Effect of Liver Fibrosis on Oral and Gut Microbiota in the Japanese General Population Determined by Evaluating the FibroScan–Aspartate Aminotransferase Score

• Published in: International journal of molecular sciences Vol. 24; no. 17; p. 13470
• Main Authors: Sato, Satoshi, Iino, Chikara, Chinda, Daisuke, Sasada, Takafumi, Tateda, Tetsuyuki, Kaizuka, Masatoshi, Nomiya, Hiroki, Igarashi, Go, Sawada, Kaori, Mikami, Tatsuya, Nakaji, Shigeyuki, Sakuraba, Hirotake, Fukuda, Shinsaku
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-09-2023; MDPI
• Subjects: Alcohol; Analysis; Antigens; Bacteria; Biopsy; Body mass index; Diabetes; Discriminant analysis; Epidemiology; FibroScan–asparate aminotransferase (FAST) score; Fibrosis; gut microbiota; Hepatitis B; Hepatitis C; Inflammation; Insulin resistance; Liver; Liver cirrhosis; Liver diseases; liver fibrosis; Metabolism; Microbiota; Microbiota (Symbiotic organisms); Multivariate analysis; oral microbiota; Oxidative stress; Pathogens; Type 2 diabetes; Japan
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms241713470

The association between liver fibrosis and oral or gut microbiota has been studied before. However, epidemiological studies in the general population are limited owing to the difficulty of noninvasive liver-fibrosis assessment. FibroScan–asparate aminotransferase (FAST) scores can be used to accurately and non-invasively evaluate liver fibrosis. This study aimed to determine the association between liver fibrosis and oral or gut microbiota using the FAST score in the general population. After propensity score matching of 1059 participants based on sex, age, body mass index, homeostasis model assessment of insulin resistance, and triglyceride levels, 125 (non-liver-fibrosis group, 100; liver fibrosis group, 25) were included. The diversity of gut microbiota differed significantly between the two groups; however, no significant differences were noted in their oral microbiota. The liver fibrosis group showed an increase in the relative abundance of Fusobacteria strains and a decrease in the relative abundance of Faecalibacterium, with the presence of Fusicatenibacter in the gut microbiota. Feacalibacterium was not identified as an independent factor of liver fibrosis in adjusting the fatty liver index. In the general population, gut microbiota may be more involved in liver fibrosis than oral microbiota.