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Published on: August 8, 2022
[Association between methylthioadenosine phosphorylase gene single nucleotide polymorphisms and myocardial infarction
Qi Zhang1, Shuang-shuang Cheng, Jie Yan
1Department of Cardiology, the Affiliated Hospital of North China Coal Medical College, Tangshan 063000, China.
Insights
Methylthioadenosine phosphorylase (MTAP) gene single nucleotide polymorphisms (SNPs) were studied for association with myocardial infarction (MI) in Chinese Han individuals. A specific SNP, rs7027989, showed increased MI risk in males.
Area of Science:
- Genetics
- Cardiovascular Disease Epidemiology
- Pharmacogenomics
Background:
- Myocardial infarction (MI) is a leading cause of mortality globally.
- Genetic factors play a role in MI susceptibility.
- The methylthioadenosine phosphorylase (MTAP) gene is a potential candidate for influencing cardiovascular health.
Purpose of the Study:
- To examine the association between single nucleotide polymorphisms (SNPs) in the MTAP gene and the risk of MI.
- To investigate this relationship specifically within the Chinese Han population.
Main Methods:
- A case-control study involving 432 MI patients and 430 healthy controls.
- Genotyping of nine tag SNPs within the MTAP gene.
- Stratified analysis based on gender.
Main Results:
- No overall significant association was found between the selected MTAP SNPs and MI across all participants.
- However, a significant association was detected for the rs7027989 SNP in male subjects.
- Male carriers of the minor allele at rs7027989 had a 26% increased risk of MI (P = 0.005), even after adjusting for confounders.
Conclusions:
- The MTAP gene, particularly the rs7027989 polymorphism, may contribute to the development of MI in the Chinese Han male population.
- Further research is warranted to elucidate the precise mechanisms linking MTAP to MI etiology.
Objective:
To investigate the association between methylthioadenosine phosphorylase (MTAP) gene single nucleotide polymorphisms (SNP) and myocardial infarction (MI) in the Chinese Han ethnicity.
Methods:
432 patients suffered from myocardial infarction and 430 controls were involved for case and control groups, respectively. Nine tag SNPs in MTAP gene were selected and genotyped.
Results:
We found no significant association of selected tag SNPs with MI in all of the samples. However, in stratified analysis, significant association was observed at rs7027989 in male subjects. The risk of MI increased by 26% (P = 0.005) for male subjects of minor allele carriers in a dominant model. The increased risk of MI at rs7027989 remained significant after adjusting for confounding factors.
Conclusion:
MTAP gene might be involved in the etiology of MI in Chinese Han ethnicity.
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