Changes in gut microbiota in patients with metabolic-associated fatty liver disease

O.Y. Komarytsia, O.M. Radchenko, K.A. Moskva, M.O. Borovets
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Abstract

Background. Modern science considers changes in the gut microbiota as a pathogenetic factor in the development of many di­seases, including metabolic-associated fatty liver disease (MAFLD) and liver steatosis. Although dysbiosis is present at every stage of fatty liver disease, typical signs have not been identified separately for MAFLD that determines the relevance and expedien­cy of our research. This investigation purposed to evaluate the state of the gut microbiota in patients with MAFLD. Materials and methods. In total, 19 patients were observed. Among them, 14 had metabolic syndrome and MAFLD and 5 were without metabolic syndrome with intact liver. These two groups differed significantly only in body mass index, had similar gender-age distribution, blood pressure, parameters of lipid and carbohydrate metabolism. Metagenomic analysis of the intestinal microbiome was performed by polymerase chain reaction in a certified laboratory in addition to standard cli­nical and laboratory examinations. Patients were treated and exa­mined according to regulatory documents and the Declaration of Helsinki. Digital results were processed statistically, the level of significance was p < 0.05. Results. In patients with MAFLD, the changes in the gut microbiota began already at the stage of steatosis. They manifested by an increase in the total bacterial mass by a third, a lower number of obligate strains (Lactobacillus, Bifidobacterium, Bacteroides thetaiotaomicron, Akkermansia muciniphila) and an increased content of opportunistic pathogens (Сlostridium perfringens, Klebsiella pneumoniae, Klebsiella oxytoca, enterоpathogenic Escherichia coli, Shigella, Proteus, Salmonella) in contrast to patients with an intact liver. The bulk of bacterial DNA were DNA of Bacteroidetes (50.66 % compared to intact liver; Δ = +8.29 %) and Firmicutes (31.97 ± 3.19 %; Δ = –10.87 %) and Actinobacteria DNA (Δ = +40.41 %) made up 7.47 ± 2.69 %. Changes in the metagenomic status of the gut microbiota are associated with body weight, systemic blood circulation, lipid and carbohydrate metabolism. Conclusions. Alterations in the gut microbiota with an increase in total bacterial mass, a lower number of obligate and increased amount of opportunistic strains already at the stage of steatosis have been shown to correlate with the development and progression of fatty liver disease due to metabolic effects.
代谢性脂肪性肝病患者肠道菌群的变化
背景。现代科学认为肠道微生物群的变化是许多疾病发展的一个致病因素,包括代谢性脂肪性肝病(MAFLD)和肝脏脂肪变性。虽然失调存在于脂肪肝疾病的每个阶段,但尚未单独确定MAFLD的典型体征,这决定了我们研究的相关性和便捷性。本研究旨在评估MAFLD患者肠道菌群的状态。材料和方法。共观察19例患者。其中有代谢综合征和MAFLD的14例,无代谢综合征且肝脏完整的5例。这两组仅在体重指数、性别年龄分布、血压、脂质和碳水化合物代谢参数等方面存在显著差异。除了标准的临床和实验室检查外,还在认证实验室通过聚合酶链反应对肠道微生物组进行宏基因组分析。根据监管文件和赫尔辛基宣言对患者进行治疗和检查。数字结果进行统计学处理,显著性水平为p <0.05. 结果。在MAFLD患者中,肠道菌群的变化早在脂肪变性阶段就开始了。与肝脏完整的患者相比,它们表现为总细菌质量增加了三分之一,专性菌株(乳酸杆菌、双歧杆菌、拟杆菌、嗜粘杆菌)数量减少,机会致病菌(Сlostridium产气荚膜菌、肺炎克雷伯菌、氧化克雷伯菌、肠道致病性大肠杆菌、志贺氏菌、变形杆菌、沙门氏菌)含量增加。与完整肝脏相比,大部分细菌DNA为拟杆菌门DNA (50.66%);Δ = + 8.29%)和厚壁菌门(31.97±3.19%);Δ = - 10.87%),放线菌DNA (Δ = + 40.41%)占7.47±2.69%。肠道微生物群宏基因组状态的变化与体重、全身血液循环、脂质和碳水化合物代谢有关。结论。肠道菌群的改变与细菌总质量的增加、专性菌株数量的减少和已经处于脂肪变性阶段的机会性菌株数量的增加已被证明与代谢作用导致的脂肪肝疾病的发生和进展相关。
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0.50
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60
审稿时长
6 weeks
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