TY - JOUR
T1 - Characterization of the gut-liver-muscle axis in cirrhotic patients with sarcopenia
AU - Ponziani, Francesca Romana
AU - Picca, Anna
AU - Marzetti, Emanuele
AU - Calvani, Riccardo
AU - Conta, Giorgia
AU - Del Chierico, Federica
AU - Capuani, Giorgio
AU - Faccia, Mariella
AU - Fianchi, Francesca
AU - Funaro, Barbara
AU - Josè Coelho-Junior, Helio
AU - Petito, Valentina
AU - Rinninella, Emanuele
AU - Paroni Sterbini, Francesco
AU - Reddel, Sofia
AU - Vernocchi, Pamela
AU - Cristina Mele, Maria
AU - Miccheli, Alfredo
AU - Putignani, Lorenza
AU - Sanguinetti, Maurizio
AU - Pompili, Maurizio
AU - Gasbarrini, Antonio
PY - 2021
Y1 - 2021
N2 - Background & Aim: Sarcopenia is frequent in cirrhosis and is associated with unfavourable outcomes. The role of the gut-liver-muscle axis in this setting has been poorly investigated. The aim of this study was to identify gut microbiota, metabolic and inflammatory signatures associated with sarcopenia in cirrhotic patients. Methods: Fifty cirrhotic patients assessed for the presence of sarcopenia by the quantification of muscle mass and strength were compared with age- and sex-matched controls. A multiomic analysis, including gut microbiota composition and metabolomics, serum myokines and systemic and intestinal inflammatory mediators, was performed. Results: The gut microbiota of sarcopenic cirrhotic patients was poor in bacteria associated with physical function (Methanobrevibacter, Prevotella and Akkermansia), and was enriched in Eggerthella, a gut microbial marker of frailty. The abundance of potentially pathogenic bacteria, such as Klebsiella, was also increased, to the detriment of autochthonous ones. Sarcopenia was associated with elevated serum levels of pro-inflammatory mediators and of fibroblast growth factor 21 (FGF21) in cirrhotic patients. Gut microbiota metabolic pathways involved in amino acid, protein and branched-chain amino acid metabolism were up-regulated, in addition to ethanol, trimethylamine and dimethylamine production. Correlation networks and clusters of variables associated with sarcopenia were identified, including one centred on Klebsiella/ethanol/FGF21/Eggerthella/Prevotella. Conclusions: Alterations in the gut-liver-muscle axis are associated with sarcopenia in patients with cirrhosis. Detrimental but also compensatory functions are involved in this complex network.
AB - Background & Aim: Sarcopenia is frequent in cirrhosis and is associated with unfavourable outcomes. The role of the gut-liver-muscle axis in this setting has been poorly investigated. The aim of this study was to identify gut microbiota, metabolic and inflammatory signatures associated with sarcopenia in cirrhotic patients. Methods: Fifty cirrhotic patients assessed for the presence of sarcopenia by the quantification of muscle mass and strength were compared with age- and sex-matched controls. A multiomic analysis, including gut microbiota composition and metabolomics, serum myokines and systemic and intestinal inflammatory mediators, was performed. Results: The gut microbiota of sarcopenic cirrhotic patients was poor in bacteria associated with physical function (Methanobrevibacter, Prevotella and Akkermansia), and was enriched in Eggerthella, a gut microbial marker of frailty. The abundance of potentially pathogenic bacteria, such as Klebsiella, was also increased, to the detriment of autochthonous ones. Sarcopenia was associated with elevated serum levels of pro-inflammatory mediators and of fibroblast growth factor 21 (FGF21) in cirrhotic patients. Gut microbiota metabolic pathways involved in amino acid, protein and branched-chain amino acid metabolism were up-regulated, in addition to ethanol, trimethylamine and dimethylamine production. Correlation networks and clusters of variables associated with sarcopenia were identified, including one centred on Klebsiella/ethanol/FGF21/Eggerthella/Prevotella. Conclusions: Alterations in the gut-liver-muscle axis are associated with sarcopenia in patients with cirrhosis. Detrimental but also compensatory functions are involved in this complex network.
KW - cirrhosis
KW - ethanol
KW - gut microbiota
KW - metabolomics
KW - sarcopenia
KW - cirrhosis
KW - ethanol
KW - gut microbiota
KW - metabolomics
KW - sarcopenia
UR - http://hdl.handle.net/10807/179381
U2 - 10.1111/liv.14876
DO - 10.1111/liv.14876
M3 - Article
SN - 1478-3223
SP - N/A-N/A
JO - Liver International
JF - Liver International
ER -