The Neurobiology of Psychotherapy: Emotional Reactivity and Regulation in PTSD
心理治疗的神经生物学:创伤后应激障碍的情绪反应和调节
基本信息
- 批准号:8724560
- 负责人:
- 金额:$ 26.6万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-09-01 至 2016-08-31
- 项目状态:已结题
- 来源:
- 关键词:AftercareAmygdaloid structureAnimal ModelAnteriorAnxietyAnxiety DisordersAwarenessBase of the BrainBiological MarkersBrainClinicalConflict (Psychology)ConsciousDataDevelopmentDiseaseDorsalDown-RegulationEmotionalEmotionsEvidence based treatmentFaceFrightFunctional Magnetic Resonance ImagingFutureGoalsInferior frontal gyrusInterventionKnowledgeLateralLeftLifeLocationMapsMedialMental disordersMood DisordersNational Institute of Mental HealthNeurobiologyNeurosciencesOutcomePatientsPatternPlaguePost-Traumatic Stress DisordersPrefrontal CortexProcessPsychiatryPsychopathologyPsychotherapyPublic HealthRegulationResearchRouteSiteSolutionsStimulusStrategic PlanningSystemTherapeuticTranscranial magnetic stimulationTranslatingTranslationsWaiting Listsbasedesigneffective therapyemotion regulationevidence basefollow-upneural circuitneurobiological mechanismneuroimagingneuromechanismnovelprogramsrelating to nervous systemresponsetooltreatment response
项目摘要
Psychotherapy remains a cornerstone of treatment for many psychiatric disorders, and
can be highly highly effective for a portion of patients. Very little, however, is understood about the
neurobiological mechanisms of action of psychotherapy, nor are there biological markers for
who is likely to respond. For some disorders, such as posttraumatic stress disorder (PTSD),
psychotherapy is also the only evidence-based treatment, leaving non-responders with no
effective treatment alternative. A lot is known, by contrast, about the neural basis of PTSD.
Despite this, there is a large gap between our understanding of the neural basis of
psychopathology in PTSD and the mechanisms of therapeutic change, and an even larger gap
between those and an ability to use information from neuroimaging studies to guide the
development of novel, neurocircuitry-targeting treatments. This latter issue is one, in fact, that
plagues neuroimaging studies of psychiatric disorders more generally. Development of such
novel treatments is a major goal of the Strategic Plan of the NIMH, and thus the BRAINS RFA,
and may bring new hope to the treatment of severe illnesses, such as PTSD.
The overall goal of this research program is to apply functional magnetic resonance
imaging (fMRI) to elucidate the brain circuitry underlying improvement in response to
psychotherapy, and to leverage this knowledge to develop a novel, personalized, neurocircuitrytargeting
treatment using transcranial magnetic stimulation (TMS). One potential mechanism of
action of psychotherapy is the alteration of patterns of dysfunctional emotional processing.
Numerous studies with healthy subjects has delineated the neural circuitry for reacting to and
regulating negative emotion, and how it is perturbed in psychopathology. We propose to build
on this knowledge and study psychotherapeutic change and its pretreatment predictors by
systematically probing emotional reactivity and regulation using fMRI in patients with PTSD
before and after treatment with prolonged exposure psychotherapy (PE), versus wait list. Before
receiving PE, all patients will undergo mapping of the prefrontal cortex using concurrent TMS
and fMRI. Patterns of brain activation induced and modulated by TMS at a variety of prefrontal
sites will be compared to those associated with successful PE, thereby forming the basis for a
future neuroimaging-guided TMS intervention strategy that is directly informed by an
understanding of the neurocircuitry of treatment response. A successful outcome in this study
may therefore produce a paradigm shift in the translation of clinical neuroscience to brain circuitbased
interventions.
心理治疗仍然是许多精神疾病治疗的基石,
对一部分患者非常有效。然而,人们对这一点知之甚少。
心理治疗的神经生物学作用机制,也没有生物学标志物,
谁可能会回应。对于一些疾病,如创伤后应激障碍(PTSD),
心理治疗也是唯一的循证治疗,使无反应者没有
有效的治疗方法。相比之下,关于PTSD的神经基础,我们已经知道了很多。
尽管如此,在我们对神经基础的理解之间存在着很大的差距。
PTSD的精神病理学和治疗变化的机制,甚至更大的差距
以及利用神经影像学研究的信息来指导
开发新的神经回路靶向治疗。事实上,后一个问题是,
更普遍地困扰着精神疾病的神经影像学研究。发展这种
新的治疗方法是NIMH战略计划的主要目标,因此也是BRAINS RFA的主要目标,
并可能为创伤后应激障碍等严重疾病的治疗带来新的希望。
这项研究计划的总体目标是将功能性磁共振技术应用于
功能性磁共振成像(fMRI),以阐明大脑回路的改善,
心理治疗,并利用这些知识来开发一种新的,个性化的,神经回路靶向
使用经颅磁刺激(TMS)治疗。一种潜在的机制
心理治疗的作用是改变功能失调的情绪处理模式。
对健康受试者的许多研究已经描绘了神经回路,
调节负面情绪,以及它在精神病理学中是如何被扰乱的。我们提出建设
在此基础上,研究心理治疗变化及其治疗前预测因素,
使用功能磁共振成像系统地探索PTSD患者的情绪反应和调节
治疗前和治疗后的长期暴露心理治疗(PE),与等待名单。之前
接受PE,所有患者将使用并行TMS进行前额叶皮层标测
和功能磁共振成像经颅磁刺激诱发和调节的不同前额叶皮层的脑激活模式
将与成功PE相关的站点进行比较,从而为
未来的神经成像引导的TMS干预策略,直接由
了解治疗反应的神经回路。这项研究的成功结果
因此,可能会在临床神经科学向基于脑回路的翻译中产生范式转变。
干预措施。
项目成果
期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Emotional processing in anterior cingulate and medial prefrontal cortex.
- DOI:10.1016/j.tics.2010.11.004
- 发表时间:2011-02
- 期刊:
- 影响因子:19.9
- 作者:Etkin, Amit;Egner, Tobias;Kalisch, Raffael
- 通讯作者:Kalisch, Raffael
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Amit Etkin其他文献
Amit Etkin的其他文献
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{{ truncateString('Amit Etkin', 18)}}的其他基金
Validating of Machine Learning-Based EEG Treatment Biomarkers in Depression
验证基于机器学习的脑电图治疗抑郁症生物标志物
- 批准号:
10009501 - 财政年份:2020
- 资助金额:
$ 26.6万 - 项目类别:
Validating of Machine Learning-Based EEG Treatment Biomarkers in Depression
验证基于机器学习的脑电图治疗抑郁症生物标志物
- 批准号:
10116492 - 财政年份:2020
- 资助金额:
$ 26.6万 - 项目类别:
Validating of Machine Learning-Based EEG Treatment Biomarkers in Depression
验证基于机器学习的脑电图治疗抑郁症生物标志物
- 批准号:
10366060 - 财政年份:2020
- 资助金额:
$ 26.6万 - 项目类别:
Assessing an electroencephalography (EEG) biomarker of response to transcranial magnetic stimulation for major depression
评估重度抑郁症对经颅磁刺激反应的脑电图 (EEG) 生物标志物
- 批准号:
9933192 - 财政年份:2020
- 资助金额:
$ 26.6万 - 项目类别:
A "Circuits-First" Platform for Personalized Neurostimulation Treatment
用于个性化神经刺激治疗的“电路优先”平台
- 批准号:
10214488 - 财政年份:2019
- 资助金额:
$ 26.6万 - 项目类别:
A "Circuits-First" Platform for Personalized Neurostimulation Treatment
用于个性化神经刺激治疗的“电路优先”平台
- 批准号:
10000142 - 财政年份:2019
- 资助金额:
$ 26.6万 - 项目类别:
A "Circuits-First" Platform for Personalized Neurostimulation Treatment
用于个性化神经刺激治疗的“电路优先”平台
- 批准号:
10019435 - 财政年份:2019
- 资助金额:
$ 26.6万 - 项目类别:
A Circuit Approach to Mechanisms and Predictors of Topiramate Response
托吡酯反应机制和预测因子的电路方法
- 批准号:
10473684 - 财政年份:2018
- 资助金额:
$ 26.6万 - 项目类别:
A Circuit Approach to Mechanisms and Predictors of Topiramate Response
托吡酯反应机制和预测因子的电路方法
- 批准号:
10237286 - 财政年份:2018
- 资助金额:
$ 26.6万 - 项目类别:
A “Circuits-First” Platform for Personalized Neurostimulation Treatment
用于个性化神经刺激治疗的“电路优先”平台
- 批准号:
9552929 - 财政年份:2017
- 资助金额:
$ 26.6万 - 项目类别: