Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
BMJ Open. 2019 Feb 22;8(11):e021508. doi: 10.1136/bmjopen-2018-021508.
This meta-analysis of randomised placebo-controlled clinical trials aimed to assess the effect of fenofibrate on apolipoprotein C-III (apo C-III), a key regulator of triglyceride metabolism.
Randomised placebo-controlled trials investigating the impact of fenofibrate treatment on apo C-III levels were searched in PubMed-Medline, Scopus, Web of Science and Google Scholar databases from inception to 18 August 2017. Quantitative data synthesis was determined by a random-effects model and generic inverse variance method. Sensitivity analysis was conducted using the leave-one-out method. A weighted random-effects meta-regression was performed to evaluate glycaemic parameter confounders.
Meta-analysis of 10 clinical trials involving 477 subjects showed fenofibrate therapy decreased apo C-III levels (weighted mean difference (WMD) -4.78 mg/dL, 95% CI -6.95 to -2.61, p<0.001; I66.87%). Subgroup analysis showed that fenofibrate reduced plasma apo C-III concentrations in subgroups of trials with treatment durations of either <12 weeks (WMD -4.50 mg/dL, p=0.001) or ≥12 weeks (WMD: -4.73 mg/dL, p=0.009) and doses of fenofibrate <200 mg/day (WMD -6.33 mg/dL, p<0.001) and >200 mg/day (p=0.006), with no significant difference between the subgroups.
This meta-analysis found that fenofibrate therapy significantly decreases apo C-III levels, an effect evident with both short-term treatment and doses less than 200 mg/day.
本荟萃分析对随机安慰剂对照临床试验进行了研究,旨在评估非诺贝特对载脂蛋白 C-III(apo C-III)的影响,apo C-III 是甘油三酯代谢的关键调节因子。
在 PubMed-Medline、Scopus、Web of Science 和 Google Scholar 数据库中搜索了从成立到 2017 年 8 月 18 日为止的旨在研究非诺贝特治疗对 apo C-III 水平影响的随机安慰剂对照试验。采用随机效应模型和通用倒数方差法进行定量数据综合。采用剔除一个研究的方法进行敏感性分析。采用加权随机效应荟萃回归评估血糖参数混杂因素。
对 10 项涉及 477 名受试者的临床试验进行荟萃分析,结果表明非诺贝特治疗可降低 apo C-III 水平(加权均数差(WMD)-4.78mg/dL,95%CI-6.95 至-2.61,p<0.001;I66.87%)。亚组分析显示,非诺贝特降低了治疗持续时间<12 周(WMD-4.50mg/dL,p=0.001)或≥12 周(WMD:-4.73mg/dL,p=0.009)、非诺贝特剂量<200mg/天(WMD-6.33mg/dL,p<0.001)和>200mg/天(p=0.006)的试验亚组中的血浆 apo C-III 浓度。各亚组之间无显著差异。
本荟萃分析发现,非诺贝特治疗可显著降低 apo C-III 水平,这一效应在短期治疗和剂量<200mg/天的情况下均存在。