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Multicenter Study
. 2014 Jul 3:349:g4120.
doi: 10.1136/bmj.g4120.

Implications of expanding indications for drug treatment to prevent fracture in older men in United States: cross sectional and longitudinal analysis of prospective cohort study

Affiliations
Multicenter Study

Implications of expanding indications for drug treatment to prevent fracture in older men in United States: cross sectional and longitudinal analysis of prospective cohort study

Kristine E Ensrud et al. BMJ. .

Abstract

Objectives: To quantify incremental effects of applying different criteria to identify men who are candidates for drug treatment to prevent fracture and to examine the extent to which fracture probabilities vary across distinct categories of men defined by these criteria.

Design: Cross sectional and longitudinal analysis of a prospective cohort study.

Setting: Multicenter Osteoporotic Fractures in Men (MrOS) study in the United States.

Participants: 5880 untreated community dwelling men aged 65 years or over classified into four distinct groups: osteoporosis by World Health Organization criteria alone; osteoporosis by National Osteoporosis Foundation (NOF) but not WHO criteria; no osteoporosis but at high fracture risk (at or above NOF derived FRAX intervention thresholds recommended for US); and no osteoporosis and at low fracture risk (below NOF derived FRAX intervention thresholds recommended for US).

Main outcome measures: Proportion of men identified for drug treatment; predicted 10 year probabilities of hip and major osteoporotic fracture calculated using FRAX algorithm with femoral neck bone mineral density; observed 10 year probabilities for confirmed incident hip and major osteoporotic (hip, clinical vertebral, wrist, or humerus) fracture events calculated using cumulative incidence estimation, accounting for competing risk of mortality.

Results: 130 (2.2%) men were identified as having osteoporosis by using the WHO definition, and an additional 422 were identified by applying the NOF definition (total osteoporosis prevalence 9.4%). Application of NOF derived FRAX intervention thresholds led to 936 (15.9%) additional men without osteoporosis being identified as at high fracture risk, raising the total prevalence of men potentially eligible for drug treatment to 25.3%. Observed 10 year hip fracture probabilities were 20.6% for men with osteoporosis by WHO criteria alone, 6.8% for men with osteoporosis by NOF (but not WHO) criteria, 6.4% for men without osteoporosis but classified as at high fracture risk, and 1.5% for men without osteoporosis and classified as at low fracture risk. A similar pattern was noted in observed fracture probabilities for major osteoporotic fracture. Among men with osteoporosis by WHO criteria, observed fracture probabilities were greater than FRAX predicted probabilities (20.6% v 9.5% for hip fracture and 30.0% v 17.4% for major osteoporotic fracture).

Conclusions and relevance: Choice of definition of osteoporosis and use of NOF derived FRAX intervention thresholds have major effects on the proportion of older men identified as warranting drug treatment to prevent fracture. Among men identified with osteoporosis by WHO criteria, who comprised 2% of the study population, actual observed fracture probabilities during 10 years of follow-up were highest and exceeded FRAX predicted fracture probabilities. On the basis of findings from randomized trials in women, these men are most likely to benefit from treatment. Expanding indications for treatment beyond this small group has uncertain value owing to lower observed fracture probabilities and uncertain benefits of treatment among men not selected on the basis of WHO criteria.

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Conflict of interest statement

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf (available on request from the corresponding author) and declare: KEE serves as a consultant on a data monitoring committee for Merck Sharpe & Dohme; WDL has served as a speaker for Amgen, Eli Lilly, and Novartis and received research grants from Novartis, Amgen, and Genzyme; ESO receives research support from Merck Sharpe & Dohme and Eli Lilly and provides consultation to Amgen, Merck Sharpe & Dohme, and Eli Lilly; no other relationships or activities that could appear to have influenced the submitted work.

Figures

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Fig 1 Observed versus predicted 10 year probability of hip fracture according to definition and fracture risk. 26 hip fractures occurred among 130 men with osteoporosis by WHO criteria alone, 28 among 422 men with osteoporosis by National Osteoporosis Foundation (NOF) (but not WHO) criteria, 59 among 936 men without osteoporosis but at high risk of fracture, and 64 among 4392 men without osteoporosis and at low risk of fracture
None
Fig 2 Observed versus predicted 10 year probability of major osteoporotic fracture according to definition and fracture risk. 38 major osteoporotic fractures occurred among 130 men with osteoporosis by WHO criteria alone, 74 among 422 men with osteoporosis by National Osteoporosis Foundation (NOF) (but not WHO) criteria, 111 among 936 men without osteoporosis but at high risk of fracture, and 206 among 4392 men without osteoporosis but at low risk of fracture

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