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持续皮下胰岛素输注后1型糖尿病患者胰岛素敏感性得到改善。

Improved insulin sensitivity in patients with type I diabetes mellitus after CSII.

作者信息

Simonson D C, Tamborlane W V, Sherwin R S, Smith J D, DeFronzo R A

出版信息

Diabetes. 1985 Aug;34 Suppl 3:80-6. doi: 10.2337/diab.34.3.s80.

Abstract

Tissue sensitivity to insulin was studied using the euglycemic insulin clamp technique (delta plasma insulin above basal 90 microU/ml) in eight patients with type I diabetes mellitus (IDDM) before and after 4-8 mo of continuous subcutaneous insulin infusion (CSII) and in 36 age-matched control subjects. Institution of CSII was associated with significant improvements in glycosylated hemoglobin (HbA1) (11.2 +/- 0.6% versus 8.1 +/- 0.4%; P less than 0.001) and mean 24-h plasma glucose concentrations (239 +/- 23 mg/dl versus 106 +/- 18 mg/dl; P less than 0.001). Insulin-mediated glucose metabolism in the diabetic patients pre-CSII (3.92 +/- 0.36 mg/kg X min) was reduced by 44% compared with controls (7.03 +/- 0.22 mg/kg X min; P less than 0.001). After 4-8 mo of improved glycemic control, improved tissue sensitivity to insulin was observed (5.33 +/- 0.75 mg/kg X min; P less than 0.05 versus pre-CSII). However, insulin-mediated glucose utilization still remained significantly below control values (P less than 0.01). During hyperinsulinemia, hepatic glucose production (3-3H-glucose) was suppressed by over 90% in diabetic patients (pre- and post-CSII) and in control subjects. We conclude that near-normalization of glucose metabolism with CSII partially corrects, but does not restore to normal, insulin-stimulated glucose uptake in IDDM. Our failure to totally reverse the impaired response of peripheral tissues to insulin in IDDM patients may be attributed to inadequate metabolic correction, the peripheral route of insulin administration, or a primary defect in glucose metabolism.

摘要

采用正常血糖胰岛素钳夹技术(基础血浆胰岛素水平以上增加90微单位/毫升),对8例1型糖尿病(IDDM)患者在持续皮下胰岛素输注(CSII)4 - 8个月前后以及36例年龄匹配的对照者进行了组织对胰岛素敏感性的研究。实施CSII与糖化血红蛋白(HbA1)显著改善相关(从11.2±0.6%降至8.1±0.4%;P<0.001),24小时平均血浆葡萄糖浓度也显著改善(从239±23毫克/分升降至106±18毫克/分升;P<0.001)。糖尿病患者在CSII前胰岛素介导的葡萄糖代谢(3.92±0.36毫克/千克·分钟)与对照者相比降低了44%(对照者为7.03±0.22毫克/千克·分钟;P<0.001)。在血糖控制改善4 - 8个月后,观察到组织对胰岛素的敏感性有所改善(5.33±0.75毫克/千克·分钟;与CSII前相比P<0.05)。然而,胰岛素介导的葡萄糖利用仍显著低于对照值(P<0.01)。在高胰岛素血症期间,糖尿病患者(CSII前后)和对照者的肝脏葡萄糖生成(3 - 3H - 葡萄糖)均被抑制超过90%。我们得出结论,CSII使葡萄糖代谢接近正常化可部分纠正,但不能恢复至正常,IDDM患者中胰岛素刺激的葡萄糖摄取。我们未能完全逆转IDDM患者外周组织对胰岛素反应受损的情况,可能归因于代谢纠正不足、胰岛素的外周给药途径或葡萄糖代谢的原发性缺陷。

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