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Statin reduces mortality and morbidity in systemic lupus erythematosus patients with hyperlipidemia: A nationwide
Hsin-Hui Yu1, Pau-Chung Chen2, Yao-Hsu Yang1
1Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Insights
Statin use in patients with systemic lupus erythematosus (SLE) and hyperlipidemia significantly lowers mortality and cardiovascular risks. High-dose statins showed the most substantial risk reduction for death, heart disease, stroke, and kidney disease.
Area of Science:
- Rheumatology
- Cardiology
- Nephrology
Background:
- Systemic lupus erythematosus (SLE) is associated with increased cardiovascular and renal morbidity.
- The role of statins in mitigating these risks in SLE patients with hyperlipidemia is not fully understood.
Purpose of the Study:
- To investigate the association between statin use and outcomes in SLE patients with hyperlipidemia.
- To test the hypothesis that statin use reduces mortality and morbidity in this patient population.
Main Methods:
- A population-based cohort study using the Taiwan National Health Insurance Research Database (1997-2008).
- Included 4095 SLE patients with hyperlipidemia, with a nested matched cohort of 935 never-users and statin users (1:2 ratio).
- Cox proportional hazards regression analyzed associations with all-cause mortality, coronary artery disease (CAD), cerebrovascular disease (CVD), and end-stage renal disease (ESRD).
Main Results:
- Statin users showed a reduced risk of all-cause mortality (HR 0.67; 95% CI, 0.54-0.83) compared to never-users.
- High-dose statins significantly decreased the risk of all-cause mortality (HR 0.44), CAD (HR 0.20), CVD (HR 0.14), and ESRD (HR 0.22).
- Results were consistent in the nested matched cohort analysis.
Conclusions:
- Statin therapy may be beneficial in reducing mortality, cardiovascular disease, and end-stage renal disease risks for SLE patients with hyperlipidemia.
- Further large-scale prospective studies with long-term follow-up are warranted to confirm these findings.
Objective:
The anti-inflammatory and cardiovascular protective effects of statin for patients with systemic lupus erythematosus (SLE) are not clear. We tested the hypothesis that statin use is associated with reduced mortality and morbidity in SLE patients with hyperlipidemia.
Methods:
We included 4095 patients with SLE and hyperlipidemia from the entire population using the Taiwan National Health Insurance Research Database between 1997 and 2008. A total of 935 matching sets (1:2) of patients who had never used lipid-lowering medications and statin users were included in the nested matched cohort. Cox proportional hazards regression was used to calculate the hazard ratios (HR) and 95% confidence intervals (CI) for the association between statin and all-cause mortality, coronary artery disease (CAD), cerebrovascular disease (CVD) and end-stage renal disease (ESRD), conditional for matching sets in the matched cohort.
Results:
The multivariate adjusted hazard ratios (HR) for statin users, as compared with patients had never used lipid-lowering medications, were 0.67 (95% CI, 0.54 to 0.83) for death from any cause. High-dose statins (>365 cumulative defined daily dose) significantly reduced risk of all-cause mortality (HR 0.44, 95% CI 0.32 to 0.60); CAD (HR 0.20, 95% CI 0.13 to 0.31); CVD (HR 0.14, 95% CI 0.08 to 0.25); and ESRD (HR 0.22, 95% CI, 0.16 to 0.29), with similar results in the nested matched study.
Conclusion:
Statin therapy in SLE patients with hyperlipidemia may reduce the risk of mortality, cardiovascular disease and ESRD. The effect of statins needs to be demonstrated in large prospective studies with long-term follow-up.
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