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role of rankl inhibition in osteoporosisrankl抑制在骨质疏松症中的作用
Available online /content/9/S1/S3
Review
Role of RANKL inhibition in osteoporosis
Michael McClung
Oregon Osteoporosis Center, NE Hoyt Street, Portland, Oregon 97213, USA
Corresponding author: Michael McClung, mmcclung@
Published: 29 June 2007 Arthritis Research Therapy 2007, 9(Suppl 1):S3 (doi:10.1186/ar2167)
This article is online at /content/9/S1/S3
© 2007 BioMed Central Ltd
Abstract about 20% [3]. One-third of hip fractures occur in men. A
When the rate of bone resorption exceeds that of bone formation, healthy 50-year-old woman has a 40% to 50% chance of
destruction of bone tissue occurs, resulting in a fragile skeleton. The experiencing an osteoporosis-related fracture over the
clinical consequences, namely osteoporosis and fragility fractures, remainder of her lifetime, whereas approximately 20% of men
are common and costly problems. Treatments that normalize the will experience fragility fractures.
balance of bone turnover by inhibiting bone resorption preserve
bone mass and reduce fracture risk. The discovery of receptor
Caring for patients with these fractures is expensive; the
activator of nuclear factor-κB ligand (RANKL) as a pivotal regulator
of osteoclast activity provides a new therapeutic target. Early annual direct care expenditure on caring for patients with
studies have demonstrated that denosumab, an investigational, osteoporotic fractures was US$12 to 18 billion in 2002 [3].
hig
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