Elevated systemic total bile acids escalate susceptibility to alcohol-associated liver disease

Excessive alcohol consumption is a major global health problem. Individuals with alcoholic liver disease often exhibit elevated serum total bile acids (TBAs). Nevertheless, the extent to which high TBA contributes to alcohol-associated liver disease (AALD) remains elusive. To investigate this, wild-type mice were categorized into normal (nTBA) and high (hTBA) TBA groups. Both groups underwent chronic-binge ethanol feeding for 4 weeks, followed by additional weekly ethanol doses. Ethanol feeding worsened AALD in both male and female mice with elevated serum TBA, characterized by liver dysfunction and steatosis. Decreased hepatic expression of genes involved in mitochondrial β-oxidation and lipid transport in ethanol-fed hTBA mice suggests that altered fatty acid metabolism contributed to AALD. Our findings, which represent the first to link high serum TBA to increased AALD susceptibility, underscore the importance of proactive serum TBA screening as a valuable tool for identifying individuals at high risk of developing AALD.

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Publication Details

Journal
iScience
Published
2024-09-13
DOI
https://doi.org/10.1016/j.isci.2024.110940
Citations
6
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
2.32

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article

Elevated systemic total bile acids escalate susceptibility to alcohol-associated liver disease

Fuhua Hao, Devendra Paudel, Umesh K. Goand, Yuan Tian et al.
6 citations
iScience
Liver Disease Diagnosis and Treatment
2.32
article

Elevated systemic total bile acids escalate susceptibility to alcohol-associated liver disease

Fuhua Hao, Devendra Paudel, Umesh K. Goand, Yuan Tian, Sangshan Tian, Andrew D. Patterson, Anthony Koehle, Vishal Singh, Loi V Nguyen
article en
6 citations

Abstract

Excessive alcohol consumption is a major global health problem. Individuals with alcoholic liver disease often exhibit elevated serum total bile acids (TBAs). Nevertheless, the extent to which high TBA contributes to alcohol-associated liver disease (AALD) remains elusive. To investigate this, wild-type mice were categorized into normal (nTBA) and high (hTBA) TBA groups. Both groups underwent chronic-binge ethanol feeding for 4 weeks, followed by additional weekly ethanol doses. Ethanol feeding worsened AALD in both male and female mice with elevated serum TBA, characterized by liver dysfunction and steatosis. Decreased hepatic expression of genes involved in mitochondrial β-oxidation and lipid transport in ethanol-fed hTBA mice suggests that altered fatty acid metabolism contributed to AALD. Our findings, which represent the first to link high serum TBA to increased AALD susceptibility, underscore the importance of proactive serum TBA screening as a valuable tool for identifying individuals at high risk of developing AALD.

iScienceVol. 27(10)
Pennsylvania State University (US)
National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 11%
Liver Disease Diagnosis and Treatment
2.32
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Elevated systemic total bile acids escalate susceptibility to alcohol-associated liver disease — Fuhua Hao, Devendra Paudel, et al. · iScience (2024) | TGRS Research Map | TGRS