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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.

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