The neural bases of placebo effects and their relation to regulatory processes
安慰剂效应的神经基础及其与调节过程的关系
基本信息
- 批准号:10539287
- 负责人:
- 金额:$ 70.06万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-07-01 至 2024-10-31
- 项目状态:已结题
- 来源:
- 关键词:Acupuncture TherapyAddressAffectAffectiveAffective SymptomsAlcohol abuseAnxietyAreaBrainBrain DiseasesCardiovascular DiseasesCaringCellular PhoneClinicalClinical ResearchClinical TreatmentClinical TrialsCognitiveConceptionsDeceptionDiseaseDrug abuseEmotionsExpectancyFailureFunctional Magnetic Resonance ImagingFundingFutureGrantIndividualInterventionJointsLearningLinkLiteratureMachine LearningMajor Depressive DisorderMediatingMediatorMental DepressionMental HealthMental disordersModelingMotivationNaloxoneNeural PathwaysNeurobiologyNeurologicNeuronal PlasticityOperative Surgical ProceduresOutcomePainParkinson DiseaseParticipantPathway interactionsPatientsPatternPattern RecognitionPersonsPharmaceutical PreparationsPharmacological TreatmentPharmacotherapyPhysiologyPlacebo EffectPlacebosPredispositionProcessPsyche structurePsychotherapyPublic HealthRandomizedRecording of previous eventsRegulationResearchRisk FactorsRoleShapesSleepSocial Anxiety DisorderSubstance Use DisorderSuggestionSymptomsSystemTaste PerceptionTestingTimeVisualWorkactive methodbasebrain pathwayclinical painclinical practiceclinically relevantclinically significantendogenous opioidsexpectationexperienceexperimental studyfollow-upgastrointestinal functionimprovednegative affectneuralneurochemistryneuroimagingneuromechanismneuroregulationpatient expectationpharmacologicplacebo analgesiapreventprogramspsychologicresilienceresponsesocialsocial influencesocial modelsuccesstheoriestranslational potentialtreatment response
项目摘要
Placebo treatments can induce clinically significant benefits, compared with no-treatment
controls, across a variety of disorders. But placebo treatments themselves are pharmacologically
and physically inert: Their benefits result from active brain and psychological responses to the
treatment context. Neuroscientific studies have established that placebo treatments influence
cortical-subcortical brain pathways and neurochemical systems relevant for expectation,
appraisals of personal and social meaning, and value-driven learning. These systems are also
related to symptom progression across mental health disorders and several other neurological
and substance use disorders. Understanding the brain and psychological mechanisms of placebo
effects will help improve psychological and neurological (e.g., neuromodulation-based)
treatments across disorders.
This R01 renewal funds an ongoing program of research that has made fundamental contributions
to this literature. It has also identified several significant gaps that are particularly important for
connecting placebo research to mental health. One gap is that our understanding of the brain
mechanisms underlying placebo effects comes almost purely from studies of pain. The proposed
studies extend previous work to study the brain pathways underlying placebo effects in anxiety
and social rejection, negative affective processes directly relevant for multiple mental health
disorders. Pattern-recognition (machine learning) analyses identify the most symptom-relevant
pathways, and test effects of placebo and other context interventions on these pathways. In Aim
1 (Experiments 1-3), we develop models across multiple affective symptoms, parsing affective
pathways into those that are symptom-specific and those that generalize across multiple
symptoms and outcomes. We also address the role of endogenous opioids, strongly linked to
placebo analgesia, in other negative affective experiences. Another gap is that most previous
studies of the context variables that drive strong placebo effects—including social influences,
treatment history—have not been studied extensively at the brain level. In Aim 2, we study the
brain pathways underlying several promising context interventions that enhance the strength of
placebo effects, including social modeling of successful or unsuccessful treatment response,
initial experiences of treatment success or failure, and the match between placebo suggestions
and a person’s predisposition to be receptive to them.
与不治疗相比,安慰剂治疗可诱导临床显著获益
控制,在各种疾病。但安慰剂治疗本身是不安全的,
和身体惰性:他们的好处来自活跃的大脑和心理反应,
治疗背景。神经科学研究已经证实,安慰剂治疗会影响
皮质-皮质下脑通路和与预期相关的神经化学系统,
对个人和社会意义的评价,以及价值驱动的学习。这些系统也
与精神健康障碍和其他几种神经系统疾病的症状进展相关
和物质使用障碍。了解安慰剂的大脑和心理机制
效果将有助于改善心理和神经(例如,基于神经调节)
治疗各种疾病。
R 01的更新资助了一项正在进行的研究计划,该计划做出了重要贡献
这些文学。它还查明了一些重大差距,
将安慰剂研究与心理健康联系起来一个差距是我们对大脑的理解
安慰剂效应的潜在机制几乎完全来自于疼痛研究。拟议
研究扩展了先前的工作,研究焦虑中安慰剂效应的大脑通路
社会排斥、负性情感过程与多重心理健康直接相关
紊乱模式识别(机器学习)分析确定最相关的
途径,并测试安慰剂和其他背景干预对这些途径的影响。在Aim中
1(实验1-3),我们开发了跨多种情感症状的模型,解析情感
这些途径分为特定于特定的途径和跨多个
症状和结果。我们还讨论了内源性阿片类药物的作用,与
安慰剂镇痛,在其他负面的情感体验。另一个差距是,
对驱动强烈安慰剂效应的背景变量的研究,包括社会影响,
治疗史-尚未在大脑水平上进行广泛研究。在目标2中,我们研究
几种有前景的背景干预措施的大脑通路,
安慰剂效应,包括成功或不成功治疗反应的社会建模,
治疗成功或失败的初步经验,以及安慰剂建议之间的匹配
以及一个人接受这些的倾向。
项目成果
期刊论文数量(73)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A neuroimaging biomarker for sustained experimental and clinical pain.
- DOI:10.1038/s41591-020-1142-7
- 发表时间:2021-01
- 期刊:
- 影响因子:82.9
- 作者:Lee JJ;Kim HJ;Čeko M;Park BY;Lee SA;Park H;Roy M;Kim SG;Wager TD;Woo CW
- 通讯作者:Woo CW
Predicting individual differences in placebo analgesia: contributions of brain activity during anticipation and pain experience.
- DOI:10.1523/jneurosci.3420-10.2011
- 发表时间:2011-01-12
- 期刊:
- 影响因子:0
- 作者:Wager TD;Atlas LY;Leotti LA;Rilling JK
- 通讯作者:Rilling JK
Brain mediators of biased social learning of self-perception in social anxiety disorder.
- DOI:10.1038/s41398-023-02587-z
- 发表时间:2023-09-02
- 期刊:
- 影响因子:6.8
- 作者:Koban, Leonie;Andrews-Hanna, Jessica R.;Ives, Lindsay;Wager, Tor D.;Arch, Joanna J.
- 通讯作者:Arch, Joanna J.
The placebo effect: advances from different methodological approaches.
- DOI:10.1523/jneurosci.4099-11.2011
- 发表时间:2011-11-09
- 期刊:
- 影响因子:0
- 作者:Meissner K;Bingel U;Colloca L;Wager TD;Watson A;Flaten MA
- 通讯作者:Flaten MA
Common and distinct neural representations of aversive somatic and visceral stimulation in healthy individuals.
- DOI:10.1038/s41467-020-19688-8
- 发表时间:2020-11-23
- 期刊:
- 影响因子:16.6
- 作者:Van Oudenhove L;Kragel PA;Dupont P;Ly HG;Pazmany E;Enzlin P;Rubio A;Delon-Martin C;Bonaz B;Aziz Q;Tack J;Fukudo S;Kano M;Wager TD
- 通讯作者:Wager TD
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{{ truncateString('TOR D. WAGER', 18)}}的其他基金
Psychosocial risk factors for chronic pain: Characterizing brain and genetic pathways and variation across understudied populations
慢性疼痛的心理社会危险因素:描述大脑和遗传途径以及未充分研究人群的差异
- 批准号:
10599396 - 财政年份:2022
- 资助金额:
$ 70.06万 - 项目类别:
The neural bases of placebo effects and their relation to regulatory processes
安慰剂效应的神经基础及其与调节过程的关系
- 批准号:
10358505 - 财政年份:2019
- 资助金额:
$ 70.06万 - 项目类别:
The neural bases of placebo effects and their relation to regulatory processes
安慰剂效应的神经基础及其与调节过程的关系
- 批准号:
10056222 - 财政年份:2019
- 资助金额:
$ 70.06万 - 项目类别:
fMRI-based Biomarkers for Multiple Components of Pain
基于功能磁共振成像的多种疼痛生物标志物
- 批准号:
8826094 - 财政年份:2013
- 资助金额:
$ 70.06万 - 项目类别:
fMRI-based Biomarkers for Multiple Components of Pain
基于功能磁共振成像的多种疼痛生物标志物
- 批准号:
9245657 - 财政年份:2013
- 资助金额:
$ 70.06万 - 项目类别:
fMRI-based Biomarkers for Multiple Components of Pain
基于功能磁共振成像的多种疼痛生物标志物
- 批准号:
8481081 - 财政年份:2013
- 资助金额:
$ 70.06万 - 项目类别:
fMRI-based Biomarkers for Multiple Components of Pain
基于功能磁共振成像的多种疼痛生物标志物
- 批准号:
8701264 - 财政年份:2013
- 资助金额:
$ 70.06万 - 项目类别:
fMRI-based Biomarkers for Multiple Components of Pain
基于功能磁共振成像的多种疼痛生物标志物
- 批准号:
9039027 - 财政年份:2013
- 资助金额:
$ 70.06万 - 项目类别:
fMRI-based Biomarkers for Multiple Components of Pain
基于功能磁共振成像的多种疼痛生物标志物
- 批准号:
8916319 - 财政年份:2013
- 资助金额:
$ 70.06万 - 项目类别:
Learning to avoid pain: Computational mechanisms and application to methamphetami
学习避免疼痛:计算机制及其在甲基苯丙胺中的应用
- 批准号:
7922059 - 财政年份:2009
- 资助金额:
$ 70.06万 - 项目类别:
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