Dankovtseva E N, Zateĭshchikov D A, Chudakova D A, Koroleva O S, Brovkin A N, Nosikov V V, Gaĭdukova N V, Tishchenko V A, Sidorenko B A
Kardiologiia. 2005;45(12):17-24.
To study polymorphisms of genes of factors of the system of hemostasis in young patients with ischemic heart disease (IHD).
Two groups of patients participated in the study: patients with first manifestation of IHD at the age < or = 50 years (men) or < or = 55 years (women) (n=158), and patients with first IHD manifestation at the age > or = 70 years (n=92).
We studied polymorphic markers of genes encoding clotting factors V (F5) and VII (F7), subunit IIIa of platelet integrin (ITGB3), beta-chain of fibrinogen (FGB) and tissue plasminogen activator type 1 (PLANH1).
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]; p<0.001) and presence of genotype TT of C(-426)T polymorphic marker of F5 gene (OR=9.410 [1.074-82.459]; p=0.043).
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.
研究青年缺血性心脏病(IHD)患者止血系统因子基因的多态性。
两组患者参与了本研究:IHD首次发病年龄≤50岁(男性)或≤55岁(女性)的患者(n = 158),以及IHD首次发病年龄≥70岁的患者(n = 92)。
我们研究了编码凝血因子V(F5)和VII(F7)、血小板整合素亚基IIIa(ITGB3)、纤维蛋白原β链(FGB)和组织纤溶酶原激活物1型(PLANH1)的基因的多态性标记。
在分离出无前驱性心绞痛的心肌梗死患者亚组后,我们发现因子V基因多态性标记C(-426)T基因型频率分布存在显著差异:年轻患者(14.9%)中基因型TT的频率显著高于老年患者(2%)(p = 0.008)。多因素逻辑回归显示,早期IHD与吸烟(比值比6.112 [2.567 - 14.552];p < 0.001)以及F5基因C(-426)T多态性标记基因型TT的存在(比值比 = 9.410 [1.074 - 82.459];p = 0.043)独立相关。
因此,我们获得的数据表明,IHD风险与青年心肌梗死表现之间存在独立关联,与F5基因多态性标记C(-426)T的基因型TT以及IHD的传统风险因素有关。