Association of gut microbiota with portal vein pressure in patients with liver cirrhosis undergoing living donor liver transplantation

Author:

Toshida Katsuya1ORCID,Itoh Shinji1ORCID,Kosai‐Fujimoto Yukiko1,Ishikawa Takuma1,Nakayama Yuki1,Tsutsui Yuriko1,Iseda Norifumi1,Izumi Takuma1,Bekki Yuki1,Yoshiya Shohei1,Toshima Takeo1ORCID,Nakamuta Makoto2,Yoshizumi Tomoharu1

Affiliation:

1. Department of Surgery and Science, Graduate School of Medical Sciences Kyushu University Fukuoka Japan

2. Department of Gastroenterology, Kyushu Medical Center National Hospital Organization Fukuoka Japan

Abstract

AbstractBackground and AimMany recent studies have shown a relationship between various systemic diseases and the gut microbiota (GM), with the gut–liver axis receiving particular attention. In contrast, no report has comprehensively shown the effects of GM on the pathophysiology of patients undergoing living donor liver transplantation (LDLT).MethodWe enrolled 16 recipients who underwent LDLT for liver cirrhosis, and 17 donors constituted the reference group. We examined the differences in GM between recipients and donors. We also examined the relationships between GM, short‐chain fatty acids, and portal vein pressure (PVP) in recipients.ResultsThere was no significant difference in alpha‐diversity between the recipients and donors, but there was variation in beta‐diversity among the recipients. The abundance of the phylum Bacteroidetes was significantly higher in recipients than in donors (P = 0.016), and it was positively correlated with PVP (r = 0.511, P = 0.043). Propionic acid, which is a component of short‐chain fatty acids, was positively correlated with PVP (r = 0.544, P = 0.0295), the phylum Bacteroidetes (r = 0.677, P = 0.004), and total bilirubin concentration (r = 0.501, P = 0.048). Propionic acid was negatively correlated with serum albumin concentration (r = −0.482, P = 0.043).ConclusionOur findings suggest relationships between fecal Bacteroidetes levels, propionic acid concentrations, and PVP in patients with liver cirrhosis undergoing LDLT.

Publisher

Wiley

Subject

Gastroenterology,Hepatology

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