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Signal Recovery in Susceptibility Based Functional MRI

Signal Recovery in Susceptibility Based Functional MRI
基于磁敏度的功能 MRI 信号恢复
批准号:
6656395
负责人:
DOUGLAS C NOLL
金额:
$28.93万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-10 至 2007-06-30

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项目成果

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中文摘要
翻译
描述(由申请人提供):本项目将开发、分析和评价能够有效使用功能性磁共振成像(MRI)的方法,该方法使用血氧水平依赖(BOLD)对比度,在靠近与空气或骨骼的组织界面的大脑区域中进行。该项目的动机是由组织和空气或骨骼之间的磁化率差异引起的大信号空洞和图像失真。这些伪影在功能磁共振成像中普遍存在于许多脑下部结构,例如,眶额皮质、下颞叶和内侧颞叶、脑干结构和额极。该项目的进一步动机是fh4RI倾向于使用更高的磁场系统,这提高了大脑许多部位的灵敏度,但也加剧了伪影。许多去除这些失真的当前技术在用于检测激活的时间分辨率或灵敏度方面具有很大的成本。作为研究计划的一部分,将开发减少可重复性引起的伪影但保留标准单次fMRI技术的速度、对运动和生理噪声的鲁棒性以及对比灵敏度的方法。与许多其他方法不同,我们将解决平面内和通过平面的伪影来源。正在调查的方法包括三维定制的激励脉冲和不对称的自旋回波采集信号空隙的减少,和迭代图像重建方法和并行接收线圈成像的成像失真的减少。将评价这些方法在减少易诱发伪影方面的有效性、视觉和运动区激活的可靠性、对鼻窦附近杏仁核结构激活的敏感性以及时间准确性。该项目的成功将导致有价值的新功能磁共振成像方法,能够探测所有主要的大脑结构的方式是敏感的功能激活和强大的文物。这些方法将是快速和敏感的BOLD对比,允许常见的功能磁共振成像技术,如事件相关的研究,用于整个大脑。此外,它们将极大地帮助研究与各种神经,精神和行为障碍有关的大脑区域,包括疼痛障碍,情感障碍,精神分裂症,酒精和药物滥用。
英文摘要
DESCRIPTION (provided by applicant): This project will develop, analyze and evaluate methods that enable the efficient use of functional Magnetic Resonance Imaging (MRI) using blood oxygenation level dependent (BOLD) contrast in regions of the brain that are proximal to tissue interfaces with air or bone. This project is motivated by the large signal voids and image distortions caused by magnetic susceptibility differences between tissue and air or bone. These artifacts are ubiquitous in fMRI for many inferior brain structures, for example, orbito-frontal cortex, inferior and medial temporal lobes, brain stem structures and the frontal pole. This project is further motivated by a trend in fh4RI towards using higher magnetic field systems, which improves sensitivity in many parts of the brain, but also exacerbates the artifacts. Many current techniques to remove these distortions have a large cost in terms of temporal resolution or sensitivity for detection of activation. As part of the research plan, methods will be developed that reduce the susceptibility-induced artifact but preserve the speed, robustness to motion and physiological noise, and contrast sensitivity of standard single- shot fMRI techniques. Unlike many other approaches, we will address both in-plane and through-plane sources of artifact. The methods under investigation include three-dimensional tailored excitation pulses and asymmetric spin-echo acquisitions for reduction of signal voids, and iterative image reconstruction methods and parallel receiver coil imaging for reduction of imaging distortions. These methods will be evaluated with respect to effectiveness in reducing susceptibility-induced artifact, reliability of activation in visual and motor areas, sensitivity to activation in the amygdala structure near the paranasal sinus, and temporal accuracy. Success in this project will lead to valuable new fMRI methods capable of probing all major brain structures in a manner that is sensitive to functional activation and robust to artifacts. The methods will be fast and sensitive to BOLD contrast, allowing common fMRI techniques, like event-related studies, to be used over the entire brain. In addition, they will dramatically aid in the study of brain regions implicated in a wide variety of neurological, psychiatric, and behavioral disorders, including pain disorders, affective disorders, schizophrenia, and alcohol and drug abuse.
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