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Statin Use, Bone Mineral Density, and Fracture Risk
Geelong Osteoporosis Study
Julie A. Pasco, PhD;
Mark A. Kotowicz, MBBS, FRACP;
Margaret J. Henry, PhD;
Kerrie M. Sanders, MNutr, PhD;
Geoffrey C. Nicholson, MBBS, PhD, FRACP, FRCP
Arch Intern Med. 2002;162:537-540.
Background Recent data suggest that 3-hydroxy-3-methylglutaryl coenzyme A reductase
inhibitors (statins) decrease fracture risk and increase bone mineral density
(BMD).
Methods This cross-sectional study is set in southeastern Australia. We evaluated
the association between statin use, fracture risk, and BMD in 1375 women (573
with incident fractures and 802 without incident fracture, all drawn from
the same community). Fractures were identified radiologically. Medication
use and lifestyle factors were documented by questionnaire.
Results Unadjusted odds ratio for fracture associated with statin use was 0.40
(95% confidence interval [CI], 0.23-0.71). Adjusting for BMD at the femoral
neck, spine, and whole body increased the odds ratio to 0.45 (95% CI, 0.25-0.80),
0.42 (95% CI, 0.24-0.75), and 0.43 (95% CI, 0.24-0.78), respectively. Adjusting
for age, weight, concurrent medications, and lifestyle factors had no substantial
effect on the odds ratio for fracture. Statin use was associated with a 3%
greater adjusted BMD at the femoral neck (P = .08),
and BMD tended to be greater at the spine and whole body but did not achieve
statistical significance.
Conclusion The substantial 60% reduction in fracture risk associated with statin
use is greater than would be expected from increases in BMD alone.
From the Department of Clinical and Biomedical SciencesBarwon
Health, The University of Melbourne, Geelong Hospital, Geelong, Australia.
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