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西酞普兰治疗暴饮暴食症:一项安慰剂对照试验。

Citalopram in the treatment of binge-eating disorder: a placebo-controlled trial.

作者信息

McElroy Susan L, Hudson James I, Malhotra Shishuka, Welge Jeffrey A, Nelson Erik B, Keck Paul E

机构信息

Division of Psychopharmacology Research and Eating Disorders, Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0559, USA.

出版信息

J Clin Psychiatry. 2003 Jul;64(7):807-13. doi: 10.4088/jcp.v64n0711.

Abstract

BACKGROUND

Binge-eating disorder is a newly recognized eating disorder characterized by recurrent episodes of binge eating without compensatory weight loss behaviors. It commonly co-occurs with depressive disorders and obesity. Citalopram is a highly selective serotonin reuptake inhibitor antidepressant. The purpose of this study was to assess the efficacy and safety of citalopram in the treatment of binge-eating disorder.

METHOD

Thirty-eight outpatients with a DSM-IV diagnosis of binge-eating disorder were enrolled in the study between August 2000 and July 2001 and were randomly assigned to receive either citalopram (N = 19) or placebo (N = 19) in a 6-week, double-blind, flexible-dose (20-60 mg/day) study. The primary measure of efficacy was frequency of binge-eating episodes. Secondary measures included frequency of binge days, body mass index (BMI), weight, Clinical Global Impressions-Severity of Illness scale scores, Yale-Brown Obsessive Compulsive Scale Modified for Binge Eating (YBOCS-BE) scores, Hamilton Rating Scale for Depression (HAM-D) scores, and response categories. The outcome measures were analyzed using 2 random regression methods, with a time trend analysis (primary analysis) and an endpoint analysis. In addition, response categories were analyzed using an exact trend test.

RESULTS

Compared with placebo-treated subjects, subjects receiving citalopram (mean dose of 57.9 mg/day) had a significantly greater rate of reduction in frequency of binge eating (p =.003), frequency of binge days (p <.001), BMI (p <.001), weight (p <.001), severity of illness (p =.028), and YBOCS-BE score (p =.007) and a marginally significant rate of reduction in HAM-D score (p =.053). Differences between groups in response categories were marginally significant (p =.068 for intent-to-treat analysis).

CONCLUSION

In a 6-week, placebo-controlled, flexible-dose trial, citalopram was efficacious in reducing binge-eating frequency, weight, and severity of illness and was generally well tolerated in subjects with binge-eating disorder.

摘要

背景

暴饮暴食症是一种新被认识的饮食失调症,其特征为反复出现暴饮暴食发作且无代偿性体重减轻行为。它常与抑郁症和肥胖症同时出现。西酞普兰是一种高选择性5-羟色胺再摄取抑制剂抗抑郁药。本研究的目的是评估西酞普兰治疗暴饮暴食症的疗效和安全性。

方法

2000年8月至2001年7月期间,38名符合《精神疾病诊断与统计手册》第四版(DSM-IV)暴饮暴食症诊断标准的门诊患者被纳入研究,并被随机分配接受西酞普兰(N = 19)或安慰剂(N = 19),进行为期6周的双盲、灵活剂量(20 - 60毫克/天)研究。疗效的主要衡量指标是暴饮暴食发作的频率。次要衡量指标包括暴饮暴食天数的频率、体重指数(BMI)、体重、临床总体印象-疾病严重程度量表评分、针对暴饮暴食进行改良的耶鲁-布朗强迫量表(YBOCS-BE)评分、汉密尔顿抑郁量表(HAM-D)评分以及反应类别。使用两种随机回归方法对结果指标进行分析,包括时间趋势分析(主要分析)和终点分析。此外,使用精确趋势检验对反应类别进行分析。

结果

与接受安慰剂治疗的受试者相比,接受西酞普兰治疗(平均剂量为57.9毫克/天)的受试者在暴饮暴食频率(p = 0.003)、暴饮暴食天数的频率(p < 0.001)、BMI(p < 0.001)、体重(p < 0.001)、疾病严重程度(p = 0.028)以及YBOCS-BE评分(p = 0.007)方面的降低率显著更高,在HAM-D评分方面的降低率有边缘显著性(p = 0.053)。两组在反应类别上的差异有边缘显著性(意向性治疗分析的p = 0.068)。

结论

在一项为期6周的安慰剂对照、灵活剂量试验中,西酞普兰在降低暴饮暴食频率、体重和疾病严重程度方面有效,并且在暴饮暴食症患者中总体耐受性良好。

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