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Published on: June 8, 2022
Inflammatory myositis in systemic lupus erythematosus
Nicole Bitencourt1, E Blair Solow1, Tracey Wright1,2
1Division of Rheumatic Diseases, University of Texas Southwestern Medical Center, Dallas, USA.
Inflammatory myositis affects 6.3% of systemic lupus erythematosus (SLE) patients, particularly those of Black race and with childhood-onset SLE. Routine screening for myositis is recommended in these high-risk SLE populations.
Area of Science:
- Rheumatology
- Immunology
- Internal Medicine
Background:
- The co-occurrence of inflammatory myositis within systemic lupus erythematosus (SLE) requires further investigation.
- Understanding the incidence, types, and risk factors of myositis in SLE patients is crucial.
Purpose of the Study:
- To determine the incidence of inflammatory myositis in a cohort of pediatric and adult SLE patients.
- To identify distinct types of inflammatory myositis and associated risk factors in SLE.
- To describe clinical, laboratory, and pathological features of myositis in SLE.
Main Methods:
- Retrospective analysis of SLE patients diagnosed with myositis between 2010-2019.
- Inclusion of data from two pediatric and one adult hospital.
- Collection and descriptive statistical analysis of demographic, clinical, laboratory, and pathological features.
Main Results:
- 6.3% of 1718 SLE patients (108 individuals) had coexisting inflammatory myositis.
- Higher prevalence observed in Black individuals and those with childhood-onset SLE.
- Concurrent onset of SLE and myositis occurred in 68%; common features included systemic sclerosis overlap (48%), dermatomyositis rashes (33%), arthralgias/arthritis (>90%), and thrombotic events/pregnancy morbidity (>33%).
- Frequent laboratory findings included lymphopenia, hypocomplementemia, and positive RNP antibodies.
- Myositis-specific antibodies (MSA) and myositis-associated antibodies (MAA) were present in over 40% of patients.
- Muscle biopsy revealed diverse pathology, including nonspecific changes, dermatomyositis, polymyositis, and necrotizing autoimmune myopathy.
Conclusions:
- Inflammatory myositis is a significant comorbidity in 6.3% of SLE patients.
- Clinical manifestations like dermatomyositis rashes, systemic sclerosis overlap, arthralgias/arthritis, and cytopenias are common.
- Elevated frequency of RNP, MSA, and MAA supports their role in SLE-myositis.
- Black individuals and those with childhood-onset SLE exhibit higher myositis prevalence.
- Routine myositis screening is advised for Black SLE patients, childhood-onset SLE, and those with MSA/MAA.
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