Chow C C, Ko G T, Tsang L W, Yeung V T, Chan J C, Cockram C S
Department of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, N.T.
Diabetes Care. 1997 Jul;20(7):1122-7. doi: 10.2337/diacare.20.7.1122.
To investigate the safety, efficacy, and metabolic effects of dexfenfluramine in obese Chinese NIDDM patients.
Thirty-two patients, mean (+/- SD) body weight 76.2 +/- 8.5 kg with corresponding BMI 31.1 +/- 2.1 kg/m2, were randomized into a two-phase study, after a 2-week single-blind run-in period on placebo. Phase 1 was a randomized 3-month double-blind placebo-controlled trial during which either dexfenfluramine or placebo was added to the existing treatment regimens of diet plus or minus sulfonylureas without metformin. Phase 2 was a further 3-month single-blind trial during which the placebo group was given dexfenfluramine without patients' knowledge of changing to active medication, while the active group continued with dexfenfluramine. Body weight, glycemic control, blood pressure, lipids, and quality of life were assessed before and at 3 and 6 months after randomization. A total of 27 patients were also followed for an additional period of 6-12 months (215 +/- 53 days) after dexfenfluramine treatment was withdrawn.
During the run-in period, both groups were comparable for all parameters measured. At 3 months, mean changes in BMI were -1.2 +/- 1.0 kg/m2 (dexfenfluramine) vs. -0.1 +/- 0.5 kg/m2 (placebo) (P < 0.001). The mean changes in fasting plasma glucose were -1.14 +/- 0.99 vs. 0.51 +/- 1.34 mmol/l (dexfenfluramine vs. placebo, P = 0.004). HbA(1c) also significantly improved in the dexfenfluramine group (-0.80 +/- 0.53 vs. 0.25 +/- 0.64%, P < 0.001). During the 3-month single-blind dexfenfluramine treatment in the ex-placebo group, there were similar improvements in body weight and glycemic indexes. After cessation of dexfenfluramine therapy at 6 months, significant increases in body weight and glycemic indexes, almost back to the baseline, were observed for both groups.
Dexfenfluramine aids weight loss and improves glycemic control in obese Chinese NIDDM patients over a 3- to 6-month period. These effects are emphasized after withdrawal of treatment and further support the longer-term use of dexfenfluramine for chronic complicated obesity.
研究右芬氟拉明对中国肥胖型非胰岛素依赖型糖尿病(NIDDM)患者的安全性、疗效及代谢影响。
32例患者,平均(±标准差)体重76.2±8.5kg,相应体重指数(BMI)为31.1±2.1kg/m²,在接受为期2周的安慰剂单盲导入期后,随机分为两阶段研究。第1阶段为为期3个月的随机双盲安慰剂对照试验,在此期间,将右芬氟拉明或安慰剂添加到现有的饮食加或减磺脲类药物(不含二甲双胍)治疗方案中。第2阶段为为期3个月的单盲试验,在此期间,安慰剂组在患者不知情的情况下换用右芬氟拉明,而治疗组继续使用右芬氟拉明。在随机分组前及随机分组后3个月和6个月时评估体重、血糖控制、血压、血脂及生活质量。共有27例患者在停用右芬氟拉明治疗后还进行了6 - 12个月(215±53天)的随访。
在导入期,两组所有测量参数均具有可比性。3个月时,BMI的平均变化为-1.2±1.0kg/m²(右芬氟拉明组)对比-0.1±0.5kg/m²(安慰剂组)(P<0.001)。空腹血糖的平均变化为-1.14±0.99对比0.51±1.34mmol/L(右芬氟拉明组对比安慰剂组,P = 0.004)。右芬氟拉明组糖化血红蛋白(HbA₁c)也显著改善(-0.80±0.53对比0.25±0.64%,P<0.001)。在前安慰剂组接受3个月单盲右芬氟拉明治疗期间,体重和血糖指标有类似改善。6个月停用右芬氟拉明治疗后,两组体重和血糖指标均显著增加,几乎回到基线水平。
右芬氟拉明在3至6个月期间有助于中国肥胖型NIDDM患者减轻体重并改善血糖控制。停药后这些作用更为明显,进一步支持右芬氟拉明用于慢性复杂性肥胖的长期治疗。