Evidence map›Paper›PMID 26562495›Full record

ArticleGenetic testing and molecular biomarkers2016

Identification of a CYP19 Gene Single-Nucleotide Polymorphism Associated with a Reduced Risk of Coronary Heart Disease.

Bei Wang, Zhen-Yan Fu, Yi-Tong Ma, Ding Huang, Fen Liu, Chun-Lan Dong, Ting Wang, Ya-Jie Meng

Abstract read
In one paragraph

Article in Genetic testing and molecular biomarkers, 2016. 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
0.7field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

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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, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Genetic association ofCardiovascular endocrinology & metabolism · 2021
    Article
  5. Article
  6. Article
  7. Review
  8. Sex-specific association ofOncotarget · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Bei WangDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Zhen-Yan FuDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Yi-Tong MaDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Ding HuangDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Fen LiuDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Chun-Lan DongDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Ting WangDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Ya-Jie MengDepartment of Cardiovascular Medicine, The First Affiliated Hospital of Xinjiang Medical University , Urumqi, China .
Xinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAn imbalance in sex hormone ratios has been identified in coronary heart disease (CHD), and as a key enzyme in the conversion of androgen to estrogen, aromatase plays an important role in the balance of sex hormone levels. However, there is a paucity of research into the potential roles of aromatase in CHD. In this study, we investigated associations between single-nucleotide polymorphisms (SNPs) in the CYP19 gene, which encodes aromatase, and CHD.

methodsWe collected 1706 blood samples from CHD patients and control participants and used propensity score matching techniques to match case and control groups with respect to confounding factors. In a final study population, including 596 individuals, we conducted a case-control study to identify associations between three SNPs in CYP19 and CHD using χ(2) or Fisher exact tests, and binary logistic regression analysis. Differences in lipid levels and parameters of echocardiography among individuals with different genotypes were assessed by one-way analysis of variance.

resultsThe distributions of rs2289105 alleles in the CYP19 gene differed significantly between the CHD and control groups (p = 0.014), and the heterozygote CT genotype was associated with a significantly lower risk of CHD compared to the homozygous wild-type CC genotype (p = 0.0063 and odds ratio = 0.575). However, blood lipid levels and echocardiographic parameters among individuals with different genotypes did not differ between the CHD and control groups.

conclusionsThe CT genotype of the rs2289105 polymorphism in the CYP19 gene is associated with a decreased risk of CHD and may be a genetic marker of protection from CHD.

Indexed as

GenotypePolymorphism, Single NucleotideAdultAgedAromataseCoronary DiseaseFemaleGenetic MarkersHumansMaleMiddle AgedRisk FactorsAromataseCYP19A1 protein, humanGenetic Markers

Identifiers

PMID26562495
PMCPMC4742981
OpenAlexW2178205986

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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.