The Role of Intestinal Microbiota, Endotoxemia and Systemic Inflammation in the Pathogenesis of Nonalcoholic Fatty Liver Disease

G. Fadieienko, А. Gridnev, I. Kushnir, T. Solomentseva, V. Chernova, V. Galchіnskaya
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Abstract

Introduction. Currently there are few and contradictory data concerning the influence of intestinal microbiota (IM) disturbances on the nature and severity of inflammatory processes in the liver tissue, the role of microbial metabolites in the activation of steatosis and fibrosis processes in patients with non-alcoholic fatty liver disease (NAFLD). The aim of the study. To clarify the role of intestinal microbiota, endotoxemia and systemic inflammation in the development and progression of nonalcoholic fatty liver disease. Materials and methods. 108 patients with NAFLD were examined, control group included 30 people. Detection of CRP and TNF-alpha levels, endotoxin in blood serum was carried out by the immunoenzymatic method. Determination of IM composition at the level of the main phylotypes was carried out by the method of quantitative polymerase chain reaction in real time. Results. A weak direct correlation between TNF-alpha, CRP and endotoxin with Firmicutes content (F), and an inverse correlation between CRP with Bacteroidetes content (B) was revealed. The dependence of the ratio of main intestinal phyla (F/B) on markers of systemic inflammation in NAFLD patients with different levels of endotoxin was evaluated. In patients with NAFLD, as endotoxin concentration increased, a deeper imbalance of IM was observed. In the group of patients with NAFLD with a high level of endotoxin, the maximum values of the F/B index were observed. Also, the increase in the intestinal permeability of the mucous barrier depended not only on changes in the IM, but also on systemic inflammation. The highest levels of endotoxemia were observed in patients with a high F/B index and increased activity of pro-inflammatory markers. In patients with NAFLD with varying degrees of fatty infiltration of the liver, an imbalance of IM was detected in comparison with the control group. As the degree of steatosis increased in NAFLD patients, an increase in Firmicutes content was observed. The maximum shift in the balance of the main phyla towards a decrease in the relative content of Bacteroidetes and an increase in Firmicutes was determined in patients with 3rd degree of steatosis (p-value less than 0.05). In the group of patients with a low and moderate degree of steatosis, a similar trend of IM disorders was observed, but these changes were insignificant. The relative number of Actinobacteria exposed no differences between the examined patients. The analysis of changes in IM in patients with NAFLD depending on the stage of liver fibrosis revealed no significant differences both from the control group and between groups with different degrees of fibrosis. The obtained data indicate that the imbalance of IM makes a significant contribution to the development of liver steatosis, while other important factors are involved in the formation of fibrosis processes, in particular, inflammation, the activity of intestinal metabolites and regulatory molecules. Conclusions.The imbalance of the intestinal microbiota towards an increase in Firmicutes leads to an increase in the production of intestinal metabolites with subsequent initiation of systemic inflammation, which stimulates the accumulation of fat in hepatocytes, affecting the progression of steatosis and the processes of fibrosis in the liver.
肠道菌群、内毒素血症和全身性炎症在非酒精性脂肪肝发病中的作用
介绍。目前,关于肠道微生物群(IM)紊乱对肝组织炎症过程的性质和严重程度的影响,以及微生物代谢物在非酒精性脂肪性肝病(NAFLD)患者脂肪变性和纤维化过程激活中的作用,数据很少且相互矛盾。研究的目的。阐明肠道菌群、内毒素血症和全身性炎症在非酒精性脂肪性肝病发生和进展中的作用。材料和方法。对108例NAFLD患者进行检查,对照组30例。采用免疫酶法检测血清CRP、tnf - α、内毒素水平。采用实时定量聚合酶链反应法测定主要种型水平的IM组成。结果。tnf - α、CRP和内毒素与厚壁菌门含量(F)呈微弱的直接相关,而CRP与拟杆菌门含量(B)呈负相关。评价不同内毒素水平NAFLD患者主肠门比值(F/B)对全身性炎症标志物的依赖性。在NAFLD患者中,随着内毒素浓度的升高,IM的失衡程度加深。在内毒素水平较高的NAFLD组,观察F/B指数的最大值。此外,肠粘膜屏障通透性的增加不仅取决于IM的变化,还与全身炎症有关。在高F/B指数和促炎标志物活性增加的患者中观察到最高水平的内毒素血症。在不同程度的脂肪浸润肝脏的NAFLD患者中,与对照组相比,检测到IM失衡。随着NAFLD患者脂肪变性程度的增加,观察到厚壁菌门含量增加。在3度脂肪变性患者中,主要门的平衡向拟杆菌门相对含量下降和厚壁菌门相对含量增加的最大方向移动(p值小于0.05)。在低中度脂肪变性患者组中,观察到类似的IM障碍趋势,但这些变化不显著。放线菌暴露的相对数量在检查的患者之间没有差异。分析NAFLD患者IM随肝纤维化分期的变化,结果显示与对照组及不同纤维化程度组间无显著差异。所获得的数据表明,IM的失衡对肝脏脂肪变性的发展有重要贡献,而其他重要因素也参与了纤维化过程的形成,特别是炎症、肠道代谢物的活性和调节分子。结论。肠道菌群失衡导致厚壁菌门增加,导致肠道代谢物产生增加,随后引发全身性炎症,刺激肝细胞脂肪积累,影响脂肪变性的进展和肝脏纤维化过程。
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