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:

Myositis-specific autoantibodies

Autoantibody	Effect	Association	Percentage
Histidyl-tRNA synthetase (anti-Jo-1)	myositis, interstitial lung disease, mechanic’s hands, and arthritis	Antisynthetase syndrome
Chromodomain helicase DNA binding protein 4 (Mi-2)
Signal recognition particle (anti-SRP)
Alanyl-tRNA synthetase (PL-12)
Transcriptional intermediary factor 1-gamma (TIF-1γ)
Nuclear matrix protein (NXP-2)
Anti-small ubiquitin-like modifier activating enzyme (anti-SAE)
Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR)	immune-mediated necrotizing myopathies	statin-associated necrotizing autoimmune myopathy (SANAM)	6%