Lupus & antiphospholipid syndrome

Pancarditis and fibrosis as hallmarks of lupus myocarditis: clinical features, imaging findings and outcomes

Rheumatology (Oxford)Published Retrospective cohort study

Authors' conclusion

LM is a distinct and severe phenotype of SLE, characterized by pancarditis and unique imaging features.

Study context

Population
Lupus myocarditis (LM) patients diagnosed 2005–2022, matched with active systemic lupus erythematosus (SLE)-non-LM and AM-non-AI32 LM patients
Exposure
LM vs active SLE without myocarditis vs acute non-autoimmune myocarditis
  • LMn = 32
Outcome
Wall motion abnormalities on echocardiography
Methodological detailsmatched 1:1 by age and sex, 2-year follow-up
  • Matched 1:1 by age and sex
  • 2-year follow-up

Main finding

As reported in the abstract

P < 0.001

Observational data: associations, not effects.

Further findings

OutcomeLMAM-non-AIP value
Reduced LV ejection fractionLM vs AM-non-AI56.3%18.8%P = 0.002
Pulmonary hypertensionLM vs AM-non-AI37.5%3.1%P = 0.001
Valvular abnormalitiesLM vs AM-non-AI65.5%3.1%P < 0.001
Late gadolinium enhancement on CMRLM vs AM-non-AI · comparator group not named for this result in the abstract65.6%37.5%P = 0.024
PancarditisLM vs AM-non-AI65.6%0%P < 0.001
ICU admissionLM vs AM-non-AI28.1%6.3%P = 0.043
Invasive mechanical ventilationLM vs AM-non-AI25.0%3.1%P = 0.027
  • Pancarditis: identified exclusively in LM; comparator not named in the abstract

Mortality · 2 years

Comparable between LM and AM-non-AI

Original publication

Pancarditis and fibrosis as hallmarks of lupus myocarditis: clinical features, imaging findings and outcomes. Rheumatology (Oxford). Published 3 February 2026. doi:10.1093/rheumatology/keag067

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