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2型(非胰岛素依赖型)糖尿病患者口服降糖药继发失效后,联合使用胰岛素和磺脲类药物治疗后胰岛素分泌及作用的部分恢复。

Partial recovery of insulin secretion and action after combined insulin-sulfonylurea treatment in type 2 (non-insulin-dependent) diabetic patients with secondary failure to oral agents.

作者信息

Del Prato S, Vigili de Kreutzenberg S, Riccio A, Maifreni L, Duner E, Lisato G, Iavicoli M, Tiengo A

机构信息

Cattedra di Malattie del Ricambio, University of Padova, Italy.

出版信息

Diabetologia. 1990 Nov;33(11):688-95. doi: 10.1007/BF00400571.

Abstract

Metabolic control, insulin secretion and insulin action were evaluated in seven Type 2 (non-insulin-dependent) diabetic patients with secondary failure to oral antidiabetic agents before and after two months of combined therapy with supper-time insulin (Ultratard: 0.4 U/kg body weight/day) plus premeal glibenclamide (15 mg/day). Metabolic control was assessed by 24 h plasma glucose, NEFA, and substrate (lactate, alanine, glycerol, ketone bodies) profile. Insulin secretion was evaluated by glucagon stimulation of C-peptide secretion, hyperglycaemic clamp (+ 7 mmol/l) and 24 h free-insulin and C-peptide profiles. The repeat studies, after two months of combined therapy, were performed at least 72 h after supper-time insulin withdrawal. Combining insulin and sulfonylurea agents resulted in a reduction in fasting plasma glucose (12.9 +/- 7 vs 10.4 +/- 1.2 mmol/l; p less than 0.05) and hepatic glucose production (13.9 +/- 1.1 vs 11.1 +/- 1.1 mumol.kg-1.min-1; p less than 0.05). Mean 24 h plasma glucose was also lower (13.7 +/- 1.2 vs 11.1 +/- 1.4 mmol/l; p less than 0.05). Decrements in fasting plasma glucose and mean 24 h profile were correlated (r = 0.90; p less than 0.01). HbA1c also improved (11.8 +/- 0.8 vs 8.9 +/- 0.5%; p less than 0.05). Twenty-four hour profile for NEFA, glycerol, and ketone bodies was lower after treatment, while no difference occurred in the blood lactate and alanine profile. Insulin secretion in response to glucagon (C-peptide = +0.53 +/- 0.07 vs +0.43 +/- 0.07 pmol/ml) and hyperglycaemia (freeinsulin = 13.1 +/- 2.0 vs 12.3 +/- 2.2 mU/l) did not change.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对7例2型(非胰岛素依赖型)糖尿病患者进行了评估,这些患者口服抗糖尿病药物继发失效,在接受晚餐时胰岛素(优泌林NPH:0.4U/千克体重/天)加餐前格列本脲(15毫克/天)联合治疗两个月前后,评估了代谢控制、胰岛素分泌和胰岛素作用。通过24小时血浆葡萄糖、非酯化脂肪酸(NEFA)和底物(乳酸、丙氨酸、甘油、酮体)谱评估代谢控制。通过胰高血糖素刺激C肽分泌、高血糖钳夹(+7毫摩尔/升)以及24小时游离胰岛素和C肽谱评估胰岛素分泌。在联合治疗两个月后进行的重复研究,在晚餐时停用胰岛素至少72小时后进行。联合使用胰岛素和磺脲类药物导致空腹血糖降低(12.9±7对10.4±1.2毫摩尔/升;P<0.05)以及肝脏葡萄糖生成减少(13.9±1.1对11.1±1.1微摩尔·千克-1·分钟-1;P<0.05)。24小时平均血浆葡萄糖也较低(13.7±1.2对11.1±1.4毫摩尔/升;P<0.05)。空腹血糖降低和24小时平均谱降低具有相关性(r=0.90;P<0.01)。糖化血红蛋白(HbA1c)也有所改善(11.8±0.8对8.9±0.5%;P<0.05)。治疗后NEFA、甘油和酮体的24小时谱降低,而血乳酸和丙氨酸谱无差异。对胰高血糖素的胰岛素分泌反应(C肽=+0.53±0.07对+0.43±0.07皮摩尔/毫升)和对高血糖的反应(游离胰岛素=13.1±2.0对12.3±2.2毫单位/升)未发生变化。(摘要截短于250字)

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