Six-month efficacy and safety of amfepramone in obese Mexican patients: a double-blinded, randomized, controlled trial

被引:14
|
作者
Soto-Molina, Herman [1 ]
Pizarro-Castellanos, Mariel [2 ]
Rosado-Perez, Juana [3 ]
Rizzoli-Cordoba, Antonio [2 ]
Lara-Padilla, Eleazar [4 ]
del Valle-Laisequilla, Cecilia Fernandez [4 ]
Gerardo Reyes-Garcia, Juan [4 ]
机构
[1] Univ Autonoma Metropolitana Xochimilco, Mexico City, DF, Mexico
[2] Hosp Infantil Mexico Dr Federico Gomez, Direcc Invest, Mexico City, DF, Mexico
[3] Univ Nacl Autonoma Mexico, Fac Estudios Super Zaragoza, Mexico City 04510, DF, Mexico
[4] Inst Politecn Nacl, Escuela Super Med, Secc Estudios Posgrad & Invest, Mexico City 11340, DF, Mexico
关键词
amfepramone; diethylpropion; Mexican; noradrenaline-releasing drug; obesity; PRIMARY PULMONARY-HYPERTENSION; DIETHYLPROPION; EPIDEMIOLOGY; TENUATE;
D O I
10.5414/CP202135
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Amfepramone, also known as diethylpropion, is an anorectic drug used for the short-term treatment of obesity; however, its efficacy and safety during periods greater than 3 months has been scarcely studied. To evaluate the 6-month efficacy and safety of amfepramone treatment in obese adult Mexican patients resistant to diet and exercise, a double-blinded, randomized, and placebo-controlled clinical trial study was designed on 156 volunteers with a body mass index (BMI) greater than 30 kg/m(2) and less than 45 kg/m(2). Patients were randomized to receive a 75 mg tablet of amfepramone or placebo daily for 6 months. Primary outcome was the absolute body weight loss, whereas secondary outcomes were the percentage of patients who achieved at least 5% or 10% weight loss, as well as the improvement of anthropometric and metabolic parameters. Amfepramone treatment produced a superior efficacy to decrease body weight than placebo at 3 months (-4.9 +/- 0.25 kg vs. 0.7 +/- 0.32 kg) and 6 months (-7.7 +/- 0.52 kg vs. -1.1 +/- 0.7 kg). In addition, 64 and 34 patients achieved at least 5% or 10% weight loss, respectively, with amfepramone at 6 months, compared with 8 and 0 patients on placebo. Amfepramone also significantly improved BMI and waist circumference, but it only showed a favorable tendency in the waist-hip index (WHI), glucose, total cholesterol, low-density lipoproteins (LDL), high-density lipoproteins (HDL), triglycerides, heart rate, systolic blood pressure, and diastolic blood pressure at 3 and 6 months. Amfepramone produced only mild adverse events, and they were presented in a greater number than placebo only at 3 months, dry mouth being the the main adverse event. Data suggest that amfepramone is effective and well tolerated in obese Mexican patients during a 6-month regimen.
引用
收藏
页码:541 / 549
页数:9
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