What is an Autoimmune Myopathy/Myositis (Inflammatory Myopathy) panel?

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Last updated: March 25, 2025View editorial policy

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From the Guidelines

An Autoimmune Myopathy/Myositis panel is a crucial diagnostic tool that includes tests for myositis-specific autoantibodies, which may define subgroups of patients with idiopathic inflammatory myositis and suggest specific extramuscular organ involvement, as highlighted in a study published in the Mayo Clinic Proceedings 1. The panel typically includes tests for myositis-specific antibodies (MSAs) like anti-Jo-1, anti-Mi-2, anti-SRP, anti-MDA5, and anti-TIF1-gamma, as well as myositis-associated antibodies (MAAs) such as anti-PM-Scl and anti-Ku. Key features of the panel include:

  • Detection of specific antibodies associated with inflammatory muscle diseases
  • Diagnosis of conditions like polymyositis, dermatomyositis, inclusion body myositis, and immune-mediated necrotizing myopathy
  • Guidance on treatment approaches, which may include corticosteroids, immunosuppressants, or biologics depending on the specific condition identified, as discussed in the study 1 The presence of specific antibodies can help physicians diagnose and manage autoimmune myopathies, which can be difficult to diagnose based on symptoms alone. Early diagnosis using the Autoimmune Myopathy/Myositis panel allows for prompt treatment that can prevent muscle damage and disability, emphasizing the importance of this diagnostic tool in clinical practice 1.

From the Research

Definition of Autoimmune Myopathy/Myositis Panel

  • An Autoimmune Myopathy/Myositis panel is a diagnostic tool used to evaluate patients with suspected idiopathic inflammatory myopathy (IIM) 2, 3, 4, 5, 6.
  • The panel typically includes a range of tests to detect myositis-specific autoantibodies, which can help diagnose and classify different subtypes of IIM, such as dermatomyositis, polymyositis, and inclusion body myositis 2, 3, 5.

Components of the Panel

  • The panel may include tests for various autoantibodies, such as anti-Mi-2, anti-Jo-1, and anti-signal recognition particle (SRP) antibodies 4, 5, 6.
  • The results of the panel can provide diagnostic and prognostic information, helping clinicians to identify patients at higher risk for certain complications, such as interstitial lung disease or cancer-associated myositis 5, 6.

Clinical Utility of the Panel

  • The myositis autoantibody panel can be used to diagnose and monitor disease progression in patients with IIM 4, 6.
  • The panel can also help guide treatment decisions, such as the use of corticosteroids, immunosuppressive agents, or biologics 2, 3, 6.
  • Specific factors associated with positive results on the panel, such as chronic corticosteroid use and sclerodermoid skin changes, can help identify patients at higher risk for IIM 4.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Autoimmune Myopathies: Updates on Evaluation and Treatment.

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2018

Research

The Clinical Features of Myositis-Associated Autoantibodies: a Review.

Clinical reviews in allergy & immunology, 2017

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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