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Gut microbiome and metabolome signatures in liver cirrhosis-related complications.
Sharma, Satya Priya; Gupta, Haripriya; Kwon, Goo-Hyun; Lee, Sang Yoon; Song, Seol Hee; Kim, Jeoung Su; Park, Jeong Ha; Kim, Min Ju; Yang, Dong-Hoon; Park, Hyunjoon; Won, Sung-Min; Jeong, Jin-Ju; Oh, Ki-Kwang; Eom, Jung A; Lee, Kyeong Jin; Yoon, Sang Jun; Ham, Young Lim; Baik, Gwang Ho; Kim, Dong Joon; Suk, Ki Tae.
Afiliación
  • Sharma SP; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Gupta H; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Kwon GH; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Lee SY; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Song SH; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Kim JS; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Park JH; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Kim MJ; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Yang DH; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Park H; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Won SM; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Jeong JJ; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Oh KK; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Eom JA; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Lee KJ; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Yoon SJ; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Ham YL; Department of Nursing Daewon University College Jecheon, Republic of Korea 27135.
  • Baik GH; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
  • Kim DJ; Department of Internal Medicine, Hallym University College of Medicine, Chuncheon, Republic of Korea 24253.
  • Suk KT; Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea 24253.
Clin Mol Hepatol ; 2024 Jul 25.
Article en En | MEDLINE | ID: mdl-39048520
ABSTRACT
Background/

Aims:

Shifts in the gut microbiota and metabolites are interrelated with liver cirrhosis progression and complications. However, causal relationships have not been evaluated comprehensively. Here, we identified complication-dependent gut microbiota and metabolic signatures in patients with liver cirrhosis.

Methods:

Microbiome taxonomic profiling was performed on 194 stool samples (52 controls and 142 cirrhosis patients) via V3-V4 16S rRNA sequencing. Next, 51 samples (17 controls and 34 cirrhosis patients) were selected for fecal metabolite profiling via gas chromatography mass spectrometry and liquid chromatography coupled to time-of-flight-mass spectrometry. Correlation analyses were performed targeting the gut- microbiota, metabolites, clinical parameters, and presence of complications (varices, ascites, peritonitis, encephalopathy, hepatorenal syndrome, hepatocellular carcinoma, and deceased).

Results:

Veillonella bacteria, Ruminococcus gnavus, and Streptococcus pneumoniae are cirrhosis-related microbiotas compared with control group. Bacteroides ovatus, Clostridium symbiosum, Emergencia timonensis, Fusobacterium varium, and Hungatella_uc were associated with complications in the cirrhosis group. The areas under the receiver operating characteristic curve (AUROCs) for the diagnosis of cirrhosis, encephalopathy, hepatorenal syndrome, and deceased were 0.863, 0.733, 0.71, and 0.69, respectively. The AUROCs of mixed microbial species for the diagnosis of cirrhosis and complication were 0.808 and 0.847, respectively. According to the metabolic profile, 5 increased fecal metabolites in patients with cirrhosis were biomarkers (AUROC > 0.880) for the diagnosis of cirrhosis and complications. Clinical markers were significantly correlated with the gut microbiota and metabolites.

Conclusion:

Cirrhosis-dependent gut microbiota and metabolites present unique signatures that can be used as noninvasive biomarkers for the diagnosis of cirrhosis and its complications.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Mol Hepatol Año: 2024 Tipo del documento: Article Pais de publicación: Corea del Sur

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Mol Hepatol Año: 2024 Tipo del documento: Article Pais de publicación: Corea del Sur