Heart-Brain Interactions In Human Acute Ischemic Stroke
人类急性缺血性中风的心脑相互作用
基本信息
- 批准号:7585368
- 负责人:
- 金额:$ 37.96万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-05-15 至 2014-04-30
- 项目状态:已结题
- 来源:
- 关键词:AcuteAcute Brain InjuriesAddressAdoptedAdrenal GlandsAffectAnatomyAtrial FibrillationBlood GlucoseBrainBrain DiseasesBrain regionCardiacCerebral IschemiaCerebrumCongenital Heart DefectsCoronary ArteriosclerosisDataData SetDevelopmentDiagnosisEducational process of instructingElectrocardiogramEnzymesEventFunctional Magnetic Resonance ImagingGoalsHeartHeart DiseasesHumanHyperglycemiaInfarctionInjuryInsula of ReilIschemiaIschemic StrokeKnowledgeLeadLinkLocationMagnetic Resonance ImagingMapsMediatingMethodologyMethodsModelingMorbidity - disease rateMultivariate AnalysisMyocardialNervous System TraumaNeurological outcomeOutcomePathway interactionsPatientsPlayPopulationPrevalencePrevention strategyPreventiveResearchResearch PersonnelRiskRoleSerumSiteStatistical MethodsStrokeSubgroupSudden DeathSympathetic Nervous SystemTechniquesTestingTextbooksTissuesTroponinTroponin TWorkacute stressacute strokebasebiological adaptation to stresscohortimprovedmortalitypatient populationprospectivepublic health relevancerelating to nervous systemresponse
项目摘要
DESCRIPTION (provided by applicant): Acute brain infarcts can lead to injury to the heart in the absence of primary cardiac causes, with serious outcomes ranging from myocardial damage to sudden death. Our research aims to investigate the neuroanatomic substrate of myocardial injury and acute stress response occurring after ischemic stroke and link this localization to tissue outcome in cerebral ischemia. Identification of a cerebral site for stroke-related myocardial injury and acute stress response could facilitate development of preventive strategies and improve neurological outcome and survival. However, there are unresolved issues in the study of heart-brain interactions due to inability to differentiate between neurogenic and cardiogenic mechanisms of myocardial injury and the bias caused by using a-priori anatomic assumptions in the study of cerebral localization. We have recently demonstrated that the permutation method originally developed for functional MRI analysis is a feasible approach in the study of heart-brain interactions. The method is free from the bias of an a-priori hypothesis as to any specific location and tests the null hypothesis at the voxel level in a statistically valid manner for correlation with an externally defined event. Using this methodology we have demonstrated that infarction in the right insula is associated with elevated serum troponin-T level indicating acute myocardial injury. Here we propose to first validate our findings in a prospective dataset, and then extend this work by developing an anatomical map for acute stress response defined by acute stress hyperglycemia in acute ischemic stroke. Specifically, we will: 1) Test the hypothesis that there are focal brain regions that when infarcted are associated with cardiac troponin-T elevation indicative of myocardial injury. 2) Test the hypothesis that there are focal brain regions that when infarcted are associated with acute stress response characterized by acute stress hyperglycemia. 3) Identify whether the neural substrate linked to cardiac and systemic alterations confers an independent risk for myocardial injury and acute stress response in acute ischemic stroke. If proven, the information gained from this research could be used to generate models that can accurately assess the risk for cardiac and systemic complications in a given stroke patient. PUBLIC HEALTH RELEVANCE:
Acute brain injury can independently lead to injury to the heart in the absence of primary cardiac causes, often with serious outcomes ranging from myocardial damage to sudden death. The goal of our research is to investigate the brain anatomy of neurogenic myocardial injury in acute ischemic stroke. Identification of a cerebral site that is linked to stroke-related myocardial injury could facilitate development of preventive strategies and allow the timely management of cardiac complications and thus lead to improved neurological outcomes and survival in stroke patients.
描述(由申请人提供):急性脑梗死可在无原发心脏原因的情况下导致心脏损伤,其严重后果从心肌损伤到猝死不等。我们的研究旨在探讨缺血性脑卒中后心肌损伤和急性应激反应的神经解剖学基础,并将这种定位与脑缺血的组织结局联系起来。确定脑卒中相关心肌损伤和急性应激反应的大脑部位有助于制定预防策略,改善神经预后和生存率。然而,由于无法区分心肌损伤的神经源性和心源性机制,以及在脑定位研究中使用先验解剖学假设造成的偏差,在心脑相互作用的研究中存在未解决的问题。我们最近已经证明,排列方法最初开发的功能MRI分析是一种可行的方法,在心脏-大脑相互作用的研究。该方法没有对任何特定位置的先验假设的偏见,并以统计有效的方式在体素级别测试与外部定义事件的相关性的零假设。使用这种方法,我们已经证明了右岛梗死与血清肌钙蛋白- t水平升高有关,这表明急性心肌损伤。在这里,我们建议首先在前瞻性数据集中验证我们的发现,然后通过开发急性缺血性卒中急性应激高血糖定义的急性应激反应解剖图来扩展这项工作。具体来说,我们将:1)验证脑局灶性区域在梗死时与心肌肌钙蛋白- t升高相关的假设,这表明心肌损伤。2)验证脑局灶区梗死时与急性应激反应相关的假设,急性应激性高血糖为特征。3)确定与心脏和全身改变相关的神经底物是否在急性缺血性卒中中具有心肌损伤和急性应激反应的独立风险。如果得到证实,从这项研究中获得的信息可用于生成模型,以准确评估特定中风患者的心脏和全身并发症的风险。公共卫生相关性:
项目成果
期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
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Hakan Ay其他文献
Hakan Ay的其他文献
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{{ truncateString('Hakan Ay', 18)}}的其他基金
Heart-Brain Interactions In Human Acute Ischemic Stroke
人类急性缺血性中风的心脑相互作用
- 批准号:
8460864 - 财政年份:2009
- 资助金额:
$ 37.96万 - 项目类别:
Heart-Brain Interactions In Human Acute Ischemic Stroke
人类急性缺血性中风的心脑相互作用
- 批准号:
7835519 - 财政年份:2009
- 资助金额:
$ 37.96万 - 项目类别:
Heart-Brain Interactions In Human Acute Ischemic Stroke
人类急性缺血性中风的心脑相互作用
- 批准号:
8064699 - 财政年份:2009
- 资助金额:
$ 37.96万 - 项目类别:
Heart-Brain Interactions In Human Acute Ischemic Stroke
人类急性缺血性中风的心脑相互作用
- 批准号:
8257955 - 财政年份:2009
- 资助金额:
$ 37.96万 - 项目类别: