Evidence map›Paper›PMID 39837620›Full record

ArticleRMD open2025

Predictive value of myositis antibodies: role of semiquantitative classification and positivity for more than one autoantibody.

Anne M Kerola, Annukka Pietikäinen, Julia Barantseva, Annaleena Pajander, Arno Hänninen

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Article in RMD open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Anne M KerolaInstitute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland anne.kerola@helsinki.fi.ORCID 0000-0003-2257-3291
Annukka PietikäinenInstitute of Biomedicine, Faculty of Medicine, University of Turku, Turku, Finland.ORCID 0000-0003-3554-0683
Julia BarantsevaDepartment of Internal Medicine, Kuopio University Hospital, Kuopio, Finland.ORCID 0000-0002-9695-8971
Annaleena PajanderTYKS laboratories, Clinical Microbiology, Turku University Hospital, Turku, Finland.
Arno HänninenTYKS laboratories, Clinical Microbiology, Turku University Hospital, Turku, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe assessed the positive predictive value (PPV) of 17 myositis antibodies for having a diagnosis of myositis and other myositis-spectrum conditions (interstitial lung disease (ILD), connective tissue diseases (CTD), malignancy) and evaluated the impact of semiquantitative classification and antibody overlap on the PPVs. MATERIALS AND

methodsWe retrospectively identified 1068 individuals ≥18 years who tested positive for ≥1 antibody in the EUROLINE myositis line blot assay or positive for anti-3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) in an ELISA-based test between 2015 and 2020 in 15 out of the 20 hospital districts in Finland. We extracted clinical diagnoses from the Care Register for Health Care between January 2013 and June 2022.

resultsThe PPV for a myositis diagnosis (ever during data collection) was highest for anti-HMGCR antibodies (94%), followed by anti-MDA5, anti-Jo-1 and anti-TIF1-γ (49-54%). Regarding other myositis antibodies, 18-42% of cases had myositis. Anti-synthetase antibodies, anti-MDA5, anti-PM-Scl100, anti-SAE1 and anti-Ro52 had a PPV for ILD of 25-47%. A PPV for CTD was highest for anti-Ro52 (57%). The PPV for malignancy was highest for anti-TIF1-γ (38%), followed by anti-PL-7 (32%). Stronger antibody band intensity was associated with higher PPVs for myositis and CTD but not for ILD or malignancies. Simultaneous positivity for ≥2 antibodies compared with single antibody was associated with higher PPVs for myositis, CTD and ILD.

conclusionThe PPV of myositis antibodies for diagnoses of myositis or other myositis spectrum diseases vary considerably between individual autoantibodies. Higher PPVs can be expected with stronger band intensities and with the presence of ≥2 overlapping myositis antibodies.

Indexed as

AutoantibodiesMyositisAdultAgedBiomarkersEnzyme-Linked Immunosorbent AssayFemaleFinlandHumansHydroxymethylglutaryl CoA ReductasesMaleMiddle AgedPredictive Value of TestsRetrospective StudiesAutoantibodiesBiomarkersHydroxymethylglutaryl CoA ReductasesAutoantibodiesDermatomyositisPolymyositis

Identifiers

PMID39837620
PMCPMC11749618

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.