Non-invasive Multi-modal Parcellation of the Human Cerebral Cortex
Non-invasive Multi-modal Parcellation of the Human Cerebral Cortex
批准号:
8647004
负责人:
Matthew Frederick Glasser
金额:
$4.77万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-04-01 至 2015-03-31
关键词:
AlgorithmsArchitectureAreaBase of the BrainBehavioral SciencesBiological MarkersBrainCerebral cortexCerebrumComputer softwareConsensusDataData QualityDiffusionDiseaseEuclidean SpaceFunctional Magnetic Resonance ImagingGeneric DrugsGoalsHealthHumanImageIndividualKnowledgeLiteratureMacacaMagnetic Resonance ImagingMapsMeasuresMental disordersMethodsMinorityModalityMorphologic artifactsMyelinNational Institute of Mental HealthNeurophysiology - biologic functionOutcomePTPN6 genePatternPopulationPositioning AttributePropertyPublishingResearch PersonnelResolutionRestRunningScanningScientistSignal TransductionSourceStimulusStrategic PlanningStudy SubjectSurfaceSystemTechniquesTestingThickWeightbaseimprovedinterestneuroimagingnonhuman primatereconstructionresponsevisual mapwhite matter
中文摘要
描述(由申请人提供):大脑皮层区域构成了人类大脑皮层功能和解剖组织的一个重要和可接近的水平。在对非人类灵长类动物的侵入性研究中,皮质区域的定义使用了功能(对外部或内部刺激的神经活动模式)、结构(皮质每个区域内CLL和连接的组织)、连接性(不同区域之间连接的差异)和地形(某些皮质区域存在的空间、身体等地图)的差异。基于我们对猕猴的广泛了解和对人类的有限了解,人类大脑皮层包含150到200个皮质区域,这些区域可以使用多模式神经成像方法进行最佳识别。该项目的目标有两个:1)改进一种基于MRI的非侵入性结构技术-髓鞘映射,我们最近展示的这种技术可以在组平均数据中定义许多皮质区域。人工制品破坏了群体平均数据的某些区域,而个人拥有更多的人工制品。我们将使用改进的算法来检测和纠正更高质量数据中的这些伪像。预期的结果是更好的髓鞘图谱和定义个体皮质区域的能力。2)确定静息功能磁共振成像(R-fMRI)数据中可重现的皮质区域和区域边界。我们将改进基于梯度的R-fMRI分割,并将其应用于人类连接组计划获取的高分辨率7T R-fMRI数据。这一目标应该产生更详细的皮质区域和区域边界地图,显示不同扫描、不同受试者、不同受试者以及与其他模式相比的一致性。预期的结果是一张更详细的皮质区域地图,由R-fMRI功能连接性定义,并与已发表的解剖学和功能研究相关。健康和疾病中大脑连接和功能的研究将大大受益于将解剖和功能数据定位到大脑皮层区域的改进方法。准确定义个人和群体的皮质区域将使研究精神障碍的科学家能够更好地比较他们在个人、群体和研究中的结果。它还将使对与疾病直接相关的皮质区的具体研究成为可能。NIMH战略计划反复提到神经成像和人脑区域。人类大脑皮质区域地图的改进,以及在非侵入性研究中准确定义个体区域的能力,将极大地有助于解释神经成像模式。皮质区域的准确定义还允许将其用作疾病的生物标记物(或作为测量其他非侵入性生物标记物的神经生物学标志物,如髓鞘含量、功能连接性或弥漫性纤维束造影术)。NIMH基础脑和行为科学优先项目也强调在神经成像研究中使用良好的解剖学信息,这项提案旨在提供这一点。
英文摘要
DESCRIPTION (provided by applicant): Cortical areas constitute an important and accessible level of functional and anatomical organization of the human cortex. In invasive studies of nonhuman primates, cortical areas have been defined using differences in Function (neural activity patterns in response to external or internal stimuli), Architecture (the organization of clls and connections within each area of the cortex), Connectivity (differences in connections between different areas), and Topography (maps of space, the body, etc present in some cortical areas). Based on our extensive knowledge in the macaque and limited knowledge in the human, the human cerebral cortex contains between 150 and 200 cortical areas that can best be identified using a mutli-modal neuroimaging approach. The project aims are twofold: 1) To improve upon a non-invasive MRI-based architectonic technique, myelin mapping, that we recently showed can define many cortical areas in group-average data. Artifacts corrupt some regions of the group average data and individuals have more artifacts. We will use improved algorithms to detect and correct these artifacts in higher quality data. The anticipated outcomes are better myelin maps and the ability to define cortical areas in individuals. 2) To identify reproducible cortical areas and areal boundaries in resting state fMRI (R-fMRI) data. We will improve gradient-based R-fMRI parcellation and apply it to high-resolution 7T R-fMRI data acquired by the Human Connectome Project. This aim should yield more detailed maps of cortical areas and areal borders that show consistency across scans, within subjects, across subjects, and when compared to other modalities. The anticipated outcome is a more detailed map of cortical areas defined by R-fMRI functional connectivity and related to published anatomical and functional studies. The study of brain connectivity and function in heath and disease will benefit greatly from improved methods for localizing anatomical and functional data to the cortical areas. Accurately defining cortical areas in individuals and groups will allow scientists studying mental disorders to better compare their results across individuals, groups, and studies. It will also enable specific study of those cortical areas directly implicated in the disease. The NIMH Strategic Plan mentions neuroimaging and human brain areas repeatedly. Interpreting neuroimaging patterns will be greatly aided by improved maps of human cortical areas across populations and the ability to accurately define areas in the individuals being studied non-invasively. Accurate definition of cortical areas also allows for their use as biomarkers of diseases (or as neurobiologically grounded landmarks for measuring other non-invasive biomarkers such as myelin content, functional connectivity, or diffusion tractography). The NIMH Priorities for Basic Brain and Behavioral Science also emphasizes the use of good anatomical information in neuroimaging studies, which this proposal aims to provide.
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会议论文
Non-invasive Multi-modal Parcellation of the Human Cerebral Cortex
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批准号:8310694
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项目类别:
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资助金额:$2.85万
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财政年份:2012
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负责人:Matthew Frederick Glasser
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依托单位:
Non-invasive Multi-modal Parcellation of the Human Cerebral Cortex
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批准号:8453641
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项目类别:
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资助金额:$2.85万
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财政年份:2012
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负责人:Matthew Frederick Glasser
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依托单位:
海外基金