Evidence map›Paper›PMID 25047496›Full record

ArticlePloS one2014

Synergistic association between two alcohol metabolism relevant genes and coronary artery disease among Chinese hypertensive patients.

Yuefei Wang, Fengxia Du, Hongye Zhao, Xiaohong Yu, Jun Liu, Yu Xiao, Changzhu Lu, Xue Li, Yanli Wang, Bin Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Observational
  6. Article
  7. Review
  8. Association between theInternational journal of clinical and experimental pathology · 2018
    Article
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 at 4 institutions in 1 country.

Yuefei WangDepartment of Physiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Fengxia DuDepartment of Etiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Hongye ZhaoDepartment of Physiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Xiaohong YuDepartment of Cardiology, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Jun LiuDepartment of Cardiology, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Yu XiaoDepartment of Physiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Changzhu LuDepartment of Physiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Xue LiDepartment of Physiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Yanli WangThe Third Division of Cardiology, Department of Internal Medicine, The Second Affiliated Hospital of Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Bin WangDepartment of Physiology, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Wenquan NiuState Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Shanghai Institute of Hypertension, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Qiqihar Medical University · CNDalian Medical University · CNFirst Affiliated Hospital of Dalian Medical University · CNShanghai Institute of Hypertension · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCoronary artery disease (CAD) is a multifactorial and polygenic disease. The aim of this study was to examine the association between six polymorphisms of four alcohol metabolism relevant genes (ADH1B, ADH1C, ALDH1b1, ALDH2) and the risk of CAD in Han Chinese. METHODS AND

resultsThis was a hospital-based case-control study involving 1365 hypertensive patients. All study subjects were angiographically confirmed. Genotypes were determined with ligase detection reaction method. There was no observable deviation from the Hardy-Weinberg equilibrium for six examined polymorphisms in controls. The genotype and allele distributions of ALDH1b1 rs2073478 and ALDH2 rs671 polymorphisms differed significantly between the two groups (P≤0.005), even after the Bonferroni correction. The most common allele combination was A-C-C-G-C-G (alleles in order of rs1229984, rs1693482, rs2228093, rs2073478, rs886205, rs671) and its frequency was slightly higher in controls than in CAD patients (P = 0.067). After assigning the most common allele combination as a reference, allele combination A-C-C-T-C-A, which simultaneously possessed the risk alleles of rs2073478 and rs671 polymorphisms, was associated with a 1.80-fold greater risk of CAD. Further, a two-locus model including rs2073478 and rs671 that had a maximal testing accuracy of 0.598 and a cross-validation consistency of 10 (P = 0.008) was deemed as the overall best MDR model, which was further validated by classical Logistic regression model.

conclusionOur findings provide clear evidence for both individual and interactive associations of ALDH1b1 and ALDH2 genes with the development of CAD in Han Chinese.

Indexed as

AgedAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAldehyde Dehydrogenase, MitochondrialAllelesAsian PeopleCase-Control StudiesChinaCoronary Artery DiseaseFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHaplotypesHumansHypertensionAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAldehyde Dehydrogenase, MitochondrialALDH1B1 protein, humanALDH2 protein, human

Identifiers

PMID25047496
PMCPMC4105442
OpenAlexW1969653324

What OpenQuestion holds

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LicenceCC BY
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.