Brain Research and Innovation Centre, Ministry of Defence, Utrecht, the Netherlands.
Department of Translational Neuroscience, UMC Utrecht Brain Center, Utrecht University, Utrecht, The Netherlands.
Transl Psychiatry. 2023 Dec 7;13(1):376. doi: 10.1038/s41398-023-02660-7.
Current evidence-based treatments for post-traumatic stress disorder (PTSD) are efficacious in only part of PTSD patients. Therefore, novel neurobiologically informed approaches are urgently needed. Clinical and translational neuroscience point to altered learning and memory processes as key in (models of) PTSD psychopathology. We extended this notion by clarifying at a meta-level (i) the role of information valence, i.e. neutral versus emotional/fearful, and (ii) comparability, as far as applicable, between clinical and preclinical phenotypes. We hypothesized that cross-species, neutral versus emotional/fearful information processing is, respectively, impaired and enhanced in PTSD. This preregistered meta-analysis involved a literature search on PTSD+Learning/Memory+Behavior, performed in PubMed. First, the effect of information valence was estimated with a random-effects meta-regression. The sources of variation were explored with a random forest-based analysis. The analyses included 92 clinical (N = 6732 humans) and 182 preclinical (N = 6834 animals) studies. A general impairment of learning, memory and extinction processes was observed in PTSD patients, regardless of information valence. Impaired neutral learning/memory and fear extinction were also present in animal models of PTSD. Yet, PTSD models enhanced fear/trauma memory in preclinical studies and PTSD impaired emotional memory in patients. Clinical data on fear/trauma memory was limited. Mnemonic phase and valence explained most variation in rodents but not humans. Impaired neutral learning/memory and fear extinction show stable cross-species PTSD phenotypes. These could be targeted for novel PTSD treatments, using information gained from neurobiological animal studies. We argue that apparent cross-species discrepancies in emotional/fearful memory deserve further in-depth study; until then, animal models targeting this phenotype should be applied with utmost care.
目前针对创伤后应激障碍(PTSD)的循证治疗方法对部分 PTSD 患者有效。因此,迫切需要新的神经生物学指导方法。临床和转化神经科学表明,改变学习和记忆过程是 PTSD 病理模型的关键。我们通过在元水平上澄清(i)信息效价(即中性与情感/恐惧)的作用,以及(ii)临床和临床前表型之间的可比性(在适用的情况下),扩展了这一概念。我们假设,跨物种的中性与情感/恐惧信息处理在 PTSD 中分别受损和增强。这项预先注册的元分析涉及在 PubMed 上进行 PTSD+学习/记忆+行为的文献检索。首先,使用随机效应元回归估计信息效价的影响。使用基于随机森林的分析探索变异源。分析包括 92 项临床研究(N=6732 人)和 182 项临床前研究(N=6834 种动物)。无论信息效价如何,PTSD 患者都表现出学习、记忆和遗忘过程的普遍受损。在 PTSD 动物模型中也存在中性学习/记忆和恐惧遗忘受损的情况。然而,PTSD 模型在临床前研究中增强了恐惧/创伤记忆,而 PTSD 则损害了患者的情绪记忆。关于恐惧/创伤记忆的临床数据有限。记忆阶段和效价解释了啮齿动物中大部分的变异,但在人类中则不然。中性学习/记忆受损和恐惧遗忘显示出稳定的跨物种 PTSD 表型。这些可以成为针对 PTSD 的新型治疗方法的目标,利用从神经生物学动物研究中获得的信息。我们认为,情绪/恐惧记忆中明显的跨物种差异值得进一步深入研究;在那之前,应该谨慎应用针对该表型的动物模型。