机构地区:[1]同济大学附属上海市第十人民医院内分泌科,上海200072 [2]上海市医学会
出 处:《上海医学》2005年第12期1018-1023,共6页Shanghai Medical Journal
摘 要:目的观察2型糖尿病患者进食不同剂量葡甘聚糖后,空腹血糖(FBG)、餐后2 h血糖(P2hBG)、空腹胰岛素、餐后2 h胰岛素和血脂的变化,并评价其安全性.方法选择140例2型糖尿病患者,均分为4组.伏格列波糖组予伏格列波糖口服;低、中、高剂量组分别予葡甘聚糖10、20和30 g/d口服.4组患者均供给含纤维素量基本一致的蔬菜500 g/d,个体膳食纤维的摄入量为10 g/d,以保证个体间纤维素量一致.结果①血糖、胰岛素:治疗12周后,4组患者的FBG、P2hBG、糖化血红蛋白(HbA1c)、空腹胰岛素、餐后2 h胰岛素均显著下降(P<0.01),以伏格列波糖组的降幅最大,低、中剂量组的降幅均显著小于高剂量组(P值均<0.05).②血脂:治疗12周后,4组患者的胆固醇(TCh)、低密度脂蛋白-胆固醇(LDL-C)水平均显著下降(P值均<0.01),低、中剂量组的降幅显著小于高剂量组(P值均<0.05),高剂量组显著小于伏格列波糖组(P<0.05).③体重指数(BMI)、腰臀比(WHR):治疗12周后,低、中、高剂量组的BMI、WHR均明显下降(P值均<0.01),以高剂量组的降幅最大,而伏格列波糖组治疗前、后的差异无显著性.④不良反应:高剂量组4例(11.42%)有轻度腹胀,1例轻度腹泻,3~6 d后自然好转;3例出现饥饿感,可自然适应,无需增加进食量.中剂量组2例(5.71%)有轻度腹胀,3~6 d后自然好转.结论葡甘聚糖低、中、高3个剂量均具有降低血糖、胰岛素、血脂和减肥的疗效,其安全性、耐受性良好.与中、低剂量的葡甘聚糖相比,高剂量葡甘聚糖对控制FBG、P2hBG及降低胰岛素、血脂水平的疗效更好.Objective To investigate the changes of fasting blood glucose level (FBG), 2 hours postprandial blood glucose level (2hBG), fasting serum insulin concentration (Fins), 2 hours postprandial serum insulin concentration (2hIns) and lipid profile in type 2 diabetics with different doses of water soluble fiber (glucoman nan), and to evaluate its safety as well. Methods A total of 140 subjects participated in the clinical trial and were randomized into 4 groups, namely, positive control group with Voglibose, low dose group with glucomannan 10 g/d, median-dose group with glucomannan 20 g/d, and high dose group with glucomannan 30 g/d. The diets of all participantes were previously adjusted according to the guideline individually and were asked to eat various kinds of vegetables 500 g/d to ensure the amount of basal daily dietary fiber intake approximately 10 g. Results① After 12 weeks of intervention, FBG, 2hBG, HbA1 c, Fins and 2hIns decreased markedly in all 4 groups (P〈 0.01), with maximal reduction in the positive control group. The amplitude of the reduction in the low dose and median-dose groups were all lower than that in the high-dose group (P〈0.05). ② Lipid profile. After 12 weeks of intervention, TCh and LDL1c decreased markedly in all 4 groups (P〈0.01). The amplitude of the reduction in the low dose and median-dose groups were all lower than the high-dose group (P〈0.05) but higher than the positive control group. ③ BMI and WHR: With the exception of positive control group, BMI and EHR lowered in all groups with different doses of glucomannan (P〈0.01), with maximal reduction in the high dose group. ④ Adverse events: In the high dose group, 4 cases complained of mild abdominal distension (11.42%), and 1 case with mild diarrhea which disappeared after 3-6 days automatically, 3 cases fell hungry and no further diet modifi cation was needed. In the media-dose group, 2 cases complained of mild abdominal distension (5.71%) and disappeared after 3
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