Department of Psychiatry, Cooper University Hospital and Cooper Medical School of Rowan University, Camden, NJ, USA.
Bio-analytical Chemistry and Drug Discovery Section of the National Institute on Aging (NIA), National Institute of Health (NIH), Bethesda, MD, USA.
Biochim Biophys Acta Proteins Proteom. 2018 Jul;1866(7):831-839. doi: 10.1016/j.bbapap.2018.03.006. Epub 2018 Mar 18.
Post-traumatic stress disorder (PTSD) is a chronic and debilitating condition that is often refractory to standard frontline antidepressant therapy. A promising new approach to PTSD therapy is administration of a single sub-anesthetic dose of (R,S)-ketamine (Ket). The treatment produces rapid and significant therapeutic response, which lasts for only 4-7 days. In one of our studies, the mean duration of response was increased to 33 days when Ket administration was combined with a mindfulness-based cognitive therapy, Trauma Interventions using Mindfulness Based Extinction and Reconsolidation (TIMBER). We now report the results from a 20-patient study, which examined the duration of sustained response with combined TIMBER-Ket therapy, TIMBER-K arm, relative to the response observed in a placebo-controlled arm, TIMBER-P. A significant difference in the duration of response was observed between TIMBER-K and TIMBER-P arms: 34.44 ± 19.12 days and 16.50 ± 11.39 days, respectively (p = 0.022). Previous studies identified a negative correlation between antidepressant response to Ket and basal plasma concentrations of d-serine (DSR). In this study, the basal DSR levels positively correlated with the pre-treatment severity of PTSD symptoms (Pearson's r = 0.42, p = 0.07) and patients with basal DSR level ≥ 3.5 μM displayed not only higher PTSD severity but also shorter duration of response. The data indicate that basal DSR levels may serve as a biomarker of the severity of PTSD symptoms and as a predictor of clinical response. This article is part of a Special Issue entitled: d-Amino acids: biology in the mirror, edited by Dr. Loredano Pollegioni, Dr. Jean-Pierre Mothet and Dr. Molla Gianluca.
创伤后应激障碍(PTSD)是一种慢性和衰弱性疾病,通常对标准的一线抗抑郁治疗无效。一种有前途的 PTSD 治疗新方法是给予单次亚麻醉剂量的(R,S)-氯胺酮(Ket)。该治疗方法产生快速而显著的治疗反应,持续时间仅为 4-7 天。在我们的一项研究中,当 Ket 给药与正念认知疗法相结合时,创伤干预使用基于正念的灭绝和再巩固(TIMBER)时,反应的平均持续时间增加到 33 天。我们现在报告一项 20 例患者研究的结果,该研究检查了联合 TIMBER-Ket 治疗、TIMBER-K 臂的持续反应持续时间,与安慰剂对照臂、TIMBER-P 的反应相比。在 TIMBER-K 和 TIMBER-P 臂之间观察到反应持续时间的显著差异:分别为 34.44±19.12 天和 16.50±11.39 天(p=0.022)。先前的研究表明,Ket 对抗抑郁反应与基础血浆中 D-丝氨酸(DSR)浓度之间存在负相关。在这项研究中,基础 DSR 水平与 PTSD 症状的治疗前严重程度呈正相关(Pearson r=0.42,p=0.07),并且基础 DSR 水平≥3.5μM 的患者不仅表现出更高的 PTSD 严重程度,而且反应持续时间更短。这些数据表明,基础 DSR 水平可以作为 PTSD 症状严重程度的生物标志物,并作为临床反应的预测指标。本文是一个特刊的一部分,该特刊题为:D-氨基酸:镜像中的生物学,由 Loredano Pollegioni 博士、Jean-Pierre Mothet 博士和 Molla Gianluca 博士编辑。