...
首页> 外文期刊>Кардиология >Associations of Hemostasis Factors Genes With Early Development of Ischemic Heart Disease and Manifestation of Myocardial Infarction in Young Age.
【24h】

Associations of Hemostasis Factors Genes With Early Development of Ischemic Heart Disease and Manifestation of Myocardial Infarction in Young Age.

机译:年轻人中,止血因子基因与缺血性心脏病的早期发展和心肌梗塞的表现相关。

获取原文
获取原文并翻译 | 示例
           

摘要

AIM: To study polymorphisms of genes of factors of the system of hemostasis in young patients with ischemic heart disease (IHD). MATERIAL: Two groups of patients participated in the study: patients with first manifestation of IHD at the age capital JE, Serbian50 years (men) or capital JE, Serbian55 years (women) (n=158), and patients with first IHD manifestation at the age small i, Ukrainian70 years (n=92). METHODS: We studied polymorphic markers of genes encoding clotting factors V (F5) and VII (F7), subunit IIIa of platelet integrin (ITGB3), b-chain of fibrinogen (FGB) and tissue plasminogen activator type 1 (PLANH1). RESULTS: After separation of a subgroup of patients with MI without preceding angina we revealed significant differences in distribution of frequencies of genotypes of polymorphic marker C(–426)T of factor V gene: genotype TT was significantly more frequent in young (14.9%) than in old (2%) patients (p=0.008). Multifactorial logistic regression revealed independent association of early IHD with smoking (OR 6.112 [2.567—14.552]; p0.001) and presence of genotype TT of C(-426)T polymorphic marker of F5 gene (OR=9.410 [1.074—82.459]; p=0.043). CONCLUSION: Thus we obtained data on the presence of independent association between IHD risk and manifestation of MI in young age with genotype TT of polymorphic marker C(-426)T of F5 gene as well as with traditional risk factors of IHD.
机译:目的:研究年轻缺血性心脏病(IHD)患者止血系统因子基因的多态性。材料:两组患者参加了研究:年龄在首都JE,塞尔维亚人50岁(男性)或首都JE,塞尔维亚55岁(妇女)(158岁)年龄段中首次出现IHD的患者,以及在年龄小i,乌克兰人70岁(n = 92)。方法:我们研究了编码凝血因子V(F5)和VII(F7),血小板整联蛋白IIIa亚基(ITGB3),纤维蛋白原b链(FGB)和1型组织纤溶酶原激活物(PLANH1)的基因的多态标记。结果:分离出亚型的无心绞痛的MI患者亚组后,我们发现因子V基因多态性标记C(–426)T基因型的频率分布存在显着差异:年轻人中TT基因型的频率更高(14.9%)高于老年患者(2%)(p = 0.008)。多因素logistic回归分析显示早期IHD与吸烟(OR 6.112 [2.567-14.552]; p <0.001)和F5基因C(-426)T多态性标记的基因型TT存在独立相关性(OR = 9.410 [1.074-82.459]) ; p = 0.043)。结论:因此,我们获得了有关FHD基因多态性标记C(-426)T的基因型TT以及传统IHD危险因素的IHD危险与年轻MI的独立相关性的数据。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号