Agomelatine Prevents Relapse in Generalized Anxiety Disorder: A 6-Month Randomized, Double-Blind, Placebo-Controlled Discontinuation Study

被引:60
作者
Stein, Dan J. [1 ]
Ahokas, Antti [2 ]
Albarran, Cristina [3 ]
Olivier, Valerie [3 ]
Allgulander, Christer [4 ]
机构
[1] Groote Schuur Hosp, Dept Psychiat, ZA-7925 Cape Town, South Africa
[2] Mehilainen Clin, Helsinki, Finland
[3] IRIS, Suresnes, France
[4] Univ Hosp, Karolinska Inst, Sect Psychiat, Dept Clin Neurosci, Huddinge, Sweden
关键词
MAJOR DEPRESSIVE DISORDER; LONG-TERM TREATMENT; CLINICAL-TRIALS; EFFICACY; VENLAFAXINE; PAROXETINE; SYMPTOMS; TIME;
D O I
10.4088/JCP.11m07493
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: This study evaluated the efficacy and tolerability of agomelatine in the prevention of relapse in patients with generalized anxiety disorder (GAD). Method: Patients with GAD (Hamilton Anxiety Rating Scale [HARS] >= 22, with items 1 and 2 >= 2, item 1 + 2 >= 5; Montgomery-Asberg Depression Rating Scale [MADRS] <= 16; and < 20% decrease in HARS total score between screening and baseline) who responded to a 16-week course of agomelatine 25-50 mg/d treatment were randomly assigned to receive continuation treatment with agomelatine (n = 113) or placebo (n = 114) for 26 weeks. The main outcome measure was time to relapse during this maintenance period. The estimated risk of relapse was calculated using the Kaplan-Meier method, and groups were compared using a log-rank test stratified for country. The study was undertaken in 31 clinical centers in Canada, Denmark, Estonia, Finland, Hungary, and Sweden from November 2007 to September 2009. Results: During the 6-month maintenance period, the proportion of patients that relapsed during the double-blind period in the agomelatine group (22 patients, 19.5%) was lower than in the placebo group (35 patients, 30.7%). The risk of relapse over time was significantly lower for patients who continued treatment than for those switched to placebo (P=.046, log-rank test stratified for country). Agomelatine was also superior to placebo in preventing relapse in the subset of more severe patients with baseline HARS total score >= 25 and CGI-S score >= 5. The tolerability of agomelatine was good throughout the study, and there were no differences in discontinuation symptoms after withdrawal of agomelatine in comparison to maintenance on agomelatine. Conclusions: The present study extends the positive findings of an earlier short-term study of agomelatine in GAD, demonstrating that agomelatine is effective and well-tolerated in the longer-term treatment of this chronic disorder.
引用
收藏
页码:1002 / 1008
页数:7
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