Banerji M A, Chaiken R L, Lebovitz H E
Department of Medicine, State University of New York Health Science Center, Brooklyn.
Diabetes. 1995 Apr;44(4):466-70. doi: 10.2337/diab.44.4.466.
Microvascular and neuropathic complications of diabetes mellitus can be significantly decreased by long-term, near-normoglycemic regulation in patients with insulin-dependent diabetes mellitus. Prevention or delay of onset of hyperglycemia in non-insulin-dependent diabetes mellitus (NIDDM) patients should reduce morbidity and mortality from these complications. NIDDM can be nearly normoglycemic when diagnosed by screening before its symptomatic stage or when clinically hyperglycemic NIDDM goes into remission. One potential strategy to delay the onset of hyperglycemia in individuals at high risk is chronic low-dose sulfonylurea therapy. Thirty black NIDDM subjects who recently had developed near-normoglycemia were followed with no treatment or were randomly assigned to a 3-year, double-blind glipizide or placebo treatment. Baseline and follow-up parameters included fasting plasma glucose (FPG), HbA1c, plasma insulin, and glucose responses to an oral glucose tolerance test and insulin action, as determined by the euglycemic insulin clamp. Baseline FPG and HbA1c for all three groups were 107 mg/dl and 4.7%, respectively. Relapse to hyperglycemia was defined as an FPG level > or = 140 mg/dl on several consecutive visits or an FPG level > or = 140 mg/dl and symptoms of hyperglycemia. During the course of the treatment and follow-up, hyperglycemia occurred in 6 of 10 subjects in the no treatment group, 6 of 10 in the placebo group, and 2 of 10 in the glipizide treatment group. Prolongation of near-normoglycemia was significantly (P < 0.05) increased by low-dose (2.5 mg/day) glipizide compared with placebo treatment.(ABSTRACT TRUNCATED AT 250 WORDS)
在胰岛素依赖型糖尿病患者中,长期接近正常血糖水平的调控可显著降低糖尿病的微血管和神经病变并发症。在非胰岛素依赖型糖尿病(NIDDM)患者中预防或延迟高血糖的发生应能降低这些并发症导致的发病率和死亡率。当在症状出现前通过筛查诊断NIDDM,或临床高血糖的NIDDM进入缓解期时,血糖可接近正常。对于高危个体,延缓高血糖发生的一个潜在策略是慢性低剂量磺脲类药物治疗。30名近期血糖接近正常的黑人NIDDM受试者,一部分未接受治疗进行随访,另一部分被随机分配接受为期3年的双盲格列吡嗪或安慰剂治疗。基线和随访参数包括空腹血糖(FPG)、糖化血红蛋白(HbA1c)、血浆胰岛素,以及口服葡萄糖耐量试验的血糖反应和胰岛素作用(通过正常血糖胰岛素钳夹法测定)。三组的基线FPG和HbA1c分别为107mg/dl和4.7%。血糖复发定义为连续几次就诊时FPG水平≥140mg/dl,或FPG水平≥140mg/dl且伴有高血糖症状。在治疗和随访过程中,未治疗组10名受试者中有6名出现高血糖,安慰剂组10名中有6名,格列吡嗪治疗组10名中有2名。与安慰剂治疗相比,低剂量(2.5mg/天)格列吡嗪显著(P<0.05)延长了接近正常血糖的时间。(摘要截选至250词)