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           酒精性肌病相关炎性因子和氧化应激标志物水平的

           Meta 分析

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           汪楠  1,2 ,Oleksandr Motuziuk ,Iryna Mishchenko ,周颖婷   2                              查看原文
               【摘要】 背景 酒精中毒会引发酒精性肌病。目前,评价酒精性肌病的标志物有 10 种以上,但这些标志物的
           评价价值尚存争议。目的 系统评价酒精性肌病相关炎性因子和氧化应激标志物水平的影响。方法 检索维普网(VIP)、
           万方数据知识服务平台(Wanfang Data)、中国知网(CNKI)、Web of Science、PubMed、Embase、Cochrane Library 等
           数据库,筛选关于酒精性肌病相关炎性因子和氧化应激标志物的动物干预研究,检索时间为 1990-02-01 至 2021-08-
           31。采用 RevMan 5.4.1 进行 Meta 分析。结局指标包括还原型谷胱甘肽(GSH)、丙二醛(MDA)、胰岛素样生长因子
           1(IGF-1)及白介素 6(IL-6)mRNA 表达水平。结果 最终纳入 17 项动物干预试验,Meta 分析结果表明,试验组
           IGF-1 mRNA 表达水平〔SMD=-3.09,95%CI(-5.75,-0.43),P=0.02〕和 GSH 水平〔SMD=-4.20,95%CI(-6.24,-2.17),
           P<0.000 01〕低于对照组;试验组 IL-6 mRNA 表达水平〔SMD=3.75,95%CI(2.93,4.57),P<0.000 01〕和 MDA 水
           平〔SMD=0.97,95%CI(0.64,1.29),P<0.000 01〕高于对照组。结论 发生酒精性肌病时 IGF-1 mRNA 表达水平和
           GSH 水平降低,IL-6 mRNA 表达水平和 MDA 水平升高。
               【关键词】 肌病;慢性酒精性肌病;氧化应激;炎性因子浸润;系统评价;Meta 分析
               【中图分类号】 R 685 R 595.6 【文献标识码】 A DOI:10.12114/j.issn.1007-9572.2022.0214
               汪楠,Oleksandr Motuziuk,Iryna Mishchenko,等 . 酒精性肌病相关炎性因子和氧化应激标志物水平的 Meta 分析[J].
           中国全科医学,2022,25(33):4123-4129. [www.chinagp.net]
               WANG N,OLEKSANDR M,IRYNA M,et al. Levels of relevant inflammatory factors and oxidative stress markers in
           alcoholic myopathy:a Meta-analysis[J]. Chinese General Practice,2022,25(33):4123-4129.

           Levels of Relevant Inflammatory Factors and Oxidative Stress Markers in Alcoholic Myopathy:a Meta-analysis
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           WANG Nan 1,2 ,OLEKSANDR Motuziuk ,IRYNA Mishchenko ,ZHOU Yingting 2
           1.Biomedical Research and Evidence-Based Center,Lesya Ukrainka Volyn National University,Lutsk 43025,Ukraine
           2.Department of basic medicine,Jiangsu Vocational College of Medicine,Yancheng 224000,China
           3.Volyn Medical Institute,Lutsk 43025,Ukraine
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           Corresponding author:OLEKSANDR Motuziuk,Associate professor,Doctoral supervisor;E-mail:cmoplutsk@gmail.com
               【Abstract】 Background Alcoholism can lead to alcoholic myopathy. Although there are over ten biomarkers used to
           evaluate this disease,their diagnostic value remains controversial. Objective To systematically evaluate the effects of alcoholic
           myopathy on levels of relevant inflammatory factors and oxidative stress markers. Methods The VIP Database for Chinese
           Technical Periodicals,Wanfang Data Knowledge Service Platform,China National Knowledge Infrastructure,Web of Science,
           PubMed,Embase and Cochrane Library databases were searched for animal intervention studies on inflammatory factors and
           oxidative stress markers in alcoholic myopathy from February 1,1990 to August 31,2021 to retrieve. RevMan 5.4.1 was used
           for Meta-analysis. Outcome measures included reduced glutathione(GSH)and malondialdehyde (MDA) levels as well as the
           mRNA expression levels of insulin-like growth factor 1(IGF-1)and interleukin 6(IL-6). Results Ultimately,17 animal
           interventionstudies were included,and the results of Meta-analysis showed that the levels of IGF-1 mRNA expression〔SMD=-3.09,
           95%CI(-5.75,-0.43),P=0.02〕and GSH levels〔SMD=-4.20,95%CI(-6.24,-2.17),P<0.000 01〕in the experimental
           group were lower than those in the control group. The levels of IL-6 mRNA expression〔SMD=3.75,95%CI(2.93,4.57),
           P<0.000 01〕and MDA levels〔SMD=0.97,95%CI(0.64,1.29),P<0.000 01〕were higher in the experimental group than those
           in the control group. Conclusion Animals with alcoholic myopathy show decreased IGF-1 mRNA expression and GSH levels but
           increased IL-6 mRNA expression and MDA levels.
               【Key words】 Myopathy;Chronic alcoholic myopathy;Oxidative stress;Inflammatory factor infiltration;Systematic
           evaluation;Meta analysis

               1.43025 乌克兰,卢茨克市,乌克兰沃伦国立大学生物医学研究与循证中心 2.224000 江苏省盐城市,江苏医药职业学院基础医
           学部 3.43025 乌克兰,卢茨克市,沃伦医学院
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               通信作者:Oleksandr Motuziuk,副教授,博士生导师;E-mail:cmoplutsk@gmail.com
               本文数字出版日期:2022-08-05
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