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Published on: February 20, 2019
Accelerated atherosclerosis in patients with SLE--mechanisms and management
Brian J Skaggs1, Bevra H Hahn, Maureen McMahon
1Division of Rheumatology, David Geffen School of Medicine, University of California, Los Angeles, 32-59 Rehab Center, 1000 Veteran Avenue, Los Angeles, CA 90095, USA. bskaggs@mednet.ucla.edu
Insights
Systemic lupus erythematosus (SLE) patients face accelerated atherosclerosis due to autoimmunity, not just traditional risk factors. Understanding immune dysfunction is key to managing cardiovascular disease (CVD) risk in these individuals.
Area of Science:
- Immunology
- Cardiovascular Medicine
- Rheumatology
Background:
- Systemic lupus erythematosus (SLE) is associated with a significantly higher incidence and earlier onset of cardiovascular disease (CVD) compared to the general population.
- Traditional CVD risk factors do not fully account for the elevated risk in SLE patients, indicating a role for autoimmunity.
- Immune system dysfunction is a primary driver of atherosclerosis initiation and progression in SLE.
Purpose of the Study:
- To review the epidemiology of CVD in SLE.
- To explore the impact of immune system dysfunction on atherosclerosis development and progression in SLE.
- To discuss the implications for monitoring and treatment of atherosclerosis in SLE patients.
Main Methods:
- Literature review and synthesis of existing research on CVD in SLE.
- Analysis of the role of various autoimmune manifestations (cytokines, autoantibodies, oxidative stress) in atherosclerosis.
- Discussion of the influence of SLE therapeutics on cardiovascular risk.
Main Results:
- Autoimmunity, through mechanisms like altered cytokines, autoantibodies, and oxidative stress, significantly contributes to accelerated atherosclerosis in SLE.
- Both SLE and its treatments can influence the development and progression of atherosclerosis.
- There is a need for SLE-specific cardiovascular risk factors and biomarker panels.
Conclusions:
- Immune system dysfunction is central to accelerated atherosclerosis in SLE patients.
- Developing comprehensive biomarker panels is crucial for identifying and managing high-risk individuals.
- Further research into SLE-specific CVD risk factors and targeted therapies is warranted.
Abstract:
Rapid-onset cardiovascular disease (CVD) is a major concern for many patients with systemic lupus erythematosus (SLE). Cardiovascular events occur more frequently and with earlier onset in patients with SLE compared with healthy individuals. Traditional risk factors, such as altered lipid levels, aging and smoking, do not fully explain this increased risk of CVD, strongly suggesting that autoimmunity contributes to accelerated atherosclerosis. Altered immune system function is recognized as the primary contributor to both the initiation and progression of atherosclerosis. Multiple manifestations of autoimmunity, including changes in cytokine levels and innate immune responses, autoantibodies, adipokines, dysfunctional lipids, and oxidative stress, could heighten atherosclerotic risk. In addition, multiple SLE therapeutics seem to affect the development and progression of atherosclerosis both positively and negatively. SLE-specific cardiovascular risk factors are beginning to be discovered by several groups, and development of a comprehensive, clinically feasible biomarker panel could be invaluable for identification and treatment of patients at risk of developing accelerated atherosclerosis. Here, we discuss the epidemiology of CVD in SLE and the implications of immune system dysfunction on the development and progression, monitoring and treatment of atherosclerosis in individuals with this disease.
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