Mechanism of cell death in acute-on-chronic liver failure: a clinico-pathologic-biomarker study

• Published in: Liver international 2015-12, Vol.35 (12), p.2564-2574
• Main Authors: Adebayo, Danielle, Morabito, Vincenzo, Andreola, Fausto, Pieri, Giulia, Luong, Tu-Vin, Dhillon, Amar, Mookerjee, Rajeshwar, Jalan, Rajiv
• Format: Article
• Language: English
• Subjects: Acute-On-Chronic Liver Failure - metabolism; Acute-On-Chronic Liver Failure - pathology; Acute-On-Chronic Liver Failure - physiopathology; Adult; apoptosis; Apoptosis - physiology; Biomarkers - metabolism; Caspase 3 - metabolism; cell death; Cell Death - physiology; Female; Humans; Keratin-18 - blood; Liver - metabolism; Liver - pathology; liver failure; Male; Middle Aged; necrosis; Peptide Fragments - blood; Statistics as Topic
• ISSN: 1478-3223; 1478-3231
• DOI: 10.1111/liv.12850

Background & Aims Mortality of patients who develop acute‐on‐chronic liver failure (ACLF) is unacceptably high but the predominant mode of cell death is unknown. The aim of this study was to evaluate whether plasma levels of caspase‐cleaved cytokeratin M30 (marker of apoptosis) and uncleaved cytokeratin M65 (marker of total cell death) are altered in ACLF patients and relate this to liver histology. Methods Twenty‐seven patients with acute decompensation of liver disease were divided into two groups: no‐ACLF (n = 11) or ACLF (n−16). Healthy controls (n = 8) and acute liver failure (ALF) patients (n = 10) were also enrolled. Cell death was assessed in plasma using an ELISA kit (M30 and M65). Simultaneous biopsy samples were analysed for M30 and caspase‐3 staining. Results Plasma M30 value was significantly elevated in ACLF patients compared with healthy volunteers (P = 0.0001), it was also significantly higher in ACLF patients compared with no‐ACLF patients (P = 0.002). M65 levels were higher in ALF compared with ACLF patients (P = 0.002) but the apoptotic index defined by M30/M65 ratio was significantly higher in ACLF patients. Patients with extra‐hepatic failure had higher M30 levels compared with patients without organ failure (P = 0.03). M30 staining in liver was more marked in the patients with ACLF and was observed in all the patients that died. Conclusions The results of this study suggest that hepatocyte apoptosis is the predominant mode of cell death in ACLF, which can be identified in the peripheral blood. Further studies are required to validate our findings and to determine whether M30 can be used as a biomarker of apoptosis or as a target for therapy.