Center for Anxiety Disorders Overwaal, Institution for Integrated Mental Health Care Pro Persona, Nijmegen, The Netherlands; Radboud University, Behavioural Science Institute, NijCare, Nijmegen, the Netherlands.
The University of Texas at Austin, Department of Psychology and Institute for Mental Health Research, Austin, TX, United States.
J Anxiety Disord. 2015 Aug;34:63-7. doi: 10.1016/j.janxdis.2015.06.005. Epub 2015 Jun 14.
Augmentation of exposure therapy with d-cycloserine (DCS) has proven efficacious across anxiety disorders, although results in PTSD have been mixed. Work in animals and anxiety-disordered patients suggest that the potentiating effects of DCS are dependent on the level of extinction learning during extinction training and exposure treatment, respectively. The aim of the current study was to replicate and extend previous work by examining the association between the degree of extinction learning and DCS efficacy in our randomized clinical trial on DCS (50 mg) versus placebo enhancement of exposure therapy in a chronic mixed-trauma PTSD sample (N=67; de Kleine, Hendriks, Kusters, Broekman, & van Minnen, 2012). The decline in subjective units of distress ratings collected during and across the exposure sessions were evaluated as indices of extinction learning. First, we examined whether extinction learning during an exposure session moderated DCS effects on self-reported PTSD symptoms at the next session. Second, we examined whether averaged extinction learning over the course of treatment interacted with group assignment to predict change over time and post treatment outcome. We did not find evidence that DCS effects were moderated by the degree of extinction learning, although, extinction learning was related to outcome regardless of group assignment. In PTSD, not one extinction-learning index has been consistently linked to DCS enhanced exposure treatment outcome. More (experimental) work needs to been done to unravel the complex interplay between extinction learning and DCS enhancement, especially in PTSD patients.
用 D-环丝氨酸 (DCS) 增强暴露疗法已被证明在各种焦虑障碍中有效,尽管在 PTSD 中的效果参差不齐。动物和焦虑障碍患者的研究表明,DCS 的增强作用分别取决于在消退训练和暴露治疗期间的消退学习程度。本研究的目的是复制和扩展之前的工作,通过检查在我们的一项关于 DCS(50mg)与安慰剂增强慢性混合创伤后应激障碍(PTSD)样本暴露治疗的随机临床试验中,消退学习程度与 DCS 疗效之间的关联,来检验在我们的一项关于 DCS(50mg)与安慰剂增强慢性混合创伤后应激障碍(PTSD)样本暴露治疗的随机临床试验中,消退学习程度与 DCS 疗效之间的关联(N=67;de Kleine、Hendriks、Kusters、Broekman 和 van Minnen,2012)。在暴露治疗期间和整个暴露治疗过程中收集的主观痛苦单位评分的下降被评估为消退学习的指标。首先,我们检查了在暴露治疗过程中,一个治疗疗程的消退学习是否会调节 DCS 对下一次治疗疗程中自我报告的 PTSD 症状的影响。其次,我们检查了治疗过程中平均消退学习是否与分组相互作用,以预测随时间的变化和治疗后的结果。我们没有发现 DCS 效果受到消退学习程度调节的证据,尽管无论分组如何,消退学习都与结果有关。在 PTSD 中,没有一个消退学习指标与 DCS 增强的暴露治疗结果一直有关。需要进行更多(实验性)工作来揭示消退学习和 DCS 增强之间的复杂相互作用,特别是在 PTSD 患者中。