Kelly C M, Fantus I G
Department of Medicine, Royal Victoria Hospital, McGill University, Montreal, Quebec, Canada.
Metabolism. 1995 Apr;44(4):506-12. doi: 10.1016/0026-0495(95)90059-4.
Insulin binding has been reported to be decreased in non-insulin-dependent diabetes mellitus (NIDDM). Although elevated basal insulin concentrations have been correlated with decreased insulin binding in obesity, this relationship has not been found in NIDDM. To determine the potential cause(s) of the decrease, we measured 125I-insulin binding to circulating monocytes isolated from 31 non-insulin-treated patients with NIDDM who had a fasting plasma glucose (FPG) concentration greater than 7.8 mmol/L and 13 control subjects. We examined the influence of obesity, insulin concentration, glycemic control, and treatment with oral hypoglycemic agents on insulin binding in a cross-sectional study. Insulin binding was significantly decreased in the entire NIDDM group (mean +/- SEM, %/10(7) monocytes: 4.65 +/- 0.33) as compared with controls (6.45 +/- .70, P < .02). Subgroups defined by obesity (relative body weight > 1.2) and poor glycemic control (FPG > 11.1 mmol/L) and those not taking oral hypoglycemic agents had significantly lower insulin binding (P < .02). However, neither relative body weight nor insulin concentrations (basal or stimulated) correlated with insulin binding. Stepwise linear regression analysis showed that only FPG significantly correlated with insulin binding (r = -.45, P = .002) even when oral hypoglycemic agent-treated patients were removed from the analysis (r = -.50, P = .003). There was no significant contribution to explain insulin binding by the other variables, including diagnosis of diabetes, obesity, insulin concentration, or treatment with oral hypoglycemic agents. We conclude that poor metabolic control is associated with an alteration in insulin receptor regulation in NIDDM.
据报道,非胰岛素依赖型糖尿病(NIDDM)患者的胰岛素结合能力下降。虽然在肥胖症中基础胰岛素浓度升高与胰岛素结合能力下降相关,但在NIDDM中未发现这种关系。为了确定这种下降的潜在原因,我们测量了从31名空腹血糖(FPG)浓度大于7.8 mmol/L的未接受胰岛素治疗的NIDDM患者和13名对照受试者中分离出的循环单核细胞与125I-胰岛素的结合情况。我们在一项横断面研究中检查了肥胖、胰岛素浓度、血糖控制和口服降糖药治疗对胰岛素结合的影响。与对照组(6.45±0.70)相比,整个NIDDM组的胰岛素结合能力显著下降(平均值±标准误,%/10(7)单核细胞:4.65±0.33,P<0.02)。由肥胖(相对体重>1.2)、血糖控制不佳(FPG>11.1 mmol/L)定义的亚组以及未服用口服降糖药的亚组胰岛素结合能力显著降低(P<0.02)。然而,相对体重和胰岛素浓度(基础或刺激后)均与胰岛素结合无关。逐步线性回归分析表明,即使将接受口服降糖药治疗的患者排除在分析之外,只有FPG与胰岛素结合显著相关(r = -0.45,P = 0.002)(r = -0.50,P = 0.003)。包括糖尿病诊断、肥胖、胰岛素浓度或口服降糖药治疗在内的其他变量对解释胰岛素结合没有显著贡献。我们得出结论,代谢控制不佳与NIDDM患者胰岛素受体调节改变有关。