4.5 Article

Performance of FRAX in a cohort of community-dwelling, ambulatory older men: the Osteoporotic Fractures in Men (MrOS) study

Journal

OSTEOPOROSIS INTERNATIONAL
Volume 24, Issue 4, Pages 1185-1193

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s00198-012-2215-3

Keywords

Fracture; Men; Prediction; Risk assessment

Funding

  1. National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
  2. National Institute on Aging (NIA)
  3. National Center for Research Resources (NCRR)
  4. NIH Roadmap for Medical Research [U01 AR45580, U01 AR45614, U01 AR45632, U01 AR45647, U01 AR45654, U01 AR45583, U01 AG18197, U01-AG027810, UL1 RR024140]
  5. National Institutes of Health [AR053351]
  6. Foundation for Osteoporosis Research and Education (FORE)

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We evaluated performance of FRAX in older men who participated in the Osteoporotic Fractures in Men (MrOS) study. FRAX has been extensively studied in women, but there are few studies of its performance in men. FRAX estimates for 10-year hip fracture and major osteoporotic fracture (MOF; either hip, clinical spine, forearm, or shoulder) were calculated from data obtained from MrOS participants and compared to observed 10-year fracture cumulative incidence calculated using product limit estimate methods, accounting for competing mortality risk. Five thousand eight hundred ninety-one men were followed for an average of 8.4 years. Without bone mineral density (BMD) in the FRAX model, the mean 10-year predicted fracture probabilities for hip and MOF were 3.5 % and 8.9 %, respectively; addition of BMD to the calculations reduced these estimates to 2.3 % and 7.6 %. Using FRAX without BMD, predicted quintile probabilities closely estimated cumulative incidence of hip fracture (range of observed to predicted ratios 0.9-1.1). However, with BMD in the FRAX calculation, observed to predicted hip fracture probabilities were not close to unity and varied markedly across quintiles of predicted probability. For MOF, FRAX without BMD overestimated observed cumulative incidence (range of observed to predicted ratios 0.7-0.9) and addition of BMD did not improve this discrepancy (range of observed to predicted ratios 0.7-1.1). Addition of BMD to the calculation had mixed effects on the discriminatory performance of FRAX, depending on the analysis tool applied. Among this cohort of community-dwelling older men, the FRAX risk calculator without BMD was well calibrated to hip fracture but less well to MOF.

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