High D Allele Frequency of ACE I/D Gene Polymorphism in Familial Hypertension in Javanese Indonesian

F. Irijanto, Herjanti Rahajeng, Sutarso Kamajaya, Mochammad Sja’bani, A. Sadewa, Y. Shimizu, Y. Tomino
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引用次数: 1

Abstract

Family studies demonstrated the contribution of genetic factor to the development of essential hypertension. While the familial component of blood pressure(BP) is well described, the risk of hypertension developing as a result of family history has not been well quantified . The heritage portion of blood pressure is estimated to range between 35% and 65% . Genetic polymorphisms are related to hypertension. Genes coded in the components of renin-angiotensin-aldosteron system(RAAS) are crucial in the pathogenesis of essensial hypertension via the blood pressure management. Epidemiological studies have suggested that nucleotide sequence variations of genes such as angiotensinogen(AGT), renin(REN), angiotensin-converting enzyme (ACE), angiotensin II receptor type I(AT─1R) and aldosterone synthase(CYP11B2) are associated with the risk of essensial hypertension . The ACE insertion/deletion(I/D) gene polymorphism and a predisposition to hypertension have been shown in many studies. More than 100 polyOriginal Articles
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爪哇印度尼西亚人家族性高血压ACE I/D基因多态性的高等位基因频率
家庭研究表明遗传因素对原发性高血压的发生有一定的影响。虽然血压(BP)的家族成分被很好地描述,但由于家族史而导致高血压的风险尚未得到很好的量化。血压的遗传部分估计在35%到65%之间。遗传多态性与高血压有关。肾素-血管紧张素-醛固酮系统(RAAS)中编码的基因在高血压的发病机制中起着至关重要的作用。流行病学研究表明,血管紧张素原(AGT)、肾素(REN)、血管紧张素转换酶(ACE)、血管紧张素II受体I型(AT─1R)和醛固酮合成酶(CYP11B2)等基因的核苷酸序列变异与原发性高血压的风险有关。许多研究表明,ACE插入/缺失(I/D)基因多态性与高血压易感性有关。超过100篇多原创文章
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