Fernández-Real J M, Vendrell J, Ricart W, Broch M, Gutiérrez C, Casamitjana R, Oriola J, Richart C
Diabetes Unit, Endocrinology and Nutrition, University Hospital of Girona Dr. Josep Trueta, Barcelona, Spain.
Diabetes Care. 2000 Jun;23(6):831-7. doi: 10.2337/diacare.23.6.831.
Mice lacking the tumor necrosis factor-alpha receptor 2 (TNFR2) gene fed a high-fat diet gain less weight and display reduced leptin and insulin levels. In humans, plasma levels of the soluble fraction of TNFR2 (sTNFR2) circulate in proportion to the degree of insulin resistance. The purpose of this study was to evaluate a polymorphism in the 3' untranslated region of the TNFR2 gene on chromosome 1 in relation to BMI, leptin levels, and insulin resistance.
Using single-strand conformation polymorphism, the polymorphism was analyzed in 107 nondiabetic subjects (60 women, 47 men) and in 110 consecutive patients with type 2 diabetes (79 women, 31 men). In a subset of 33 healthy subjects, insulin sensitivity (minimal model analysis) was also evaluated.
Four alleles of the TNFR2 gene were identified (A1, A2, A3, and A4). BMI and serum leptin levels were significantly increased in young carriers of the A2 allele. Plasma sTNFR2 levels were similar among the different TNFR2 gene variants. However, in subjects who did not carry the A2 allele, in young subjects, and in women, plasma sTNFR2 levels were proportional to BMI and leptin levels. In the study sample, carriers of the A2 allele (n = 18) showed significantly increased BMI, fat mass, waist-to-hip ratio, serum total and VLDL triglyceride levels, and leptin levels and had a lower insulin sensitivity index than noncarriers of the A2 variant (n = 15). The frequency of the different alleles among diabetic subjects was similar to that in the control population. However, diet-treated diabetic subjects (n = 49) who were carriers of the A2 allele exhibited significantly higher BMI and leptin levels than diet-treated noncarriers of the A2 allele.
The presence of the A2 allele in the TNFR2 gene may predispose subjects to obesity and higher leptin levels, which may in turn predispose them to insulin resistance or vice versa. The TNFR2 gene may be involved in weight-control mechanisms.
喂食高脂饮食的缺乏肿瘤坏死因子-α受体2(TNFR2)基因的小鼠体重增加较少,且瘦素和胰岛素水平降低。在人类中,TNFR2可溶性部分(sTNFR2)的血浆水平与胰岛素抵抗程度成比例循环。本研究的目的是评估1号染色体上TNFR2基因3'非翻译区的一个多态性与体重指数(BMI)、瘦素水平和胰岛素抵抗的关系。
采用单链构象多态性分析,对107名非糖尿病受试者(60名女性,47名男性)和110名连续的2型糖尿病患者(79名女性,31名男性)进行该多态性分析。在33名健康受试者的一个亚组中,还评估了胰岛素敏感性(最小模型分析)。
鉴定出TNFR2基因的四个等位基因(A1、A2、A3和A4)。A2等位基因的年轻携带者的BMI和血清瘦素水平显著升高。不同TNFR2基因变体之间的血浆sTNFR2水平相似。然而,在未携带A2等位基因的受试者、年轻受试者和女性中,血浆sTNFR2水平与BMI和瘦素水平成比例。在研究样本中,A2等位基因携带者(n = 18)的BMI、脂肪量、腰臀比、血清总甘油三酯和极低密度脂蛋白甘油三酯水平以及瘦素水平显著升高,且胰岛素敏感性指数低于A2变体非携带者(n = 15)。糖尿病受试者中不同等位基因的频率与对照人群相似。然而,接受饮食治疗的A2等位基因携带者糖尿病受试者(n = 49)的BMI和瘦素水平显著高于接受饮食治疗的A2等位基因非携带者。
TNFR2基因中A2等位基因的存在可能使受试者易患肥胖症和更高的瘦素水平,这反过来可能使他们易患胰岛素抵抗,反之亦然。TNFR2基因可能参与体重控制机制。