D-Cycloserine Augmentation of Exposure Therapy for Post-Traumatic Stress Disorder: A Pilot Randomized Clinical Trial

被引:153
作者
Difede, JoAnn [1 ,2 ]
Cukor, Judith [1 ,2 ]
Wyka, Katarzyna [1 ]
Olden, Megan [1 ,2 ]
Hoffman, Hunter [3 ,4 ]
Lee, Francis S. [1 ,2 ]
Altemus, Margaret [1 ,2 ]
机构
[1] Weill Cornell Med Coll, Dept Psychiat, New York, NY 10065 USA
[2] NewYork Presbyterian Hosp, New York, NY USA
[3] Univ Washington, Dept Mech Engn, Human Interface Technol Lab, Seattle, WA 98195 USA
[4] Univ Washington, Human Photon Lab, Seattle, WA 98195 USA
关键词
post-traumatic stress disorder; exposure therapy; virtual reality; D-cycloserine; translational research; terrorism; PLACEBO-CONTROLLED TRIAL; SOCIAL ANXIETY DISORDER; RECEPTOR COMPLEX; EXTINCTION; FEAR; INDIVIDUALS; IMIPRAMINE; RATS;
D O I
10.1038/npp.2013.317
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Viewing post-traumatic stress disorder (PTSD) as a disorder of emotional learning, this study used a cognitive enhancer synergistically with virtual reality exposure (VRE) therapy for the treatment of PTSD. The main objective was to determine if a novel pharmacotherapy, D-cycloserine (DCS), enhanced the efficacy of the psychotherapy. Pre-clinical studies suggest that when fear extinction occurs during DCS administration, neuroplasticity may be enhanced. VRE therapy is a particularly promising format to test the hypothesis that DCS enhances extinction learning, as sensory fear cues are standardized across patients. In a pilot randomized, double-blind, placebo-controlled trial, 100 mg of DCS or placebo was administered 90 min before each weekly VRE session, to ensure peak plasma concentrations during the sessions in 25 patients with chronic PTSD. The primary outcome measure was the Clinician Administered PTSD Scale (CAPS). Secondary outcome measures included the Beck Depression Inventory-II and the State-Trait Anger Expression Inventory-2. Assessments occurred at pre-treatment, following sessions 3, 6, 10, post-treatment, and at 6 months. The difference in CAPS between the VRE-DCS (n = 13) and VRE-placebo (n = 12) groups increased over time beginning at 6 weeks, with medium to large between-group effect sizes immediately post-treatment and 6 months later (d = 0.68 and d = 1.13, respectively). A similar pattern was observed for depression, anger expression, and sleep. PTSD remission rates were significantly greater for the VRE-DCS group (46% vs 8% at post-treatment; 69% vs 17% at 6 months). Patients in the VRE-DCS group showed earlier and greater improvement in PTSD symptoms compared with the VRE-placebo group. These results suggest a promising new treatment for PTSD.
引用
收藏
页码:1052 / 1058
页数:7
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