Risk of Osteoporotic Fractures With Angiotensin II Receptor Blockers Versus Angiotensin-Converting Enzyme Inhibitors in Hypertensive Community-Dwelling Elderly

被引:21
作者
Butt, Debra A. [1 ,2 ]
Mamdani, Muhammad [3 ,4 ,5 ,6 ]
Gomes, Tara [3 ,4 ,5 ,6 ]
Lix, Lisa [7 ]
Lu, Hong [3 ]
Tu, Karen [1 ,3 ,8 ]
机构
[1] Univ Toronto, Dept Family & Community Med, Res Dept, Toronto, ON M5S 1A1, Canada
[2] Scarborough Gen Hosp, Scarborough, ON, Canada
[3] Inst Clin Evaluat Sci, Toronto, ON, Canada
[4] St Michaels Hosp, Appl Hlth Res Ctr, Li Ka Shing Knowledge Inst, Toronto, ON M5B 1W8, Canada
[5] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[6] Univ Toronto, Leslie Dan Fac Pharm, Toronto, ON, Canada
[7] Univ Manitoba, Dept Community Hlth Sci, Winnipeg, MB R3T 2N2, Canada
[8] Toronto Western Hosp, Family Hlth Team, Toronto, ON M5T 2S8, Canada
基金
加拿大健康研究院;
关键词
ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; ANGIOTENSIN II RECEPTOR BLOCKERS; HYPERTENSION; OSTEOPOROSIS-RELATED FRACTURES; ELDERLY;
D O I
10.1002/jbmr.2271
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) are used to treat hypertension; however, in vivo and clinical studies suggest that ARBs and ACE inhibitors may exert different effects on bone. The association between long-term use of ARBs and ACE inhibitors and fracture requiring medical attention is limited. We conducted a population-based, retrospective cohort study with propensity score matching using administrative databases in Ontario, Canada, to examine the risk of osteoporosis-related fractures in hypertensive elderly treated with ARBs versus ACE inhibitors. We identified a cohort of newly treated hypertensive patients aged 66 years and older who initiated an ACE inhibitor from May 1, 2004, to March 31, 2012, and matched them to ARB users on propensity score, sex, and age at drug initiation. The primary outcome was hip fracture, and secondary outcomes were non-hip major osteoporotic fractures (other femoral, clinical vertebral, forearm, wrist, humerus) and other osteoporotic fractures (pelvis, clavicle, patella, shoulder, upper arm, tibia, fibula, ankle, scapula, ribs, sternum, trunk). We calculated hazard ratios (HRs) using Cox proportional hazards model with robust standard errors. Of the 87,635 patients who initiated treatment, 28,819 (32.9%) started ARBs and 58,816 (67.1%) started ACE inhibitors. Among new ARB users, 27,815 (96.5%) were successfully matched to ACE inhibitor users. Without dose adjustment, no significant association was observed for ARBs relative to ACE inhibitor users for hip fractures (HR=0.88; 95% confidence interval [CI] 0.70-1.11), with a decreased risk of other major osteoporotic fractures (HR=0.81; CI 0.70-0.93) and no significant association for other osteoporotic fractures (HR=0.88; CI 0.74-1.05). When adjusted for dosage, there was no significant difference between the effects of ARBs and ACE inhibitors on hip (HR=0.99; CI 0.78-1.25), other major osteoporotic (HR=0.87; CI 0.75-1.01), and other osteoporotic fractures (HR=0.90; CI 0.74-1.08). (c) 2014 American Society for Bone and Mineral Research.
引用
收藏
页码:2483 / 2488
页数:6
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