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We read with interest the article by the European League Against Rheumatism/American College of Rheumatology on the classification criteria for adult and juvenile idiopathic inflammatory myopathies (IIM) and their major subgroups.1 While we believe these criteria will help with the diagnosis of most of the major subgroups of idiopathic inflammatory myopathies, we anxiously await society guidelines that direct physicians on how best to individualise the treatment for specific subgroups of this disease.
For example, one subgroup we seek immediate direction is on the treatment of patients with antibodies directed against the melanoma differentiation associated protein 5 (anti-MDA5). This antibody is typically identified in patients with clinically amyopathic dermatomyositis (CADM), and it is now increasingly appreciated that some of these individuals …
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