Structural and functional neural alterations in suicidality among Veterans with PTSD
患有创伤后应激障碍 (PTSD) 的退伍军人自杀倾向的结构和功能神经改变
基本信息
- 批准号:10417101
- 负责人:
- 金额:--
- 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:2019-01-01 至 2024-09-30
- 项目状态:已结题
- 来源:
- 关键词:AffectAfghanistanAgeAnatomyArchitectureAreaAtrophicBehaviorBehavior assessmentBiological MarkersBrainBrain regionCause of DeathCessation of lifeCharacteristicsClinicalCognitionDataDiagnosticDiffusionDiffusion Magnetic Resonance ImagingEnvironmentFeeling suicidalFoundationsFrequenciesFunctional disorderFundingFutureGoalsGraphIndividualInfrastructureInjuryInsula of ReilInterventionInvestigationIraqLeadLimbic SystemLiteratureLocationMagnetic Resonance ImagingMeasuresMental DepressionMental Health ServicesMental disordersMentorsMentorshipMilitary PersonnelModelingMoodsNeurobiologyNeurosciencesParietalParticipantPathologyPatternPharmacologyPost-Traumatic Stress DisordersPrevalencePreventionRecording of previous eventsResearchRestRiskSeveritiesStressSuicideSuicide attemptSuicide preventionSymptomsSynapsesTechnologyThickTimeTrainingTraumaTraumatic Brain InjuryVeteransWarWorkbasebiomarker identificationbrain circuitrycareercohortcomorbiditycostdesigndisorder preventiondrug developmentexperiencegray matterideationimprovedimproved outcomeloved onesmild traumatic brain injurymood regulationmultimodal neuroimagingneuromechanismnovelnovel therapeuticsprogramsrelating to nervous systemresiliencesexsocioeconomicsstatisticsstress related disordersuicidal morbidity
项目摘要
PROJECT SUMMARY/ABSTRACT
Research: Veterans of the U.S. military die by suicide at a rate of two to six times that of their civilian
counterparts. Suicidal ideation (SI) and suicide attempts (SA), cardinal precursors to death by suicide, occur at
significantly greater frequency than death and cause immense individual and societal burden, yet relatively
little is known about their pathophysiology. This is especially so in posttraumatic stress disorder (PTSD), a
signature injury of the wars in Iraq and Afghanistan. High rates of comorbidity and inflated prevalence of both
suicidality and PTSD in Veterans, highlights the urgency of advancing understanding of the shared and
distinguishing neural mechanisms between these. Evidence of trauma- and stress-related synaptic loss and
large-scale alterations in intrinsic connectivity networks in brain regions implicated in mood, cognition, and
behavior exists in both SI/SA and PTSD literature. However, a major obstacle in field is the scarcity of
neurobiologically-based studies of SI/SA in PTSD cohorts. Preliminary data supports the notion that the
location and pattern of synaptic alterations may interact with individual and environmental characteristics to
affect clinical presentation and symptom severity. Specifically, Veterans with PTSD endorsing SI appear to
have a neural signature of synaptic alterations distinct from PTSD symptom severity, depression, and age.
Extending this work, state-of-the-art multimodal neuroimaging and behavioral assessment sessions will be
conducted in 96 Veterans across 3 study groups (n=32/group): PTSD only; PTSD+SI; PTSD+SA. Robust,
complimentary evidence of a unique pattern and location of synaptic alterations will be demonstrated using (a)
whole-brain vertex-wise structural magnetic resonance imaging (MRI) to measure cortical thickness, (b)
resting-state functional connectivity MRI (rs-fcMRI) to measure global brain connectivity (GBC), and (c)
diffusion MRI to measure diffusion GBC (dGBC), a measure of microstructural architecture and connectivity.
Veterans will be matched on age, sex, PTSD symptom severity, and history of traumatic brain injury. This study
may identify biomarkers of treatment targets in two of the operational priority areas for the VA – suicide and
PTSD, inform novel drug development of efficacious pharmacologic interventions, and ultimately advance the
field making way to alleviate suffering of millions of individuals – Veteran and civilian alike - struggling with
suicidality.
Candidate: Dr. Averill has demonstrated an unwavering commitment to improving Veterans’ mental health
care, with emphasis on PTSD and suicide prevention for well over a decade. Short-term goals include receipt of
the CDA-2 to both advance her expertise through rigorous training objectives (focused on the neurobiology of
SI/SA, multimodal neuroimaging, and statistics) and to provide data for future funding as she establishes a
niche program of research in the National Center for PTSD-Clinical Neurosciences Division (NCPTSD-CND).
Long-term goals include becoming a thought leader in the areas of suicide prevention and PTSD in Veterans
through empirical investigations aimed at informing novel drug development and improved prevention,
diagnostics, identification of biomarkers of risk and resilience in SI/SA, and treatment options.
Environment: The infrastructure, quality of mentors, supplementary funding support, technology, and
Veteran-focused research environment available at the National Center for PTSD-Clinical Neurosciences
Division and Yale are unparalleled. This offers unique opportunity to support Dr. Averill in her transition to
independence though exceptional targeted training/mentorship and to conduct a low cost/high yield study
with great potential to advance the field, lead to improved outcomes for Veterans, and set a foundation for a
successful VA-centric career.
项目摘要/摘要
研究:美军退伍军人自杀率是平民自杀率的两到六倍
对口单位。自杀意念(SI)和自杀未遂(SA)是自杀死亡的主要前兆,发生在
比死亡频率高得多,造成巨大的个人和社会负担,但相对
人们对它们的病理生理学知之甚少。这在创伤后应激障碍(PTSD)中尤其如此,
伊拉克和阿富汗战争中的标志性伤势。两者的高共患率和夸大的患病率
退伍军人中的自杀和创伤后应激障碍,突出了促进对共同和
区分这两者之间的神经机制。与创伤和应激相关的突触丢失和
大脑区域内固有连接网络的大规模变化与情绪、认知和
行为在SI/SA和创伤后应激障碍文献中都存在。然而,实地工作的一个主要障碍是缺乏
创伤后应激障碍队列中SI/SA的神经生物学研究。初步数据支持这样一种观点,即
突触改变的位置和模式可能与个体和环境特征相互作用
影响临床表现和症状严重程度。具体地说,患有创伤后应激障碍的退伍军人似乎支持SI
有突触改变的神经特征,不同于创伤后应激障碍症状的严重程度、抑郁和年龄。
扩展这项工作,最先进的多模式神经成像和行为评估会议将是
对96名退伍军人进行了3组研究(n=32/组):单纯创伤后应激障碍;创伤后应激障碍+SI;创伤后应激障碍+SA。健壮,
将使用(A)证明突触改变的独特模式和位置的补充证据
全脑顶端结构磁共振成像(MRI)测量皮质厚度,(B)
静息状态功能连通性磁共振成像(RS-fcMRI),用于测量全球大脑连通性(GBC),以及(C)
弥散磁共振成像测量弥散GBC(DGBC),这是微结构架构和连通性的测量。
退伍军人将在年龄、性别、创伤后应激障碍症状严重程度和创伤性脑损伤病史方面进行匹配。本研究
可在退伍军人自杀和退伍军人事务部的两个操作优先领域确定治疗目标的生物标记物
创伤后应激障碍,告知新药开发有效的药理干预措施,并最终促进
为缓解数百万人--老兵和平民--的痛苦而让路
自杀。
候选人:埃弗里尔博士表现出了对改善退伍军人心理健康的坚定承诺
护理,重点是创伤后应激障碍和自杀预防,长达十多年。短期目标包括收到
CDA-2通过严格的培训目标提高她的专业知识(重点是
SI/SA、多模式神经成像和统计学),并为未来的资金提供数据,因为她建立了
国家创伤后应激障碍中心-临床神经科学部(NCPTSD-CND)的利基研究计划。
长期目标包括成为退伍军人自杀预防和创伤后应激障碍领域的思想领袖
通过旨在为新药开发和改进预防提供信息的实证调查,
诊断、确定SI/SA风险和恢复能力的生物标记物,以及治疗选择。
环境:基础设施、导师的质量、补充资金支持、技术和
国家创伤后应激障碍临床神经科学中心提供以退伍军人为重点的研究环境
分部和耶鲁是无与伦比的。这提供了独特的机会来支持Averill博士过渡到
通过特殊的有针对性的培训/指导独立,并进行低成本/高收益的研究
具有推动这一领域的巨大潜力,为退伍军人带来更好的结果,并为
以退伍军人管理局为中心的成功职业生涯。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Lynnette Astrid Averill其他文献
Lynnette Astrid Averill的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Lynnette Astrid Averill', 18)}}的其他基金
Structural and functional neural alterations in suicidality among Veterans with PTSD
患有创伤后应激障碍 (PTSD) 的退伍军人自杀倾向的结构和功能神经改变
- 批准号:
10389495 - 财政年份:2019
- 资助金额:
-- - 项目类别:
Structural and functional neural alterations in suicidality among Veterans with PTSD
患有创伤后应激障碍 (PTSD) 的退伍军人自杀倾向的结构和功能神经改变
- 批准号:
10292415 - 财政年份:2019
- 资助金额:
-- - 项目类别:
Structural and functional neural alterations in suicidality among Veterans with PTSD
患有创伤后应激障碍 (PTSD) 的退伍军人自杀倾向的结构和功能神经改变
- 批准号:
9854738 - 财政年份:2019
- 资助金额:
-- - 项目类别:
Structural and functional neural alterations in suicidality among Veterans with PTSD
患有创伤后应激障碍 (PTSD) 的退伍军人自杀倾向的结构和功能神经改变
- 批准号:
10610389 - 财政年份:2019
- 资助金额:
-- - 项目类别:
相似海外基金
Drought and Climate Resilience of Smallholders in Afghanistan: Needs and Preferences Analysis
阿富汗小农的干旱和气候抵御能力:需求和偏好分析
- 批准号:
24K16366 - 财政年份:2024
- 资助金额:
-- - 项目类别:
Grant-in-Aid for Early-Career Scientists
'Diaspora States' in Somalia and Afghanistan: New Perspectives on Post-War Politics, Dual Citizenship and International Statebuilding
索马里和阿富汗的“侨民国家”:战后政治、双重国籍和国际国家建设的新视角
- 批准号:
EP/X022048/1 - 财政年份:2023
- 资助金额:
-- - 项目类别:
Fellowship
Improving learning outcomes in Afghanistan and Pakistan in the midst of COVID-19 through Community based system dynamics and project-based learning
通过基于社区的系统动态和基于项目的学习,在 COVID-19 期间改善阿富汗和巴基斯坦的学习成果
- 批准号:
ES/X014088/1 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Research Grant
On Politics and Justice: British Military Justice following War Crimes Allegations in Iraq and Afghanistan, 2001-present
论政治与司法:2001 年至今,伊拉克和阿富汗战争罪指控后的英国军事司法
- 批准号:
2745904 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Studentship
U.S and Afghanistan - why the nation-building project failed?
美国和阿富汗——国家建设项目为何失败?
- 批准号:
22K01385 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Grant-in-Aid for Scientific Research (C)
Market Economy and Conflict; Disjuncture between the Politics and Economics of Statebuilding in Afghanistan during 2001-2021
市场经济与冲突;
- 批准号:
ES/X006832/1 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Fellowship
Analysis of the structure of conflict between ethnicities in the transformation of national integration policy in Afghanistan
阿富汗民族融合政策转型中的族群冲突结构分析
- 批准号:
19K20529 - 财政年份:2019
- 资助金额:
-- - 项目类别:
Grant-in-Aid for Early-Career Scientists
Neurosteroid Intervention for PTSD in Iraq/Afghanistan-era Veterans
神经类固醇干预伊拉克/阿富汗时期退伍军人的创伤后应激障碍
- 批准号:
10417141 - 财政年份:2019
- 资助金额:
-- - 项目类别:
Neurosteroid Intervention for PTSD in Iraq/Afghanistan-era Veterans
神经类固醇干预伊拉克/阿富汗时期退伍军人的创伤后应激障碍
- 批准号:
10589071 - 财政年份:2019
- 资助金额:
-- - 项目类别:
A pilot assessment of miltefosine's efficacy and tolerability for treating cutaneous Leishmania tropica in Afghanistan
在阿富汗对米替福辛治疗皮肤热带利什曼原虫的疗效和耐受性进行初步评估
- 批准号:
MR/R018391/1 - 财政年份:2018
- 资助金额:
-- - 项目类别:
Research Grant














{{item.name}}会员




