Treatments with Alzheimer's Disease, Vascular Dementia, and Other Dementias

被引:178
作者
Davies, Neil M. [2 ,3 ]
Kehoe, Patrick G. [1 ]
Ben-Shlomo, Yoav [2 ]
Martin, Richard M. [2 ,3 ]
机构
[1] Univ Bristol, Frenchay Hosp, John James Labs, Sch Clin Sci,Fac Med & Dent,Dementia Res Grp, Bristol BS16 1LE, Avon, England
[2] Univ Bristol, Fac Med & Dent, Sch Social & Community Med, Bristol BS16 1LE, Avon, England
[3] Univ Bristol, MRC Ctr Causal Anal Translat Epidemiol CAiTE, Bristol BS16 1LE, Avon, England
基金
英国医学研究理事会;
关键词
All cognitive disorders/dementia; Alzheimer's disease; case control studies; risk factors in epidemiology; vascular dementia; ANGIOTENSIN-CONVERTING ENZYME; BLOOD-PRESSURE; COGNITIVE FUNCTION; BRAIN; HYPERTENSION; DECLINE; MEDICATIONS; INHIBITORS; ENALAPRIL; RELEASE;
D O I
10.3233/JAD-2011-110347
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated whether angiotensin II receptor blockers (ARBs) and angiotensin converting enzyme inhibitors (ACE-Is) are more strongly associated with Alzheimer's disease (AD), vascular dementia (VaD), and other dementias, than other anti-hypertensive drugs. We conducted a nested case-control analysis within the UK general practice research database, with prospectively recorded anti-hypertensive prescribing data. We sampled cases aged >= 60 years and diagnosed between 1997-2008 (5,797 with AD, 2,186 with VaD, 1,214 with unspecified/other dementia) which were matched to up to four controls by age, general practice and gender. We computed odds-ratios and dose response effects for AD, vascular and unspecified/other dementia, comparing those prescribed ARBs or ACE-Is for at least six months with patients prescribed other anti-hypertensives. We controlled for matching factors, co-morbidities, smoking status, an area measure of socioeconomic status, consultation rate and blood pressure and accounted for reverse causality by introducing time-lags of up to eight years prior to diagnosis/index date. Patients diagnosed with AD, vascular and unspecified/other dementia had fewer prescriptions for ARBs and ACE-Is. Inverse associations with AD were strongest for ARBs (odds-ratio; 0.47, 95%CI: 0.37-0.58) compared with ACE-Is (odds-ratio; 0.76, 95%CI: 0.69-0.84) (p(difference)<0.001). Associations of ARBs with AD were stronger than for vascular dementia (p(difference)=0.01) and unspecified/other dementia (p(difference)=0.23). There were inverse dose-response relationships between ARBs and ACE-Is with AD (both p(trend)<0.01). The inverse association of ACE-Is with AD diminished when using longer time lags but the ARB-AD association persisted. Patients with AD were around half as likely to be prescribed ARBs. Further randomized controlled trial evidence is required to rigorously test these findings.
引用
收藏
页码:699 / 708
页数:10
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