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Published on: October 22, 2014
ARB users exhibit a lower fracture incidence than ACE inhibitor users among older hypertensive men
Timothy Kwok1, Jason Leung2, Elizabeth Barrett-Connor3
1Department of Medicine & Therapeutics, the Chinese University of Hong Kong.
Insights
Angiotensin receptor blockers (ARBs) and angiotensin-converting enzyme (ACE) inhibitors reduce fracture risk in older men. ARBs showed a significantly greater reduction in non-vertebral fractures compared to ACE inhibitors.
Area of Science:
- Gerontology
- Pharmacology
- Orthopedics
Background:
- The renin-angiotensin system (RAS) plays a role in bone metabolism.
- Angiotensin II can induce bone loss.
- RAS-inhibiting drugs may mitigate bone loss and fracture risk.
Purpose of the Study:
- To compare fracture incidence in older hypertensive men using ACE inhibitors or ARBs versus calcium channel blockers (CCBs) and non-users.
- To evaluate the long-term effects of ACE inhibitors and ARBs on fracture incidence.
Main Methods:
- A cohort of 2,573 US men aged 65+ from the MrOS study with bone density data were analyzed.
- Fracture incidence was followed for an average of 6.8 years.
- Cox regression was used to assess the association between medication use and non-vertebral fractures.
Main Results:
- Long-term users of ACE inhibitors (N=619) and ARBs (N=182) had significantly lower non-vertebral fracture incidence than non-users.
- ARB users had a 3-fold lower hazard ratio for non-vertebral fractures compared to ACE inhibitor users (0.194 vs. 0.620).
- A trend towards greater fracture risk reduction with longer ARB use duration was observed.
Conclusions:
- In older hypertensive men, ARB use was linked to a lower incidence of non-vertebral fractures compared to ACE inhibitors and CCBs.
- ARBs appear more effective than ACE inhibitors in reducing non-vertebral fracture risk in this population.
Introduction:
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.
Methods:
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).
Results:
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.
Conclusions:
In older hypertensive men, ARBs use was associated with lower incidence of non-vertebral fracture than ACE inhibitors or CCBs.
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