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Submitted on January 9, 2008
Accepted on March 19, 2008
Endocrine Research Unit (S.K.) and Division of Rheumatology (S.A.), College of Medicine, Mayo Clinic, Rochester, MN (S.K., S.A.); and Division of Endocrinology, Oregon Health Sciences University, Portland, Oregon (E.O.)
* To whom correspondence should be addressed. E-mail: khosla.sundeep{at}mayo.edu.
With the aging of the population, there is a growing recognition that osteoporosis and fractures in men are a significant public health problem, and both hip and vertebral fractures are associated with increased morbidity and mortality in men. Osteoporosis in men is a heterogeneous clinical entity: while most men experience bone loss with aging, some men develop osteoporosis at a relatively young age, often for unexplained reasons (idiopathic osteoporosis). Declining sex steroid levels and other hormonal changes likely contribute to age-related bone loss, as do impairments in osteoblast number and/or activity. Secondary causes of osteoporosis also play a significant role in pathogenesis. While there is ongoing controversy regarding whether osteoporosis in men should be diagnosed based on female or male-specific reference ranges (since some evidence indicates that the risk of fracture is similar in women and men for a given level of bone mineral density), a diagnosis of osteoporosis in men is generally made based on male-specific reference ranges. Treatment consists both of non-pharmacological (lifestyle factors, calcium and vitamin D supplementation) and pharmacological (most commonly bisphosphonates or parathyroid hormone) approaches, with efficacy similar to that seen in women. Increasing awareness of osteoporosis in men among physicians and the lay public is critical for the prevention of fractures in our aging male population.
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