Lewitt M S, Yu V K, Rennie G C, Carter J N, Marel G M, Yue D K, Hooper M J
Department of Endocrinology, Repatriation General Hospital, Sydney, Australia.
Diabetes Care. 1989 Jun;12(6):379-83. doi: 10.2337/diacare.12.6.379.
We conducted a double-blind crossover study to determine which patient characteristics best predict a beneficial response to combined insulin-glyburide therapy. Glyburide (15 mg/day) or placebo was added to the treatment regimen of 31 insulin-treated type II (non-insulin-dependent) diabetic subjects. During glyburide therapy, there was a significant improvement in glycemic control with a reduction in glycosylated hemoglobin from 9.9 +/- 1.3 to 9.1 +/- 1.3% (P less than .001). Patients who responded had higher fasting C-peptide levels (P less than .001) and shorter durations of insulin therapy (P less than .01) than those who did not respond. Glyburide withdrawal was associated with a greater than expected deterioration in glycemic control. Patients on insulin therapy for greater than 8 yr are unlikely to benefit significantly from the addition of glyburide to their treatment regimen.
我们进行了一项双盲交叉研究,以确定哪些患者特征最能预测对胰岛素与格列本脲联合治疗的有益反应。将格列本脲(15毫克/天)或安慰剂添加到31名接受胰岛素治疗的II型(非胰岛素依赖型)糖尿病患者的治疗方案中。在格列本脲治疗期间,血糖控制有显著改善,糖化血红蛋白从9.9±1.3%降至9.1±1.3%(P<0.001)。有反应的患者空腹C肽水平较高(P<0.001),胰岛素治疗时间较短(P<0.01),而无反应的患者则不然。停用格列本脲与血糖控制恶化程度超过预期有关。接受胰岛素治疗超过8年的患者,在治疗方案中添加格列本脲不太可能显著获益。