Masuo Kazuko, Katsuya Tomohiro, Fu Yuxiao, Rakugi Hiromi, Ogihara Toshio, Tuck Michael L
Human Neurotransmitter Laboratory, Baker Heart Research Institute, Melbourne, Victoria, Australia.
Am J Hypertens. 2005 Jul;18(7):1009-14. doi: 10.1016/j.amjhyper.2005.01.006.
The genes responsible for insulin resistance are also candidate genes for insulin resistance-related diseases, such as obesity and hypertension. Functional polymorphisms in the beta2- and beta3-adrenergic receptors have been reported to be associated with diabetes, hypertension, and obesity. To clarify the relevance of the beta-adrenergic receptor polymorphisms to insulin resistance, we studied their association with polymorphisms of beta2 (Arg16Gly, Gln27Glu) and beta3 (Trp64Arg) adrenoceptor genes.
We studied 155 young, nonobese Japanese men using the homeostasis model assessment of insulin resistance (HOMA-IR) to divide individuals into insulin-sensitive and insulin-resistant groups. Insulin resistance in the participants was defined as HOMA-IR equal to or greater than the average plus 1 SD of 3.1. There were 69 men who were insulin resistant and 86 men who were insulin sensitive. Body mass index (BMI), blood pressure (BP), plasma glucose, insulin, leptin, norepinephrine (NE) levels, and the polymorphisms of Arg16Gly and Gln27Glu of the beta2- and Trp64Arg of the beta3-adrenoceptor polymorphisms were measured in all participants.
The insulin-resistant group had higher frequency of the Gly16 allele of Arg16Gly compared with the insulin-sensitive group, whereas the frequencies of genotypes or alleles of Gln27Glu and Trp64Arg were similar. The insulin-resistant group had a higher mean HOMA-IR, fasting insulin, NE, and total fat mass compared with levels in the insulin-sensitive group, but the BMI and leptin levels were similar. The subjects carrying the Gly16 allele of the beta2-adrenoceptor gene had a higher mean HOMA-IR, fasting insulin, NE, body fat mass, and BP than those without the Gly16 allele.
The Gly16 mutation of the beta2-adrenoceptor gene is associated with increased insulin resistance, adiposity, and BP accompanied by higher plasma NE levels early in the metabolic disease in developing obesity. These findings show an important role of beta2-adrenoceptor gene polymorphisms in the association of insulin resistance in hypertension and obesity.
负责胰岛素抵抗的基因也是胰岛素抵抗相关疾病(如肥胖症和高血压)的候选基因。据报道,β2和β3肾上腺素能受体的功能性多态性与糖尿病、高血压和肥胖症有关。为了阐明β肾上腺素能受体多态性与胰岛素抵抗的相关性,我们研究了它们与β2(Arg16Gly、Gln27Glu)和β3(Trp64Arg)肾上腺素能受体基因多态性的关联。
我们使用胰岛素抵抗的稳态模型评估(HOMA-IR)对155名年轻、非肥胖的日本男性进行了研究,以将个体分为胰岛素敏感组和胰岛素抵抗组。参与者的胰岛素抵抗定义为HOMA-IR等于或大于3.1的平均值加1个标准差。其中有69名胰岛素抵抗男性和86名胰岛素敏感男性。对所有参与者测量了体重指数(BMI)、血压(BP)、血浆葡萄糖、胰岛素、瘦素、去甲肾上腺素(NE)水平,以及β2肾上腺素能受体的Arg16Gly的Gly16等位基因和Gln27Glu以及β3肾上腺素能受体的Trp64Arg的多态性。
与胰岛素敏感组相比,胰岛素抵抗组中Arg16Gly的Gly16等位基因频率更高,而Gln27Glu和Trp64Arg的基因型或等位基因频率相似。与胰岛素敏感组相比,胰岛素抵抗组的平均HOMA-IR、空腹胰岛素、NE和总脂肪量更高,但BMI和瘦素水平相似。携带β2肾上腺素能受体基因Gly16等位基因的受试者的平均HOMA-IR、空腹胰岛素、NE、体脂肪量和血压高于不携带Gly16等位基因的受试者。
β2肾上腺素能受体基因的Gly16突变与胰岛素抵抗增加、肥胖和血压升高有关,且在肥胖症发展过程中的代谢疾病早期伴有较高的血浆NE水平。这些发现表明β2肾上腺素能受体基因多态性在高血压和肥胖症中胰岛素抵抗的关联中起重要作用。