激素治疗对肾移植后胰岛素依赖糖尿病患者胰岛素敏感性的影响

Agneta V. Ekstrand
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引用次数: 14

摘要

关于胰岛素依赖型糖尿病(IDDM)患者肾移植后接受免疫抑制的葡萄糖和能量代谢的信息很少。因此,我们测量了(a) 8例肾移植后接受类固醇治疗的IDDM患者、(b) 10例无肾病的IDDM患者、(c) 10例肾移植后非糖尿病患者和(d) 10例健康对照者的胰岛素敏感性(正糖胰岛素夹夹联合间接量热法和输注氚化葡萄糖)。与非糖尿病肾移植受体和健康对照(2.8±0.2和2.7±0.1 mg/kg LBM·min)相比,类固醇治疗的IDDM移植患者(4.8±0.6 mg/kg瘦体重(LBM)·min)和无并发症的IDDM患者(3.8±0.2 mg/kg LBM·min)的肝糖生成均有所增加;p & lt;0.01)。与健康对照组相比,胰岛素刺激的葡萄糖处置在移植和非移植IDDM患者和非糖尿病移植患者中减少(6.6±0.8、5.7±0.7和7.5±0.6 vs 9.3±0.6 mg/kg LBM·min);p & lt;0.05)。这种减少主要是由于非氧化糖代谢的损害,即糖原合成(3.1±0.6、2.7±0.4和3.3±0.5 vs 5.0±0.5 mg/kg LBM·min);p & lt;与健康对照组相比,0.05)。结论:无肾病的IDDM患者表现为肝脏和外周胰岛素抵抗。在IDDM患者中,皮质类固醇治疗引起的胰岛素抵抗的进一步增加可以通过增加胰岛素剂量来纠正。然而,非糖尿病类固醇治疗的肾移植受者表现出与IDDM患者相当的胰岛素抵抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of steroid-therapy on insulin sensitivity in insulin-dependent diabetic patients after kidney transplantation

Little information is available on glucose and energy metabolism in insulin-dependent diabetes mellitus (IDDM) patients receiving immunosuppression after kidney transplantation. We therefore measured insulin sensitivity (euglycemic insulin clamp in combination with indirect calorimetry and infusion of tritiated glucose) in (a) eight steroid-treated IDDM patients after kidney transplantation, (b) ten IDDM patients without nephropathy, (c) ten nondiabetic patients after kidney transplantation, and (d) ten healthy control subjects. Hepatic glucose production was enhanced in both steroid-treated transplanted IDDM patients [4.8 ± 0.6 mg/kg lean body mass (LBM)·min] and IDDM patients without complications (3.8 ± 0.2 mg/kg LBM·min) compared with nondiabetic renal graft recipients and with healthy controls (2.8 ± 0.2 and 2.7 ± 0.1 mg/kg LBM·min; p < 0.01). Insulin-stimulated glucose disposal was reduced in transplanted and non-transplanted IDDM patients and nondiabetic transplanted patients versus healthy controls (6.6 ± 0.8, 5.7 ± 0.7, and 7.5 ± 0.6 versus 9.3 ± 0.6 mg/kg LBM·min; p < 0.05). This reduction was mainly due to an impairment in nonoxidative glucose metabolism, i.e., glycogen synthesis (3.1 ± 0.6, 2.7 ± 0.4, and 3.3 ± 0.5 versus 5.0 ± 0.5 mg/kg LBM·min; p < 0.05 versus healthy controls). It is concluded that IDDM patients without nephropathy show both hepatic and peripheral insulin resistance. In IDDM patients a further increase of insulin resistance caused by treatment with corticosteroids can be corrected by increased insulin doses. However, nondiabetic steroid-treated renal graft recipients show insulin resistance comparable to IDDM patients.

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