» Articles » PMID: 31938159

Association of Rs1333040 SNPs with Susceptibility, Risk Factors, and Clinical Characteristics of Acute Myocardial Infarction Patients in a Chinese Han Population

Overview
Specialty Pathology
Date 2020 Jan 16
PMID 31938159
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

This study aimed to examine the association of rs1333040 SNPs and several risk and environmental factors with acute myocardial infarction (AMI). The association of rs1333040 single nucleotide polymorphisms (SNPs) within the cyclin-dependent kinase inhibitor 2B antisense RNA1 (CDKN2B-AS1) gene with AMI has been confirmed in some European populations. However, at the time this study was initiated, no rs1333040 SNPs had been associated with AMI in Chinese individuals. Genotypes of rs1333040 were determined in 334 AMI patients and 334 healthy controls from a Chinese Han population by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP), and then confirmed by direct sequencing. The TT genotype of rs1333040 was positively correlated with AMI risk ( < 0.001). The frequency of the C allele of rs1333040 in patients with diagnosis time (DT) > 12 h was lower than that in patients with shorter DT ( < 0.05), with no differences in typical symptoms, serious complications, and infarction location ( > 0.05 for each). There were interactions between the rs1333040 SNP genotype (TT, TC, or CC), and patients who smoked ≥ 20 cigarettes/day ( < 0.017). The rs1333040 TT genotype was positively correlated with the risk of AMI. For the first time, we discovered that the C allele of rs1333040 was significantly correlated with DT ≤ 12 h of AMI. Also, the interaction between the minor C allele of rs1333040 and smoking appears to increase the risk of AMI.

Citing Articles

Identifying potential drug targets for myocardial infarction through Mendelian randomization.

Yu X, Liu S PLoS One. 2024; 19(12):e0313770.

PMID: 39715222 PMC: 11665999. DOI: 10.1371/journal.pone.0313770.

References
1.
Musunuru K, Kathiresan S . Genetics of coronary artery disease. Annu Rev Genomics Hum Genet. 2010; 11:91-108. DOI: 10.1146/annurev-genom-082509-141637. View

2.
Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C . Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. Nature. 2010; 464(7287):409-12. PMC: 2938076. DOI: 10.1038/nature08801. View

3.
Folkersen L, Kyriakou T, Goel A, Peden J, Malarstig A, Paulsson-Berne G . Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants. PLoS One. 2009; 4(11):e7677. PMC: 2765615. DOI: 10.1371/journal.pone.0007677. View

4.
Barnett R, Larson G . A phenol-chloroform protocol for extracting DNA from ancient samples. Methods Mol Biol. 2012; 840:13-9. DOI: 10.1007/978-1-61779-516-9_2. View

5.
Dogra R, Das R, Ahluwalia J, Kumar R, Talwar K . Prothrombotic gene polymorphisms and plasma factors in young North Indian survivors of acute myocardial infarction. J Thromb Thrombolysis. 2012; 34(2):276-82. DOI: 10.1007/s11239-012-0734-6. View