Urhammer S A, Hansen T, Borch-Johnsen K, Pedersen O
Steno Diabetes Center and Hagedorn Research Institute, Copenhagen, Denmark.
J Clin Endocrinol Metab. 2000 Sep;85(9):3151-4. doi: 10.1210/jcem.85.9.6790.
This study examined whether the simultaneous presence of the previously identified Trp/Arg64 polymorphism of the beta3-adrenergic receptor (BAR) gene and the -3826 A-->G nucleotide variant of the uncoupling protein-1 (UCP1) gene are associated with obesity, insulin resistance, or alterations in size at birth in a Danish study population comprising 379 unrelated young Caucasian subjects. All study participants underwent an iv glucose tolerance test with addition of tolbutamide after 20 min. In addition, a number of biochemical and anthropometric measures were performed on each subject. The subjects were genotyped for the 2 polymorphisms by applying PCR-restriction fragment length polymorphism. The subjects were divided into 4 groups according to their BAR and UCP1 genotype: wild-type carriers (n = 184), only Trp/Arg64 carriers (n = 29), only A-->G UCP1 carriers (n = 146), and carriers of both genetic variants (n = 20). There were no differences across the genotype groups with respect to body mass index, fat mass, waist to hip ratio, birth weight or length, ponderal index, or weight gain during childhood or adolescence, nor was the combined genotype related to alterations in fasting serum levels of lipids, insulin, or C peptide or the insulin sensitivity index. In conclusion, the present study failed to demonstrate an additive or synergistic effect of the Trp/Arg64 variant of the BAR gene and the -3826 A-->G variant of the UCP1 gene on the development of obesity and insulin resistance among randomly recruited Danish Caucasian subjects.
本研究在一个由379名无亲缘关系的年轻白种人组成的丹麦研究人群中,检验了先前确定的β3 - 肾上腺素能受体(BAR)基因的Trp/Arg64多态性与解偶联蛋白 - 1(UCP1)基因的 - 3826 A→G核苷酸变体同时存在是否与肥胖、胰岛素抵抗或出生时的体型改变有关。所有研究参与者均接受了静脉葡萄糖耐量试验,并在20分钟后加用甲苯磺丁脲。此外,对每个受试者进行了多项生化和人体测量。通过应用聚合酶链反应 - 限制性片段长度多态性对受试者的这两种多态性进行基因分型。根据受试者的BAR和UCP1基因型将其分为4组:野生型携带者(n = 184)、仅Trp/Arg64携带者(n = 29)、仅A→G UCP1携带者(n = 146)以及两种基因变体的携带者(n = 20)。在基因型组之间,关于体重指数、脂肪量、腰臀比、出生体重或身长、体重 ponderal指数或儿童期或青春期体重增加均无差异,并且联合基因型与空腹血清脂质、胰岛素或C肽水平或胰岛素敏感性指数的改变也无关。总之,本研究未能证明BAR基因的Trp/Arg64变体和UCP1基因的 - 3826 A→G变体对随机招募的丹麦白种人受试者肥胖和胰岛素抵抗的发展具有累加或协同作用。