Test Directory
| Test Code | ||||
| MYO11 | ||||
| Test Name | ||||
| Myositis Specific 11 Antibody Panel | ||||
| CPT Codes | ||||
| 84182 X 6, 86235 X 5 | ||||
| Included Tests | ||||
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| Expected Turnaround Time | ||||
| 3 - 5 days | ||||
| Clinical Utility | ||||
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Myositis-specific autoantibodies (MSAs) are highly selective, usually exclusive and are associated with particular clinical phenotypes within the myositis spectrum. Myositis-specific autoantibodies to cytoplasmic enzymes that catalyze the binding of specific amino acids to their cognate tRNA define the anti-synthetase syndrome characterized by myositis and lung inflammation, and include autoantibodies to Jo-1 (antihistidyl-tRNA synthetase), PL-7 (threonyl), PL-12 (alanyl), EJ (glycyl), and OJ (isoleucyl). A further subset of myositis patients is characterized by the presence of autoantibodies directed against the signal recognition particle (SRP). Autoantibodies to Mi-2 (Mi-2/nucleosome remodeling and deacetylase (NuRD) complex) are detected in patients with hallmark dermatomyositis features. Autoantibody to a cytoplasmic 140-kDa protein, melanoma-differentiation associated gene 5 (MDA5), also known as anti-CADM140, identified patients with clinically amyopathic dermatomyositis (CADM) and rapidly progressive lung disease. Autoantibodies to transcriptional intermediary factor 1-gamma (TIF-1 y), a p155/140 nuclear protein involved in cellular differentiation, have been reported in adult and juvenile dermatomyositis; in adults, it is associated with malignancy. Autoantibodies to nuclear matrix protein NXP-2, another 140-kDa protein, is found in juvenile dermatomyositis (JDM). Anti-TIF-1 y and anti-NXP-2, two novel serological subsets in JDM, occur collectively in >40% of children and appear to identify those with more severe disease. |
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| Specimen and Container Info | ||||
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Specimen Type: Serum Preferred Collection Container: Red Top, Plain Alternate Collection Container: Gold Top, Serum Separator Desired Specimen Volume: 0.5 mL |
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| Collection Instructions | ||||
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| Processing and Submission Instructions | ||||
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| Patient Preparation | ||||
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For patients receiving STRENSIQ, consideration should be given to using alternate methods. |
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| Transport Instructions | ||||
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Transport to the laboratory refrigerated. |
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| Stability Requirements | ||||
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| Methodology | ||||
| Line Blot | ||||
| Reference Intervals | ||||
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See patient report. |
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| Limitations | ||||
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Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. |
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| Reference Lab | ||||
| Quest Diagnostics Nichols Institute | ||||
| Testing Schedule | ||||
| Routine, 5 times per week | ||||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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