激活物抑制剂纤溶酶原1基因(pai-1) 4g / 5g多态性对深静脉血栓形成的影响

M. Pođanin, Herzegovina, R. Terzić, A. Avdić, A. Jusic
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摘要

分析PAI-1基因4G/5G多态性与其他诱发静脉血栓栓塞发生的遗传及外部危险因素的相互作用,可用于静脉血栓栓塞发生的风险评估。研究人员对来自波斯尼亚东北部的202名18岁以上的男女考生进行了调查。实验组包括100名诊断为深静脉血栓的受检者和101名在抽样前未诊断为深静脉血栓的受检者。在DVT组中,基因型频率确定如下:27%的考生为正常基因型5G/5G, 68%为杂合子,5%为突变纯合子4G/4G。在对照组中,PAI-1基因4G/5G多态性频率为:42.6%的考生为5G/5G基因型,55.4%的考生为4G/5G杂合子,2%的考生为4G/4G基因型。这些结果支持了PAI-1与其他遗传和外部危险因素相互作用可能诱导静脉血栓栓塞发生的假设。
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THE INFLUNECE OF 4G/5G POLYMORPHISM OF ACTIVATOR INHIBITOR PLASMINOGEN 1 GENE (PAI-1) ON DEVELOPEMENT DEEP VEIN THROMBOSIS
Analysis of 4G/5G polymorphisms of PAI-1 gene in interaction with other genetic and external risk factors that induce development of venous thromboembolism can be used for risk assessment for development of venous thromboembolism. Research was conducted on 202 examinees of both genders, older than 18, from north-eastern Bosnia. Experimental group included 100 examinees with diagnosed DVT and 101 examinees who until the sampling procedure did not have diagnosed DVT. In DVT group, following genotype frequencies were determined: 27% of examinees had a normal genotype 5G/5G, 68% are heterozygotes and 5% are mutated homozygotes 4G/4G. In the control group, frequencies of 4G/5G polymorphisms of PAI-1 gene were: 42.6% of examinees have 5G/5G genotype, 55.4% are heterozygotes 4G/5G and 2% are 4G/4G genotype. Obtained results support the hypothesis that PAI-1 in interaction with other genetic and external risk factors probably induces the development of venous thromboembolism.
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