Biomarkers of Frailty in Patients with Advanced Chronic Liver Disease Undergoing a Multifactorial Intervention Consisting of Home Exercise, Branched-Chain Amino Acids, and Probiotics
Luca Laghi,
Maria Àngels Ortiz,
Giacomo Rossi,
Eva Román,
Carlo Mengucci,
Elisabet Cantó,
Lucia Biagini,
Elisabet Sánchez,
Maria Mulet,
Álvaro García-Osuna,
Eulàlia Urgell,
Naujot Kaur,
Maria Poca,
Josep Padrós,
Maria Josep Nadal,
Berta Cuyàs,
Edilmar Alvarado,
Silvia Vidal,
Elena Juanes,
Andreu Ferrero-Gregori,
Àngels Escorsell,
German Soriano
Affiliations
Luca Laghi
Department of Agricultural and Food Sciences, University of Bologna, 47521 Cesena, Italy
Maria Àngels Ortiz
Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain
Giacomo Rossi
School of Veterinary Medical Sciences, University of Camerino, 62032 Camerino, Italy
Eva Román
CIBERehd (Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Instituto de Salud Carlos III, 28029 Madrid, Spain
Carlo Mengucci
Department of Agricultural and Food Sciences, University of Bologna, 47521 Cesena, Italy
Elisabet Cantó
Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain
Lucia Biagini
School of Veterinary Medical Sciences, University of Camerino, 62032 Camerino, Italy
Elisabet Sánchez
Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain
Maria Mulet
Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain
Álvaro García-Osuna
Department of Biochemistry, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
Eulàlia Urgell
Department of Biochemistry, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
Naujot Kaur
Department of Gastroenterology, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
Maria Poca
CIBERehd (Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Instituto de Salud Carlos III, 28029 Madrid, Spain
Josep Padrós
Department of Physical Medicine and Rehabilitation, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
Maria Josep Nadal
Department of Physical Medicine and Rehabilitation, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
Berta Cuyàs
CIBERehd (Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Instituto de Salud Carlos III, 28029 Madrid, Spain
Edilmar Alvarado
CIBERehd (Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Instituto de Salud Carlos III, 28029 Madrid, Spain
Silvia Vidal
Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain
Elena Juanes
Department of Pharmacy, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
Andreu Ferrero-Gregori
Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain
Àngels Escorsell
Department of Gastroenterology, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
German Soriano
CIBERehd (Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Instituto de Salud Carlos III, 28029 Madrid, Spain
Frailty in cirrhosis or advanced chronic liver disease (ACLD) is a relevant prognostic factor. In the present study, we aimed to analyze potential biomarkers associated with frailty and its improvement in patients with ACLD. We analyzed the serum of outpatients with ACLD who participated in a previous study (Román, Hepatol Commun 2024) in which frailty was assessed using the liver frailty index (LFI), and patients who were frail or prefrail were randomized to a multifactorial intervention (home exercise, branched-chain amino acids, and probiotics) or control for 12 months. We determined a biomarker battery of inflammation, bacterial translocation, and liver damage in blood and urine and blood metabolomics by 1H-NMR. Thirty-seven patients were included. According to the LFI, 32 patients were frail or prefrail, and 5 were robust. At baseline, LFI correlated with LBP, sCD163, mtDNA, FGF-21, urinary NGAL, urinary claudin-3, and the metabolites mannose, ethanol, and isoleucine. During the study, patients in the intervention group showed an improvement in LFI and a decrease in CRP, LBP, sCD163, and ccK18 compared to the control group. Metabolomics showed a decrease in dimethyl sulfone and creatinine and an increase in malonate, ornithine, isoleucine, and valine in the intervention group. We conclude that frailty in patients with ACLD is associated with biomarkers of systemic inflammation, bacterial translocation, and liver damage, and alterations of amino acid and short-chain fatty acid metabolism.