ArticleClinical and experimental rheumatology2025
Infections preceding diagnosis associated with myositis phenotypes in a national patient registry.
Article in Clinical and experimental rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
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12 authors.
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Abstract
objectivesWe investigated the association of antecedent infections with clinical subgroups and phenotypes in the idiopathic inflammatory myopathies (IIMs).
methodsAdult IIM patients (362 with dermatomyositis (DM), 250 with polymyositis (PM), and 256 with inclusion body myositis (IBM)) enrolled in a national myositis patient registry. One hundred thirty-four patients had symptoms of lung disease plus fever and/or arthritis (LD+), and 103 with systemic autoimmune rheumatic disease-associated overlap myositis (OM). Self-reported infections and antibiotic usage within 12 months prior to IIM diagnosis were examined. Adjusted odds ratios (ORs) and 95% confidence intervals (CIs) were calculated across IIMs. LD+ and OM analyses were performed excluding IBM patients.
resultsInfections before IIM diagnosis were more frequent in DM and PM than IBM. Febrile illness and gastroenteritis were more frequent in DM than IBM (OR 2.82 and 3.30, respectively), and in PM than IBM (OR 3.27 and 3.26, respectively). Patients with LD+ and OM had higher odds of reported infections than those without these phenotypes, with pneumonia the most strongly associated infection (OR 5.26 95% CI 2.59-10.71 in LD+, OR 2.75, 95% CI 1.25-6.06 in OM). Antibiotic usage within 1 year before diagnosis did not differ among DM, PM and IBM patients, nor in OM. Antibiotics were used more frequently used in patients with LD+ compared to no LD, but this was attenuated after adjusting for infections.
conclusionsAntecedent infections, particularly respiratory and gastrointestinal infections may contribute to adult IIM phenotypes. Pneumonia showed the strongest association with myositis phenotypes accompanied by frequent lung disease.
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