[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.197.142.219. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
April 9, 1997

Prevention of Nonvertebral Fractures by AlendronateA Meta-analysis

Author Affiliations

for the Alendronate Osteoporosis Treatment Study Groups
From the Merck Research Laboratories, Rahway, NJ (Drs Karpf, Shapiro, Santora, Hirsch, Oppenheimer, and Thompson); AustinHospital,Heidelberg,Victoria,Australia (DrSeeman); University of Minnesota and VA Medical Center, Minneapolis (Dr Ensrud); Indiana University School of Medicine, Indianapolis (Dr Johnston); Centro Ospedaliero Clinicizzato di Valeggio, Verona, Italy (Dr Adami); and University of California, San Francisco (Dr Harris). Dr Karpf is now with Roche Global Development, Palo Alto, Calif;

JAMA. 1997;277(14):1159-1164. doi:10.1001/jama.1997.03540380073035
Abstract

Objective.  —To evaluate the effect of treatment with alendronate sodium, a potent aminobisphosphonate, on the incidence of nonvertebral fractures in postmenopausal women with osteoporosis.

Data Sources.  —Published data and data on file at Merck Research Laboratories.

Study Selection.  —All completed prospective, randomized, placebo-controlled alendronate trials of at least 2 years' duration (5 studies).

Data Extraction.  —All subjects were women with osteoporosis between the ages of 42 and 85 years, postmenopausal at least 4years with lumbar spine bone mineral density (measured using dual-energy x-ray absorptiometry) at least 2.0 SD below the mean for young adult women. All women randomized to treatment with placebo or alendronate at a dose higher than 1 mg per day for at least 2 years were included.

Data Synthesis.  —In the placebo group (n=590), 60 women reported nonvertebral fractures during 1347 patient-years at risk (overall rate, 4.45 women with fractures per 100 patient-years at risk). In the alendronate group (n=1012), 73 women reported nonvertebral fractures during 2240 patient-years at risk (overall rate, 3.26 women with fractures per 100 patient-years at risk). The estimated cumulative incidence of nonvertebral fractures after 3 years was 12.6% in the placebo group and 9.0% in alendronate group. The relative risk for nonvertebral fracture estimated using the Cox proportional hazards model was 0.71 (95% confidence interval,0.502-0.997) (P=.048). A reduction in risk was consistent across each of the studies and at each major site of osteoporotic fracture, including the hip and wrist.

Conclusion.  —In postmenopausal women with osteoporosis, treatment with alendronate reduces the risk of nonvertebral fractures over at least 3 years.

×