Department of Medicine & Therapeutics, the Chinese University of Hong Kong.
Jockey Club Centre for Osteoporosis Care and Control, the Chinese University of Hong Kong.
Age Ageing. 2017 Jan 10;46(1):57-64. doi: 10.1093/ageing/afw150.
Angiotensin II, a major effector protein of the renin angiotensin system (RAS), induces bone loss under certain conditions. Drugs that block the RAS may therefore reduce bone loss and fracture incidence. The fracture incidence in older hypertensive men with long-term use of angiotensin-converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARBs) were compared with the incidence in users of calcium channel blockers (CCBs) and non-users.
A total of 5,994 US men aged 65 years or older who had bone mineral density measured at baseline in the Osteoporotic Fractures in Men Study (MrOS) were followed for fracture incidence for an average of 6.8 years. Men with follow-up dual-energy X-ray absorptiometry bone mineral density data and who reported hypertension at any visit, or use of antihypertensive medications at any visit among those with non-missing mediation data were included in the study (N = 2,573).
Six hundred and nineteen men had taken ACE inhibitors, while 182 took ARBs for at least 4 years. Using Cox regression for the incidence of non-vertebral fractures, we found that long-term users of ACE inhibitors and ARBs each had a significantly lower fracture incidence than non-users. The hazard ratio of non-vertebral fractures was three times lower in ARB users than ACE inhibitor users (Hazard ratio (95% confidence interval): 0.194 (0.079–0.474) versus 0.620 (0.453–0.850), P = 0.0168). There was a trend of greater fracture risk reduction with longer duration of ARB use, but not for ACE inhibitor use.
In older hypertensive men, ARBs use was associated with lower incidence of non-vertebral fracture than ACE inhibitors or CCBs.
血管紧张素 II 是肾素-血管紧张素系统 (RAS) 的主要效应蛋白,在某些情况下会导致骨质流失。因此,阻断 RAS 的药物可能会减少骨质流失和骨折的发生率。本研究比较了长期使用血管紧张素转换酶 (ACE) 抑制剂或血管紧张素受体阻滞剂 (ARB) 的老年高血压男性与钙通道阻滞剂 (CCB) 使用者和未使用者的骨折发生率。
共纳入 5994 名年龄在 65 岁及以上的美国男性,他们在男性骨质疏松性骨折研究 (MrOS) 中基线时进行了骨密度测量,平均随访 6.8 年骨折发生率。本研究纳入了有随访双能 X 射线吸收法骨密度数据且在任何一次就诊时报告有高血压或在非缺失药物数据的就诊时报告有使用降压药物的男性 (n=2573)。
619 名男性服用 ACE 抑制剂,182 名男性至少服用 4 年 ARB。使用 Cox 回归分析非椎体骨折的发生率,我们发现长期使用 ACE 抑制剂和 ARB 的男性骨折发生率均显著低于未使用者。ARB 使用者的非椎体骨折风险比 ACE 抑制剂使用者低 3 倍 (危险比 (95%置信区间):0.194 (0.079-0.474) 比 0.620 (0.453-0.850),P=0.0168)。ARB 使用时间越长,骨折风险降低的趋势越明显,但 ACE 抑制剂的使用则无此趋势。
在老年高血压男性中,ARB 的使用与 ACE 抑制剂或 CCB 相比,非椎体骨折的发生率较低。