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首页> 外文期刊>Russian journal of genetics >Association of T3111C polymorphism in 3'-untranslated region of the Clock gene with the risk of essential arterial hypertension and coronary artery disease in the Russian population (Residents of Karelia)
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Association of T3111C polymorphism in 3'-untranslated region of the Clock gene with the risk of essential arterial hypertension and coronary artery disease in the Russian population (Residents of Karelia)

机译:Clock基因的3'-非翻译区T3111C多态性与俄罗斯人群原发性高血压和冠心病风险的关联(卡累利阿居民)

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摘要

Allele and genotype distributions of the T3111C polymorphism in 3'-untranslated region of the Clock gene were examined in the groups of Russian patients with essential arterial hypertension (EAH) and coronary artery disease (CAD), and in control group of Russia residents of the Republic of Karelia. The genotype frequency distributions of the polymorphism examined in the EAH and CAD patients were statistically significantly different from that in the individuals without clinical signs of these diseases. The CC genotype frequency in EAH and CAD males was higher, and in the corresponding females it was lower than in males and females from the control group. Male CC carriers were characterized by a possible increased risk of EAH: OR (95% CI) = 1.42 (0.56; 3.58). Moreover, the presence of the CC genotype in males could increase the risk of CAD: OR (95% CI) = 1.58 (0.63; 3.93).
机译:在俄罗斯原发性高血压(EAH)和冠心病(CAD)患者组以及俄罗斯居民的对照组中,检查了Clock基因3'-非翻译区T3111C多态性的等位基因和基因型分布卡累利阿共和国。在EAH和CAD患者中检查的多态性的基因型频率分布与没有这些疾病临床症状的个体在统计学上显着不同。 EAH和CAD男性的CC基因型频率较高,相应的女性低于对照组的男性和女性。男性CC携带者的特征在于可能增加EAH风险:OR(95%CI)= 1.42(0.56; 3.58)。此外,男性CC基因型的存在会增加CAD的风险:OR(95%CI)= 1.58(0.63; 3.93)。

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