Polymorphisms in the GCK gene increase the risk of clopidogrel resistance in stable coronary artery disease (SCAD) patients

被引:1
|
作者
Xu, Hongyu [1 ]
Yu, Qinglin [2 ]
Zhou, Honglin [3 ]
Yang, Jin [3 ]
Zheng, Nan [3 ]
Xu, Zhifeng [4 ]
Su, Jia [3 ]
机构
[1] Ningbo 1 Hosp, Dept Geratol, Ningbo, Peoples R China
[2] Ningbo 1 Hosp, Dept Tradit Chinese Internal Med, Ningbo, Peoples R China
[3] Ningbo 1 Hosp, Dept Cardiol, Ningbo, Peoples R China
[4] Zhenhai Peoples Hosp Zhejiang Prov, Dept Cardiol, Ningbo, Peoples R China
关键词
Polymorphisms; coronary artery disease; platelet aggregation inhibitors; RESIDUAL PLATELET REACTIVITY; PROMOTER DNA METHYLATION; MYOCARDIAL-INFARCTION; ANTIPLATELET; IMPACT;
D O I
10.1080/16078454.2021.1945789
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Diabetes mellitus is a major factor in clopidogrel resistance (CR), and the glucokinase (GCK) gene plays a pivotal role in glucose homeostasis. This study investigated the contribution of GCK polymorphisms to CR risk. Methods Two hundred SCAD patients were recruited, and their platelet functions were detected by the Verify-Now P2Y12 assay. The polymorphisms of GCK were tested based on the methods of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). We investigated the associations of GCK polymorphisms and CR. Multivariate logistic regression was performed to analyse the correlations between GCK polymorphisms and clinical values. Results Our study found that the SNPs rs4607517 and rs6975024 were associated with CR. Additionally, patients with the G allele of rs4607517had a greater CR risk, but the C allele of rs6975024 might be a protective factor. Finally, logistic regression revealed that CC + TC (rs6975024) as well as the values of albumin were correlated with a decreased risk of CR, and higher levels of uric acid (UA) may be positively associated with CR. Conclusion The GCK gene polymorphisms might increase the CR risk in SCAD patients. Meanwhile, higher albumin levels and lower UA values might decrease the risk.
引用
收藏
页码:447 / 452
页数:6
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