Zhu Haidong, Wang Xiaoling, Lu Yanhui, Poola Joseph, Momin Zamena, Harshfield Gregory A, Snieder Harold, Dong Yanbin
Georgia Prevention Institute, Department of Pediatrics, Medical College of Georgia, 1120 15th Street, HS-1640, Augusta, GA 30912-3715, USA.
Curr Hypertens Rep. 2006 Apr;8(1):23-9. doi: 10.1007/s11906-006-0037-4.
The classic candidate gene approach continues to be the most prevalent tool in the search for the genetic basis of essential hypertension. With the list of candidate genes for this disorder steadily increasing, the pertussis toxin-sensitive inhibitory G protein (Gi) protein beta3 subunit (GNB3) gene has remained "sizzling," challenging the domination of the renin-angiotensin system. Is the genetic variability of GNB3 a causative factor underlying the pathogenesis of essential hypertension? Is the "functional" polymorphism, C825T, only "another" of the countless single nucleotide polymorphisms (SNP) for this disorder after all? As such, does its presence merely reinforce our confidence that essential hypertension is indeed polygenic? Should the C825T polymorphism be used in clinical practice and individualized antihypertensive treatment? Currently, there are still more questions than answers. In this review, in conjunction with our own research, we bring readers up to date on the latest developments of GNB3 polymorphisms in the field of hypertension.
经典的候选基因方法仍然是寻找原发性高血压遗传基础时最常用的工具。随着该疾病候选基因列表的不断增加,百日咳毒素敏感的抑制性G蛋白(Gi)蛋白β3亚基(GNB3)基因一直备受关注,对肾素-血管紧张素系统的主导地位构成挑战。GNB3的基因变异性是原发性高血压发病机制的潜在致病因素吗?“功能性”多态性C825T究竟只是该疾病无数单核苷酸多态性(SNP)中的“另一个”吗?如此一来,它的存在是否仅仅增强了我们对原发性高血压确实是多基因疾病的信心?C825T多态性是否应用于临床实践和个体化降压治疗?目前,问题仍然多于答案。在这篇综述中,结合我们自己的研究,我们向读者介绍高血压领域中GNB3多态性的最新进展。