摘要
目的:探讨江苏地区急性心肌梗死与肿瘤坏死因子样凋亡微弱诱导剂(tumor necrosis factor-like weak inducer of apoptosis,TWEAK)基因多态性rs12937543、rs4968211、rs11552708位点单核苷酸基因多态性的相关性。方法:收集本院2016-07-2017-07收住急性心肌梗死患者267例为病例组,另选取健康体检者281例为对照组,采用聚合酶链反应-限制性片段长度多态性方法检测TWEAK基因多态位点rs12937543、rs4968211、rs11552708的基因型和等位基因分布频率。结果:TWEAK基因多态性位点rs12937543基因频率在病例组与对照组中分布差异具有统计学意义(P<0.05);T等位基因能显著增加急性心肌梗死的危险,且与TWEAK血浆表达水平相关(P<0.05)。rs4968211、rs11552708位点均无统计学差异。结论:TWEAK基因多态性位点rs12937543与江苏地区急性心肌梗死存在相关性。
Objective:To investigate the association between rs12937543,rs4968211 and rs11552708 single nucleotide polymorphism in TWEAK and acute myocardial infarction in Jiangsu province.Method:A total of 261 patients with acute myocardial infarction(AMI group)and 281 healthy cases(control group)from July 2016 to July2017 in Zhongda Hospital were included.Polymerase chain reaction-restriction fragment length polymorphisms was used to identify genotypes and alleles of rs12937543,rs4968211 and rs11552708.Result:Frequencies of rs12937543 genotype and allele were statistically significant different between AMI group and control group(P0.05).The exist of T allele increased the risk of AMI and had a correlation with the plasma level ofTWEAK(P0.05).There was no relationship in rs4968211 and rs11552708 between AMI and control group.Conclusion:The TWEAK gene polymorphism site rs12937543 is associated with acute myocardial infarction in Jiangsu province.
出处
《临床心血管病杂志》
CAS
CSCD
北大核心
2018年第2期123-126,共4页
Journal of Clinical Cardiology
基金
国家自然科学基金资助项目(No:81400225
81400219
81500204)
江苏省青年医学人才项目(No:QNRC2016815)