Evidence map›Paper›PMID 29779728›Full record

Trial reportThe American journal of the medical sciences2018

Association Between Aldehyde Dehydrogenase 2 Glu504Lys Polymorphism and Alcoholic Liver Disease.

Binxia Chang, Shuli Hao, Longyu Zhang, Miaomiao Gao, Ying Sun, Ang Huang, Guangju Teng, Baosen Li, David W Crabb, Praveen Kusumanchi and 3 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in The American journal of the medical sciences, 2018. 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
1.2field-weighted citation impact, top 23% 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, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Genetic Polymorphisms ofInternational journal of molecular sciences · 2025
    Review
  4. Article
  5. Contribution of Genetic Polymorphisms in Human Health.International journal of environmental research and public health · 2023
    Review
  6. [Research progress of acetaldehyde dehydrogenase 2 in liver diseases].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2022
    Article
  7. Review
  8. Article
  9. Article
  10. Role of ALDH2 in Hepatic Disorders: Gene Polymorphism and Disease Pathogenesis.Journal of clinical and translational hepatology · 2021
    Review
  11. Article
  12. Review
  13. Aldehyde Dehydrogenase, Liver Disease and Cancer.International journal of biological sciences · 2020
    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

13 authors at 5 institutions in 2 countries.

Binxia ChangThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
Shuli HaoThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
Longyu ZhangThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
Miaomiao GaoThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
Ying SunThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
Ang HuangThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
Guangju TengThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
Baosen LiThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China.
David W CrabbDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana; Eskenazi Health, Indianapolis, Indiana.
Praveen KusumanchiDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Li WangDepartment of Physiology and Neurobiology, and The Institute for Systems Genomics, University of Connecticut, Storrs, Connecticut; Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut; Department of Internal Medicine, Section of Digestive Diseases, Yale University, New Haven, Connecticut; School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Suthat LiangpunsakulDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana; Roudebush Veterans Administration Medical Center, Indianapolis, Indiana. Electronic address: zszou302@163.com.
Zhengsheng ZouThe Center for Diagnosis and Treatment of Noninfectious Liver Disease, Institute of Alcoholic Liver Disease, Beijing, China. Electronic address: zszou302@163.com.
302 Military Hospital of China · CNEskenazi HealthIndiana University – Purdue University Indianapolis · USRichard L. Roudebush VA Medical Center · USVA Connecticut Healthcare System · US

Funding

Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI MICHAEL H NATHANSON, Mario Strazzabosco · 1986 to 2026
$31.1M
Translational Research and Evolving Alcoholic hepatitis Treatment (TREAT-IU)U01AA021840 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI NAGA P CHALASANI, Olawale Ojo · 2012 to 2026
$8.1M
Genetic risk factors for alcoholic cirrhosis - genome-wide case-control studyU01AA018389 · NIAAA · SOUTHERN CALIFORNIA INST FOR RES/EDUC · PI CORDELL, HEATHER JANE, DALY, ANN · 2011 to 2018
$3.0M
SHP-regulation of Lipid and Lipoprotein MetabolismR01DK080440 · NIDDK · UNIVERSITY OF UTAH · PI WANG, LI · 2008 to 2015
$2.3M
Novel biomarkers as a clinical tool for excessive alcohol use screeningR01AA025208 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI LIANGPUNSAKUL, SUTHAT, TU, WANZHU · 2016 to 2020
$1.7M
LncRNA as a New Mediator of Bile Acid HomeostasisR01DK104656 · NIDDK · UNIVERSITY OF CONNECTICUT STORRS · PI WANG, LI · 2015 to 2018
$1.7M
Sestrin3 in the pathogenesis of alcoholic and non-alcoholic fatty liver diseaseR01DK107682 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI DONG, X. CHARLIE, LIANGPUNSAKUL, SUTHAT · 2016 to 2019
$1.4M
Molecular Basis of Cancer Cell Metabolic ReprogrammingR01ES025909 · NIEHS · UNIVERSITY OF CONNECTICUT STORRS · PI WANG, LI · 2015 to 2017
$1.0M
Long noncoding RNAs in alcoholic liver diseaseR21AA024935 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI LIANGPUNSAKUL, SUTHAT, WANG, LI · 2016 to 2017
$431k
Alcohol, nuclear receptor signaling, and circadian clocksR21AA022482 · NIAAA · UNIVERSITY OF CONNECTICUT STORRS · PI WANG, LI · 2015 to 2016
$415k
Non-coding RNAs in serrated polyps identify patients with high colon cancer riskR21CA191507 · NCI · UNIVERSITY OF UTAH · PI DELKER, DON A, KANTH, PRIYANKA · 2015 to 2016
$371k
Circadian Clock Regulation of Alcoholic Liver DiseaseI01BX002634 · VA · VA CONNECTICUT HEALTHCARE SYSTEM · PI WANG, LI · 2016 to 2019
–
BLRD VA I01 BX002634CSRD VA I01 CX000361NCI NIH HHS R21 CA191507NIAAA NIH HHS R01 AA025208NIAAA NIH HHS R21 AA022482NIAAA NIH HHS R21 AA024935NIAAA NIH HHS U01 AA018389NIAAA NIH HHS U01 AA021840NIDDK NIH HHS P30 DK034989NIDDK NIH HHS R01 DK080440NIDDK NIH HHS R01 DK104656NIDDK NIH HHS R01 DK107682NIEHS NIH HHS R01 ES025909
6 · The paper itself

Abstract

backgroundOnly a subset of patients with excessive alcohol use develop alcoholic liver disease (ALD), though the exact mechanism is not completely understood. Once ingested, alcohol is metabolized by 2 key oxidative enzymes, alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH). There are 2 major ALDH isoforms, cytosolic and mitochondrial, encoded by the aldehyde ALDH1 and ALDH2 genes, respectively. The ALDH2 gene was hypothesized to alter genetic susceptibility to alcohol dependence and alcohol-induced liver diseases. The aim of this study is to determine the association between aldehyde dehydrogenase 2 (rs671) glu504lys polymorphism and ALD.

methodsALDH2 genotyping was performed in 535 healthy controls and 281 patients with ALD.

resultsThe prevalence of the common form of the single nucleotide polymorphism rs671, 504glu (glu/glu) was significantly higher in patients with ALD (95.4%) compared to that of controls (73.7%, P < 0.0001). Among controls, 23.7% had the heterozygous (glu/lys) genotype compared to 4.6% in those with ALD (odds ratio [OR] = 0.16, 95% CI: 0.09-0.28). The allele frequency for 504lys allele in patients with ALD was 2.3%, compared to 14.5% in healthy controls (OR = 0.13, 95% CI: 0.07-0.24).

conclusionsPatients with ALDH2 504lys variant were less associated with ALD compared to those with ALDH2 504glu using both genotypic and allelic analyses.

Indexed as

Gene FrequencyGenetic Predisposition to DiseaseLiver Cirrhosis, AlcoholicMutation, MissensePolymorphism, Single NucleotideAdultAldehyde Dehydrogenase, MitochondrialAmino Acid SubstitutionHumansMaleMiddle AgedPrevalenceAldehyde Dehydrogenase, MitochondrialALDH2 protein, humanAlcoholic liver diseaseAldehyde dehydrogenaseGene polymorphismRisk

Identifiers

PMID29779728
PMCPMC6063768
OpenAlexW2790290129

What OpenQuestion holds

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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.