Evidence map›Paper›PMID 35456053›Full record

ReviewCells2022

Key Signaling in Alcohol-Associated Liver Disease: The Role of Bile Acids.

Grayson W Way, Kaitlyn G Jackson, Shreya R Muscu, Huiping Zhou

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  11. HostFrontiers in microbiology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Grayson W WayCenter for Clinical and Translational Research, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID 0000-0002-5765-2064
Kaitlyn G JacksonDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID 0000-0003-2663-9593
Shreya R MuscuDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Huiping ZhouDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID 0000-0002-0050-372X
Virginia Commonwealth University · US

Funding

Regulation of Hepatic SphK2 by Bile Acids: Effects on Lipid MetabolismR01DK057543 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI HYLEMON, PHILLIP B, ZHOU, HUIPING ROSE · 2001 to 2015
$4.4M
LncRNA H19 in Cholestatic Liver DiseasesR01DK115377 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI HYLEMON, PHILLIP B, ZHOU, HUIPING ROSE · 2018 to 2021
$2.1M
Bile Acid and Sphingosine-1-phosphate Receptor-mediated Signaling in CholestasisR01DK104893 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI HYLEMON, PHILLIP B, ZHOU, HUIPING ROSE · 2016 to 2020
$2.0M
Sphingosine-1 phosphate signaling in alcoholic liver diseaseR21AA026629 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI ZHOU, HUIPING ROSE · 2019 to 2020
$407k
BLR&D Research Career Scientist Award ApplicationIK6BX004477 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI HUIPING ZHOU · 2019 to 2026
–
The ShEEP request for Waters Xevo TQ-XS Liquid Chromatography Mass Spectrometer SystemIS1BX004777 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI ZHOU, HUIPING ROSE · 2019 to 2019
–
Mechanisms of Berberine for the Treatment of Non-Alcoholic Fatty Liver DiseaseI01BX004033 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI ZHOU, HUIPING ROSE · 2018 to 2021
–
BLRD VA I01 BX004033BLRD VA I01 BX005730BLRD VA IK6 BX004477BLRD VA IS1 BX004777NIAAA NIH HHS R21 AA026629NIDDK NIH HHS R01 DK057543NIDDK NIH HHS R01 DK104893NIDDK NIH HHS R01 DK115377
6 · The paper itself

Abstract

Alcohol-associated liver disease (ALD) is a spectrum of diseases, the onset and progression of which are due to chronic alcohol use. ALD ranges, by increasing severity, from hepatic steatosis to alcoholic hepatitis (AH) and alcohol-associated cirrhosis (AC), and in some cases, can lead to the development of hepatocellular carcinoma (HCC). ALD continues to be a significant health burden and is now the main cause of liver transplantations in the United States. ALD leads to biological, microbial, physical, metabolic, and inflammatory changes in patients that vary depending on disease severity. ALD deaths have been increasing in recent years and are projected to continue to increase. Current treatment centers focus on abstinence and symptom management, with little in the way of resolving disease progression. Due to the metabolic disruption and gut dysbiosis in ALD, bile acid (BA) signaling and metabolism are also notably affected and play a prominent role in disease progression in ALD, as well as other liver disease states, such as non-alcoholic fatty liver disease (NAFLD). In this review, we summarize the recent advances in the understanding of the mechanisms by which alcohol consumption induces hepatic injury and the role of BA-mediated signaling in the pathogenesis of ALD.

Indexed as

Carcinoma, HepatocellularLiver Diseases, AlcoholicLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseBile Acids and SaltsDisease ProgressionHumansBile Acids and Saltsalcohol-associated liver diseasebile acidscirrhosisethanolsteatohepatitissteatosis

Identifiers

PMID35456053
PMCPMC9031669
OpenAlexW4224262013

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.