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Published on: June 20, 2014
Clinical characteristics of lupus myocarditis in Korea
Jae-Wook Chung1, Dai-Yeol Joe, Han-Jung Park
1Department of Allergy and Rheumatology, Ajou University School of Medicine, Suwon, South Korea.
Insights
Systemic lupus erythematosus (SLE) can cause rare but severe lupus myocarditis leading to heart dysfunction. Early immunosuppressive treatment, particularly high-dose corticosteroids, improves outcomes and prevents recurrence in most patients.
Area of Science:
- Cardiology
- Rheumatology
- Immunology
Background:
- Systemic lupus erythematosus (SLE) is a complex autoimmune disease.
- Clinically significant myocarditis is an uncommon manifestation of SLE.
- Severe left ventricular dysfunction can occur in SLE patients.
Observation:
- This study details five SLE patients with severe left ventricular dysfunction attributed to lupus myocarditis.
- Patient demographics included four females with a mean age of 36.4 years.
- Comorbidities such as lupus nephritis were present in three patients.
- Immunological markers like anti-dsDNA antibodies and anticardiolipin antibodies were evaluated.
Findings:
- Four patients received high-dose corticosteroids, one received intravenous pulse methylprednisolone, and another received intravenous immunoglobulin with pulse cyclophosphamide and corticosteroids.
- Marked improvement in left ventricular function was observed in four patients.
- No recurrence of lupus myocarditis was noted during a follow-up period of up to 33 months.
- One patient did not improve and unfortunately expired from sudden cardiac arrest.
Implications:
- Lupus myocarditis requires prompt immunosuppressive therapy, primarily high-dose corticosteroids.
- Early and aggressive treatment is associated with favorable prognosis and reduced recurrence rates.
- This highlights the importance of monitoring cardiac function in SLE patients.
Abstract:
Clinically important myocarditis is an unusual feature in systemic lupus erythematosus (SLE). We describe the clinical characteristics, management and outcomes of five SLE patients who developed severe left ventricular dysfunction. Four patients were female with mean age of 36.4 years. Three patients had both lupus myocarditis and lupus nephritis. Four patients had raised anti-dsDNA antibody titer and low complement level and two patients had positive IgG anticardiolipin antibody. Three patients were treated by high-dose corticosteroids, one patient by intravenous pulse methylprednisolone, and one patient by intravenous immunoglobulin and pulse cyclophosphamide with high dose corticosteroids. Left ventricular function improved markedly in four patients and all of them had no recurrence of lupus myocarditis up to follow-up of 33 months. However, one patient, who showed no improvement of left ventricular function, was expired due to sudden cardiac arrest. Lupus myocarditis should be treated by immunosuppressive therapy with high-dose corticosteroids and mostly the prognosis might be good with early treatment.
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