The Cognitive and Negative Symptoms in Schizophrenia, Trial (CONSIST): The efficacy of glutamatergic agents for negative symptoms and cognitive impairments

被引:301
|
作者
Buchanan, Robert W.
Javitt, Daniel C.
Marder, Stephen R.
Schooler, Nina R.
Gold, James M.
McMahon, Robert P.
Heresco-Levy, Uriel
Carpenter, William T.
机构
[1] Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Baltimore, MD 21228 USA
[2] Nathan S Kline Inst Psychiat Res, Orangeburg, NY 10962 USA
[3] Univ Calif Los Angeles, Los Angeles, CA USA
[4] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA
[5] Zucker Hillside Hosp, Glen Oaks, NY USA
[6] Hebrew Univ Jerusalem, Hadassah Med Sch, Ezrath Nashim Herzog Mem Hosp, IL-91010 Jerusalem, Israel
[7] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Psychiat, IL-91010 Jerusalem, Israel
来源
AMERICAN JOURNAL OF PSYCHIATRY | 2007年 / 164卷 / 10期
关键词
D O I
10.1176/appi.ajp.2007.06081358
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
objective: Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N-methyl-D-aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments. Method: The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine, D-cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores. Results: There were no significant differences in change in the SANS total score between glycine and placebo subjects or D-cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving D-cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or D-cycloserine and placebo subjects on the average cognition z score. Conclusions: The study results suggest that neither glycine nor D-cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments.
引用
收藏
页码:1593 / 1602
页数:10
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