Instituto de Biomedicina, Universidad de León, España.
Universidad de León.
Rev Esp Enferm Dig. 2019 Apr;111(4):275-282. doi: 10.17235/reed.2019.6068/2018.
increasing evidence suggests a role of intestinal dysbiosis in obesity and non-alcoholic fatty liver disease (NAFLD). The advances in recent years with regard to the role of the gut microbiota raise the potential utility of new therapeutic approaches based on the modification of the microbiome.
the aim of this study was to compare the bacterial communities in obese patients with or without NAFLD to those of healthy controls.
the fecal microbiota composition of 20 healthy adults, 36 obese patients with NAFLD and 17 obese patients without NAFLD was determined by 16S ribosomal RNA sequencing using the Illumina MiSeq system.
the results highlighted significant differences in the phylum Firmicutes between patients with and without NAFLD, which was a determining factor of the disease and supported its possible role as a marker of NAFLD. At the genus level, the relative abundance of Blautia, Alkaliphilus, Flavobacterium and Akkermansia was reduced in obese patients, both with or without NAFLD, compared to healthy controls. Furthermore, the number of sequences from the genus Streptococcus was significantly higher in patients with NAFLD in comparison with individuals without the disease, constituting another possible marker. Comparison of bacterial communities at the genus level by a principal coordinate analysis indicated that the bacterial communities of patients with NAFLD were dispersed and did not form a group.
in conclusion, these results indicate the role of intestinal dysbiosis in the development of NAFLD associated with obesity. There was a differential microbiota profile between obese patients, with and without NAFLD. Thus, supporting gut microbiota modulation as a therapeutic alternative for the prevention and treatment of NAFLD.
越来越多的证据表明肠道菌群失调与肥胖和非酒精性脂肪性肝病(NAFLD)有关。近年来,肠道微生物组在疾病中作用的相关研究进展,提高了基于微生物组修饰的新治疗方法的潜在应用价值。
本研究旨在比较肥胖伴或不伴 NAFLD 患者与健康对照者的肠道细菌群落。
采用 Illumina MiSeq 系统对 20 名健康成年人、36 名肥胖伴 NAFLD 患者和 17 名肥胖不伴 NAFLD 患者的粪便微生物群落组成进行 16S 核糖体 RNA 测序。
结果突出了 NAFLD 患者与非 NAFLD 患者之间厚壁菌门的显著差异,这是疾病的决定因素,并支持其作为 NAFLD 标志物的可能作用。在属水平上,与健康对照组相比,肥胖患者(伴或不伴 NAFLD)中 Blautia、Alkaliphilus、Flavobacterium 和 Akkermansia 的相对丰度降低。此外,与无该病患者相比,NAFLD 患者中链球菌属的序列数量显著更高,构成了另一个可能的标志物。通过主坐标分析对属水平的细菌群落进行比较,表明 NAFLD 患者的细菌群落分散且未形成一个群组。
总之,这些结果表明肠道菌群失调在肥胖相关的 NAFLD 发展中起作用。肥胖伴或不伴 NAFLD 患者的微生物群组成存在差异。因此,支持肠道微生物群调节作为预防和治疗 NAFLD 的治疗选择。