Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Jul 1;54(4):408-416.
doi: 10.1093/alcalc/agz036.

Alcoholic Hepatitis: A Review

Affiliations
Review

Alcoholic Hepatitis: A Review

Nooshin Hosseini et al. Alcohol Alcohol. .

Abstract

Alcoholic liver disease (ALD) represents a spectrum of injury, ranging from simple steatosis to alcoholic hepatitis to cirrhosis. Regular alcohol use results in fatty changes in the liver which can develop into inflammation, fibrosis and ultimately cirrhosis with continued, excessive drinking. Alcoholic hepatitis (AH) is an acute hepatic inflammation associated with significant morbidity and mortality that can occur in patients with steatosis or underlying cirrhosis. The pathogenesis of ALD is multifactorial and in addition to genetic factors, alcohol-induced hepatocyte damage, reactive oxygen species, gut-derived microbial components result in steatosis and inflammatory cell (macrophage and neutrophil leukocyte) recruitment and activation in the liver. Continued alcohol and pro-inflammatory cytokines induce stellate cell activation and result in progressive fibrosis. Other than cessation of alcohol use, medical therapy of AH is limited to prednisolone in a subset of patients. Given the high mortality of AH and the progressive nature of ALD, there is a major need for new therapeutic intervention for this underserved patient population.

Keywords: ABIC score; MELD score; alcoholic hepatitis; alcoholic liver disease; alcoholic steatohepatitis; glascow alcoholic hepatitis score; lille score; maddrey score; pro-inflammatory cytokines; stellate cell activation.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Pathomechanisms of alcohol-induced liver injury involving the gut-liver access.
Fig. 2.
Fig. 2.
Treatment algorithm for corticosteroids in alcoholic hepatitis using Maddrey, GAH, and Lille scores.
Fig. 3.
Fig. 3.
Maddrey Discriminant Function (MDF). Scores are used to predict mortality and for guiding treatment with coritcosteroids.
Fig. 4.
Fig. 4.
Model for End-stage liver disease (MELD) scoring system.

References

    1. (NIAAA) NIoAAaA (2014) NIAAA Council Approves Definition of Binge Drinking. NIAAA Newsletter, No. 3, Winter 2004.
    1. (SAMHSA) SAaMHSA (2014) National Survey on Drug Use and Health (NSDUH). Table 2.41B—Alcohol use in lifetime, past year, and past month among persons aged 18 or older, by demographic characteristics: Percentages, 2013 and 2014.
    1. Addolorato G, Leggio L, Ferrulli A, et al. (2007) Effectiveness and safety of baclofen for maintenance of alcohol abstinence in alcohol-dependent patients with liver cirrhosis: randomised, double-blind controlled study. Lancet 370:1915–22. - PubMed
    1. Agriculture USDoHaHSaUSDo (2015) Dietary Guidelines for Americans 2015-2020.
    1. Alcohol Alert Brief Interventions. National Institute of Health. National Institute on Alcohol Abuse and Alcoholism. 2005. (66). https://pubs.niaaa.nih.gov/publications/aa66/aa66.htm

MeSH terms

Substances