Banarer Salomon, Cryer Philip E
Division of Endocrinology, Metabolism, and Lipid Research, General Clinical Research Center, Washington University School of Medicine, 660 S. Euclid Avenue, St. Louis, MO 63110, USA.
Diabetes. 2003 May;52(5):1195-203. doi: 10.2337/diabetes.52.5.1195.
Given that iatrogenic hypoglycemia often occurs during the night in people with type 1 diabetes, we tested the hypothesis that physiological, and the resulting behavioral, defenses against developing hypoglycemia-already compromised by absent glucagon and attenuated epinephrine and neurogenic symptom responses-are further compromised during sleep in type 1 diabetes. To do so, we studied eight adult patients with uncomplicated type 1 diabetes and eight matched nondiabetic control subjects with hyperinsulinemic stepped hypoglycemic clamps (glucose steps of approximately 85, 75, 65, 55, and 45 mg/dl) in the morning (0730-1230) while awake and at night (2100-0200) while awake throughout and while asleep from 0000 to 0200 in random sequence. Plasma epinephrine (P = 0.0010), perhaps norepinephrine (P = 0.0838), and pancreatic polypeptide (P = 0.0034) responses to hypoglycemia were reduced during sleep in diabetic subjects (the final awake versus asleep values were 240 +/- 86 and 85 +/- 47, 205 +/- 24 and 148 +/- 17, and 197 +/- 45 and 118 +/- 31 pg/ml, respectively), but not in the control subjects. The diabetic subjects exhibited markedly reduced awakening from sleep during hypoglycemia. Sleep efficiency (percent time asleep) was 77 +/- 18% in the diabetic subjects, but only 26 +/- 8% (P = 0.0109) in the control subjects late in the 45-mg/dl hypoglycemic steps. We conclude that autonomic responses to hypoglycemia are reduced during sleep in type 1 diabetes, and that, probably because of their reduced sympathoadrenal responses, patients with type 1 diabetes are substantially less likely to be awakened by hypoglycemia. Thus both physiological and behavioral defenses are further compromised during sleep. This sleep-related hypoglycemia-associated autonomic failure, in the context of imperfect insulin replacement, likely explains the high frequency of nocturnal hypoglycemia in type 1 diabetes.
鉴于医源性低血糖常在1型糖尿病患者夜间发生,我们检验了如下假设:针对低血糖发生的生理防御以及由此产生的行为防御——已因胰高血糖素缺乏、肾上腺素及神经源性症状反应减弱而受损——在1型糖尿病患者睡眠期间会进一步受损。为此,我们对8例无并发症的成年1型糖尿病患者和8例匹配的非糖尿病对照者进行了研究,采用高胰岛素血症阶梯式低血糖钳夹试验(血糖阶梯约为85、75、65、55和45mg/dl),在上午(0730 - 1230)清醒时、夜间(2100 - 0200)全程清醒时以及0000至0200睡眠期间随机进行。糖尿病患者睡眠期间对低血糖的血浆肾上腺素反应(P = 0.0010)、可能还有去甲肾上腺素反应(P = 0.0838)以及胰多肽反应(P = 0.0034)均降低(最终清醒与睡眠时的值分别为240±86和85±47、205±24和148±17、197±45和118±31pg/ml),但对照者未出现这种情况。糖尿病患者在低血糖期间睡眠中醒来的次数明显减少。在45mg/dl低血糖阶梯后期,糖尿病患者的睡眠效率(睡眠时间百分比)为77±18%,而对照者仅为26±8%(P = 0.0109)。我们得出结论,1型糖尿病患者睡眠期间对低血糖的自主反应降低,而且可能由于其交感肾上腺反应减弱,1型糖尿病患者被低血糖唤醒的可能性大幅降低。因此,生理和行为防御在睡眠期间均进一步受损。在胰岛素替代不完善的情况下,这种与睡眠相关的低血糖相关自主神经功能衰竭可能解释了1型糖尿病患者夜间低血糖的高发生率。