Evidence map›Paper›PMID 36270295›Full record

ReviewAnnual review of pathology2023

Recent Advances in Understanding of Pathogenesis of Alcohol-Associated Liver Disease.

Xiaoqin Wu, Xiude Fan, Tatsunori Miyata, Adam Kim, Christina K Cajigas-Du Ross, Semanti Ray, Emily Huang, Moyinoluwa Taiwo, Rakesh Arya, Jianguo Wu and 1 more

Abstract readReview
In one paragraph

Review in Annual review of pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

140 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  12. Therapeutics for Alcohol-Associated Liver Disease.Annual review of pharmacology and toxicology · 2026
    Review
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80 more citing papers are in PubMed but not listed here.

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

11 authors.

Xiaoqin WuNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Xiude FanNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Tatsunori MiyataNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Adam KimNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Christina K Cajigas-Du RossNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Semanti RayNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Emily HuangNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Moyinoluwa TaiwoNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Rakesh AryaNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Jianguo WuNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.
Laura E NagyNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, Ohio, USA; email: nagyL3@ccf.org.

Funding

Project Two - Exercise Training Decreases Alcohol Drinking by an FGF21-Dependent MechanismP50AA024333 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI Thomas M McIntyre · 2016 to 2026
$19.6M
The Cleveland Digestive Diseases Research Core Center (DDRCC)P30DK097948 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI Fabio Cominelli · 2015 to 2026
$15.6M
Transcriptional and non-transcriptional functions of IRF3 in ALDR01AA027456 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI LAURA E. NAGY · 2019 to 2026
$3.5M
IRAKM and Mincle in ALDR01AA023722 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI LI, XIAOXIA, NAGY, LAURA E. · 2015 to 2019
$2.2M
Microbial metabolites and Innate Immunity in AH: Biomarkers of injury and repairU01AA026938 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2018 to 2023
$1.4M
The role of PDK4 in alcohol-associated liver diseaseK01AA029474 · NIAAA · NORTHEAST OHIO MEDICAL UNIVERSITY · PI WU, JIANGUO · 2021 to 2025
$932k
C-Type Lectins and Immune Surveillance in ALDR00AA028048 · NIAAA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KIM, ADAM · 2022 to 2024
$892k
Role of MLKL in Alcohol-associated Liver DiseaseR00AA029146 · NIAAA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, XIAOQIN · 2023 to 2025
$747k
Role of MLKL in Alcohol-associated Liver DiseaseK99AA029146 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI WU, XIAOQIN · 2021 to 2022
$341k
C-Type Lectins and Immune Surveillance in ALDK99AA028048 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI KIM, ADAM · 2019 to 2021
$308k
IRF3 activation promotes fibrotic liver injury in alcohol-associated-liver diseaseF32AA029290 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI DU ROSS, CHRISTINA KATHERINE · 2021 to 2023
$192k
NIAAA NIH HHS F32 AA029290NIAAA NIH HHS K01 AA029474NIAAA NIH HHS K99 AA028048NIAAA NIH HHS K99 AA029146NIAAA NIH HHS P50 AA024333NIAAA NIH HHS R00 AA028048NIAAA NIH HHS R00 AA029146NIAAA NIH HHS R01 AA023722NIAAA NIH HHS R01 AA027456NIAAA NIH HHS U01 AA026938NIDDK NIH HHS P30 DK097948
6 · The paper itself

Abstract

Alcohol-associated liver disease (ALD) is one of the major diseases arising from chronic alcohol consumption and is one of the most common causes of liver-related morbidity and mortality. ALD includes asymptomatic liver steatosis, fibrosis, cirrhosis, and alcohol-associated hepatitis and its complications. The progression of ALD involves complex cell-cell and organ-organ interactions. We focus on the impact of alcohol on dysregulation of homeostatic mechanisms and regulation of injury and repair in the liver. In particular, we discuss recent advances in understanding the disruption of balance between programmed cell death and prosurvival pathways, such as autophagy and membrane trafficking, in the pathogenesis of ALD. We also summarize current understanding of innate immune responses, liver sinusoidal endothelial cell dysfunction and hepatic stellate cell activation, and gut-liver and adipose-liver cross talk in response to ethanol. In addition,we describe the current potential therapeutic targets and clinical trials aimed at alleviating hepatocyte injury, reducing inflammatory responses, and targeting gut microbiota, for the treatment of ALD.

Indexed as

Liver Diseases, AlcoholicEthanolFibrosisHepatocytesHumansLiverEthanolalcohol-associated liver diseaseALDcomplementgut-liver axispattern recognition receptorsPCDprogrammed cell deathPRR

Identifiers

PMID36270295
PMCPMC10060166

What OpenQuestion holds

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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.