Fujisawa T, Ikegami H, Yamato E, Hamada Y, Kamide K, Rakugi H, Higaki J, Murakami H, Shimamoto K, Ogihara T
Department of Geriatric Medicine, Osaka University Medical School, Japan.
Am J Hypertens. 1997 Jan;10(1):101-5. doi: 10.1016/s0895-7061(96)00297-x.
A putative pathogenic mutation in the beta3-adrenergic receptor gene (Trp64Arg) has been reported to be associated with higher diastolic blood pressure as well as clinical features of the insulin resistance syndrome and an earlier onset of non-insulin-dependent diabetes mellitus (NIDDM) in Pima Indians and Finns. Because essential hypertension is reported to be associated with insulin resistance, we studied the mutation in Japanese patients with essential hypertension to clarify associations of this mutation with hypertension, insulin resistance, and basal adrenergic state in hypertensive subjects. The allele frequency of the mutation (Arg) in patients with essential hypertension was similar to that in control subjects (35 of 202 alleles [17.3%] v 27 of 146 [18.5%], respectively, P > .7). Insulin sensitivity measured by hyperinsulinemic euglycemic glucose clamp and plasma norepinephrine and epinephrine levels were also similar in hypertensive subjects with and without the mutation. These data suggest that Trp64Arg mutation in the beta3-adrenergic receptor gene does not play a major role in susceptibility to essential hypertension or in insulin resistance and basal adrenergic state in hypertension.
据报道,β3-肾上腺素能受体基因中的一个假定致病突变(色氨酸64精氨酸)与舒张压升高、胰岛素抵抗综合征的临床特征以及皮马印第安人和芬兰人非胰岛素依赖型糖尿病(NIDDM)的较早发病有关。由于据报道原发性高血压与胰岛素抵抗有关,我们对日本原发性高血压患者的该突变进行了研究,以阐明该突变与高血压、胰岛素抵抗以及高血压患者基础肾上腺素能状态之间的关联。原发性高血压患者中该突变(精氨酸)的等位基因频率与对照组相似(分别为202个等位基因中的35个[17.3%]和146个中的27个[18.5%],P>.7)。通过高胰岛素正常血糖钳夹测量的胰岛素敏感性以及血浆去甲肾上腺素和肾上腺素水平在有和没有该突变的高血压患者中也相似。这些数据表明,β3-肾上腺素能受体基因中的色氨酸64精氨酸突变在原发性高血压易感性、胰岛素抵抗以及高血压患者基础肾上腺素能状态中不起主要作用。