
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions β written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Alcoholic hepatitis pathophysiology
Introduction
Overview
Overview
The pathophysiology of Alcoholic Hepatitis is caused by interplay between alcohol metabolism, inflammation and innate immunity. Alcohol metabolism leads to depletion of NAD and subsequent lipogenesis. Additionally, increased endotoxemia causes translocation of lipopolysaccharide from intestine to hepatocytes. In hepatocytes, lipopolysaccharide activates kupffer cells. Therefore, activated cells release inflammatory markers which lead to Alcoholic hepatitis.
Pathophysiology
Pathophysiology
Pathogenesis
- The pathogenesis of Alcoholic Hepatitis is multifactorial.
- Alcoholic Hepatitis is caused by interplay between alcohol metabolism, inflammation and innate immunity. [1]
- Ethanol metabolism in the liver is carried out mainly by two enzymes:[2]
- Both of these enzymes use NAD+ as a cofactor. Alcohol is converted to acetaldehyde and acetaldehyde is then further oxidized to acetate. Acetaldehyde is the toxic metabolite in this process.
- The Alcohol metabolism leads to a reduced ratio of the nicotinamide adenine dinucleotide (NAD) to NADH. The NAD depletion inhibit fatty acid oxidation and causes fat accumulation in hepatocytes associated with lipogenesis. [1]
- Due to increased intestinal permeability in patients with Alcoholic Hepatitis, high levels of Endotoxemia is recognized.[1]
- Endotoxin binds to lipopolysaccharide and translocate from intestine to hepatocytes.[3]
- In hepatocytes, lipopolysaccharide bindes to CD14 molecule and toll-like receptor 4 on surface of Kupffer cells.[4]
- These bindings activate Kupffer cells to release reactive oxygen species.[3]
- This activation release tumor necrosis factor-alpha (TNF alpha), interleukin-8, monocyte chemotactic protein 1 (MCP-1), andplatelet-derived growth factor (PDGF) which are responsible for characterized symptoms including malaise, fever, and peripheral neutrophil leukocytosis. [5] [6]
Genetics
Genetics
- Genetic predisposition in alcoholism and developing alcohol -related liver injury:[7]
- There is a significant association between ADH2, ADH3, and ALDH2 alleles and the risk of alcoholism
- The ADH2 and ADH3 alleles are associated with alcoholism in East Asians population
- The ADH2 allele is associated with alcoholism in Caucasians
- The association between genetic predisposition and development of alcoholic liver injury is unknown
- There is a significant association between ADH2, ADH3, and ALDH2 alleles and the risk of alcoholism
Associated Conditions
Associated Conditions
Conditions associated with alcoholic liver disease include:[2][8]
- Obesity
- Chronic viral hepatitis
- Iron overload
- Cirrhosis
- Hepatocellular carcinoma
Microscopic Pathology
Microscopic Pathology
On microscopic histopathological analysis characteristic findings of Alcoholic Hepatitis include:
- Steatosis
- Macrovesicular steatosis – the cytoplasm of hepatocytes is occupied by large lipid droplets that end up displacing the nucleus and other organelles peripherally
- Mallory body
- A condition where pre-keratin filaments accumulate in hepatocytes. This sign is not limited to alcoholic liver disease.[9]
- Ballooning degeneration
- Hepatocytes in the setting of alcoholic change often swell up with excess fat, water and protein. Accompanied with ballooning, there is necrotic damage. The swelling blocks biliary ducts, leading to diffuse cholestasis.[9]
- Inflammation
- If chronic liver disease is also present:
References
References
- β 1.0 1.1 1.2 Gao, Bin; Bataller, Ramon (2011). “Alcoholic Liver Disease: Pathogenesis and New Therapeutic Targets”. Gastroenterology. 141 (5): 1572β1585. doi:10.1053/j.gastro.2011.09.002. ISSNΒ 0016-5085.
- β 2.0 2.1 Ceni E, Mello T, Galli A (2014). “Pathogenesis of alcoholic liver disease: role of oxidative metabolism”. World J. Gastroenterol. 20 (47): 17756β72. doi:10.3748/wjg.v20.i47.17756. PMCΒ 4273126. PMIDΒ 25548474.
- β 3.0 3.1 Bautista, Abraham P (2001). “Impact of alcohol on the ability of Kupffer cells to produce chemokines and its role in alcoholic liver disease“. Journal of Gastroenterology and Hepatology. 15 (4): 349β356. doi:10.1046/j.1440-1746.2000.02174.x. ISSNΒ 0815-9319.
- β Suraweera DB, Weeratunga AN, Hu RW, Pandol SJ, Hu R (2015). “Alcoholic hepatitis: The pivotal role of Kupffer cells”. World J Gastrointest Pathophysiol. 6 (4): 90β8. doi:10.4291/wjgp.v6.i4.90. PMCΒ 4644891. PMIDΒ 26600966.
- β Bird G (1994). “Interleukin-8 in alcoholic liver disease”. Acta Gastroenterol Belg. 57 (3β4): 255β9. PMIDΒ 7810274.
- β Laso FJ, LapeΓ±a P, Madruga JI, San Miguel JF, Orfao A, Iglesias MC; et al. (1997). “Alterations in tumor necrosis factor-alpha, interferon-gamma, and interleukin-6 production by natural killer cell-enriched peripheral blood mononuclear cells in chronic alcoholism: relationship with liver disease and ethanol intake”. Alcohol Clin Exp Res. 21 (7): 1226β31. PMIDΒ 9347083.
- β Zintzaras E, Stefanidis I, Santos M, Vidal F (2006). “Do alcohol-metabolizing enzyme gene polymorphisms increase the risk of alcoholism and alcoholic liver disease?”. Hepatology. 43 (2): 352β61. doi:10.1002/hep.21023. PMIDΒ 16440362.
- β Lucey, Michael R.; Mathurin, Philippe; Morgan, Timothy R. (2009). “Alcoholic Hepatitis”. New England Journal of Medicine. 360 (26): 2758β2769. doi:10.1056/NEJMra0805786. ISSNΒ 0028-4793.
- β 9.0 9.1 9.2 Cotran. Robbins Pathologic Basis of Disease. Philadelphia: W.B Saunders Company. 0-7216-7335-X. Unknown parameter
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shadan Mehraban, M.D.[2]Prashanth Saddala M.B.B.S
