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Analysis of the Association Between MicroRNA Biogenesis Gene Polymorphisms and Venous Thromboembolism in Koreans

机译:朝鲜族MicroRNA生物发生基因多态性与静脉血栓栓塞之间的关联性分析

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摘要

Venous thromboembolism (VTE) involves the formation of a blood clot, typically in the deep veins of the leg or arm (deep vein thrombosis), which then travels via the circulatory system and ultimately lodges in the lungs, resulting in pulmonary embolism. A number of microRNAs (miRNAs) are well-known regulators of thrombosis and thrombolysis, and mutations in miRNA biogenesis genes, such as DICER1, DROSHA have been implicated in miRNA synthesis and function. We investigated the genetic association between polymorphisms in four miRNA biogenesis genes, DICER1 rs3742330A > G, DROSHA rs10719T > C, RAN rs14035C > T and XPO5 rs11077A > C, and VTE in 503 Koreans: 300 controls and 203 patients. Genotyping was assessed with polymerase chain reaction-restriction fragment length polymorphism assays. We detected associations between polymorphisms in RAN and XPO5 and VTE prevalence (RAN rs14035CC + CT versus TT: p = 0.018; XPO5 rs11077AA + AC versus CC: p < 0.001). Analysis of allele combinations of all four polymorphisms (DICER1, DROSHA, RAN, XPO5) revealed that A-T-T-A was associated with decreased VTE prevalence (p = 0.0002), and A-T-C-C was associated with increased VTE prevalence (p = 0.027). Moreover, in subjects with provoked VTE, the DROSHA rs10719T > C, polymorphism was associated with increased disease prevalence (TT versus TC + CC: p < 0.039). Our study demonstrates that RAN and XPO5 polymorphisms are associated with risk for VTE in Korean subjects.
机译:静脉血栓栓塞症(VTE)涉及血栓的形成,通常在腿或手臂的深静脉(深静脉血栓形成)中形成,然后通过循环系统传播并最终滞留在肺部,导致肺栓塞。许多microRNA(miRNA)是众所周知的血栓形成和溶栓调节剂,miRNA生物发生基因(如DICER1,DROSHA)的突变与miRNA的合成和功能有关。我们在503名韩国人中对300个对照组和203例患者的四个miRNA生物发生基因DICER1 rs3742330A> G,DROSHA rs10719T> C,RAN rs14035C> T和XPO5 rs11077A> C和VTE之间的遗传关联进行了研究。用聚合酶链反应-限制性片段长度多态性分析评估基因分型。我们检测到RAN和XPO5中的多态性与VTE患病率之间存在关联(RAN rs14035CC + CT与TT:p = 0.018; XPO5 rs11077AA + AC与CC:p <0.001)。对所有四个多态性(DICER1,DROSHA,RAN,XPO5)的等位基因组合进行分析后发现,ATTA与VTE患病率降低( p = 0.0002)相关,ATCC与VTE患病率升高( > p = 0.027)。此外,在患有诱发性VTE的受试者中, DROSHA rs10719T> C,多态性与疾病患病率升高相关(TT与TC + CC: p <0.039)。我们的研究表明, RAN XPO5 多态性与韩国受试者发生VTE的风险有关。

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