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膜微粒在非酒精性脂肪性肝炎中的诊断价值

陈俊 李良平 付万智

引用本文:
Citation:

膜微粒在非酒精性脂肪性肝炎中的诊断价值

DOI: 10.3969/j.issn.1001-5256.2019.09.028
详细信息
  • 中图分类号: R575.5

Value of microparticles in the diagnosis of nonalcoholic steatohepatitis

  • 摘要:

    目的探讨血浆中CD14+细胞群和恒定自然杀伤T淋巴细胞(iNKT)源性膜微粒(MP)水平在非酒精性脂肪性肝炎(NASH)中的诊断价值。方法纳入2015年3月-2015年11月四川省人民医院消化内科、肝胆外科接受肝活组织检查的非酒精性脂肪性肝病(NAFLD)患者(36例),根据NAFLD活动度积分(NAS)和肝纤维化分期,分为NASH组(n=22)和非NASH组(n=14)。对照组为年龄、性别等因素匹配的健康体检者(n=15)。采用流式细胞术检测受试者血浆CD14+细胞和iNKT细胞的MP水平。符合正态分布的计量资料2组间比较采用t检验;多组间比较采用单因素方差分析,进一步两两比较采用LSD-t检验;非正态分布的计量资料2组间比较采用Mann-Whitney U检验。计数资料2组间比较采用χ2检验,两变量相关采用Pearson相关性分析。应用受试者工作特征曲线(ROC曲线)评价MP的诊断价值。结果 NAFLD组血浆CD14+细胞MP水平高于对照组[(5. 92±0. 62)个/μl vs (4. 52±0. 42)个/μl,t=7. 160,P <0. 001]、iNKT细胞MP水...

     

  • [1] FAZEL Y, KOENIG AB, SAYINER M, et al. Epidemiology and natural history of non-alcoholic fatty liver disease[J]. Metabolism, 2016, 65 (8) :1017-1025.
    [2] Group of Fatty Liver and Alcoholic Liver Diseases, Society of Hepatology, Chinese medical Association. Guidelines for management of non-alcoholic fatty liver disease[J]. J Clin Hepatol, 2010, 26 (2) :120-124. (in Chinese) 中华医学会肝脏病学分会脂肪肝和酒精性肝病学组.非酒精性脂肪性肝病诊疗指南[J].临床肝胆病杂志, 2010, 26 (2) :120-124.
    [3] KHAN FZ, PERUMPAIL RB, WONG RJ, et al. Advances in hepatocellular carcinoma:Nonalcoholic steatohepatitis-related hepatocellular carcinoma[J]. World J Hepatol, 2015, 7 (18) :2155-2161.
    [4] SERFATY L, LEMOINE M. Definition and natural history of metabolic steatosis:Clinical aspects of NAFLD, NASH and cirrhosis[J]. Diabetes Metab, 2008, 34 (6 Pt 2) :634-637.
    [5] GOH GB, CHANG PE, TAN CK. Changing epidemiology of hepatocellular carcinoma in Asia[J]. Best Pract Res Clin Gastroenterol, 2015, 29 (6) :919-928.
    [6] WONG VW, WONG GL, CHOI PC, et al. Disease progression of non-alcoholic fatty liver disease:A prospective study with paired liver biopsies at 3 years[J]. Gut, 2010, 59 (7) :969-974.
    [7] BAN LA, SHACKEL NA, MCLENNAN SV. Extracellular vesicles:A new frontier in biomarker discovery for non-alcoholic fatty liver disease[J]. Int J Mol Sci, 2016, 17 (3) :1-14.
    [8] CHAN WK, STHANESHWER P, NIK MN, et al. Limited utility of plasma M30 in discriminating non-alcoholic steatohepatitis from steatosis-a comparison with routine biochemical markers[J]. PLo S One, 2014, 9 (9) :e105903.
    [9] OROZCO AF, LEWIS DE. Flow cytometric analysis of circulating microparticles in plasma[J]. Cytometry A, 2010, 77 (6) :502-514.
    [10] PATZ S, TRATTNIG C, GRUNBACHER G, et al. More than cell dust:Microparticles isolated from cerebrospinal fluid of brain injured patients are messengers carrying mRNAs, miRNAs, and proteins[J]. J Neurotrauma, 2013, 30 (14) :1232-1242.
    [11] EL AS, MAGER I, BREAKEFIELD XO, et al. Extracellular vesicles:Biology and emerging therapeutic opportunities[J]. Nat Rev Drug Discov, 2013, 12 (5) :347-357.
    [12] BEYER C, PISETSKY DS. The role of microparticles in the pathogenesis of rheumatic diseases[J]. Nat Rev Rheumatol, 2010, 6 (1) :21-29.
    [13] WU ZH, JI CL, LI H, et al. Membrane microparticles and diseases[J]. Eur Rev Med Pharmacol Sci, 2013, 17 (18) :2420-2427.
    [14] BARTENEVA NS, FASLER-KAN E, BERNIMOULIN M, et al.Circulating microparticles:Square the circle[J]. BMC Cell Biol, 2013, 14:23.
    [15] FRITZSCHING B, SCHWER B, KARTENBECK J, et al. Release and intercellular transfer of cell surface CD81 via microparticles[J]. J Immunol, 2002, 169 (10) :5531-5537.
    [16] ROZMYSLOWICZ T, MAJKA M, KIJOWSKI J, et al. Plateletand megakaryocyte-derived microparticles transfer CXCR4receptor to CXCR4-null cells and make them susceptible to infection by X4-HIV[J]. AIDS, 2003, 17 (1) :33-42.
    [17] EGUCHI A, MULYA A, LAZIC M, et al. Microparticles release by adipocytes act as “find-me”signals to promote macrophage migration[J]. PLo S One, 2015, 10 (4) :e123110.
    [18] KORNEK M, POPOV Y, LIBERMANN T A, et al. Human T cell microparticles circulate in blood of hepatitis patients and induce fibrolytic activation of hepatic stellate cells[J]. Hepatology, 2011, 53 (1) :230-242.
    [19] SUTTI S, BRUZZI S, ALBANO E. The role of immune mechanisms in alcoholic and nonalcoholic steatohepatitis:A 2015 update[J]. Expert Rev Gastroenterol Hepatol, 2016, 10 (2) :243-253.
    [20] KLEINER DE, BRUNT EM, VAN NM, et al. Design and validation of a histological scoring system for nonalcoholic fatty liver disease[J]. Hepatology, 2005, 41 (6) :1313-1321.
    [21] STEPIEN E, GRUSZCZYNSKI K, KAPUSTA P, et al. Plasma centrifugation does not influence thrombin-antithrombin and plasmin-antiplasmin levels but determines platelet microparticles count[J]. Biochem Med (Zagreb) , 2015, 25 (2) :222-229.
    [22] JEEN YM, JIN SY. Pathology of nonalcoholic steatohepatitis[J]. Korean J Hepatol, 2009, 15 (2) :122-130.
    [23] ZHANG ZL, HUANG YS, FAN YD, et al. Effect of Xuezhikang on hepatitis and oxidative stress in rats with nonalcoholic fatty liver diseases[J]. Chin J Med Offic, 2018, 46 (6) :605-609. (in Chinese) 张子龙, 黄樱硕, 范煜东, 等.血脂康对非酒精性脂肪性肝病大鼠肝炎症及氧化应激影响[J].临床军医杂志, 2018, 46 (6) :605-609.
    [24] SA R, ZHANG W, GE J, et al. Discovering a critical transition state from nonalcoholic hepatosteatosis to nonalcoholic steatohepatitis by lipidomics and dynamical network biomarkers[J].J Mol Cell Biol, 2016, 8 (3) :195-206.
    [25] KORNEK M, POPOV Y, LIBERMANN TA, et al. Human T cell microparticles circulate in blood of hepatitis patients and induce fibrolytic activation of hepatic stellate cells[J]. Hepatology, 2011, 53 (1) :230-242.
    [26] POVERO D, EGUCHI A, NIESMAN IR, et al. Lipid-induced toxicity stimulates hepatocytes to release angiogenic microparticles that require Vanin-1 for uptake by endothelial cells[J].Sci Signal, 2013, 6 (296) :1897-1904.
    [27] POVERO D, EGUCHI A, LI H, et al. Circulating extracellular vesicles with specific proteome and liver microRNAs are potential biomarkers for liver injury in experimental fatty liver disease[J]. PLo S One, 2014, 9 (12) :e113651.
    [28] WITEK RP, YANG L, LIU R, et al. Liver cell-derived microparticles activate hedgehog signaling and alter gene expression in hepatic endothelial cells[J]. Gastroenterology, 2009, 136 (1) :320-330.
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  • 收稿日期:  2019-04-24
  • 出版日期:  2019-09-20
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