Vanuk John R, Pace-Schott Edward F, Bullock Ayla, Esbit Simon, Dailey Natalie S, Killgore William D S
Department of Psychiatry, College of Medicine, University of Arizona, Tucson, AZ, United States.
Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, United States.
Front Behav Neurosci. 2022 Sep 12;16:886816. doi: 10.3389/fnbeh.2022.886816. eCollection 2022.
Disrupted sleep is a major feature in numerous clinical disorders and is related to decrements in affective memory processing. The prevalence of sleep disruption in post-traumatic stress disorder (PTSD) is suggested to be a key feature that exacerbates the impaired ability to recall extinction memories during experimental fear conditioning. We hypothesized that an intervention employing blue-wavelength light therapy (BLT) to regulate sleep and stabilize circadian rhythms in patients with PTSD (i.e., via regulated morning exposure) would be associated with PTSD symptom improvement, decreased sleep-related complaints, as well as improved consolidation and retention of extinction memories relative to a fear conditioning/extinction paradigm. Eighty-two individuals with PTSD underwent a well-validated fear conditioning/extinction protocol with subsequent assignment to receive morning BLUE (BLT) or placebo AMBER (ALT) light therapy daily for 30-min over 6-weeks. Participants returned after the intervention for post-treatment extinction recall, comprised of exposure to the previously conditioned stimuli, with the difference in skin conductance response between the "extinguished" and the "never-extinguished" stimuli at follow-up. Participants also viewed previously conditioned stimuli in a novel context during a functional magnetic resonance imaging (fMRI) scan. BLUE light therapy was associated with improvements relative to correlated decreases between PTSD symptoms and sleep-related complaints. Participants receiving BLT also sustained retention of the extinction memory, while those in the placebo amber light treatment group showed impairment, characterized by the restoration of the extinguished fear response after 6-weeks. Participants in the ALT also demonstrated greater reactivity in the left insula when viewing the previously extinguished fear-conditioned stimuli in a novel context. Daily BLUE-wavelength morning light exposure was associated with greater retention of extinction learning in patients with PTSD when compared to ALT, as supported by both autonomic and neurobiological reactivity. We speculate that improved sleep facilitated by a stabilized circadian rhythm, after fear-learning, led to greater consolidation of the fear extinction memory, decreased PTSD symptom presentation, and associated decreases in sleep-related complaints. Prominent exposure treatments for PTSD incorporate principles of fear extinction, and our findings suggest that blue light treatment may facilitate treatment gains by promoting the consolidation of extinction memories via improved sleep.
睡眠中断是众多临床疾病的一个主要特征,并且与情感记忆处理能力的下降有关。创伤后应激障碍(PTSD)中睡眠中断的患病率被认为是一个关键特征,它会加剧在实验性恐惧条件反射过程中回忆消退记忆的受损能力。我们假设,采用蓝光疗法(BLT)来调节PTSD患者的睡眠并稳定昼夜节律(即通过规律的早晨光照暴露),将与PTSD症状改善、睡眠相关主诉减少以及相对于恐惧条件反射/消退范式而言,消退记忆的巩固和保持得到改善相关。82名PTSD患者接受了一项经过充分验证的恐惧条件反射/消退方案,随后被分配每天接受30分钟的早晨蓝光(BLT)或安慰剂琥珀光(ALT)治疗,为期6周。干预结束后,参与者返回进行治疗后消退回忆,包括暴露于先前条件化的刺激,随访时“消退”和“从未消退”刺激之间的皮肤电导反应差异。参与者还在功能磁共振成像(fMRI)扫描期间在新环境中观看先前条件化的刺激。相对于PTSD症状与睡眠相关主诉之间的相关下降,蓝光疗法带来了改善。接受BLT的参与者也维持了消退记忆,而安慰剂琥珀光治疗组的参与者则表现出受损,其特征是6周后消退的恐惧反应恢复。ALT组的参与者在新环境中观看先前消退的恐惧条件化刺激时,左侧脑岛也表现出更大的反应性。与ALT相比,每天早晨暴露于蓝光波长与PTSD患者消退学习的更好保持相关,这得到了自主神经和神经生物学反应性的支持。我们推测,恐惧学习后昼夜节律稳定促进的睡眠改善,导致恐惧消退记忆得到更好巩固,PTSD症状表现减少,以及睡眠相关主诉相应减少。PTSD的显著暴露疗法纳入了恐惧消退原则,我们的研究结果表明,蓝光治疗可能通过改善睡眠促进消退记忆的巩固来促进治疗效果。