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Risk of fractures in older adults using antihypertensive medications
Daniel H Solomon1, Helen Mogun, Katie Garneau
1Division of Rheumatology and Pharmacoepidemiology, Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA. dsolomon@partners.org
Insights
Fracture risk varies among hypertension medications. Thiazide diuretics and angiotensin receptor blockers showed lower fracture risks compared to calcium channel blockers in a large Medicare study.
Area of Science:
- Pharmacology
- Gerontology
- Epidemiology
Background:
- Hypertension and its treatments can impact bone metabolism and density.
- Existing research suggests a link between antihypertensive drugs and bone health.
- The specific fracture risk associated with different classes of antihypertensive medications requires further investigation.
Purpose of the Study:
- To evaluate the relative risk of osteoporotic fractures in hypertensive patients initiating single-drug antihypertensive therapy.
- To compare fracture risk across various classes of antihypertensive medications.
Main Methods:
- A large cohort of 376,061 Medicare beneficiaries with hypertension, new to antihypertensive medication, was assembled.
- Health care utilization data were used to track osteoporotic fracture events.
- Adjusted Cox proportional hazards regression models analyzed fracture risk by medication type.
Main Results:
- The overall fracture rate was 35.2 per 1000 person-years.
- Thiazide diuretics had the lowest fracture rate (28.5/1000 person-years), while loop diuretics had the highest (49.0/1000 person-years).
- Angiotensin receptor blockers (HR=0.76) and thiazide diuretics (HR=0.85) were associated with reduced fracture risk compared to calcium channel blockers.
Conclusions:
- The risk of osteoporotic fracture differs significantly among patients using various antihypertensive drug classes.
- Angiotensin receptor blockers and thiazide diuretics may offer a lower fracture risk profile.
- Further research into medication-specific effects on bone health in hypertensive individuals is warranted.
Abstract:
Many medications used to control blood pressure have been associated with bone metabolism. In addition, hypertension itself may be associated with reduced bone mineral density. We examined the relative risk of fracture among subjects with hypertension initiating single-drug therapy for antihypertension treatment. We assembled a large cohort of Medicare beneficiaries with a diagnosis of hypertension who had not filled a prescription for an antihypertensive medication in the prior 365 days. All subsequently began treatment with a single antihypertensive drug. These subjects were followed forward using health care utilization data to determine the risk of a typical osteoporotic fracture. Adjusted Cox proportional hazards regression models were constructed to assess the relative risk of fracture across types of antihypertensive medications. We identified 376,061 eligible subjects. Fracture rate in the total cohort was 35.2 per 1000 person-years [95% confidence interval (CI) 34.4-36.1]. Rates varied significantly across type of antihypertensive, with thiazide diuretics having the lowest rate (28.5, 95% CI 25.4-31.9) and loop diuretics the highest rate (49.0, 95% CI 46.1-52.1). In models adjusting for relevant comorbidities and comedications accessible in health care utilization data, the risk of fracture was reduced in users of angiotensin receptor blockers [hazard ratio (HR) = 0.76, 95% CI 0.68-0.86) and thiazide diuretics (HR = 0.85, 95% CI 0.76-0.97) compared with calcium channel blockers. The adjusted fracture risk was not significantly different from the reference for loop diuretics, beta blockers, and angiotensin-converting enzyme (ACE) inhibitors. It is concluded that the risk of fracture differs across users of different antihypertensive medications.
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