Optimized MR Fingerprinting for Rapid Volumetric Quantitative Neuroimaging
Optimized MR Fingerprinting for Rapid Volumetric Quantitative Neuroimaging
批准号:
10260805
负责人:
Bo Zhao
金额:
$24.9万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-09-21 至 2023-06-30
关键词:
3-DimensionalAddressAgeAgingAlzheimer&aposs DiseaseBrainCalibrationComplexDataDetectionDiseaseDisease ProgressionFingerprintFreedomGoalsHospitalsHumanImageImaging TechniquesInstitutionLongevityMRI ScansMagnetic ResonanceMagnetic Resonance ImagingMapsMeasurementModelingNoisePatientsPatternPerformancePlayProcessPropertyProtonsPublished CommentResolutionRoleScanningScheduleSchemeSeriesSliceSpeedStructureTechniquesThickThree-Dimensional ImagingTimeTissuesWeightWhite Matter Hyperintensitybasedata acquisitiondata modelingdata spacedensityexperimental studyfallsflexibilityheuristicsimage reconstructionimaging biomarkerimprovedin vivomagnetic fieldneuroimagingnovelquantitative imagingreconstructionsignal processingsimulation
中文摘要
项目总结/摘要
MRI扫描主要使用对比加权图像(例如,
具有T1、T2或质子密度加权)。该图像加权是这些中的一个或多个的非线性函数
由外部扫描仪设置和缺陷调制的固有MR组织参数。以定量
MR组织参数的映射,我们试图解开这个复杂的组合,以提供直接的
以绝对单位表示的组织参数的表征。这有可能改善直接比较,
在不同机构和/或扫描仪之间进行扫描,还有助于了解疾病进展
和治疗的时间跨度。尽管定量MRI的潜力长期以来一直受到质疑,
虽然认识到这一点,但其使用受到购置时间过长的限制。磁共振指纹(MRF)是一种
定量MRI的最新突破,可同时测量多个组织参数
在单个实验中,将采集时间显著缩短至每个成像切片约15秒,
内在的映射。然而,这仍然可能导致无法接受的高分辨率,
容积定量成像例如,MRF可能需要长达20分钟的体积全脑采集
其空间分辨率为1.2×1.2×5 mm 3,该分辨率本身福尔斯达不到结构化所需的分辨率。
神经影像学分析主要的不足是由于次优的数据采集和图像重建
目前采用的方案。
在这个应用中,我们将通过严格的
统计信号处理框架,总体目标是提高体积测量的准确性和速度
神经成像特别是,我们将利用体积采集固有的巨大灵活性/自由度
以及图像重建以提高精度和效率。具体来说,我们将解决图像
重建问题与原则的统计重建方法,包括(1)数据模型
对于多通道采集,(2)用于体积时间序列图像的低秩张量图像模型,以及(3)
统计噪声模型我们将表征重建性能(例如,误差条),
低秩张量模型下的约束Cramer-Rao边界(CRB)。我们解决数据采集
问题,通过利用受约束的CRB作为度量来优化MRF数据采集参数(例如,翻转
角度和重复时间表)和k空间轨迹(例如,螺旋轨迹堆叠),以提高SNR
效率总之,我们预计所提出的技术可以产生2倍更准确的MR组织
参数图,实现期望的分辨率(例如,各向同性0.8 mm 3)和全脑覆盖,
短的获取时间(例如,3分钟)。最后,我们将系统地验证
所提出的技术及其用于衰老研究的效用,其中通过快速,
全脑MRI正在发挥越来越重要的作用。
英文摘要
PROJECT SUMMARY/ABSTRACT
MRI scans are primarily performed and evaluated in a qualitative way using contrast-weighted images (e.g.,
with T1, T2 or proton-density weighting). This image weighting is a nonlinear function of one or more of these
intrinsic MR tissue parameters as modulated by external scanner settings and imperfections. In quantitative
mapping of MR tissue parameters, we attempt to unravel this complex combination to provide a direct
characterization of the tissue parameter in absolute units. This has potential to improve direct comparisons of
scans across different institutions and/or scanners, and also facilitates the understanding of disease progression
and treatment for a single patient across time. Although the potential of quantitative MRI has long been
recognized, its use has been limited by lengthy acquisition times. Magnetic resonance fingerprinting (MRF) is a
recent breakthrough in quantitative MRI that enables simultaneous measurements of multiple tissue parameters
in a single experiment, dramatically shortening acquisition time to ~15 sec per imaging slice and providing
intrinsically registered maps. However, this can still result in unacceptably lengthy acquisitions for high-resolution,
volumetric quantitative imaging. For example, MRF can take up to 20 min for a volumetric whole-brain acquisition
with a spatial resolution of 1.2×1.2×5 mm3, a resolution which, itself, falls short of that needed for structural
neuroimaging analysis. The major deficiency is due to the sub-optimal data acquisition and image reconstruction
schemes currently employed.
In this application, we will optimize the data acquisition and image reconstruction for MRF by a rigorous
statistical signal processing framework, with an overall goal of improving the accuracy and speed of for volumetric
neuroimaging. In particular, we will exploit the tremendous flexibility/freedom inherent to volumetric acquisition
and image reconstruction to improve accuracy and efficiency. Specifically, we will address the image
reconstruction problem with a principled statistical reconstruction approach that incorporates (1) a data model
for multi-channel acquisitions, (2) a low-rank tensor image model for volumetric time-series images, and (3) a
statistical noise model. We will characterize the reconstruction performance (e.g., error bars) by calculating the
constrained Cramer-Rao bounds (CRB) under low-rank tensor models. We address the data acquisition
problem, by utilizing the constrained CRB as metrics to optimize MRF data acquisition parameters (e.g., flip
angle and repletion time schedule) and k-space trajectories (e.g., stack-of-spiral trajectories) for improved SNR
efficiency. Together, we expect that the proposed technique produces 2x more accurate MR tissue
parameter maps, enabling a desirable resolution (e.g., isotropic 0.8 mm3) and a whole-brain coverage in
a short acquisition time (e.g., 3 minutes). Finally, we will systematically validate the performance of the
proposed technique and its utility for ageing studies, for which quantitative imaging biomarkers enabled by rapid,
whole-brain MRI are playing an increasingly important role.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Molecular Mechanisms of Aminoglycoside Ototoxicity
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批准号:10569609
-
项目类别:
-
资助金额:$55.41万
-
财政年份:2022
-
负责人:Bo Zhao
-
依托单位:
Molecular Mechanisms of Aminoglycoside Ototoxicity
-
批准号:10443277
-
项目类别:
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资助金额:$56.87万
-
财政年份:2022
-
负责人:Bo Zhao
-
依托单位:
Optimized MR Fingerprinting for Rapid Volumetric Quantitative Neuroimaging
-
批准号:10266853
-
项目类别:
-
资助金额:$24.9万
-
财政年份:2020
-
负责人:Bo Zhao
-
依托单位:
Optimized MR Fingerprinting for Rapid Volumetric Quantitative Neuroimaging
-
批准号:10450170
-
项目类别:
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资助金额:$24.9万
-
财政年份:2020
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负责人:Bo Zhao
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依托单位:
Functions of Fam65b protein complex at the basal stereocilia in hearing and deafness
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批准号:10194456
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项目类别:
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资助金额:$39.38万
-
财政年份:2018
-
负责人:Bo Zhao
-
依托单位:
Functions of Fam65b protein complex at the basal stereocilia in hearing and deafness
-
批准号:10433855
-
项目类别:
-
资助金额:$39.38万
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财政年份:2018
-
负责人:Bo Zhao
-
依托单位:
Targeting Epstein-Barr Virus Super-Enhancer
-
批准号:9970995
-
项目类别:
-
资助金额:$44.75万
-
财政年份:2016
-
负责人:Bo Zhao
-
依托单位:
Fam65b function in hearing and deafness
-
批准号:9088059
-
项目类别:
-
资助金额:$25.24万
-
财政年份:2016
-
负责人:Bo Zhao
-
依托单位:
Targeting Epstein-Barr Virus Super-Enhancer
-
批准号:10379876
-
项目类别:
-
资助金额:$44.75万
-
财政年份:2016
-
负责人:Bo Zhao
-
依托单位:
Targeting Epstein-Barr Virus Super-Enhancer
-
批准号:10596159
-
项目类别:
-
资助金额:$44.75万
-
财政年份:2016
-
负责人:Bo Zhao
-
依托单位:
Epstein-Barr Virus Nuclear Protein B Cell Growth Transformation
-
批准号:10219163
-
项目类别:
-
资助金额:$53.25万
-
财政年份:1987
-
负责人:Bo Zhao
-
依托单位:
Epstein-Barr Virus Nuclear Protein B Cell Growth Transformation
-
批准号:9977926
-
项目类别:
-
资助金额:$53.25万
-
财政年份:1987
-
负责人:Bo Zhao
-
依托单位:
海外基金