Abstract
The traditional management of psoriatic arthritis (PsA) includes NSAIDs, corticosteroids and DMARDs. Advancement in the knowledge of the immunopathogenesis of PsA has been associated with the development of biologic agents which have revolutionized the management of the disease. Among biologics drugs, there are the 4 currently available anti-TNFα blocking agents (etanercept, infliximab, adalimumab and golimumab) which are more effective than traditional DMARDs on symptoms/signs of inflammation, quality of life, function, and in inhibiting the progression of the structural joint damage. Despite of the high cost, TNF inhibitors are cost-effective on both the musculoskeletal and skin manifestations of psoriatic disease.
MeSH terms
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Adalimumab
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Antibodies, Monoclonal / therapeutic use
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Antibodies, Monoclonal, Humanized / therapeutic use
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Arthritis, Psoriatic / drug therapy*
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Arthritis, Psoriatic / economics
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Arthritis, Psoriatic / therapy
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Biological Factors / economics
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Biological Factors / therapeutic use*
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Clinical Trials as Topic
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Etanercept
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Humans
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Immunoglobulin G / therapeutic use
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Infliximab
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Interleukins / antagonists & inhibitors
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Lymphocyte Depletion
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Practice Guidelines as Topic
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RANK Ligand / antagonists & inhibitors
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Receptor Activator of Nuclear Factor-kappa B / antagonists & inhibitors
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Receptors, Tumor Necrosis Factor / therapeutic use
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Tumor Necrosis Factor-alpha / antagonists & inhibitors
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Biological Factors
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Immunoglobulin G
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Interleukins
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RANK Ligand
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Receptor Activator of Nuclear Factor-kappa B
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Receptors, Tumor Necrosis Factor
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TNFRSF11A protein, human
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TNFSF11 protein, human
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Tumor Necrosis Factor-alpha
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golimumab
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Infliximab
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Adalimumab
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Etanercept