Polymorphism of V312F locus in PCSK9 gene of patients with coronary heart disease and its clinical significance
10.7652/jdyxb201704016
- VernacularTitle:冠心病患者外周血人枯草溶菌素转化酶9基因V312F位点的多态性及其临床意义
- Author:
Mingming ZHANG
;
Xin LIU
;
Wei GAO
;
Cuigai ZHANG
;
Pei ZHAO
;
Yueqing YU
;
Huizhen WU
;
Yali LI
- Keywords:
human proprotein convertase subtilisin/kexin type 9 gene;
gene polymorphism;
coronary heart disease;
blood lipid
- From:
Journal of Xi'an Jiaotong University(Medical Sciences)
2017;38(4):549-553
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the correlation and significance of V312F locus polymorphism of PCSK9 gene in patients with coronary heart disease.Methods We selected 3560 patients with coronary heart disease who came to our hospital from January 2014 to January 2016 as the case group.They were divided into 5 subgroups:angina group,myocardial infarction group,silent myocardial ischemia group,ischemic cardiomyopathy group,and sudden death group,according to their anatomic and pathophysiological features.Data of 1 000 people for physical examination served as the control group.PCR assay combined with direct sequencing method was applied to test V312F locus polymorphism of PCSK9 gene.Logistic regression analysis was used to analyze relationship between V312F locus polymorphism of PCSK9 gene and types of coronary heart disease.The concentration of serum PCSK9 and lipids of the two groups were also measured.Results The serum levels of PCSK9,TC,TG and LDLC and ratio of positive family history in the case group were significantly higher than those in the control group,while the level of HDLC was lower than that of the controls (all P＜0.05).Indexes of sudden death subgroup in the case group showed the most significant changes,while asymptomatic myocardial ischemia subgroup showed the weakest changes.The frequency of genotype TT,GT and allele T in the case group was 3.4％,16.6％ and 11.7％,respectively,which was significantly higher than that in the control group (1.1％,10.2％ and 6.2％) (all P＜0.01).The highest frequency of genotype TT,GT and allele T was found in sudden death subgroup,and the lowest frequency of these indexes was found in asymptomatic myocardial ischemia subgroup (P＜0.05).Results of Logistic regression analysis showed that genotype TT in V312F locus of PCSK9 gene was related to the severity of coronary heart disease (OR =8.463,95％ CI from 3.505 to 17.854,P＜0.001).Conclusion The mutation of V312F (T/G)locus of PCSK9 gene might be related to the severity of coronary heart disease.
