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组织因子途径抑制物2(TFPI-2)基因多态性与急性冠脉综合征的关联性
  • ISSN号:1672-8467
  • 期刊名称:《复旦学报:医学版》
  • 时间:0
  • 分类:R541.4[医药卫生—心血管疾病;医药卫生—临床医学;医药卫生—内科学]
  • 作者机构:[1]复旦大学附属华山医院心内科,上海200040, [2]复旦大学基础医学院分子医学教育部重点实验室,上海200032
  • 相关基金:国家自然科学基金(30971249,81270278)
中文摘要:

目的探讨在中国汉族人群中基因多态性与急性冠脉综合征的关系。方法采用病例对照研究设计,选择急性冠脉综合征(acute coronary syndrome, ACS)患者140例,其中包括不稳定型心绞痛患者(unstable angina,UA)68例、急性心肌梗死患者(acute myocardium infarction, AMI)72例;另有稳定型心绞痛患者(stable angina,SA)273例,以及正常对照306例。采用聚合酶链反应产物直接测序的方法对所有纳入对象进行组织因子途径抑制物2 (tissue factor pathway inhibitor 2,TFPI-2)基因多态性分析和关联分析。结果在所有对象的TFPI-2基因中共检测出8个单核苷酸多态性位点,其中rs59805398和rs34489123位点基因型频率和等位基因频率分布在ACS组和SA组,与对照组间差异有统计学意义。rs3763473,rs59999573,rs59740167,rs34489123位点在ACS组中存在连锁不平衡,与rs59805398位点关联分析提示主要有C-C-G-GG和T-C-G-G-G两种单倍型。rs59999573,rs59740167,rs34489123位点在SA组中存在连锁不平衡,与rs59805398位点进行关联分析,主要有C-G-G-G和GA-A-A两种单倍型。ACS组与sA组之间未见明显差异。结论TFPI-2基因rs59805398位点C等位基因和rs34489123位点A等位基因与冠心病(coronaryheartdisease,CHD)发病存在关联性,其变异可能是中国人群冠心病发病的危险因子之一。TFPI-2基因SNP在冠心病患者中存在连锁不平衡。

英文摘要:

Objective To investigate the relation of tissue factor pathway inhibitor 2 (TFPI-2) gene polymorphism and acute coronary syndrome (ACS) in Chinese Han population. Methods The polymorphism of TFPI-2 gene was detected by PCR-sequencing in all people recruited, and a case control study was carried out in three groups,the ACS group consisted of 140 ACS patients (including 68 unstable angina patients and 72 acute myocardial infarction patients), the SA group included 273 stable angina (SA) patients, and the control group consisted of 306 healthy people. Results Eightsingle nucleotide polymorphism (SNP) sites were identified in TFPI-2 gene in all subjects, the allele and genotype frequencies were different on the two SNP sites:rs59805398 and rs34489123 among case and control group. Linkage disequilibrium among the SNPs of rs3763473, rs59999573, rs59740167, rs34489123 of TFPI-2 gene was found and C-C-G-G-G and T-C-G-G-G were predominant haplotypes in ACS patients. Linkage disequilibrium among the SNPs of rs59999573, rs59740167, rs34489123 of TFPI-2 gene was found and C-G-G-G and G-A-A-A were predominant haplotypes in SA patients. There was no significant difference between ACS group and SA group. Conclusions C allele in rs59805398 and A allele in rs34489123 have correlation with coronary heart disrase (CHD) ,implying that they might be a higher risk factor of CHD among Chinese Han population. There is apparent linkage disequilibrium among SNPs of TFPI-2 gene in CHD patients.

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期刊信息
  • 《复旦学报:医学版》
  • 北大核心期刊(2011版)
  • 主管单位:教育部
  • 主办单位:复旦大学
  • 主编:桂永浩
  • 地址:上海医学院路138号285信箱
  • 邮编:200032
  • 邮箱:xbyxb@shmu.edu.cn
  • 电话:021-54237164 021-54237314
  • 国际标准刊号:ISSN:1672-8467
  • 国内统一刊号:ISSN:31-1885/R
  • 邮发代号:4-262
  • 获奖情况:
  • 2008年第二届中国高校优秀科技期刊奖,2010年第三届中国高校精品科技期刊
  • 国内外数据库收录:
  • 美国化学文摘(网络版),波兰哥白尼索引,荷兰文摘与引文数据库,美国剑桥科学文摘,美国生物科学数据库,中国中国科技核心期刊,中国北大核心期刊(2004版),中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版)
  • 被引量:11703