Evidence map›Paper›PMID 30234998›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2019

Urinary acrolein metabolite levels in severe acute alcoholic hepatitis patients.

Vatsalya Vatsalya, Maiying Kong, Leila Gobejishvili, Wei-Yang Chen, Sanjay Srivastava, Shirish Barve, Craig McClain, Swati Joshi-Barve

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  13. Pathogenesis of Alcohol-Associated Liver Disease.Journal of clinical and experimental hepatology
    Review
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

8 authors at 2 institutions in 1 country.

Vatsalya VatsalyaDepartment of Medicine, University of Louisville , Louisville, Kentucky.
Maiying KongDepartment of Bioinformatics and Biostatistics, University of Louisville , Louisville, Kentucky.
Leila GobejishviliDepartment of Medicine, University of Louisville , Louisville, Kentucky.
Wei-Yang ChenDepartment of Pharmacology and Toxicology, University of Louisville , Louisville, Kentucky.
Sanjay SrivastavaDepartment of Medicine, University of Louisville , Louisville, Kentucky.
Shirish BarveDepartment of Medicine, University of Louisville , Louisville, Kentucky.
Craig McClainDepartment of Medicine, University of Louisville , Louisville, Kentucky.
Swati Joshi-BarveDepartment of Medicine, University of Louisville , Louisville, Kentucky.
University of Louisville · USLouisville VA Medical Center · US

Funding

Role of oxidized linoleic acid metabolites in the pathogenesis of alcoholic liver diseaseP20GM113226 · NIGMS · UNIVERSITY OF LOUISVILLE · PI BARVE, SHIRISH S · 2016 to 2025
$24.1M
Research Training and Education Core (Core D) P50HL120163 · NHLBI · AMERICAN HEART ASSOCIATION · PI BHATNAGAR, ARUNI, ROBERTSON, ROSE MARIE · 2013 to 2017
$20.1M
Superfund Training CoreP42ES023716 · NIEHS · UNIVERSITY OF LOUISVILLE · PI FORTNER, JOHN · 2017 to 2025
$18.1M
The Role of Nutrition in the Development/Progression of Alcohol-Induced Organ InjuryP50AA024337 · NIAAA · UNIVERSITY OF LOUISVILLE · PI SHIRISH S BARVE · 2016 to 2026
$17.9M
TBDP30GM127607 · NIGMS · UNIVERSITY OF LOUISVILLE · PI HILL, BRADFORD GUY · 2018 to 2022
$6.3M
Administrative Supplement Role of Gut Microbial Dysbiosis in Aging on HIV-associated in the Development of Alzheimer's DiseaseAssociated Dementia (ADRD).U01AA026225 · NIAAA · UNIVERSITY OF LOUISVILLE · PI BARVE, SHIRISH S, COOK, ROBERT L · 2017 to 2021
$3.4M
SAM Deficiency Mediated Epigenetic Mechanisms in Alcohol induced ImmunosuppressionR01AA024405 · NIAAA · UNIVERSITY OF LOUISVILLE · PI BARVE, SHIRISH S · 2015 to 2019
$1.6M
Lipid metabolites can both potentiate and treat alcoholic hepatitisU01AA026936 · NIAAA · UNIVERSITY OF LOUISVILLE · PI JOSHI-BARVE, SWATI, MCCLAIN, CRAIG J. · 2018 to 2022
$1.2M
Ubiquitous pollutant acrolein inhibits IFN?? antiviral signaling: relevance to HCK01ES017105 · NIEHS · UNIVERSITY OF LOUISVILLE · PI JOSHI-BARVE, SWATI · 2010 to 2014
$655k
Dietary Fat and Alcoholic Liver DiseaseI01BX002996 · VA · LOUISVILLE VA MEDICAL MEDICAL CENTER · PI MCCLAIN, CRAIG J. · 2017 to 2020
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BLRD VA I01 BX002996NHLBI NIH HHS P50 HL120163NIAAA NIH HHS P50 AA024337NIAAA NIH HHS R01 AA024405NIAAA NIH HHS U01 AA026225NIAAA NIH HHS U01 AA026936NIEHS NIH HHS K01 ES017105NIEHS NIH HHS P42 ES023716NIGMS NIH HHS P20 GM113226NIGMS NIH HHS P30 GM127607
6 · The paper itself

Abstract

Alcohol-associated liver disease (ALD) remains a major health concern worldwide. Alcohol consumption gives rise to reactive/toxic acrolein, a pathogenic mediator of liver injury in experimental ALD. Elevated acrolein adducts and metabolites are detectable in blood and urine. This study evaluates the major urinary acrolein metabolite, 3-hydroxypropylmercapturic acid (HPMA), in patients with acute alcoholic hepatitis (AAH) and examines its association with disease severity and markers of hepatic inflammation and injury. Urine HPMA was significantly higher in patients with severe [model for end-stage liver disease (MELD) ≥ 20] AAH compared with nonsevere AAH (MELD ≤ 19) or non-alcohol-consuming controls, suggesting that urine HPMA is a novel noninvasive biomarker in severe AAH. The association between HPMA and MELD in patients with AAH was nonlinear. In patients with nonsevere AAH, there was a positive trend, although not significant, whereas in severe AAH the association was negative, indicative of extensive injury and glutathione depletion. Consistent with the multifactorial etiology of ALD, our data identified strong combined effects of HPMA and proinflammatory cytokines on hepatocyte cell death, thereby supporting the pathogenic role of acrolein in liver injury. HPMA, together with IL-1β, showed robust associations with cytokeratin 18 caspase-cleaved fragment (CK18-M30; adjusted R

Indexed as

AcroleinAdultBiomarkersCytokinesFemaleHepatitis, AlcoholicHepatocytesHumansLiverLiver Diseases, AlcoholicMaleMiddle AgedTumor Necrosis Factor-alphaAcroleinBiomarkersCytokinesTumor Necrosis Factor-alphaalcoholic liver diseaseapoptosisbiomarkerdisease severityinflammation

Identifiers

PMID30234998
PMCPMC6383378
OpenAlexW2891309226

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.