Faculty of Medicine, Zagazig University, Zagazig, 44519, El-Sharkia, Egypt.
Department of Clinical Biochemistry, University College London Medical School, University College London (UCL), Royal Free Campus, London, UK.
Drugs. 2018 Mar;78(4):453-462. doi: 10.1007/s40265-018-0870-1.
BACKGROUND AND AIMS: Ezetimibe reduces plasma low-density lipoprotein cholesterol (LDL-C) levels by up to 20%. However, its effect on plasma lipoprotein(a) [Lp(a)] concentrations in patients with primary hypercholesterolemia has not been defined. OBJECTIVE: Therefore, we performed a systematic review and meta-analysis to assess this effect based on the available randomized controlled trials (RCTs). METHODS: We searched the PubMed and SCOPUS databases from inception until 28 February 2017 to identify RCTs that investigated the effect of ezetimibe monotherapy on plasma Lp(a) concentrations in patients with primary hypercholesterolemia. We pooled mean percentage changes in plasma Lp(a) concentrations as a mean difference (MD) with a 95% confidence interval (CI). RESULTS: Seven RCTs with 2337 patients met the selection criteria and were included in the analysis. Overall pooled analysis suggested that ezetimibe 10 mg significantly reduced plasma Lp(a) concentrations in patients with primary hypercholesterolemia by - 7.06% (95% CI - 11.95 to - 2.18; p = 0.005) compared with placebo. No significant heterogeneity was observed (χ = 5.34; p = 0.5). Excluding one study from the analysis resulted in insignificant differences between the two groups (p = 0.2). Meta-regression did not find a significant association between the mean percentage changes in Lp(a) and other potential moderator variables, which included the mean percentage changes of LDL-C concentrations (p = 0.06) and baseline Lp(a) mean values (p = 0.46). CONCLUSIONS: Ezetimibe monotherapy (10 mg/day) showed a small (7.06%) but statistically significant reduction in the plasma levels of Lp(a) in patients with primary hypercholesterolemia. According to current literature, this magnitude of reduction seems to have no clinical relevance. However, further studies are warranted to clarify the mechanism mediating this effect of ezetimibe and to investigate its efficacy in combination with other drugs that have shown promise in lowering Lp(a) levels.
背景和目的:依折麦布可将血浆低密度脂蛋白胆固醇(LDL-C)水平降低 20%。然而,其对原发性高胆固醇血症患者血浆脂蛋白(a)[Lp(a)]浓度的影响尚未明确。
目的:因此,我们进行了系统评价和荟萃分析,以根据现有随机对照试验(RCT)评估这种作用。
方法:我们检索了 PubMed 和 SCOPUS 数据库,检索时间从建库至 2017 年 2 月 28 日,以确定单独使用依折麦布治疗原发性高胆固醇血症患者血浆 Lp(a)浓度的 RCT。我们对血浆 Lp(a)浓度的平均百分比变化进行了汇总分析,以均数差(MD)表示 95%置信区间(CI)。
结果:7 项 RCT 共纳入 2337 例患者,符合入选标准并纳入分析。总体汇总分析表明,与安慰剂相比,依折麦布 10mg 可显著降低原发性高胆固醇血症患者的血浆 Lp(a)浓度,降幅为-7.06%(95%CI-11.95 至-2.18;p=0.005)。未观察到明显的异质性(χ2=5.34;p=0.5)。剔除分析中的一项研究后,两组间差异无统计学意义(p=0.2)。元回归未发现 Lp(a)平均百分比变化与其他潜在调节变量(包括 LDL-C 浓度的平均百分比变化[p=0.06]和基线 Lp(a)平均水平[p=0.46])之间存在显著关联。
结论:依折麦布单药治疗(10mg/天)可显著降低原发性高胆固醇血症患者的血浆 Lp(a)水平,降幅为 7.06%。根据现有文献,这种降低幅度似乎没有临床意义。但是,需要进一步的研究来阐明依折麦布介导这种作用的机制,并研究其与其他降低 Lp(a)水平有疗效的药物联合应用的疗效。
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