Pyrkosch L, Lautenbacher L M, Mumm J, Plag J, Fehm L, Fydrich T, Ströhle A
Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Psychiatry and Neurosciences, Campus Charité Mitte, Germany; Humboldt-Universität zu Berlin, Faculty of Life Sciences, Department of Psychology, Germany.
Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Psychiatry and Neurosciences, Campus Charité Mitte, Germany.
J Psychiatr Res. 2025 Jan;181:151-159. doi: 10.1016/j.jpsychires.2024.10.018. Epub 2024 Oct 20.
Combination of exposure therapy with d-cycloserine (DCS) in patients suffering from anxiety disorders yielded promising results regarding treatment outcomes. However, less is known about short-term effects of DCS during the treatment process, e. g. its potential influence on anxiety during exposure sessions. In this exploratory secondary analysis using data from a randomized, double-blind, placebo-controlled trial, we investigated longitudinal changes in anxiety during exposure in agoraphobic patients receiving DCS or placebo (PBO).
73 patients suffering from agoraphobia (with or without panic disorder) were treated with 12 sessions of individual cognitive behavioral therapy including three exposure sessions. Patients were given either PBO or 50 mg of DCS after each successful exposure. Multilevel modeling was used to analyze changes in outcomes measured in subjective units of distress (SUDS) over three time points (i.e. the exposure sessions) in the two groups.
We observed a decline in several SUDS outcomes in the DCS group, namely initial anxiety, maximum anxiety during exposure and within-session habituation, while the PBO group mostly maintained similar levels of anxiety from session to session. Anxiety at the end of exposure appeared to be stable in the DCS group as well.
Our findings suggest potential short-term effects of DCS on anxiety during exposure. Long lasting and high degree of anxiety over exposure sessions is burdensome for the patients. Thus, modifications to reduce anxiety during exposure or to accelerate the learning process while maintaining the same treatment efficacy could be desirable. However, given the exploratory nature of the analyses, confirmatory studies testing the hypothesis of a decline of SUDS in agoraphobic patients are needed before confident conclusions can be made.
在焦虑症患者中,将暴露疗法与d -环丝氨酸(DCS)联合使用在治疗效果方面产生了令人鼓舞的结果。然而,关于DCS在治疗过程中的短期影响,例如其在暴露治疗期间对焦虑的潜在影响,人们了解较少。在这项探索性的二次分析中,我们使用了一项随机、双盲、安慰剂对照试验的数据,研究了接受DCS或安慰剂(PBO)的广场恐惧症患者在暴露治疗期间焦虑的纵向变化。
73名患有广场恐惧症(伴有或不伴有惊恐障碍)的患者接受了12次个体认知行为治疗,其中包括3次暴露治疗。每次成功暴露后,患者被给予PBO或50毫克DCS。使用多水平模型分析两组在三个时间点(即暴露治疗阶段)以主观痛苦单位(SUDS)衡量的结果变化。
我们观察到DCS组的几个SUDS结果有所下降,即初始焦虑、暴露期间的最大焦虑和治疗期间的习惯化,而PBO组在各治疗阶段的焦虑水平大多保持相似。DCS组在暴露治疗结束时的焦虑似乎也稳定。
我们的研究结果表明DCS在暴露治疗期间对焦虑有潜在的短期影响。在暴露治疗期间持续存在且高度的焦虑对患者来说是沉重的负担。因此,在保持相同治疗效果的同时,进行调整以减少暴露治疗期间的焦虑或加速学习过程可能是可取的。然而,鉴于分析的探索性性质,在得出可靠结论之前,需要进行验证性研究来检验广场恐惧症患者SUDS下降的假设。