Polymyositis and dermatomyositis laboratory findings
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]
Overview
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
OR
Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
OR
[Test] is usually normal for patients with [disease name].
OR
Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].
OR
There are no diagnostic laboratory findings associated with [disease name].
Laboratory Findings
- Laboratory findings consistent with the diagnosis of polymyositis and dermatomyositis include:[1]
Myositis-specific autoantibodies
Autoantibody | Effect | Association | Percentage | |
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Histidyl-tRNA synthetase (anti-Jo-1) |
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Chromodomain helicase DNA binding protein 4 (Mi-2) |
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Signal recognition particle (anti-SRP) |
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Alanyl-tRNA synthetase (PL-12) |
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Transcriptional intermediary factor 1-gamma (TIF-1γ) |
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Nuclear matrix protein (NXP-2) |
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Anti-small ubiquitin-like modifier activating enzyme (anti-SAE) |
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Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) | immune-mediated necrotizing myopathies |
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6% | |