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在合并感染丙型肝炎病毒(HCV)和人类免疫缺陷病毒(HIV)以及单纯感染HCV且伴有胰岛素抵抗的患者中使用二甲双胍改善治疗效果和肝纤维化转归:一项随机对照试验的研究方案

Improving treatment and liver fibrosis outcomes with metformin in HCV-HIV co-infected and HCV mono-infected patients with insulin resistance: study protocol for a randomized controlled trial.

作者信息

Doyle Mary-Anne, Singer Joel, Lee Terry, Muir Miriam, Cooper Curtis

机构信息

Division of Endocrinology and Metabolism, Department of Medicine, University of Ottawa, Ottawa, ON, Canada.

Ottawa Hospital Research Institute, Ottawa, ON, Canada.

出版信息

Trials. 2016 Jul 20;17(1):331. doi: 10.1186/s13063-016-1454-6.

Abstract

BACKGROUND

Approximately 180 million people worldwide, (3 % of the world's population) are infected with hepatitis C (HCV). Insulin resistance (IR) and type 2 diabetes (T2DM) are common extrahepatic manifestations of chronic HCV infection and associated with poor treatment and liver-related outcomes. The presence of these metabolic complications have been associated with poor response to interferon-based HCV antiviral therapy and increased risk of liver-related outcomes. Metformin, an insulin sensitizer is known to improve HCV treatment response and has been associated with a reduced risk of developing hepatocellular carcinoma (HCC). This study will evaluate the effect of metformin on preventing progression or promoting regression of liver fibrosis, rate of virologic cure (SVR) and other metabolic measures in HCV-HIV co-infected and HCV mono-infected study participants who have IR and are planning on initiating HCV treatment.

METHODS

This study is a prospective 48-week single-centre, randomized, open-label, controlled trial of HIV-HCV co-infected and HCV mono-infected patients with IR (HOMA-IR ≥ 2.0) who are planning to initiate HCV antiviral therapy. Sixty participants will be recruited from The Ottawa Hospital Viral Hepatitis Clinic. Participants will be randomized in a 1:1 ratio to either arm 1, metformin 2 g (1 g twice daily) plus lifestyle, or to arm 2, lifestyle alone. The primary outcome will be the change in FibroScan® score (kPa) from baseline to week 12 (start of HCV treatment), the end of HCV treatment (week 24) and 24 weeks post HCV treatment (week 48). Secondary outcomes include changes in liver fibrosis using AST to platelet ratio index, changes in glucose and lipid levels, anthropometric measures, changes in alpha-fetoprotein levels, patient acceptability, and changes in dietary and physical activity parameters.

DISCUSSION

This pilot study will be the first to evaluate the role of metformin on liver fibrosis in HCV-HIV co-infected and HCV mono-infected patients with IR receiving DAA HCV treatment. If metformin is effective in reducing liver fibrosis in this patient population, this will represent a well-tolerated, easy-to-administer, inexpensive therapy that will protect against negative HCV outcomes. This study will also be an opportunity to evaluate the impact of insulin resistance and hyperglycemia on viral clearance in HCV-infected patients treated with interferon-free regimens.

TRIAL REGISTRATION

ClinicalTrials.gov NCT02306070 version 4.0 (June 29, 2015).

摘要

背景

全球约有1.8亿人(占世界人口的3%)感染丙型肝炎病毒(HCV)。胰岛素抵抗(IR)和2型糖尿病(T2DM)是慢性HCV感染常见的肝外表现,与治疗效果不佳及肝脏相关结局有关。这些代谢并发症的存在与基于干扰素的HCV抗病毒治疗反应不佳及肝脏相关结局风险增加有关。二甲双胍作为一种胰岛素增敏剂,已知可改善HCV治疗反应,并与肝细胞癌(HCC)发生风险降低有关。本研究将评估二甲双胍对预防HCV-HIV合并感染及HCV单一感染且有IR并计划开始HCV治疗的研究参与者肝纤维化进展或促进其逆转、病毒学治愈(SVR)率及其他代谢指标的影响。

方法

本研究是一项前瞻性、为期48周单中心、随机、开放标签、对照试验,研究对象为计划开始HCV抗病毒治疗且有IR(稳态模型评估胰岛素抵抗指数≥2.0)的HIV-HCV合并感染及HCV单一感染患者。将从渥太华医院病毒性肝炎诊所招募60名参与者。参与者将按1:1比例随机分为两组,第1组接受二甲双胍2克(每日两次,每次1克)加生活方式干预;第2组仅接受生活方式干预。主要结局指标为从基线到第12周(HCV治疗开始)、HCV治疗结束时(第24周)及HCV治疗后24周(第48周)FibroScan®评分(kPa)的变化。次要结局指标包括使用天门冬氨酸氨基转移酶与血小板比值指数评估的肝纤维化变化、血糖和血脂水平变化、人体测量指标、甲胎蛋白水平变化、患者可接受性以及饮食和身体活动参数变化。

讨论

本初步研究将首次评估二甲双胍在接受直接抗病毒药物(DAA)治疗的HCV-HIV合并感染及HCV单一感染且有IR患者中对肝纤维化的作用。如果二甲双胍对该患者群体减少肝纤维化有效,这将代表一种耐受性良好、易于给药且廉价的治疗方法,可预防HCV不良结局。本研究还将为评估胰岛素抵抗和高血糖对接受无干扰素方案治疗的HCV感染患者病毒清除的影响提供机会。

试验注册

ClinicalTrials.gov NCT02306070版本4.0(2015年6月29日)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b8c/4955144/aba530922871/13063_2016_1454_Fig1_HTML.jpg

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