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Quantitative Analysis and Characterization of Atherosclerotic Lesions in the Murine Aortic Sinus
Published on: December 8, 2013
Prevalence and correlates of accelerated atherosclerosis in systemic lupus erythematosus
Mary J Roman1, Beth-Ann Shanker, Adrienne Davis
1Division of Cardiology, Weill Medical College of Cornell University, the Hospital for Special Surgery, New York, NY 10021, USA. mroman@med.cornell.edu
Insights
Systemic lupus erythematosus (SLE) patients experience premature atherosclerosis, independent of traditional cardiovascular disease risk factors. Disease-related factors, not just age or cholesterol, significantly contribute to plaque development in SLE patients.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Immunology
Background:
- Systemic lupus erythematosus (SLE) is linked to premature myocardial infarction.
- The prevalence of atherosclerosis and its relationship to cardiovascular disease (CVD) risk factors and SLE-specific factors remain understudied in a case-control setting.
Purpose of the Study:
- To investigate the prevalence of atherosclerosis in SLE patients compared to controls.
- To examine the association of traditional CVD risk factors and SLE-related factors with atherosclerosis in SLE.
Main Methods:
- A case-control study involving 197 SLE patients and 197 matched controls.
- Carotid ultrasonography, echocardiography, and assessment of CVD risk factors were performed.
- Patients were evaluated for clinical/serologic features, inflammatory mediators, and treatment.
Main Results:
- Atherosclerosis (carotid plaque) was significantly more prevalent in SLE patients (37.1%) than controls (15.2%).
- SLE diagnosis (OR, 4.8) and higher cholesterol were independent predictors of plaque, alongside age.
- Within the SLE cohort, longer disease duration, higher damage index, and absence of anti-Smith antibodies predicted plaque presence.
Conclusions:
- Atherosclerosis occurs prematurely in SLE patients, independent of traditional CVD risk factors.
- Disease-related factors play a crucial role in atherogenesis among SLE patients.
- Further trials focusing on targeted anti-inflammatory therapies are warranted for SLE patients.
Background:
Although systemic lupus erythematosus is associated with premature myocardial infarction, the prevalence of underlying atherosclerosis and its relation to traditional risk factors for cardiovascular disease and lupus-related factors have not been examined in a case-control study.
Methods:
In 197 patients with lupus and 197 matched controls, we performed carotid ultrasonography, echocardiography, and an assessment for risk factors for cardiovascular disease. The patients were also evaluated with respect to their clinical and serologic features, inflammatory mediators, and disease treatment.
Results:
The risk factors for cardiovascular disease were similar among patients and controls. Atherosclerosis (carotid plaque) was more prevalent among patients than the controls (37.1 percent vs. 15.2 percent, P<0.001). In multivariate analysis, only older age, the presence of systemic lupus erythematosus (odds ratio, 4.8; 95 percent confidence interval, 2.6 to 8.7), and a higher serum cholesterol level were independently related to the presence of plaque. As compared with patients without plaque, patients with plaque were older, had a longer duration of disease and more disease-related damage, and were less likely to have multiple autoantibodies or to have been treated with prednisone, cyclophosphamide, or hydroxychloroquine. In multivariate analyses including patients with lupus, independent predictors of plaque were a longer duration of disease, a higher damage-index score, a lower incidence of the use of cyclophosphamide, and the absence of anti-Smith antibodies.
Conclusions:
Atherosclerosis occurs prematurely in patients with systemic lupus erythematosus and is independent of traditional risk factors for cardiovascular disease. The clinical profile of patients with lupus and atherosclerosis suggests a role for disease-related factors in atherogenesis and underscores the need for trials of more focused and effective antiinflammatory therapy.
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