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本文引用的文献

1
An Electroencephalography Connectomic Profile of Posttraumatic Stress Disorder.创伤后应激障碍的脑电图连接组学特征。
Am J Psychiatry. 2020 Mar 1;177(3):233-243. doi: 10.1176/appi.ajp.2019.18080911. Epub 2020 Jan 22.
2
Efficacy of Deep Brain Stimulation of the Ventral Anterior Limb of the Internal Capsule for Refractory Obsessive-Compulsive Disorder: A Clinical Cohort of 70 Patients.内侧囊腹前肢深部脑刺激治疗难治性强迫症的疗效:70 例临床队列研究。
Am J Psychiatry. 2020 Mar 1;177(3):265-271. doi: 10.1176/appi.ajp.2019.19060656. Epub 2020 Jan 7.
3
Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program.可复制的焦虑遗传风险位点:来自百万退伍军人计划中约 20 万名参与者的结果。
Am J Psychiatry. 2020 Mar 1;177(3):223-232. doi: 10.1176/appi.ajp.2019.19030256. Epub 2020 Jan 7.
4
Effect of CBT on Biased Semantic Network in Panic Disorder: A Multicenter fMRI Study Using Semantic Priming.认知行为疗法对惊恐障碍偏向语义网络的影响:一项使用语义启动的多中心 fMRI 研究。
Am J Psychiatry. 2020 Mar 1;177(3):254-264. doi: 10.1176/appi.ajp.2019.19020202. Epub 2019 Dec 16.
5
Individual Patterns of Abnormality in Resting-State Functional Connectivity Reveal Two Data-Driven PTSD Subgroups.静息态功能连接异常的个体模式揭示了两种数据驱动的 PTSD 亚组。
Am J Psychiatry. 2020 Mar 1;177(3):244-253. doi: 10.1176/appi.ajp.2019.19010060. Epub 2019 Dec 16.
6
The AURORA Study: a longitudinal, multimodal library of brain biology and function after traumatic stress exposure.AURORA 研究:创伤后应激暴露后大脑生物学和功能的纵向、多模态文库。
Mol Psychiatry. 2020 Feb;25(2):283-296. doi: 10.1038/s41380-019-0581-3. Epub 2019 Nov 19.
7
Changes in Dosing and Dose Timing of D-Cycloserine Explain Its Apparent Declining Efficacy for Augmenting Exposure Therapy for Anxiety-related Disorders: An Individual Participant-data Meta-analysis.D-环丝氨酸给药剂量和时间的变化解释了其增强焦虑相关障碍暴露疗法的疗效似乎逐渐下降的原因:一项个体参与者数据的荟萃分析。
J Anxiety Disord. 2019 Dec;68:102149. doi: 10.1016/j.janxdis.2019.102149. Epub 2019 Sep 23.
8
Deletion of CRH From GABAergic Forebrain Neurons Promotes Stress Resilience and Dampens Stress-Induced Changes in Neuronal Activity.从γ-氨基丁酸能前脑神经元中删除促肾上腺皮质激素释放激素可增强应激恢复力并减轻应激诱导的神经元活动变化。
Front Neurosci. 2019 Sep 20;13:986. doi: 10.3389/fnins.2019.00986. eCollection 2019.
9
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.国际 PTSD 全基因组关联研究的荟萃分析确定了性别和祖先特异性的遗传风险位点。
Nat Commun. 2019 Oct 8;10(1):4558. doi: 10.1038/s41467-019-12576-w.
10
Novel pharmacological targets in drug development for the treatment of anxiety and anxiety-related disorders.新型药理学靶点在治疗焦虑和焦虑相关障碍的药物研发中的应用。
Pharmacol Ther. 2019 Dec;204:107402. doi: 10.1016/j.pharmthera.2019.107402. Epub 2019 Aug 27.

跨电路和遗传学翻译以推进恐惧和焦虑相关障碍的进展。

Translating Across Circuits and Genetics Toward Progress in Fear- and Anxiety-Related Disorders.

机构信息

McLean Hospital, Harvard Medical School, Belmont, Mass.

出版信息

Am J Psychiatry. 2020 Mar 1;177(3):214-222. doi: 10.1176/appi.ajp.2020.20010055.

DOI:10.1176/appi.ajp.2020.20010055
PMID:32114783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7723454/
Abstract

Anxiety and fear-related disorders are common and disabling, and they significantly increase risk for suicide and other causes of morbidity and mortality. However, there is tremendous potential for translational neuroscience to advance our understanding of these disorders, leading to novel and powerful interventions and even to preventing their initial development. This overview examines the general circuits and processes thought to underlie fear and anxiety, along with the promise of translational research. It then examines some of the data-driven "next-generation" approaches that are needed for discovery and understanding but that do not always fit neatly into established models. From one perspective, these disorders offer among the most tractable problems in psychiatry, with a great deal of accumulated understanding, across species, of neurocircuit, behavioral, and, increasingly, genetic mechanisms, of how dysregulation of fear and threat processes contributes to anxiety-related disorders. One example is the progressively sophisticated understanding of how extinction underlies the exposure therapy component of cognitive-behavioral therapy approaches, which are ubiquitously used across anxiety and fear-related disorders. However, it is also critical to examine gaps in our understanding between reasonably well-replicated examples of successful translation, areas of significant deficits in knowledge, and the role of large-scale data-driven approaches in future progress and discovery. Although a tremendous amount of progress is still needed, translational approaches to understanding, treating, and even preventing anxiety and fear-related disorders offer great opportunities for successfully bridging neuroscience discovery to clinical practice.

摘要

焦虑和恐惧相关障碍很常见且具有致残性,它们会显著增加自杀和其他发病率和死亡率的风险。然而,转化神经科学有巨大的潜力来增进我们对这些障碍的理解,从而产生新的、强大的干预措施,甚至可以预防它们的最初发展。本篇综述考察了被认为是恐惧和焦虑的基础的一般回路和过程,以及转化研究的前景。然后,它检查了一些数据驱动的“下一代”方法,这些方法对于发现和理解是必要的,但并不总是符合既定模型。从一个角度来看,这些障碍提供了精神病学中最具可操作性的问题之一,具有大量跨物种的神经回路、行为以及越来越多的遗传机制的积累理解,即恐惧和威胁过程的失调如何导致与焦虑相关的障碍。一个例子是如何逐渐深入地理解,为什么消退是认知行为疗法暴露疗法的组成部分,这种方法在焦虑和恐惧相关障碍中被广泛使用。然而,检查成功转化的合理复制例子、知识的重大缺陷领域以及大规模数据驱动方法在未来进展和发现中的作用之间的理解差距也是至关重要的。尽管仍需要取得巨大的进展,但理解、治疗甚至预防焦虑和恐惧相关障碍的转化方法为成功地将神经科学发现与临床实践联系起来提供了巨大的机会。