Campbell M L, Mathys M L
College of Pharmacy, Midwestern University, Glendale, AZ, USA.
Am J Health Syst Pharm. 2001 Jul 15;58(14):1301-8. doi: 10.1093/ajhp/58.14.1301.
Past and current drug therapies for weight loss are discussed. More than 50% of Americans can be categorized as overweight or obese. Obesity is associated with increased mortality and with comorbidities such as hypertension, hyperglycemia, dyslipidemia, coronary artery disease, and certain cancers. According to guidelines for identification, evaluation, and treatment of obesity, patients with a body mass index (BMI) of > or = 30 kg/m2 should attempt to lose weight. Patients with a BMI of > or = 25 kg/m2 plus two or more risk factors or patients with an excessive waist circumference plus two or more risk factors should also attempt to lose weight. The initial goal is a 10% weight reduction in six months achieved through lifestyle changes. If lifestyle changes alone are not effective, then drug therapy may be indicated. Pharmacotherapeutic options for obesity have decreased over the past few years. Fenfluramine, dexfenfluramine, and phenylpropanolamine have been withdrawn because of severe adverse effects, leaving only sympathomimetics, sibutramine, and orlistat as anorectics with FDA-approved labeling. Phentermine has been shown to cause a 5-15% weight loss if given daily or intermittently. Compared with sibutramine and orlistat, phentermine is cheaper, and specific formulations allow once-daily administration. However, phentermine is indicated only for short-term treatment, and tolerance often develops. Common adverse effects associated with phentermine are dry mouth, insomnia, increased blood pressure, and constipation. Sibutramine increases norepinephrine and serotonin levels in the CNS and should not be taken with many antidepressants because of the risk of increased norepinephrine and serotonin levels. Its use is also contraindicated in patients with cardiovascular disease. Orlistat is not systemically absorbed; therefore, it does not cause the systemic adverse effects or drug interactions of phentermine and sibutramine. Orlistat has a cholesterol-lowering effect not seen with other diet medications. However, the three-times-daily administration and frequent gastrointestinal effects limit its use. Sibutramine, phentermine, and orlistat have both positive and negative properties. Choosing among the medications will depend on concurrent disease states and medications, ease of administration, and cost.
本文讨论了过去和当前用于减肥的药物疗法。超过50%的美国人可被归类为超重或肥胖。肥胖与死亡率增加以及高血压、高血糖、血脂异常、冠状动脉疾病和某些癌症等合并症相关。根据肥胖症的识别、评估和治疗指南,体重指数(BMI)大于或等于30kg/m²的患者应尝试减肥。BMI大于或等于25kg/m²且伴有两个或更多危险因素的患者,或腰围过大且伴有两个或更多危险因素的患者也应尝试减肥。初始目标是通过生活方式改变在六个月内减轻10%的体重。如果仅靠生活方式改变无效,则可能需要药物治疗。在过去几年中,用于肥胖症的药物治疗选择有所减少。芬氟拉明、右芬氟拉明和苯丙醇胺因严重不良反应已被撤市,仅留下拟交感神经药、西布曲明和奥利司他这几种具有美国食品药品监督管理局(FDA)批准标签的食欲抑制剂。已证明,每日或间歇服用苯丁胺可使体重减轻5%至15%。与西布曲明和奥利司他相比,苯丁胺价格更低,且特定剂型允许每日服用一次。然而,苯丁胺仅适用于短期治疗,且常出现耐受性。与苯丁胺相关的常见不良反应有口干、失眠、血压升高和便秘。西布曲明可提高中枢神经系统中的去甲肾上腺素和5-羟色胺水平,由于存在去甲肾上腺素和5-羟色胺水平升高的风险,不应与多种抗抑郁药同时服用。心血管疾病患者也禁用该药。奥利司他不会被全身吸收;因此,它不会引起苯丁胺和西布曲明的全身不良反应或药物相互作用。奥利司他具有其他节食药物所没有的降胆固醇作用。然而,每日三次给药以及频繁的胃肠道不良反应限制了其使用。西布曲明、苯丁胺和奥利司他都有其优缺点。在这些药物中进行选择将取决于并存的疾病状态和用药情况、给药便利性以及成本。