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禁食和脱水在糖尿病酮症酸中毒发病机制中的不同作用。

Differential effects of fasting and dehydration in the pathogenesis of diabetic ketoacidosis.

作者信息

Burge M R, Garcia N, Qualls C R, Schade D S

机构信息

Department of Medicine, University of New Mexico School of Medicine, Albuquerque 87131, USA.

出版信息

Metabolism. 2001 Feb;50(2):171-7. doi: 10.1053/meta.2001.20194.

Abstract

Glycemia varies widely in patients with diabetic ketoacidosis (DKA), with plasma glucose concentrations between 10 to 50 mmol/L commonly encountered. The mechanism of this glycemic variability is uncertain. Our study examined the differential effects of fasting and dehydration on hyperglycemia induced by withdrawal of insulin in type 1 diabetes. To evaluate the respective roles of dehydration and fasting in the pathogenesis of DKA, 25 subjects with type 1 diabetes were studied during 5 hours of insulin withdrawal before (control) and after either 32 hours of fasting (n = 10) or dehydration of 4.1% +/- 2.0% of baseline body weight (n = 15). Samples were obtained every 30 minutes during insulin withdrawal for substrate and counterregulatory hormone levels and rates of glucose production and disposal. Fasting resulted in reduced plasma glucose concentrations compared with the control study, while dehydration resulted in increased plasma glucose concentrations compared with the control study (P < .001). Glucose production and disposal were decreased during the fasting study and increased during the dehydration study compared with the control study. Glucagon concentrations and rates of development of ketosis and metabolic acidosis were increased during both fasting and dehydration compared with control. These data suggest that fasting and dehydration have differential effects on glycemia during insulin deficiency, with dehydration favoring the development of hyperglycemia and fasting resulting in reduced glucose concentrations. This finding is probably attributable to the differing effect of these conditions on endogenous glucose production, as well as to differences in substrate availability and counterregulatory hormone concentrations. The severity of pre-existing fasting and dehydration likely explains much of the variability in plasma glucose concentrations observed in DKA.

摘要

糖尿病酮症酸中毒(DKA)患者的血糖水平差异很大,血浆葡萄糖浓度通常在10至50 mmol/L之间。这种血糖变异性的机制尚不清楚。我们的研究探讨了禁食和脱水对1型糖尿病患者胰岛素撤药诱导的高血糖的不同影响。为了评估脱水和禁食在DKA发病机制中的各自作用,对25名1型糖尿病患者在胰岛素撤药前(对照)以及禁食32小时(n = 10)或脱水至基线体重的4.1%±2.0%(n = 15)后5小时进行了研究。在胰岛素撤药期间,每30分钟采集一次样本,检测底物和对抗调节激素水平以及葡萄糖生成和处置速率。与对照研究相比,禁食导致血浆葡萄糖浓度降低,而脱水导致血浆葡萄糖浓度升高(P <.001)。与对照研究相比,禁食研究期间葡萄糖生成和处置减少,脱水研究期间增加。与对照相比,禁食和脱水期间胰高血糖素浓度以及酮症和代谢性酸中毒的发展速率均增加。这些数据表明,禁食和脱水在胰岛素缺乏期间对血糖有不同影响,脱水有利于高血糖的发展,而禁食导致葡萄糖浓度降低。这一发现可能归因于这些情况对内源性葡萄糖生成的不同影响,以及底物可用性和对抗调节激素浓度的差异。既往禁食和脱水的严重程度可能解释了DKA患者血浆葡萄糖浓度观察到的大部分变异性。

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