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5-羟色胺能药物诱导的碳水化合物渴望型肥胖患者体重减轻

Serotoninergic drug-induced weight loss in carbohydrate craving obese patients.

作者信息

Toornvliet A C, Pijl H, Hopman E, Elte-de Wever B M, Meinders A E

机构信息

Department of General Internal Medicine, Leiden University Hospital, The Netherlands.

出版信息

Int J Obes Relat Metab Disord. 1996 Oct;20(10):917-20.

PMID:8910095
Abstract

RATIONALE

Serotoninergic neurotransmission, mainly in specific hypothalamic nuclei, plays an important role in the regulation of appetite. Dysfunction of this system has been postulated to result in the clinical picture of carbohydrate craving obesity. This subgroup of obese patients is characterized by a specific preference for high-carbohydrate and low-protein snacks. Centrally acting serotoninergic drugs, such as the serotonin re-uptake inhibitor d-fenfluramine, have been hypothesized to restore serotonin mediated control of food intake.

OBJECTIVE

To test the hypothesis that serotoninergic drugs would induce a greater weight loss in carbohydrate craving (CC) than in non-carbohydrate craving (NC) obese patients.

DESIGN

A three months open intervention study with d-fenfluramine 15 mg twice daily. In order to be able to study the effect of the drug alone, no dietary restrictions were imposed. Both the medical doctor and the patient were unaware of who was a carbohydrate craving obese patient and who was not.

SUBJECTS

10 CC and 10 NC patients, matched for sex, age, body mass index and family history of obesity.

MEASUREMENTS

Height, body weight, food intake (energy intake and macronutrient selection) and patient compliance.

RESULTS

CC patients lost 4.8 +/- 3.9 kg body weight or 15.9 +/- 13.5% of their pretreatment overweight, whereas NC patients lost 4.5 +/- 2.9 kg or 16.4 +/- 11.6% of their overweight (t-test for paired samples, P = 0.82 and P = 0.93 respectively).

CONCLUSION

We conclude that CC patients do not constitute a subgroup of obese patients that should be treated with a serotoninergic drug preferentially.

摘要

理论依据

血清素能神经传递,主要在特定的下丘脑核团中,在食欲调节中起重要作用。该系统功能障碍被认为会导致碳水化合物渴望型肥胖的临床表现。这类肥胖患者的特点是特别偏好高碳水化合物和低蛋白零食。中枢作用的血清素能药物,如血清素再摄取抑制剂右旋芬氟拉明,被假定可恢复血清素介导的食物摄入控制。

目的

检验血清素能药物在碳水化合物渴望型(CC)肥胖患者中比在非碳水化合物渴望型(NC)肥胖患者中能诱导更多体重减轻的假设。

设计

一项为期三个月的开放干预研究,每日两次服用15毫克右旋芬氟拉明。为了能够单独研究药物的效果,未施加饮食限制。医生和患者都不知道谁是碳水化合物渴望型肥胖患者,谁不是。

受试者

10名CC患者和10名NC患者,在性别、年龄、体重指数和肥胖家族史方面匹配。

测量指标

身高、体重、食物摄入量(能量摄入和常量营养素选择)以及患者依从性。

结果

CC患者体重减轻了4.8±3.9千克,或其治疗前超重的15.9±13.5%,而NC患者体重减轻了4.5±2.9千克,或其超重的16.4±11.6%(配对样本t检验,P值分别为0.82和0.93)。

结论

我们得出结论,CC患者不构成应优先使用血清素能药物治疗的肥胖患者亚组。

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