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非诺贝特对血浆载脂蛋白 C-III 水平的影响:一项随机安慰剂对照试验的系统评价和荟萃分析。

Effect of fenofibrate on plasma apolipoprotein C-III levels: a systematic review and meta-analysis of randomised placebo-controlled trials.

机构信息

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

BMJ Open. 2019 Feb 22;8(11):e021508. doi: 10.1136/bmjopen-2018-021508.

DOI:10.1136/bmjopen-2018-021508
PMID:30798284
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6278807/
Abstract

OBJECTIVES

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.

MATERIALS AND METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

材料和方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/acaeabb78e83/bmjopen-2018-021508f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/fc909a9fc68c/bmjopen-2018-021508f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/87440deb1b63/bmjopen-2018-021508f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/68ddeb3b049e/bmjopen-2018-021508f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/acaeabb78e83/bmjopen-2018-021508f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/fc909a9fc68c/bmjopen-2018-021508f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/87440deb1b63/bmjopen-2018-021508f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/68ddeb3b049e/bmjopen-2018-021508f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37b8/6278807/acaeabb78e83/bmjopen-2018-021508f04.jpg

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