Yale J F, Valiquett T R, Ghazzi M N, Owens-Grillo J K, Whitcomb R W, Foyt H L
McGill University Health Centre, 687 Pine Avenue West, Room H685, Montreal, Quebec H3A 1A1, Canada.
Ann Intern Med. 2001 May 1;134(9 Pt 1):737-45. doi: 10.7326/0003-4819-134-9_part_1-200105010-00010.
The thiazolidinediones are a new class of antidiabetes medication that enhances the actions of insulin in muscle, liver, and adipose tissue. Data have been lacking on their use in combination with both sulfonylurea and metformin among patients for whom insulin is the usual therapeutic alternative for improved glycemic control.
To determine the effects of troglitazone on hemoglobin A(1c) level in patients treated with maximum tolerated doses of sulfonylurea and metformin who have hemoglobin A(1c) levels of at least 0.085 (8.5%). This trial was completed before troglitazone was taken off the U.S. market.
Randomized, double-blind, placebo-controlled trial, followed by an open-label extension during which all patients received troglitazone.
16 outpatient clinics in Canada.
200 patients (mean age, 59 years) with type 2 diabetes mellitus and hemoglobin A(1c) levels at least 0.085 (8.5%) (mean hemoglobin A(1c) level, 0.097 [9.7%] and mean fasting plasma glucose level, 12.9 mmol/L [233 mg/dL]) while receiving maximum doses of sulfonylurea and metformin.
Levels of hemoglobin A(1c), fasting plasma glucose, total insulin, triglycerides, total cholesterol, low-density lipoprotein cholesterol, and high-density lipoprotein cholesterol.
Troglitazone, 400 mg/d, when added to sulfonylurea and metformin, significantly decreased hemoglobin A(1c) level by 0.014 +/- 0.002 (95% CI, 0.0167 to 0.0109; P < 0.001) (1.4% +/- 0.2% [CI, 1.67% to 1.09%]) and insulin by 19 +/- 4 pmol/L (CI, 30 to 10 pmol/L; P < 0.001). At 6 months, 43% of troglitazone-treated patients achieved hemoglobin A(1c) levels of 0.08 (8%) or lower compared with 6% of placebo recipients. Efficacy was maintained at 12 months.
The thiazolidinedione troglitazone, at a dosage of 400 mg/d, is effective when used in combination with sulfonylurea and metformin. Thiazolidinediones may therefore offer an effective alternative to insulin for patients treated with sulfonylurea and metformin who do not achieve adequate glycemic control.
噻唑烷二酮类是一类新型抗糖尿病药物,可增强胰岛素在肌肉、肝脏和脂肪组织中的作用。对于那些通常将胰岛素作为改善血糖控制的治疗选择的患者,关于其与磺脲类和二甲双胍联合使用的数据一直缺乏。
确定曲格列酮对接受最大耐受剂量磺脲类和二甲双胍治疗且糖化血红蛋白水平至少为0.085(8.5%)的患者糖化血红蛋白水平的影响。该试验在曲格列酮退出美国市场之前完成。
随机、双盲、安慰剂对照试验,随后进行开放标签扩展试验,在此期间所有患者均接受曲格列酮治疗。
加拿大的16家门诊诊所。
200例2型糖尿病患者(平均年龄59岁),在接受最大剂量磺脲类和二甲双胍治疗时糖化血红蛋白水平至少为0.085(8.5%)(平均糖化血红蛋白水平为0.097 [9.7%],平均空腹血糖水平为12.9 mmol/L [233 mg/dL])。
糖化血红蛋白、空腹血糖、总胰岛素、甘油三酯、总胆固醇、低密度脂蛋白胆固醇和高密度脂蛋白胆固醇水平。
当曲格列酮以400 mg/d的剂量添加到磺脲类和二甲双胍治疗中时,可使糖化血红蛋白水平显著降低0.014±0.002(95%CI,0.0167至0.0109;P<0.001)(1.4%±0.2%[CI,1.67%至1.09%]),胰岛素水平降低19±4 pmol/L(CI,30至10 pmol/L;P<0.001)。在6个月时,43%接受曲格列酮治疗的患者糖化血红蛋白水平达到0.08(8%)或更低,而接受安慰剂的患者为6%。疗效在12个月时得以维持。
曲格列酮剂量为400 mg/d时,与磺脲类和二甲双胍联合使用有效。因此,对于接受磺脲类和二甲双胍治疗但血糖控制不佳的患者,噻唑烷二酮类可能是胰岛素的有效替代药物。