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Intestinal microbiota in patients with chronic hepatitis C with and without cirrhosis compared with healthy controls

机译:与健康控制相比,慢性丙型肝炎患者肠道微生物患者,没有肝硬化

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摘要

Abstract Background & Aims The importance of the intestinal microbiota for the onset and clinical course of many diseases, including liver diseases like non‐alcoholic steatohepatitis and cirrhosis, is increasingly recognized. However, the role of intestinal microbiota in chronic hepatitis C virus ( HCV ) infection remains unclear. Methods In a cross‐sectional approach, the intestinal microbiota of 95 patients chronically infected with HCV (n=57 without cirrhosis [ NO ‐ CIR ]; n=38 with cirrhosis [ CIR ]) and 50 healthy controls ( HC ) without documented liver diseases was analysed. Results Alpha diversity, measured by number of phylotypes (S) and Shannon diversity index (H′), decreased significantly from HC to NO ‐ CIR to CIR . S and H′ correlated negatively with liver elastography. Analysis of similarities revealed highly statistically significant differences in the microbial communities between HC , NO ‐ CIR and CIR ( R =.090; P 1.0×10 ?6 ). Stratifying for HCV genotypes even increased the differences. In addition, we observed distinct patterns in the relative abundance of genera being either positive or negative correlated with diseases status. Conclusions This study shows that not only the stage of liver disease but also HCV infection is associated with a reduced alpha diversity and different microbial community patterns. These differences might be caused by direct interactions between HCV and the microbiota or indirect interactions facilitated by the immune system.
机译:抽象背景&旨在为许多疾病的发病和临床进程的重要性,包括肝脏疾病,如非酒精脂肪肝炎和肝硬化等疾病。然而,肠道微生物在慢性丙型肝炎病毒(HCV)感染中的作用仍不清楚。方法在横截面方法中,95例肠道微生物患者慢性感染HCV(n = 57,没有肝硬化[No-cir]; n = 38,肝硬化[cir])和50例健康对照(HC)没有记录肝病分析了。结果α多样性,按数量测量的数量和香农分集指数(H'),从HC到NO - CIR,从HC显着降低。 S和H'与肝脏弹性显影负相关。相似性分析揭示了HC,NO - CIR和CIR(r = .090; P& 1.0×10?6)的微生物社区的高度统计学显着差异。对HCV基因型的分层甚至增加了差异。此外,我们观察到了与疾病状态的正面或负相关的完全饱和度的不同模式。结论本研究表明,不仅具有肝病的阶段,还与HCV感染的阶段与降低的α多样性和不同的微生物群落模式相关。这些差异可能是由HCV与免疫系统促进的微生物群或微生物群或间接相互作用之间的直接相互作用引起的。

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  • 来源
    《Liver international :》 |2018年第1期|共9页
  • 作者单位

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Microbial Interactions and Processes Research GroupHelmholtz Center for Infection;

    Microbial Interactions and Processes Research GroupHelmholtz Center for Infection;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Microbial Interactions and Processes Research GroupHelmholtz Center for Infection;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Department of Gastroenterology Hepatology and EndocrinologyHannover Medical SchoolHannover Germany;

    Microbial Interactions and Processes Research GroupHelmholtz Center for Infection;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 内科学;
  • 关键词

    alpha diversity; gut microbiome; cirrhosis; liver elastography; microbial diversity;

    机译:α多样性;肠道微生物组;肝硬化;肝脏弹性成像;微生物多样性;

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