Society: AGA

Background: Alcohol-associated hepatitis (AH) is the active inflammatory state of alcohol-associated liver disease (ALD). AH varies in severity from mild to severe with mortality rates reaching 30-50% in severe AH. Prednisolone, which is a glucocorticoid receptor agonist, is the standard treatment for severe AH. The duration of treatment is based on the clinical response to prednisolone that is calculated by Lille score, where a Lille Score <0.45 at day 7 indicates that a prednisolone “responder” (AH-R) should continue treatment for 28 days. A Lille Score >0.45 indicates that a patient is a “non-responder” (AH-NR) to prednisolone and treatment should be terminated at day 7. Utilizing a proteomic approach, the current study aimed to identify hepatic proteins/pathways associated with non-responsiveness to prednisolone treatment and to characterize proteomic changes that negatively impact mortality in AH-NR.
Methods: LC/MS proteomic analysis was performed on liver biopsy samples obtained from non-ALD controls (n=10) and AH patients (n=21). Six-month survival within the AH-R was 93% (n=13 out of 14 patients) and 43% (n= 3 out of 7 patients) within the AH-NR. Significant differences in hepatic protein expression between groups were identified by a one-way ANOVA.
Results: Analysis of the hepatic proteome identified 7,944 total proteins and revealed 222 proteins that were decreased and 294 that were increased in AH-NR vs AH-R. Notably, among the significantly increased proteins in AH-NR was DHI1, an enzyme involved in metabolism of both prednisolone and prednisone. Significantly downregulated proteins in AH-NR included members of the glucocorticoid signaling pathway, GCR and GMEB2. Further, when comparing to controls, AH-R and AH-NR shared multiple protein changes but there were various proteins and pathways explicitly changed in AH-R or AH-NR. For example, the proteotoxic stress response pathway including HSF1, PSD10, RAF1, and HPBP1 was uniquely downregulated in AH-NR but not in AH-R. Next, when comparing non-survivors vs survivors within the AH-NR 113 significant proteins (57 decreased and 56 increased) were identified. Proteins involved in blood coagulation, defense response, and response to stress were significantly reduced in AH-NR non-survivors. In addition, acute inflammatory response and the expression of several acute phase proteins were downregulated in AH-NR non-survivors. For example, A1AG2, a steroid transport protein, AACT, a protease inhibitor, and AMBP, a heme homeostasis protein, among others.
Conclusion: The current study identified the specific changes in the hepatic proteins associated with non-responsiveness to prednisolone treatment and mortality in AH patients. Further studies are needed to investigate the mechanisms as to how these changes may contribute to AH patient response to prednisolone therapy and mortality.

Background: Heavy alcohol consumption leads to an increased risk of alcohol-associated liver disease (ALD), a condition associated with significant morbidity and mortality, for which there are limited treatments. ALD pathogenesis is influenced by multiple factors including dietary fatty acids. Preclinical studies in mice show that n-3 PUFA supplementation or endogenous increase attenuate experimental ALD. The goal of the current study was to examine the effects of n-3 PUFA supplementation on liver injury, systemic inflammation, and intestinal permeability in a human population of heavy drinking individuals.
Methods: Heavy drinking individuals were admitted to an NIH inpatient treatment program for 21 days. At discharge, subjects were randomized to either 2 g/day of n-3 PUFAs (EPA+DHA, n=46) or placebo (n=48) for 12 weeks. Plasma markers of liver injury (ALT, AST, and GGT) were measured at randomization (baseline) and at the conclusion of the study (final). In a subset of patients, an additional marker of liver injury (K18), systemic inflammation (TNFα, IL-8, IL-6), and intestinal permeability (flagellin, CD14, and endotoxin) were evaluated. Significant differences were determined by paired Student’s t test (p<0.05).
Results: 12-week n-3 PUFA supplementation was associated with a substantial reduction in ALT (55.15±9.52 vs35.21±4.14 U/L, p<0.05), and GGT (55.03±10.58 vs 33.25±4.89 U/L, p<0.05) levels among heavy drinkers (baseline vs. final). ALT and GGT were unchanged among the placebo group. No significant changes in AST were observed for either group. The AST:ALT ratio was unchanged for the n-3 PUFA group, but was significantly increased among the placebo group (0.85±0.05 vs 1.10±0.05, p<0.05, baseline vs final. Compared to baseline, K18 levels (specifically M65, a marker of necrosis) had a non-significant downward trend in the n-3 PUFA group (-18.94±9.14%), whereas a slight upward trend was observed for the placebo group. As an indirect marker of intestinal permeability, endotoxin levels were unchanged in the n-3 PUFA supplemented group over the course of the study, but there was a significant increase in the placebo arm (0.79±0.10 vs 1.23±0.17 EU/mL, p<0.05). CD14 and flagellin were unchanged for both groups. Lastly, levels of inflammatory cytokines IL-6, TNFα, and IL-8 had a non-significant downward trend in n-3 PUFA supplemented individuals (-32.85±13.29%; -15.35±16.60%, -8.46±20.50%, respectively). However, there was a non-significant increase for these cytokines in the placebo group (9.21%±15.69, 9.12%±11.80, 46.00%±18.17, respectively).
Conclusion: Our data suggested that n-3 PUFA supplementation in heavy drinking individuals had beneficial effects on liver injury, endotoxemia, and systemic inflammation. Further investigations are needed on the mechanistic role of n3 PUFAs in the pathogenesis of ALD.

Joe Hibbeln

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