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极低热量饮食后的药物治疗。

Drug therapy after very-low-calorie diets.

作者信息

Finer N, Finer S, Naoumova R P

机构信息

Department of Medicine, United Medical School, Guy's Hospital, London, England.

出版信息

Am J Clin Nutr. 1992 Jul;56(1 Suppl):195S-198S. doi: 10.1093/ajcn/56.1.195S.

Abstract

Very-low-calorie diets (VLCDs) are effective at reducing weight, even in patients who have often failed with conventional diets. Maintaining weight lost by means of a VLCD remains a clinical challenge. Attempts to prevent weight regain by dietary reeducation or by more formal behavior-modification techniques are not easily applicable to large numbers of patients and are not always successful; the use of drugs to maintain and improve upon initial VLCD success could be of real clinical value. Pharmacological treatment of obesity has evolved in recent years with the development and licensing of potent serotonin agonists, such as dexfenfluramine (dF), acting as nonstimulant anorectic agents. Thermogenic drugs are not yet as advanced in clinical development and evaluation but offer the prospect of increasing energy output in the reduced obese patient. Drugs used to treat obesity need to be effective, to be safe, not to exhibit drug tolerance, and ideally, to be shown to reduce morbidity or mortality from obesity, particularly because treatment will need to be prolonged. Such requirements are not unique for treating obesity, they are similar for drugs used to treat other metabolic diseases such as hypercholesterolemia or diabetes. VLCD followed by dF has been shown to be effective. A double-blind trial randomized 45 patients who had successfully completed 8 wk of treatment on the Cambridge diet to either placebo or dF 15 mg twice daily for 26 wk. Patients continued on a diet giving 60-75% of daily energy needs.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

极低热量饮食(VLCDs)在减轻体重方面很有效,即使是那些经常在传统饮食上失败的患者。通过VLCD减轻的体重维持仍是一项临床挑战。试图通过饮食再教育或更正式的行为矫正技术来防止体重反弹并不容易适用于大量患者,且并不总是成功;使用药物来维持并巩固最初VLCD的成效可能具有实际临床价值。近年来,随着强效血清素激动剂(如右芬氟拉明(dF))作为非刺激性食欲抑制剂的开发和许可,肥胖症的药物治疗有了进展。产热药物在临床开发和评估方面尚未如此先进,但有望增加肥胖症减轻患者的能量输出。用于治疗肥胖症的药物需要有效、安全、不表现出药物耐受性,理想情况下,要能证明可降低肥胖症的发病率或死亡率,特别是因为治疗需要长期进行。这些要求并非治疗肥胖症所独有,用于治疗其他代谢疾病(如高胆固醇血症或糖尿病)的药物也类似。已证明VLCD后使用dF是有效的。一项双盲试验将45名成功完成8周剑桥饮食治疗的患者随机分为接受安慰剂组或每日两次服用15毫克dF组,为期26周。患者继续食用提供每日能量需求60 - 75%的饮食。(摘要截选于250词)

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