首页> 外文期刊>Human Reproduction >Estrogen receptor 1 haplotype does not regulate oral contraceptive-induced changes in haemostasis and inflammation risk factors for venous and arterial thrombosis.
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Estrogen receptor 1 haplotype does not regulate oral contraceptive-induced changes in haemostasis and inflammation risk factors for venous and arterial thrombosis.

机译:雌激素受体1单倍型不能调节口服避孕药引起的止血和静脉和动脉血栓形成的危险因素的变化。

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BACKGROUND: Administration of oral contraceptives (OCs) has profound effects on the plasma levels of haemostasis and inflammation variables, resulting in an increased thrombosis risk. Individuals show large differences in the response of these variables to OCs. Polymorphism in the estrogen receptor-1 (ER1) gene may explain part of this inter-individual response. METHODS: We investigated the relationship between variants (c.454-397T>C and c.454-351A>G polymorphisms and the combined haplotype) in the ER1 gene in relation to changes in haemostasis and inflammation variables that are known risk factors for thrombosis in 507 healthy, nonsmoking, nulliparous women receiving six cycles of monophasic OCs with 20, 30 or 50 microg/day estrogen. RESULTS: A significant relationship was observed between the ER1 haplotype and changes in tissue-type plasminogen activator activity (P = 0.006), but no clear interaction pattern between the genotypes or between the estrogen doses was seen. No relationships were observed for the other variables, neither in the haplotype nor in the single polymorphism analysis. CONCLUSION: The ER1 haplotype does not have a strong effect on the estrogen-induced changes in haemostasis and inflammation risk markers for arterial and venous thrombosis.
机译:背景:口服避孕药(OCs)对止血和炎症变量的血浆水平具有深远影响,导致血栓形成风险增加。个人在这些变量对OC的响应上显示出很大的差异。雌激素受体1(ER1)基因的多态性可能解释了这种个体间反应的一部分。方法:我们研究了ER1基因的变异(c.454-397T> C和c.454-351A> G多态性与组合单倍型)之间的关系,这些关系涉及止血和炎症变量(已知为血栓形成的危险因素)的变化在507名健康,禁烟,未产妇中,妇女接受了六个周期的单相OC,每天服用20、30或50 microg雌激素。结果:ER1单倍型与组织型纤溶酶原激活物活性的变化之间存在显着的关系(P = 0.006),但在基因型之间或雌激素剂量之间没有清楚的相互作用模式。在单倍型和单态多态性分析中均未观察到其他变量之间的关系。结论:ER1单倍型对雌激素引起的止血变化和动脉血栓和静脉血栓形成的炎症危险标志没有明显作用。

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