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Statins for prevention of cardiovascular disease in systemic lupus erythematosus
F A Yousef Yengej1, M Limper, H L Leavis
1Department of Rheumatology and Clinical Immunology, University Medical Centre Utrecht, Utrecht, the Netherlands.
Insights
Statins may help prevent cardiovascular disease (CVD) in patients with systemic lupus erythematosus (SLE). Evidence suggests statin use reduces atherosclerosis progression and cardiac events, though more randomized trials are needed.
Area of Science:
- Rheumatology and Cardiology
- Pharmacology
Background:
- Cardiovascular disease (CVD) is a significant cause of morbidity in systemic lupus erythematosus (SLE).
- Statin therapy is a potential intervention to mitigate CVD risk in SLE patients.
Purpose of the Study:
- To review the existing evidence on the efficacy of statins in preventing CVD in patients with SLE.
Main Methods:
- A literature search was conducted on the PubMed database using keywords for SLE and statins.
- Nine relevant clinical studies were identified and analyzed.
Main Results:
- Seven studies indicated statins slightly decreased carotid intima-media thickness progression and increased flow-mediated vasodilatation.
- Two studies showed statins were associated with reduced cardiac events, coronary heart disease, cerebrovascular disease, end-stage renal disease, and mortality in SLE patients.
- Statins demonstrated a favorable safety profile in SLE patients.
Conclusions:
- Current evidence supports the use of statins for SLE patients at increased cardiovascular risk.
- Further prospective randomized studies are recommended to confirm causality and optimize statin therapy in SLE.
Objective:
In systemic lupus erythematosus (SLE), cardiovascular disease (CVD) is an important cause of long-term morbidity, which could be affected by statin use. Here we review the evidence for the use of statins for the prevention of CVD in patients with SLE.
Methods:
The PubMed database was searched using a query combining SLE and statins.
Results:
The search yielded nine relevant clinical studies. Seven studies reported on radiological findings that correlate with atherosclerosis and mainly revealed that statin treatment resulted in a slight decrease in progression of carotid intima-media thickness and an increase in flow-mediated vasodilatation. Two studies investigated CVD and mortality. In a group of SLE patients that had received a kidney transplantation, three of 23 statin-treated SLE patients experienced cardiac events compared with four of ten placebo- reated controls. Moreover, in a retrospectively studied cohort of SLE patients with dyslipidaemia, statin treatment in 777 patients was associated with a large decrease in coronary heart disease (hazard ratio [HR] = 0.20), cerebrovascular disease (HR = 0.14), end-stage renal disease (HR = 0.22) and mortality (HR = 0.44) compared with 1317 patients that had not been prescribed statins. However, the latter retrospective study was subject to bias and causality can only be proven in a randomised trial. Statins showed a good safety profile in SLE patients.
Conclusion:
Whilst awaiting new prospective randomised studies, we recommend prescription of statins in SLE patients with increased cardiovascular risk according to the current recommendations for cardiovascular risk management in rheumatoid arthritis.
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