Velussi M, Monte A D, Cernigoi A M
Azienda Sanitaria n.2 Isontina, Antidiabetic Center, S. Polo Hospital, Mon Falcone, Italy.
J Diabetes Complications. 1996 Sep-Oct;10(5):261-6. doi: 10.1016/1056-8727(96)00044-x.
A randomized double-blind study of benfluorex (150 mg x 3 daily) versus placebo was conducted over 3 months in 32 type II diabetic patients (24 men and 8 women, aged 52 +/- 8.4 years) with mild stable obesity [body-mass index (BMI) 27 +/- 1.6 kg/ m2], moderate fasting hyperglycemia (fasting blood glucose 9 +/- 0.5 mmol/L, HbA1c 6.7 +/- 0.9%) and moderate hyperinsulinemia (18.6 +/- 3.0 microU/mL) when on treatment with diet alone. After a 1-month placebo run-in period, subjects were randomized to benfluorex or placebo three tablets daily. Inclusion parameters and end-of-study measures were body weight, BMI, fasting blood glucose, glycemic profile, HbA1c, fasting insulinemia, basal and stimulated C-peptide, and an insulin tolerance test (0.1 U/kg). The groups were homogeneous at baseline, except for glycemic profile (higher postprandial glycemia in the group randomized to benfluorex). At the end of the study, the groups did not differ in body weight or BMI; however, HbA1c decreased more with benfluorex (6.0 +/- 1.0% versus 6.8 +/- 0.9%, p = 0.024), as did the mean glycemic profile (7.8 +/- 1.4 versus 8.5 +/- 1.7 mmol/L, p < 0.001), including a particular decrease in postprandial glycemia. The decreases in fasting blood glucose and insulinemia appeared larger with benfluorex (7.7 +/- 1.3 versus 8.4 +/- 1.6 mmol/L and 13.5 +/- 4.5 versus 16.1 +/- 5.1 microU/mL, respectively), but were not statistically significant. The increase in the insulin sensitivity index (Kitt) was greater with benfluorex (+0.54 +/- 1.4 versus +0.25 +/- 1.3%/mn), but the difference was not statistically significant. The same was observed for the stimulated C-peptide. In type II diabetics with mild obesity and hyperglycemia previously managed with diet alone, benfluorex has significant long-term effect on HbA1c and mean daily blood glucose, and tends to lower insulinemia.
对32例II型糖尿病患者(24例男性和8例女性,年龄52±8.4岁)进行了一项为期3个月的随机双盲研究,比较苯氟雷司(每日3次,每次150毫克)与安慰剂的效果。这些患者患有轻度稳定型肥胖症[体重指数(BMI)为27±1.6千克/平方米],中度空腹血糖升高(空腹血糖9±0.5毫摩尔/升,糖化血红蛋白A1c为6.7±0.9%),且仅通过饮食治疗时存在中度高胰岛素血症(18.6±3.0微单位/毫升)。在为期1个月的安慰剂导入期后,受试者被随机分为每日服用3片苯氟雷司或安慰剂。纳入参数和研究结束时的测量指标包括体重、BMI、空腹血糖、血糖谱、糖化血红蛋白A1c、空腹胰岛素血症、基础和刺激后的C肽,以及胰岛素耐量试验(0.1单位/千克)。除血糖谱外(随机分配到苯氟雷司组的餐后血糖较高),两组在基线时具有同质性。研究结束时,两组在体重或BMI方面没有差异;然而,苯氟雷司组的糖化血红蛋白A1c下降更多(6.0±1.0%对6.8±0.9%,p = 0.024),平均血糖谱也是如此(7.8±1.4对8.5±1.7毫摩尔/升,p < 0.001),包括餐后血糖有特别的下降。苯氟雷司组空腹血糖和胰岛素血症的下降似乎更大(分别为7.7±1.3对8.4±1.6毫摩尔/升和13.5±4.5对16.1±5.1微单位/毫升),但无统计学意义。苯氟雷司组胰岛素敏感性指数(Kitt)的增加更大(+0.54±1.4对+0.25±1.3%/分钟),但差异无统计学意义。刺激后的C肽情况也是如此。在之前仅通过饮食治疗的轻度肥胖和血糖升高的II型糖尿病患者中,苯氟雷司对糖化血红蛋白A1c和每日平均血糖有显著的长期影响,并倾向于降低胰岛素血症。