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The role of adenosine-related genes variants in susceptibility to essential hypertension.

机译:腺苷相关基因变异在原发性高血压易感性中的作用。

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OBJECTIVE: To test markers within adenosine-related genes: A1 and A2a receptors (ADORA1, ADORA2a) and adenosine deaminase (ADA) for potential involvement in essential hypertension (EH). DESIGN: Case-control association study investigating gene variants for the ADORA1, ADORA2a and ADA genes. PARTICIPANTS: The study used a cohort of 249 unrelated hypertensive individuals who were diagnosed with hypertension, and an age, sex and ethnically matched group of 249 normotensive controls. RESULTS: The association analysis indicated that both allele and genotype frequencies did not differ significantly between the case and control groups (P > 0.05) for any of the markers tested. CONCLUSION: The adenosine-related gene variants do not appear to alter susceptibility to the disease in this group of essential hypertensives. However, involvement of these genes and the adenosine system cannot be conclusively excluded from essential hypertension pathogenesis as other gene variants may still be involved.
机译:目的:测试腺苷相关基因内的标志物:A1和A2a受体(ADORA1,ADORA2a)和腺苷脱氨酶(ADA)可能参与原发性高血压(EH)。设计:病例对照协会研究,研究ADORA1,ADORA2a和ADA基因的基因变异。参与者:该研究队列使用了249名被诊断患有高血压的无关高血压个体,以及249名正常血压对照人群的年龄,性别和种族。结果:关联分析表明,病例和对照组之间的等位基因频率和基因型频率均无显着差异(P> 0.05)。结论:在这组原发性高血压患者中,腺苷相关基因变异似乎并未改变对该疾病的易感性。然而,不能将这些基因和腺苷系统的参与排除在原发性高血压的发病机制之外,因为其他基因变体仍可能参与。

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