S-adenosyl-L-methionine (SAMe) as an adjunct for resistant major depressive disorder -: An open trial following partial or nonresponse to selective serotonin reuptake inhibitors or venlafaxine

被引:67
作者
Alpert, JE
Papakostas, G
Mischoulon, D
Worthington, JJ
Petersen, T
Mahal, Y
Burns, A
Bottiglieri, T
Nierenberg, AA
Fava, M
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Psychiat,Depress Clin & Res Program, Boston, MA 02114 USA
[2] Baylor Inst Metabol Dis, Dallas, TX USA
关键词
D O I
10.1097/01.jcp.0000145339.45794.cd
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The purpose of this open trial was to evaluate the safety, tolerability, and efficacy of oral S-adenosyl-L-methionine as an antidepressant adjunct among partial and nonresponders to serotonin reuptake inhibitors or venlafaxine. Method: Thirty antidepressant-treated adult outpatients with persisting major depressive disorder received 800 to 1600 mg of S-adenoSyl-L-methionine tosylate over a 6-week trial. Results: Intent-to-treat analyses based on the Hamilton Depression Rating Scale revealed a response rate of 50% and a remission rate of 43% following augmentation with S-adenosyl-L-methionine. Gastrointestinal symptoms and headaches were the most common side effects. Conclusion: Augmentation of selective serotonin reuptake inhibitors or venlafaxine with S-adenosyl-L-methionine warrants a placebo-controlled trial in resistant depression.
引用
收藏
页码:661 / 664
页数:4
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