Sánchez Paula, Toro-Trujillo Esteban, Muñoz-Velandia Oscar M, García Angel Alberto, Fernández-Ávila Daniel G
Departamento de Medicina Interna, Facultad de Medicina, Pontificia Universidad Javeriana, Bogotá, Colombia.
Departamento de Medicina Interna, Facultad de Medicina, Pontificia Universidad Javeriana, Bogotá, Colombia.
Reumatol Clin (Engl Ed). 2019 Nov-Dec;15(6):e86-e91. doi: 10.1016/j.reuma.2017.12.013. Epub 2018 Feb 7.
There is strong evidence of a rise in cardiovascular risk in patients suffering from autoimmune diseases, especially in those with Sistemic Lupus Erythematosus. Until now, there are a few trials that assess the potencial benefit of statins on the incidence of cardiovascular events and on lipid profile of patients with SLE. This evidence has not been synthesized and assessed altogether.
We performed a search in databases of literature published until August of 2016 (Embase, MEDLINE, Cochrane Library, SciELO, Clinical Evidence, DynaMed, Cochrane Central Register of Controlled Trials, LILACS), identifying controlled clinical trials that could estimate the impact of statins on mortality, cardiovascular events, C-reactive protein and lipid profile in patients with Systemic Lupus Erythematosus. The quality of the information available was assessed with a meta-analysis, using a random effects model, employing the RevMan 5.3 software.
6 trials and 412 patients were included in the analysis. The use of statins in patients with SLE was found to significantly reduce the levels of serum total cholesterol (mean difference [MD] -31,4 mg/dL; CI 95% -43,0; -19,9), and serum low density cholesterol (MD -31,4 mg/dL; IC 95% -43,0; -19,9), but had no impact on levels of serum triglycerides (MD 4 mg/dL; IC 95% 2,49; 6,21) and C-reactive protein (MD -0,78; IC 95% -1,43; -0,13). No evidence was found about the impact on the risk of mortality or cardiovascular events.
Statins have a significant effect on the levels of serum total cholesterol, LDL cholesterol and C-reactive protein, however, more randomized controlled trials with long-term follow-up are necessary to assess the impact on mortality and cardiovascular risk.
有充分证据表明,自身免疫性疾病患者的心血管风险有所上升,尤其是系统性红斑狼疮患者。到目前为止,只有少数试验评估了他汀类药物对系统性红斑狼疮患者心血管事件发生率和血脂水平的潜在益处。这些证据尚未被综合起来进行全面评估。
我们在截至2016年8月发表的文献数据库(Embase、MEDLINE、Cochrane图书馆、SciELO、临床证据、DynaMed、Cochrane对照试验中心注册库、LILACS)中进行了检索,识别出能够评估他汀类药物对系统性红斑狼疮患者死亡率、心血管事件、C反应蛋白和血脂水平影响的对照临床试验。使用RevMan 5.3软件,采用随机效应模型,通过荟萃分析评估可用信息的质量。
分析纳入了6项试验和412名患者。研究发现,在系统性红斑狼疮患者中使用他汀类药物可显著降低血清总胆固醇水平(平均差值[MD]-31.4mg/dL;95%置信区间[-43.0;-19.9])和血清低密度胆固醇水平(MD-31.4mg/dL;95%置信区间[-43.0;-19.9]),但对血清甘油三酯水平(MD 4mg/dL;95%置信区间[2.49;6.21])和C反应蛋白水平(MD-0.78;95%置信区间[-1.43;-0.13])没有影响。未发现关于对死亡率或心血管事件风险影响的证据。
他汀类药物对血清总胆固醇、低密度脂蛋白胆固醇和C反应蛋白水平有显著影响,然而,需要更多长期随访的随机对照试验来评估对死亡率和心血管风险的影响。