Osteoporosis is a systemic skeletal disorder that causes vulnerability of bones to fracture owing to reduction in bone density and deterioration of the bone tissue microstructure. The prevalence of osteoporosis is higher in patients with autoimmune inflam-matory rheumatic diseases, including rheumatoid arthritis (RA), than in those of the general population. In this autoimmune inflammatory rheumatic disease, in addition to known risk factors for osteoporosis, various factors such as chronic inflammation, autoantibodies, metabolic disorders, drugs, and decreased physical activity contribute to additional risk. In RA, disease-related inflammation plays an important role in local or systemic bone loss, and active treatment for inflammation can help prevent os-teoporosis. In addition to conventional synthetic disease-modifying anti-rheumatic drugs that have been traditionally used for treatment of RA, biologic DMARDs and targeted synthetic DMARDs have been widely used. These agents can be employed more selectively and precisely based on disease pathogenesis. It has been reported that these drugs can inhibit bone loss by not only re-ducing inflammation in RA, but also by inhibiting bone resorption and promoting bone formation. In this review, the pathogen-esis and research results of the increase in osteoporosis in RA are reviewed, and the effects of biological agents on osteoporosis are discussed.
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Vet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Univ Utah, Sch Med, Salt Lake City, UT 84112 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Sauer, Brian C.
Teng, Chia-Chen
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Vet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Univ Utah, Sch Med, Salt Lake City, UT 84112 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Teng, Chia-Chen
He, Tao
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Vet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Univ Utah, Sch Med, Salt Lake City, UT 84112 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
He, Tao
Leng, Jianwei
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Vet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Univ Utah, Sch Med, Salt Lake City, UT 84112 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Leng, Jianwei
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Lu, Chao-Chin
Curtis, Jeffrey R.
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Univ Alabama Birmingham, Birmingham, AL USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Curtis, Jeffrey R.
Tang, Derek H.
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Amgen Inc, Thousand Oaks, CA 91320 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Tang, Derek H.
Shah, Neel
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Amgen Inc, Thousand Oaks, CA 91320 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Shah, Neel
Harrison, David J.
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Amgen Inc, Thousand Oaks, CA 91320 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Harrison, David J.
Cannon, Grant W.
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Vet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA
Univ Utah, Sch Med, Salt Lake City, UT 84112 USAVet Affairs Salt Lake City Hlth Care Syst, Salt Lake City, UT USA