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Comparative efficacy and safety of lipid-lowering agents in patients with hypercholesterolemia: A frequentist network meta-analysis

机译:高胆固醇血症患者脂降低剂的比较疗效和安全性:频繁的网络荟萃分析

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Background: The comparative efficacy and safety of PCSK9 inhibitors , statins, and ezetimibe to lower lipid levels in patients with hypercholesterolemia remain unknown. We aimed to investigate the benefits and harms of the lipid-lowering agents in these patients. Methods: PubMed, Embase, and the Cochrane Library were searched from January 1, 2000 to June 1, 2018 for relevant randomized controlled trials (RCTs). Frequentist network meta-analysis was used to pool all estimates. Ranking probabilities were used to rank the comparative effects of all drugs against placebo. Results: Eighty-four RCTs enrolled 246,706 patients were included. Most of the included were assessed as low risk of bias. The probabilities of PCSK9 inhibitors that ranked first in improving lipid outcomes were all 100%. The probability of statins that ranked first in reducing the risk of cardiovascular (CV) events was 60.6%, and the probability of PCSK9 inhibitor was 37.1%, while no significant difference of efficacy in reducing CV events was observed between the 2 agents (odds ratios [OR] 0.98, 95% CI 0.87–1.11). Statin ranked first in reducing all-cause and CV death. Compared with placebo, statins were associated with reduced risks of all-cause (OR 0.90, 95% CI 0.85–0.96) and CV death (OR 0.83, 95% CI 0.75–0.91) while PCSK9 inhibitors and ezetimibe were not. No agents caused adverse events (including neurocognitive events), except that statins therapy significantly increases the levels of alanine aminotransferase (ALT) (OR 1.89, 95% CI 1.42–2.51) and creatine kinase (CK) (OR 1.45, 95% CI 1.09–1.93) and the incidence of diabetes (OR 1.13, 95% CI 1.02–1.26). Conclusions: PCSK9 inhibitors were the most effective lipid-lowering agents in improving lipid levels. Furthermore, PCSK9 inhibitors achieved similar CV benefits like statins, while PCSK9 inhibitors were not associated with any increased risk of statin-related side-effects. Thus, PCSK9 inhibitors may also be recommended as promisingly first-line lipid-lowering treatment for patients with hypercholesterolemia , especially for these with statins intolerance or resistance.
机译:背景:PCSK9抑制剂,汀类药物和ezetimibe对高胆固醇血症患者的脂质水平的比较疗效和安全性仍然未知。我们的目标是调查这些患者脂质降低剂的益处和危害。方法:从2000年1月1日至2018年6月1日,搜查了PubMed,Embase和Cochrane图书馆,以获得相关随机对照试验(RCT)。频繁的网络元分析用于汇集所有估计。排名概率用于将所有药物对安慰剂的比较效应进行排名。结果:八十四次RCT纳入246,706名患者。随附的大部分被评估为低偏差风险。 PCSK9抑制剂首先在改善脂质成果中排名的概率均为100%。第一次在降低心血管(CV)事件风险的他汀类药物的概率为60.6%,PCSK9抑制剂的概率为37.1%,而在2个药剂之间观察到在减少CV事件中的功效显着差异(差异[或] 0.98,95%CI 0.87-1.11)。 Statin首先在减少全因和CV死亡时排名第一。与安慰剂相比,他汀类药物与所有原因(或0.90,95%CI 0.96)和Cv死亡(或0.83,95%CI 0.75-0.91)的风险降低有关,而PCSK9抑制剂和ezetimibe则没有。除了他汀类药物治疗显着增加丙氨酸氨基转移酶(ALT)(或1.89,95%CI 1.42-2.51)和肌酸激酶(或1.45,95%CI 1.09,尚未引起不良事件(包括神经成像事件)的不良事件-1.93)和糖尿病的发病率(或1.13,95%CI 1.02-1.26)。结论:PCSK9抑制剂是改善脂质水平的最有效的降脂剂。此外,PCSK9抑制剂达到了类似的CV益处,而PCSK9抑制剂与他汀类药物相关副作用的任何增加的风险无关。因此,也可以推荐PCSK9抑制剂作为高胆固醇血症患者的承诺一线脂质降低治疗,尤其是患有他汀类药物不耐受或抗性的患者。

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