Computational analysis of diffusion tensor images: application to schizophrenia
Computational analysis of diffusion tensor images: application to schizophrenia
批准号:
7596187
负责人:
Ragini Verma
金额:
$33.47万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-05-25 至 2011-03-31
关键词:
AdoptedAffectAlgorithmsAnisotropyBrainClinicalClinical TrialsCognitionComplexComputer AnalysisComputing MethodologiesControlled StudyCross-Sectional StudiesDataDatabasesDevelopmentDiffusionDiffusion Magnetic Resonance ImagingDiseaseDoctor of PhilosophyEarly DiagnosisEmotionsEquilibriumEvaluationFamily memberFiberGoalsImageImage AnalysisIndividualInvestigationLeadLearningLesionLimbic SystemLinkMagnetic ResonanceMagnetic Resonance ImagingMapsMeasurementMeasuresMethodsMicroscopicMonitorNeuroanatomyNeurodevelopmental DisorderPathologyPatientsPatternPerformancePlayPopulationProcessProtocols documentationRelative (related person)Research PersonnelResolutionRoleSchizophreniaSeveritiesSolutionsSpeedStatistical MethodsStructureSymptomsTechniquesTestingWhite Matter Diseasebasecognitive functionimage processingmyelinationneuropsychologicalprogramstoolvolunteerwater diffusionwhite matterwhite matter change
中文摘要
描述(由申请人提供):由于弥散张量成像(DTI)对白质(WM)的优越表征,它越来越多地用于多种白质疾病的研究。具体来说,DTI在非局灶性神经发育疾病(如精神分裂症)的研究中发挥着至关重要的作用,其中WM异常更为复杂和微妙,可能表现为髓鞘形成的改变或分散在整个大脑的连接中断。这导致了对DTI数据分组分析的需求不断增长,以期更好地阐明这些微妙的异常。这就产生了对用于DTI处理和分析的复杂和全自动计算神经解剖学技术的需求,这一点至关重要,因为传统的放射评估无法检测到实质性的白质差异。这种方法的发展对DTI数据具有挑战性,因为它需要解决由张量数据的高维和复杂的底层结构引起的几个数学和技术问题。虽然从张量计算的标量图像(如扩散率和各向异性图)的分析通常被用作张量数据分析的第一步,但这些图像通常从张量中提取有限的信息,因此不能捕捉到病理的全部影响。类似的和额外的限制也固有的光纤跟踪。本项目旨在通过开发直接应用于整个扩散张量数据的分析方法来缓解这些问题,而不需要中间步骤集中在标量度量上,从而将计算神经解剖学的成熟方法扩展到张量数据。该项目的关键在于为DTI数据的形态计量学分析开发一套全面的工具,旨在促进各种神经成像研究。Aim 2将开发一个用于扩散张量场统计分析的集成框架,使用流形学习技术确定DT测量的潜在流形结构,然后对这些流形进行体素统计分析。Aim 1中基于wm的DTI数据空间归一化框架的发展将极大地促进这种基于群的分析,其中张量的特征是使用定向滤波器获得的丰富而独特的形态特征。最后,在目标3中,这些方法的效用将通过研究三组之间结构连接的差异,并将其与症状严重程度的临床评分和情绪和认知的神经心理学测量的表现相关联,在一个具有良好特征的精神分裂症患者、其亲属和健康对照的大型数据库上进行测试。我们期望在成功完成该项目后,我们将开发出一套通用的、全面的、计算效率高的DTI处理和分析工具,用于大规模人群DTI研究,这套DTI分析工具可用于测试涉及白质的其他疾病的临床假设。
英文摘要
DESCRIPTION (provided by applicant): Owing to the superior characterization of white matter (WM) provided by Diffusion tensor imaging (DTI), it is being increasingly used in the investigation of several WM diseases. Specifically, DTI has a crucial role to play in the study of non-focal neurodevelopmental diseases such as schizophrenia where the WM abnormalities are more complex and subtle and may manifest as changes in myelination or disruptions in connectivity, dispersed over the whole brain. This has led to a growing need for group-based analysis of DTI data that is expected to better elucidate these subtle anomalies. This has generated the need for sophisticated and fully automated computational neuroanatomy techniques for DTI processing and analysis, crucial because the conventional radiological evaluations have failed to detect substantial white matter differences. Development of such methods is challenging for DTI data as it requires the resolution of several mathematical and technical issues arising from the high dimensionality and complex underlying structure of the tensor data. Although analysis of scalar images, such as diffusivity and anisotropy maps, that are computed from tensors is often used as a first step in analysis of tensor data, these images generally extract limited information from the tensors and therefore do not capture the full effect of pathology. Similar and additional limitations are inherent to fiber tracking also. This project seeks to alleviate these issues by developing analysis methods that apply directly to the diffusion tensor data in its entirety, without having intermediate steps concentrate on scalar measures, thereby extending well-established methods of computational neuroanatomy to tensor data. The crux of the project lies in developing a comprehensive set of tools for the morphometric analysis of DTI data, aiming at facilitating a variety of neuro-imaging studies. An integrated framework for the statistical analysis of diffusion tensor fields will be developed in Aim 2, using manifold learning techniques that determine the underlying manifold structure of the DT measures followed by voxel-wise statistical analysis on these manifolds. Such a group-based analysis will be greatly facilitated by the development of a WM-based spatial normalization framework for DTI data in Aim 1, in which tensors are characterized by rich and distinctive morphological signatures obtained using oriented filters. Finally, in Aim 3, the utility of these methods will be tested on a well characterized large database of schizophrenia patients, their relatives and healthy controls, by studying differences in structural connectivity between the three groups and correlating these with clinical ratings of symptom severity and performance on neuropsychological measurements of emotion and cognition. We expect that on successful completion of the project we will have developed a general, comprehensive and computationally efficient processing and analysis tools for large population DTI studies, set of tools for DTI analysis that can be used to test clinical hypotheses in other disorders involving white matter.
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