200 PREDICTORS OF MORTALITY & SEVERITY SCORES IN PATIENTS OF ACUTE ON CHRONIC LIVER FAILURE (ACLF)

2008 ◽  
Vol 48 ◽  
pp. S84
Author(s):  
H.K. Garg ◽  
A. Kumar ◽  
B.C. Sharma ◽  
S.K. Sarin
2015 ◽  
Vol 127 (7-8) ◽  
pp. 283-289 ◽  
Author(s):  
Ivana Mikolasevic ◽  
Sandra Milic ◽  
Mladen Radic ◽  
Lidija Orlic ◽  
Zeljka Bagic ◽  
...  

Gut ◽  
2018 ◽  
Vol 68 (10) ◽  
pp. 1872-1883 ◽  
Author(s):  
Hannelie Korf ◽  
Johannie du Plessis ◽  
Jos van Pelt ◽  
Sofie De Groote ◽  
David Cassiman ◽  
...  

ObjectiveAcute-on-chronic liver failure (ACLF) is associated with dysfunctional circulating monocytes whereby patients become highly susceptible to bacterial infections. Here, we identify the pathways underlying monocyte dysfunction in ACLF and we investigate whether metabolic rewiring reinstates their phagocytic and inflammatory capacity.DesignFollowing phenotypic characterisation, we performed RNA sequencing on CD14+CD16− monocytes from patients with ACLF and decompensated alcoholic cirrhosis. Additionally, an in vitro model mimicking ACLF patient-derived features was implemented to investigate the efficacy of metabolic regulators on monocyte function.ResultsMonocytes from patients with ACLF featured elevated frequencies of interleukin (IL)-10-producing cells, reduced human leucocyte antigen DR isotype (HLA-DR) expression and impaired phagocytic and oxidative burst capacity. Transcriptional profiling of isolated CD14+CD16− monocytes in ACLF revealed upregulation of an array of immunosuppressive parameters and compromised antibacterial and antigen presentation machinery. In contrast, monocytes in decompensated cirrhosis showed intact capacity to respond to inflammatory triggers. Culturing healthy monocytes in ACLF plasma mimicked the immunosuppressive characteristics observed in patients, inducing a blunted phagocytic response and metabolic program associated with a tolerant state. Metabolic rewiring of the cells using a pharmacological inhibitor of glutamine synthetase, partially restored the phagocytic and inflammatory capacity of in vitro generated- as well as ACLF patient-derived monocytes. Highlighting its biological relevance, the glutamine synthetase/glutaminase ratio of ACLF patient-derived monocytes positively correlated with disease severity scores.ConclusionIn ACLF, monocytes feature a distinct transcriptional profile, polarised towards an immunotolerant state and altered metabolism. We demonstrated that metabolic rewiring of ACLF monocytes partially revives their function, opening up new options for therapeutic targeting in these patients.


2016 ◽  
Vol 31 (4) ◽  
pp. 856-864 ◽  
Author(s):  
Shalimar ◽  
Dharmendra Kumar ◽  
Padmaprakash Kadavoor Vadiraja ◽  
Baibaswata Nayak ◽  
Bhaskar Thakur ◽  
...  

2018 ◽  
Vol 8 (2) ◽  
pp. 144-155 ◽  
Author(s):  
Sujay Kulkarni ◽  
Mithun Sharma ◽  
Padaki N. Rao ◽  
Rajesh Gupta ◽  
Duvvuru N. Reddy

2014 ◽  
Vol 4 ◽  
pp. S4
Author(s):  
Vinit Shah ◽  
Praveen Sharma ◽  
Rinkesh Bansal ◽  
Pankaj Tyagi ◽  
Naresh Bansal ◽  
...  

2021 ◽  
Author(s):  
Anima Sharma ◽  
Akash Roy ◽  
Madhumita Premkumar ◽  
Ajay Duseja ◽  
Sunil Taneja ◽  
...  

Abstract Background: Severe alcoholic hepatitis (SAH) presenting as acute-on-chronic liver failure (ACLF) carries a high short-term mortality. Alteration of gut microbiota is a crucial component implicated in its pathogenesis, whose modulation has been suggested as a potential therapeutic tool. We evaluated the safety of fecal microbiota transplantation (FMT) and its efficacy in improving short-term survival and clinical severity scores in patients with SAH-ACLF.Methods: Thirty-three patients [13 in the FMT arm;20 in the standard of care arm (SOC] with SAH-ACLF were included in this open-label study. A single FMT session was administered as a freshly prepared stool suspension from pre-identified healthy family member stool donors through a nasojejunal tube. Patients were followed up on days seven, twenty-eight, and ninety. Results: Survival at twenty-eight and ninety days was significantly better in the FMT arm (100% versus 60%, P=0.01; 53.84% versus 25%, P=0.02). Hepatic encephalopathy resolved in 100% versus 57.14% (FMT versus SOC, P=0.11) patients, while ascites resolved in 100% versus 40% survivors (P=0.04). Major adverse event rates, including spontaneous bacterial peritonitis and gastrointestinal bleeding, were similar in both groups (P=0.77; P=0.70). Median IL1beta decreased by21.39% (IQR -73.67-7.63) in the FMT group, whereas it increased in the SOC by 27.44% (IQR -0.88-128.11) (P=0.01). Percentage changes in bilirubin and ALT between baseline and day seven emerged as predictors of ninety-day mortality.Conclusion: FMT is safe, improves short-term and medium-term survival, and leads to improvement in clinical severity scores in patients with SAH-ACLF.


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