Kawai Toshihide, Funae Osamu, Shimada Akira, Tabata Mitsuhisa, Hirata Takumi, Atsumi Yoshihito, Itoh Hiroshi
Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Intern Med. 2008;47(13):1181-8. doi: 10.2169/internalmedicine.47.0969. Epub 2008 Jul 1.
We investigated whether or not "low dose" metformin could prevent weight gain induced by pioglitazone.
Sixty-nine patients with type 2 diabetes received 500-750 mg metformin a day for 12 weeks as an observation period before the start of the intervention. After an observation period, inadequately controlled patients (hemoglobin A1c >or=7.5%, n=34) received additional treatment with 15 mg pioglitazone (+P, M+P group). The other patients (n= 35) continued metformin monotherapy (Met group). In addition, another group consisting of 28 patients treated with 15 mg pioglitazone alone (Pio group) was observed. Body mass index (BMI), as well as several clinical parameters of glycemic control and lipid metabolism, was compared before and after 24 weeks of intervention.
BMI increased significantly in the Pio group [24.0+/-3.8 vs. 24.8+/-4.3 kg/m(2), (mean +/- SD), p<0.001], but not in the M+P group (25.1+/-3.5 vs. 25.3+/-3.4 kg/m(2), NS) and Met group (24.0+/-3.3 vs. 24.0+/-3.5 kg/m(2), NS). In addition to improvement in glycemic control, a significant reduction in the atherogenic index of plasma (AIP), defined as log [TG x0.0112/HDL-C x0.02586], was observed in the Pio group (0.06+/-0.23 vs. -0.04+/-0.27, p<0.05) and M+P group (0.08+/-0.24 vs. -0.001+/-0.252, p<0.01), but not in the Met group.
This study indicates potential benefits of the addition of pioglitazone to "low dose" metformin in terms of improvement of glucose and lipid metabolism without weight gain.
我们研究了“低剂量”二甲双胍是否能预防吡格列酮引起的体重增加。
69例2型糖尿病患者在干预开始前作为观察期,每天服用500 - 750毫克二甲双胍,为期12周。观察期后,控制不佳的患者(糖化血红蛋白≥7.5%,n = 34)接受15毫克吡格列酮的额外治疗(+P,M + P组)。其他患者(n = 35)继续二甲双胍单药治疗(Met组)。此外,观察了另一组由28例单独接受15毫克吡格列酮治疗的患者(Pio组)。在干预24周前后比较体重指数(BMI)以及血糖控制和脂质代谢的几个临床参数。
Pio组的BMI显著增加[24.0±3.8 vs. 24.8±4.3 kg/m²,(均值±标准差),p < 0.001],但M + P组(25.1±3.5 vs. 25.3±3.4 kg/m²,无显著性差异)和Met组(24.0±3.3 vs. 24.0±3.5 kg/m²,无显著性差异)未出现这种情况。除血糖控制改善外,Pio组(0.06±0.23 vs. -0.04±0.27,p < 0.05)和M + P组(0.08±0.24 vs. -0.001±0.252,p < 0.01)的血浆致动脉粥样硬化指数(AIP,定义为log [甘油三酯×0.0112/高密度脂蛋白胆固醇×0.02586])显著降低,但Met组未出现这种情况。
本研究表明,在不增加体重的情况下,“低剂量”二甲双胍联合吡格列酮在改善糖脂代谢方面具有潜在益处。