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Analytical performance of commercial myositis-specific autoantibody tests evaluated against immunoprecipitation assays as a reference standard: A systematic review and meta-analysis

  • International Myositis Assessment and Clinical Studies Group (IMACS) Myositis Autoantibody Scientific Interest Group (SIG) Study
  • Nippon Medical School
  • Vall d'Hebron University Hospital
  • VU University Medical Center
  • University of Debrecen
  • Johns Hopkins University
  • University of Crete
  • University Medical Center Utrecht
  • Siena University Hospital
  • North Bristol NHS Trust
  • University of Manchester
  • University of Birmingham Francis Crick Institute
  • Aga Khan University
  • National Institutes of Health
  • NH SRCC Children's Hospital
  • Vall d'Hebron Universitary Hospital
  • Kanazawa University
  • University of Pittsburgh
  • Uppsala University

Research output: Contribution to journalArticlepeer-review

8   Link opens in a new tab Citations (SciVal)

Abstract

OBJECTIVE: To evaluate the analytical performance of commercial myositis-specific autoantibody (MSA) assays against immunoprecipitation (IP) assays.

METHODS: A systematic literature search was conducted in PubMed, Web of Science, and Scopus through July 2024. Data were extracted on study design, participant characteristics, index tests, and 2 × 2 contingency tables for diagnostic performance. Study quality was assessed using the QUADAS-2 tool. Sensitivity and specificity were calculated for each dataset and presented as paired forest plots and summary receiver operating characteristic (SROC) curves. A hierarchical SROC model was used to estimate pooled sensitivity and specificity for meta-analysis.

RESULTS: Of 3156 articles, 23 met inclusion criteria and were judged to have low risk of bias across all QUADAS-2 domains. The most frequently evaluated commercial assay was the line blot assay (LBA; 16 studies), followed by enzyme immunoassay (EIA; 9 studies). In the meta-analyses, the highest pooled sensitivity was observed for anti-MDA5 with EIA (95.7 %), followed by anti-SAE with LBA (88.3 %), anti-PL-12 with LBA (87.2 %), and anti-Jo-1 and anti-MDA5 with LBA (82.8 %). Lower sensitivities were observed for anti-Mi-2 (67.4 %), anti-NXP2 (69.7 %), and anti-TIF1-γ (63.8 %) with LBA. Pooled specificity ranged from 94.7 % to 99.3 % across MSA assays, but a false-positive result was a common concern for LBA, except for anti-EJ.

CONCLUSION: False-positive and false-negative results remain a significant challenge in the use of commercial MSA assays.

Original languageEnglish
Article number152858
JournalSeminars in Arthritis and Rheumatism
Volume75
Early online date27 Oct 2025
DOIs
Publication statusPublished - 31 Dec 2025

Bibliographical note

Publisher Copyright:
© 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.

Keywords

  • Autoantibody
  • Diagnostic accuracy test
  • Meta-analysis
  • Myositis
  • Systematic review

ASJC Scopus subject areas

  • Rheumatology
  • Anesthesiology and Pain Medicine

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