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Cardiovascular Disease in Systemic Lupus Erythematosus: Recent Data on Epidemiology, Risk Factors and Prevention
Myrto Kostopoulou1, Dionysis Nikolopoulos1, Ioannis Parodis2
14th Department of Internal Medicine, Attikon University Hospital, Joint Rheumatology Program, National and Kapodistrian University of Athens Medical School, Athens, Greece.
Insights
Systemic Lupus Erythematosus (SLE) patients face higher cardiovascular risks due to unique inflammatory pathways. Early monitoring and tailored interventions, including hydroxychloroquine and minimizing prednisone, are crucial for managing this accelerated atherosclerosis.
Area of Science:
- Rheumatology
- Cardiology
- Immunology
Background:
- Systemic Lupus Erythematosus (SLE) significantly elevates the risk of accelerated atherosclerosis and cardiovascular (CV) events.
- CV events occur early and late in SLE patients, with younger individuals at higher risk than their age-matched peers.
- Traditional risk factors do not fully explain this increased CV risk in SLE.
Purpose of the Study:
- To review the mechanisms underlying accelerated atherosclerosis in SLE.
- To discuss current recommendations for CV risk assessment and prevention in SLE patients.
- To highlight the role of specific medications and disease management in cardiovascular health.
Main Methods:
- Literature review of pathophysiologic mechanisms in SLE-related atherosclerosis.
- Analysis of current European League Against Rheumatism recommendations.
- Evaluation of evidence regarding pharmacological interventions and preventive strategies.
Main Results:
- Pathophysiologic intermediates like type I interferons, oxidative stress, and autoantibodies contribute to endothelial injury and dyslipidemia in SLE.
- Prednisone use can aggravate these mechanisms, while hydroxychloroquine may offer antiatherogenic benefits.
- Paucity of randomized trials necessitates reliance on extrapolated evidence and risk factor monitoring.
Conclusions:
- SLE patients require regular monitoring of atherosclerotic risk factors and calculation of 10-year CV risk.
- Risk stratification should incorporate disease-related factors and guide general and SLE-specific preventive measures.
- Further research is needed on non-invasive CV assessment tools, biomarkers, and tailored risk-lowering strategies for SLE.
Abstract:
Systemic Lupus Erythematosus (SLE) is associated with increased risk for accelerated atherosclerosis and cardiovascular (CV) events including coronary heart disease, cerebrovascular and peripheral artery disease. CV events occur both early and late during the disease course, with younger patients being at much higher risk than age-matched counterparts. The risk cannot be fully accounted for by the increased prevalence of traditional atherosclerotic factors and may be due to pathophysiologic intermediates such as type I interferons and other inflammatory cytokines, oxidative stress, activated granulocytes and production of extracellular chromatin traps, antiphospholipid and other autoantibodies causing dysfunction of lipoproteins, altogether resulting in endothelial injury and pro-atherogenic dyslipidaemia. These mechanisms may be further aggravated by chronic intake of prednisone (even at doses <7.5 mg/day), whereas immunomodulatory drugs, especially hydroxychloroquine, may exert antiatherogenic properties. To date, there is a paucity of randomized studies regarding the effectiveness of preventative strategies and pharmacological interventions specifically in patients with SLE. Nevertheless, both the European League Against Rheumatism recommendations and extrapolated evidence from the general population emphasize that SLE patients should undergo regular monitoring for atherosclerotic risk factors and calculation of the 10-year CV risk. Risk stratification should include diseaserelated factors and accordingly, general (lifestyle modifications/smoking cessation, antihypertensive and statin treatment, low-dose aspirin in selected cases) and SLE-specific (control of disease activity, minimization of glucocorticoids, use of hydroxychloroquine) preventive measures be applied as appropriate. Further studies will be required regarding the use of non-invasive tools and biomarkers for CV assessment and of risk-lowering strategies tailored to SLE.
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