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首页> 外文期刊>Cellular Physiology and Biochemistry >Genetic Variations of Oxidative Stress Related Genes ALOX5, ALOX5AP and MPO Modulate Ischemic Stroke Susceptibility Through Main Effects and Epistatic Interactions in a Chinese Population
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Genetic Variations of Oxidative Stress Related Genes ALOX5, ALOX5AP and MPO Modulate Ischemic Stroke Susceptibility Through Main Effects and Epistatic Interactions in a Chinese Population

机译:氧化应激相关基因ALOX5,ALOX5AP和MPO的遗传变异通过主要效应和上位性相互作用调节缺血性中风的易感性

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>Background/Aims: To investigate the roles of the oxidative stress related-genes ALOX5, ALOX5AP and MPO in ischemic stroke susceptibility in the Han Chinese population. Methods: A total of 351 ischemic stroke patients and 417 controls were recruited. The ALOX5 rs10900213, ALOX5AP rs4293222 and MPO rs2107545 gene polymorphisms were genotyped. Results: We identified that rs2107545 of MPO gene was significantly associated with ischemic stroke susceptibility after adjusting for covariates. Furthermore, we also considered the likely complexity of oxidative stress and inflammatory process in stroke by assessing the combined effects of multiple genes. Generalized multifactor dimensionality reduction (GMDR) analysis revealed that the combination of ALOX5 rs10900213, ALOX5AP rs4293222 and MPO rs2107545 was significantly associated with increased risk of ischemic stroke (P=0.0040, OR (95% CI) =1.991 (1.241 to 3.195)). Additionally, the MPO rs2107545 genotype was significantly associated with clinical outcomes at 6 months after discharge from the hospital. Conclusion: Our study revealed that epistatic interaction among the ALOX5, ALOX5AP and MPO genes played a significant role in vulnerability to ischemic stroke. Furthermore, these results also suggest that the rs2107545 of MPO gene can be used as a biomarker for the susceptibility and prognosis of ischemic stroke patients.
机译:> 背景/目标 :研究氧化应激相关基因 ALOX5,ALOX5AP 和 MPO 在汉族人群中缺血性中风的易感性。 方法: 总共招募了351名缺血性中风患者和417名对照。对 ALOX5 rs10900213, ALOX5AP rs4293222和 MPO rs2107545基因多态性进行基因分型。 结果: 我们发现,校正协变量后, MPO 基因的rs2107545与缺血性卒中易感性显着相关。此外,我们还通过评估多个基因的综合作用,考虑了中风氧化应激和炎症过程的可能复杂性。广义多维度降维(GMDR)分析显示, ALOX5 rs10900213, ALOX5AP rs4293222和 MPO rs2107545的组合与缺血风险增加显着相关( P = 0.0040,或(95%CI)= 1.991(1.241至3.195))。此外, MPO rs2107545基因型与出院后6个月的临床结果显着相关。 结论: 我们的研究表明 ALOX5,ALOX5AP 和 MPO 基因之间的上位相互作用在脆弱性中起着重要作用缺血性中风。此外,这些结果还表明, MPO 基因的rs2107545可用作缺血性中风患者易感性和预后的生物标志物。

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