S-Adenosyl Methionine (SAMe) Augmentation of Serotonin Reuptake Inhibitors for Antidepressant Nonresponders With Major Depressive Disorder: A Double-Blind, Randomized Clinical Trial

被引:158
作者
Papakostas, George I. [1 ]
Mischoulon, David [1 ]
Shyu, Irene [1 ]
Alpert, Jonathan E. [1 ]
Fava, Maurizio [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Depress Clin & Res Program, Sch Med,Ctr Treatment Resistant Depress, Boston, MA 02114 USA
关键词
STAR-ASTERISK-D; OUTCOMES;
D O I
10.1176/appi.ajp.2009.09081198
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Despite the progressive increase in the number of antidepressants, many patients with major depressive disorder continue to be symptomatic. Clearly, there is an urgent need to develop better tolerated and more effective treatments for this disorder. The use of S-adenosyl methionine (SAMe), a naturally occurring molecule that serves as a methyl donor in human cellular metabolism, as adjunctive treatment for antidepressant nonresponders with major depressive disorder represents one such effort toward novel pharmacotherapy development. Method: Participants were 73 serotonin reuptake inhibitor (SRI) nonresponders with major depressive disorder enrolled in a 6-week, double-blind, randomized trial of adjunctive oral SAMe (target dose: 800 mg/twice daily). Patients continued to receive their SRI treatment at a stable dose throughout the 6-week trial. The primary outcome measure for the study was the response rates according to the 17-item Hamilton Depression Rating Scale (HAM D). Results: The HAM D response and remission rates were higher for patients treated with adjunctive SAMe (36.1% and 25.8%, respectively) than adjunctive placebo (17.6% versus 11.7%, respectively). The number needed to treat for response and remission was approximately one in six and one in seven, respectively. There was no statistically significant difference in the proportion of SAMe- versus placebo-treated patients who discontinued the trial for any reason (20.6% versus 29.5%, respectively), due to adverse events (5.1% versus 8.8%, respectively), or due to inefficacy (5.1% versus 11.7%, respectively). Conclusions: These preliminary results suggest that SAMe can be an effective, well-tolerated, and safe adjunctive treatment strategy for SRI nonresponders with major depressive disorder and warrant replication.
引用
收藏
页码:942 / 948
页数:7
相关论文
共 16 条
[1]   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 [J].
Alpert, JE ;
Papakostas, G ;
Mischoulon, D ;
Worthington, JJ ;
Petersen, T ;
Mahal, Y ;
Burns, A ;
Bottiglieri, T ;
Nierenberg, AA ;
Fava, M .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2004, 24 (06) :661-664
[2]  
ALPERT JE, 2008, NATURAL MED PSYCHIAT, P68
[3]   S-adenosyl-L-methionine (SAMe):: from the bench to the bedside -: molecular basis of a pleiotrophic molecule [J].
Bottiglieri, T .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 76 (05) :1151S-1157S
[4]   S-ADENOSYL-L-METHIONINE (SAME) AS ANTIDEPRESSANT - METAANALYSIS OF CLINICAL-STUDIES [J].
BRESSA, GM .
ACTA NEUROLOGICA SCANDINAVICA, 1994, 89 :7-14
[5]  
First M. B., 1995, STRUCTURED CLIN INTE
[6]  
GUY W, 1976, PUBLICATION NATL I M
[7]   A RATING SCALE FOR DEPRESSION [J].
HAMILTON, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1960, 23 (01) :56-62
[8]  
HARDY M, 2002, PUBLICATION US DEP H
[9]  
IRUELA LM, 1993, AM J PSYCHIAT, V150, P522
[10]   Diagnostic and Statistical Manual of Mental Disorders [J].
Mittal, Vijay A. ;
Walker, Elaine F. .
PSYCHIATRY RESEARCH, 2011, 189 (01) :158-159