Diabetes. 1997 Feb;46(2):271-86.
A total of 1,441 patients with IDDM were randomly assigned to receive either intensive (n = 711) or conventional (n = 730) diabetes therapy in the Diabetes Control and Complications Trial (DCCT). The patients were followed for an average of 6.5 years. Subjects were instructed to report all episodes of suspected severe hypoglycemia to their health care team. In addition, at quarterly follow-up visits, each subject was asked about the occurrence of severe hypoglycemia. There were 3,788 episodes of severe hypoglycemia (requiring assistance); 1,027 of these episodes were associated with coma and/or seizure. A total of 65% percent of patients in the intensive group vs. 35% of patients in the conventional group had at least one episode of severe hypoglycemia by the study end; the overall rates of severe hypoglycemia were 61.2 per 100 patient-years vs. 18.7 per 100 patient-years in the intensive and conventional treatment groups, respectively, with a relative risk (RR) of 3.28. The relative risk for coma and/or seizure was 3.02 for intensive therapy. The increased risk with intensive treatment persisted over each of the 9 years of follow-up in the DCCT and over the calendar years 1984-1993 during which the study was conducted. When baseline patient characteristics were examined for effects on the risk of severe hypoglycemia, the relative risk of hypoglycemia for intensive versus conventional treatment was > or = 2 for all subgroups. Several subgroups defined by baseline characteristics, including males, adolescents, and subjects with no residual C-peptide or with a prior history of hypoglycemia, had a particularly high risk of severe hypoglycemia in both treatment groups. Analyses of the cumulative incidence of successive episodes indicated that intensive treatment was also associated with an increased risk of multiple episodes within the same patient (e.g., 22% experienced five or more episodes of severe hypoglycemia within the first 5 years of follow-up vs. 4% in the conventional group). Within both treatment groups, patients who experienced severe hypoglycemia were at increased risk of subsequent episodes. Approximately 30% of patients in each group experienced a second episode within the 4 months following the first episode of severe hypoglycemia. Within each treatment group, the number of prior episodes of hypoglycemia was the strongest predictor of the risk of future episodes, followed closely by the current HbA1c value. After adjustment for the current quarterly HbA1c level, intensive treatment was still associated with a significantly increased risk of hypoglycemia, indicating that the increased risk with intensive treatment is not completely explained by differences in HbA1c values.
在糖尿病控制与并发症试验(DCCT)中,共有1441例胰岛素依赖型糖尿病(IDDM)患者被随机分配接受强化治疗(n = 711)或常规治疗(n = 730)。患者平均随访6.5年。受试者被要求向其医疗团队报告所有疑似严重低血糖发作情况。此外,在每季度的随访中,会询问每位受试者严重低血糖的发生情况。共发生3788次严重低血糖发作(需要协助);其中1027次发作伴有昏迷和/或癫痫。到研究结束时,强化治疗组65%的患者与常规治疗组35%的患者至少有一次严重低血糖发作;强化治疗组和常规治疗组严重低血糖的总体发生率分别为每100患者年61.2次和18.7次,相对风险(RR)为3.28。强化治疗导致昏迷和/或癫痫的相对风险为3.02。强化治疗增加的风险在DCCT的9年随访期以及1984 - 1993年研究开展的历年中均持续存在。在检查基线患者特征对严重低血糖风险的影响时,强化治疗与常规治疗相比,所有亚组的低血糖相对风险均≥2。一些由基线特征定义的亚组,包括男性、青少年以及无残余C肽或有低血糖既往史的受试者,在两个治疗组中严重低血糖风险都特别高。对连续发作的累积发生率分析表明,强化治疗还与同一患者多次发作的风险增加有关(例如,22%的患者在随访的前5年中经历了5次或更多次严重低血糖发作,而常规治疗组为4%)。在两个治疗组中,经历过严重低血糖的患者后续发作风险增加。每组中约30%的患者在首次严重低血糖发作后的4个月内经历了第二次发作。在每个治疗组中,既往低血糖发作次数是未来发作风险的最强预测因素,其次是当前的糖化血红蛋白(HbA1c)值。在对当前每季度的HbA1c水平进行调整后,强化治疗仍与低血糖风险显著增加相关,这表明强化治疗增加的风险不能完全由HbA1c值的差异来解释。