Journal
JOURNAL OF HEPATOLOGY
Volume 74, Issue 5, Pages 1117-1131Publisher
ELSEVIER
DOI: 10.1016/j.jhep.2020.11.035
Keywords
Multiorgan failure; Small-molecules; Biomass; Immunity; Anabolic metabolism; Dormancy
Categories
Funding
- European Foundation for the Study of Chronic Liver Failure (EF-Clif)
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In patients with ACLF, metabolite modules increased along with markers of systemic inflammation and oxidative stress. Most proteinogenic amino acids were present and increased. A metabolic network involving amino acids was activated, suggesting increased nucleotide synthesis. Certain compounds involved in antioxidant synthesis were increased. Intermediates of ketogenic amino acids catabolism were increased. Levels of spermidine, an autophagy inducer, were decreased.
Background & Aims: Systemic inflammation and organ failure(s) are the hallmarks of acute-on-chronic liver failure (ACLF), yet their pathogenesis remains uncertain. Herein, we aimed to assess the role of amino acids in these processes in patients with ACLF. Methods: The blood metabolomic database of the CANONIC study (comprising 137 metabolites, with 43% related to amino acids) - obtained in 181 patients with ACLF and 650 with acute decompensation without ACLF (AD) - was reanalyzed with a focus on amino acids, in particular 9 modules of co-regulated metabolites. We also compared blood metabolite levels between ACLF and AD. Results: The main findings in ACLF were: i) Metabolite modules were increased in parallel with increased levels of markers of systemic inflammation and oxidative stress. ii) Seventy percent of proteinogenic amino acids were present and most were increased. iii) A metabolic network, comprising the amino acids aspartate, glutamate, the serine-glycine one-carbon metabolism (folate cycle), and methionine cycle, was activated, suggesting increased purine and pyrimidine nucleotide synthesis. iv) Cystathionine, L-cystine, glutamate and pyroglutamate, which are involved in the transsulfuration pathway (a methionine cycle branch) were increased, consistent with increased synthesis of the antioxidant glutathione. v) Intermediates of the catabolism of 5 out of the 6 ketogenic amino acids were increased. vi) The levels of spermidine (a polyamine inducer of autophagy with anti-inflammatory effects) were decreased. Conclusions: In ACLF, blood amino acids fueled protein and nucleotide synthesis required for the intense systemic inflammatory response. Ketogenic amino acids were extensively catabolized to produce energy substrates in peripheral organs, an effect that was insufficient because organs failed. Finally, the decrease in spermidine levels may cause a defect in autophagy contributing to the proinflammatory phenotype in ACLF. Lay summary: Systemic inflammation and organ failures are hallmarks of acute-on-chronic liver failure (ACLF). Herein, we aimed to characterize the role of amino acids in these processes. The blood metabolome of patients with acutely decompensated cirrhosis, and particularly those with ACLF, reveals evidence of intense skeletal muscle catabolism. Importantly, amino acids (along with glucose), are used for intense anabolic, energyconsuming metabolism in patients with ACLF, presumably to support de novo nucleotide and protein synthesis in the activated innate immune system. (c) 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
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