Higashimori K, Zhao Y, Higaki J, Kamitani A, Katsuya T, Nakura J, Miki T, Mikami H, Ogihara T
Department of Geriatric Medicine, Osaka University Medical School, Japan.
Biochem Biophys Res Commun. 1993 Mar 15;191(2):399-404. doi: 10.1006/bbrc.1993.1231.
An association study of the insertion/deletion (I/D) polymorphism located in intron 16 of the ACE gene with essential hypertension in the Japanese population was performed. The 287 bp I/D polymorphism was detected by polymerase chain reaction. Derived allele frequencies for insertion and deletion were not significantly different between 133 hypertensive and 104 normotensive subjects. A significant relationship between I/D polymorphism and plasma ACE activity was observed in the normotensive group, but not in hypertensives. These results suggest that I/D polymorphism of the gene is not implicated in Japanese hypertensive subjects, and that studies involving various ethnic groups are important.
我们对日本人群中血管紧张素转换酶(ACE)基因第16内含子插入/缺失(I/D)多态性与原发性高血压进行了关联研究。采用聚合酶链反应检测287bp的I/D多态性。在133例高血压患者和104例血压正常者中,插入和缺失的衍生等位基因频率无显著差异。在血压正常组中观察到I/D多态性与血浆ACE活性之间存在显著关系,但在高血压患者中未观察到。这些结果表明,该基因的I/D多态性与日本高血压患者无关,涉及不同种族群体的研究很重要。