Garvey W T, Olefsky J M, Rubenstein A H, Kolterman O G
Department of Medicine, University of California, San Diego, La Jolla 92093.
Diabetes. 1988 May;37(5):590-9. doi: 10.2337/diab.37.5.590.
To determine whether non-insulin-dependent diabetes mellitus (NIDDM) is characterized by day-long hypoinsulinemia, we measured 24-h serum profiles for glucose, insulin, and C-peptide by use of a constant-rate blood-withdrawal technique in diabetic and control subjects fed isocaloric meals. When only lean subjects were considered, diabetic subjects (relative body weight 0.99 +/- 0.3) and control subjects (relative body weight 0.95 +/- 0.03) had similar 24-h integrated serum insulin concentrations (13.4 +/- 2.5 vs. 16.1 +/- 2.0 microU/ml, P NS) due to the offsetting effects of increased basal levels and decreased postprandial responses in NIDDM. In contrast, both basal and meal-stimulated insulin levels were decreased in obese NIDDM subjects (relative body weight 1.39 +/- 0.07) compared with obese control subjects (relative body weight 1.60 +/- 0.08), resulting in a 61% reduction in the 24-h integrated insulin value (18.7 +/- 1.5 vs. 48.4 +/- 13.7 microU/ml). Thus, the capacity to increase 24-h integrated serum insulin as a function of relative body weight was impaired in NIDDM subjects (r = 0.27, P NS) compared with control subjects (r = .70, P less than .01). In contrast, 24-h integrated C-peptide was decreased (P less than .01) in both lean (0.92 +/- 0.13 pM/ml) and obese (1.52 +/- 0.19 pM/ml) NIDDM patients compared with the respective control groups (1.50 +/- 0.13 and 3.03 +/- 0.44 pM/ml). The molar ratio of 24-h integrated C-peptide to insulin was diminished in lean but not obese NIDDM compared with control subjects. A 3-wk period of intensive insulin therapy led to normalization of the mean 24-h integrated insulin (but not integrated serum C-peptide) value in NIDDM compared with a control group that had an identical mean relative body weight. The 24-h urinary C-peptide measured on the same day as the serum profile was correlated (P less than .01) with both the 24-h integrated serum insulin (r = .69) and C-peptide (r = .67) concentrations in control subjects but not in NIDDM subjects (r = .20 and .04, respectively, P NS). Additionally, the urinary clearance of C-peptide was increased in NIDDM (38.1 +/- 7.8 vs. 20.4 +/- 1.7 ml/min in control subjects, P less than .05) and varied with treatment status (26.0 +/- 4.6 ml/min after insulin therapy).(ABSTRACT TRUNCATED AT 400 WORDS)
为了确定非胰岛素依赖型糖尿病(NIDDM)是否具有全天低胰岛素血症的特征,我们通过恒速采血技术,测量了摄入等热量餐食的糖尿病患者和对照受试者的24小时血清葡萄糖、胰岛素和C肽水平。仅考虑体型偏瘦的受试者时,糖尿病患者(相对体重0.99±0.3)和对照受试者(相对体重0.95±0.03)的24小时血清胰岛素综合浓度相似(分别为13.4±2.5和16.1±2.0微单位/毫升,P无显著差异),这是由于NIDDM患者基础水平升高和餐后反应降低的抵消作用。相比之下,肥胖的NIDDM患者(相对体重1.39±0.07)与肥胖对照受试者(相对体重1.60±0.08)相比,基础和餐食刺激后的胰岛素水平均降低,导致24小时胰岛素综合值降低61%(分别为18.7±1.5和48.4±13.7微单位/毫升)。因此,与对照受试者(r = 0.70,P<0.01)相比,NIDDM患者根据相对体重增加24小时血清胰岛素综合水平的能力受损(r = 0.27,P无显著差异)。相比之下,与各自的对照组(分别为1.50±0.13和3.03±0.44皮摩尔/毫升)相比,体型偏瘦(0.92±0.13皮摩尔/毫升)和肥胖(1.52±0.19皮摩尔/毫升)的NIDDM患者24小时C肽综合水平均降低(P<0.01)。与对照受试者相比,体型偏瘦的NIDDM患者24小时C肽与胰岛素的摩尔比降低,但肥胖的NIDDM患者未降低。与平均相对体重相同的对照组相比,为期3周的强化胰岛素治疗使NIDDM患者的平均24小时胰岛素综合值(但不是血清C肽综合值)恢复正常。与血清水平同日测量的24小时尿C肽与对照受试者的24小时血清胰岛素(r = 0.69)和C肽(r = 0.67)浓度均相关(P<0.01),但与NIDDM患者不相关(分别为r = 0.20和0.04,P无显著差异)。此外,NIDDM患者C肽的尿清除率增加(对照受试者为20.4±1.7毫升/分钟,NIDDM患者为38.1±7.8毫升/分钟,P<0.05),且随治疗状态而变化(胰岛素治疗后为26.0±4.6毫升/分钟)。(摘要截选至400字)