The Effect of Anti-rheumatic Drugs on the Skeleton

被引:0
|
作者
B. Hauser
H. Raterman
S. H. Ralston
W. F. Lems
机构
[1] Western General Hospital,Rheumatic Disease Unit
[2] University of Edinburgh,Rheumatology and Bone Disease Unit, Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer
[3] Northwest Clinics,Department of Rheumatology
[4] Amsterdam Rheumatology and Immunology Centre,undefined
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关键词
Anti-rheumatic treatment; Rheumatoid arthritis; Bone mineral density; Fracture risk; Erosion repair;
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摘要
The therapeutic armamentarium for rheumatoid arthritis has increased substantially over the last 20 years. Historically antirheumatic treatment was started late in the disease course and frequently included prolonged high-dose glucocorticoid treatment which was associated with accelerated generalised bone loss and increased vertebral and non-vertebral fracture risk. Newer biologic and targeted synthetic treatments and a combination of conventional synthetic DMARDs prevent accelerated systemic bone loss and may even allow repair of cortical bone erosions. Emerging data also gives new insight on the impact of long-term conventional synthetic DMARDs on bone health and fracture risk and highlights the need for ongoing studies for better understanding of “established therapeutics”. An interesting new antirheumatic treatment effect is the potential of erosion repair with the use of biologic DMARDs and janus kinase inhibitors. Although several newer anti-rheumatic drugs seem to have favorable effects on bone mineral density in RA patients, these effects are modest and do not seem to influence the fracture risk thus far. We summarize recent developments and findings of the impact of anti-rheumatic treatments on localized and systemic bone integrity and health.
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页码:445 / 456
页数:11
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