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Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation

机译:因子V K858R变异体的次要等位基因仅在因子V Leiden突变的非携带者中可预防静脉血栓形成

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摘要

Factor V serves an important role in the regulation of blood coagulation. The rs6025 (R534Q) and rs4524 (K858R) polymorphisms in the F5 gene, are known to influence the risk of venous thrombosis. While the rare Q534 (factor V Leiden) allele is associated with an increased risk of venous thrombosis, the minor R858 allele is associated with a lower risk of disease. However, no study has deeply examined the cumulative impact of these two variations on venous thrombosis risk. We study the association of these polymorphisms with the risk of venous thrombosis in 4 French case-control populations comprising 3719 patients and 4086 controls. We demonstrate that the Q534 allele has a dominant effect over R858. Besides, we show that in individuals not carrying the Q534 allele, the protective effect of the R858 allele acts in a dominant mode. Thrombin generation-based normalized activated protein C sensitivity ratio was lower in the 858R/R homozygotes than in the 858K/K homozygotes (1.92 ± 1.61 vs 2.81 ± 1.57, p = 0.025). We demonstrate that the R858 allele of the F5 rs4524 variant protects from venous thrombosis only in non-carriers of the Q534 allele of the F5 rs6025. Its protective effect is mediated by reduced factor VIII levels and reduced activated protein C resistance.
机译:因子V在调节血液中起着重要作用。已知F5基因中的rs6025(R534Q)和rs4524(K858R)多态性会影响静脉血栓形成的风险。罕见的Q534(因子V莱顿因子)等位基因与静脉血栓形成的风险增加相关,而次要的R858等位基因与疾病的风险较低相关。然而,尚无研究深入研究这两种变异对静脉血栓形成风险的累积影响。我们研究了这些多态性与静脉血栓形成风险的关联,该法国人群包括4个法国病例对照人群,包括3719名患者和4086名对照。我们证明Q534等位基因比R858具有主导作用。此外,我们表明,在未携带Q534等位基因的个体中,R858等位基因的保护作用以显性模式起作用。 858R / R纯合子中基于凝血酶生成的归一化活化蛋白C敏感度比858K / K纯合子低(1.92%±1.61比2.81%±1.57,p = 0.025)。我们证明F5 rs4524变体的R858等位基因仅在F5 rs6025的Q534等位基因的非携带者中保护免受静脉血栓形成。其保护作用由降低的因子VIII水平和降低的活化蛋白C抗性介导。

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