Cao Xinlu, Zolnikova Oksana, Maslennikov Roman, Reshetova Maria, Poluektova Elena, Bogacheva Arina, Zharkova Maria, Ivashkin Vladimir
Department of Internal Medicine, Gastroenterology and Hepatology, Sechenov University, 119435 Moscow, Russia.
The Interregional Public Organization "Scientific Community for the Promotion of the Clinical Study of the Human Microbiome", 119121 Moscow, Russia.
Metabolites. 2023 Jul 19;13(7):859. doi: 10.3390/metabo13070859.
The objective of this study was to investigate the metabolic activity of the gut microbiota in cirrhosis due to different variants of fatty liver disease (alcoholic vs. non-alcoholic [metabolic-associated] one [AFLD and MAFLD]). The present study included 24 patients with alcoholic liver cirrhosis, 16 patients with MAFLD-related cirrhosis, and 20 healthy controls. The level and spectrum of short-chain fatty acids (SCFAs) were determined via gas-liquid chromatography. All patients with cirrhosis showed a decrease in the total content of SCFAs ( < 0.001) and absolute content of acetate ( < 0.001), propionate ( < 0.001), butyrate ( < 0.001), and isovalerate ( < 0.001). In MAFLD cirrhosis, the metabolic activity of the microbiota was significantly altered compared to patients with alcoholic cirrhosis, as evidenced by a lower total SCFA content ( < 0.001) and absolute content of acetate ( < 0.001), propionate ( < 0.001), and butyrate ( < 0.001); a higher relative content of isovalerate ( < 0.001); and a higher IsoCn/Cn ratio ( < 0.001). Various clinical and laboratory parameters correlate differently with fecal SCFAs and their fractions in cirrhosis due to AFLD and MAFLD. SCFA-producing metabolic activity is reduced more in MAFLD cirrhosis than in alcoholic cirrhosis. According to the etiological factors of cirrhosis, disorders of this metabolic activity may be involved in different pathogenetic pathways.
本研究的目的是调查不同类型脂肪肝疾病(酒精性与非酒精性[代谢相关]脂肪肝[AFLD和MAFLD])所致肝硬化中肠道微生物群的代谢活性。本研究纳入了24例酒精性肝硬化患者、16例MAFLD相关肝硬化患者和20名健康对照者。通过气液色谱法测定短链脂肪酸(SCFAs)的水平和谱。所有肝硬化患者的SCFAs总含量(<0.001)以及乙酸盐(<0.001)、丙酸盐(<0.001)、丁酸盐(<0.001)和异戊酸盐(<0.001)的绝对含量均降低。在MAFLD肝硬化中,与酒精性肝硬化患者相比,微生物群的代谢活性发生了显著改变,表现为总SCFA含量(<0.001)以及乙酸盐(<0.001)、丙酸盐(<0.001)和丁酸盐(<0.001)的绝对含量较低;异戊酸盐的相对含量较高(<0.001);以及较高的异戊酸/总短链脂肪酸比值(<0.001)。在AFLD和MAFLD所致肝硬化中,各种临床和实验室参数与粪便SCFAs及其组分的相关性各不相同。MAFLD肝硬化中产生SCFA的代谢活性比酒精性肝硬化降低得更多。根据肝硬化的病因,这种代谢活性紊乱可能参与不同的发病机制途径。