Evidence map›Paper›PMID 37923598›Full record

ArticleDigestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver2024

Serum metabolomic analysis in cirrhotic alcohol-associated liver disease patients identified differentially altered microbial metabolites and novel potential biomarkers for disease severity.

Nathan Calzadilla, Netanel Zilberstein, Mark Hanscom, Haya T Al Rashdan, Wadih Chacra, Ravinder K Gill, Waddah A Alrefai

Open access · greenAbstract read
In one paragraph

Article in Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Nathan CalzadillaDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL, United States.
Netanel ZilbersteinDivision of Gastroenterology & Hepatology, Rush University, Chicago, IL, United States.
Mark HanscomDivision of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN, United States.
Haya T Al RashdanDivision of Gastroenterology & Hepatology, University of Illinois Chicago, Chicago, IL, United States.
Wadih ChacraDivision of Gastroenterology & Hepatology, University of Illinois Chicago, Chicago, IL, United States.
Ravinder K GillDivision of Gastroenterology & Hepatology, University of Illinois Chicago, Chicago, IL, United States.
Waddah A AlrefaiDivision of Gastroenterology & Hepatology, University of Illinois Chicago, Chicago, IL, United States; Jesse Brown VA Medical Center, Chicago, IL, United States. Electronic address: walrefai@uic.edu.
University of Illinois Chicago · USMayo Clinic in Arizona · USRush University · US

Funding

Intestinal 5-HT Transporter: A novel therapeutic target for GI disordersR01DK098170 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GILL, RAVINDER K · 2014 to 2022
$3.0M
The roles of intestinal epithelial AhR in alcohol-induced barrier dysfunction and liver injuryF30AA030222 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CALZADILLA, NATHAN · 2022 to 2024
$96k
Regulation of Intestinal Bile Acid Absorption in Health and Cholesterol-Related DisordersI01BX000152 · VA · JESSE BROWN VA MEDICAL CENTER · PI Waddah A. Alrefai · 2009 to 2026
–
BLRD Research Career Scientist Award ApplicationIK6BX005243 · VA · JESSE BROWN VA MEDICAL CENTER · PI ALREFAI, WADDAH A. · 2020 to 2025
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BLRD VA I01 BX000152BLRD VA I01 BX006177BLRD VA IK6 BX005243NIAAA NIH HHS F30 AA030222NIDDK NIH HHS R01 DK098170
6 · The paper itself

Abstract

backgroundAlcohol-Associated Liver Disease (ALD) is a leading cause of liver mortality. Mechanisms responsible for severe ALD and the roles of gut microbiota are not fully understood. Multi-omics tools have enabled a better understanding of metabolic alterations and can aid in identifying metabolites as biomarkers for severe ALD.

aimsExamine differences between cirrhotic and non-cirrhotic ALD, investigate microbial contributions to such changes, and identify potential diagnostic and prognostic metabolites for severe ALD.

methodsUntargeted metabolomics were performed on the serum of 11 non-cirrhotic and 11 cirrhotic ALD patients. Data were analyzed using MetOrigin and Metaboanalyst to identify enriched pathways.

resultsIncreased methylated nucleotides, gamma-glutamyl amino acids, bile acids, and specific metabolites kynurenine and campesterol were increased in ALD cirrhosis, whereas branched-chain amino acids, serotonin, and xanthurenate were decreased. Microbial contributions included increases in the short-chain fatty acid indolebutyrate and methionine sulfoxide in ALD cirrhosis. The analysis also identified the potential for serum levels of 3-ureidopropionate, cis-3,3-methyleneheptanoylglycine, retinol, and valine to be used as biomarkers for clinical assessment of alcohol-associated cirrhosis.

conclusionWe have identified a set of metabolites that are differentially altered in cirrhotic compared to non-cirrhotic ALD that can potentially be used as biomarkers for the severity of the disease.

Indexed as

BiomarkersMetabolomicsAdultAgedCase-Control StudiesFemaleGastrointestinal MicrobiomeHumansLiver Cirrhosis, AlcoholicLiver Diseases, AlcoholicMaleMiddle AgedSeverity of Illness IndexBiomarkersALDBiomarkersCirrhosisMetabolites

Identifiers

PMID37923598
PMCPMC11061266
OpenAlexW4388115019

What OpenQuestion holds

Textmetadata
LicenceTDM
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.