3D Quantitative-Amplified Magnetic Resonance Imaging (3D q-aMRI).

IF 3.8 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Itamar Terem, Kyan Younes, Nan Wang, Paul Condron, Javid Abderezaei, Haribalan Kumar, Hillary Vossler, Eryn Kwon, Mehmet Kurt, Elizabeth Mormino, Samantha Holdsworth, Kawin Setsompop
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引用次数: 0

Abstract

Amplified MRI (aMRI) is a promising new technique that can visualize pulsatile brain tissue motion by amplifying sub-voxel motion in cine MRI data, but it lacks the ability to quantify the sub-voxel motion field in physical units. Here, we introduce a novel post-processing algorithm called 3D quantitative amplified MRI (3D q-aMRI). This algorithm enables the visualization and quantification of pulsatile brain motion. 3D q-aMRI was validated and optimized on a 3D digital phantom and was applied in vivo on healthy volunteers for its ability to accurately measure brain parenchyma and CSF voxel displacement. Simulation results show that 3D q-aMRI can accurately quantify sub-voxel motions in the order of 0.01 of a voxel size. The algorithm hyperparameters were optimized and tested on in vivo data. The repeatability and reproducibility of 3D q-aMRI were shown on six healthy volunteers. The voxel displacement field extracted by 3D q-aMRI is highly correlated with the displacement measurements estimated by phase contrast (PC) MRI. In addition, the voxel displacement profile through the cerebral aqueduct resembled the CSF flow profile reported in previous literature. Differences in brain motion was observed in patients with dementia compared with age-matched healthy controls. In summary, 3D q-aMRI is a promising new technique that can both visualize and quantify pulsatile brain motion. Its ability to accurately quantify sub-voxel motion in physical units holds potential for the assessment of pulsatile brain motion as well as the indirect assessment of CSF homeostasis. While further research is warranted, 3D q-aMRI may provide important diagnostic information for neurological disorders such as Alzheimer's disease.

三维定量放大磁共振成像(3D q-aMRI)。
放大磁共振成像(aMRI)是一种很有前途的新技术,它能通过放大电影磁共振成像数据中子象素的运动来显示脑组织的脉动运动,但它缺乏以物理单位量化子象素运动场的能力。在此,我们介绍一种新的后处理算法,称为三维定量放大磁共振成像(3D q-aMRI)。该算法可实现脑脉冲运动的可视化和量化。3D q-aMRI 在三维数字模型上进行了验证和优化,并应用于健康志愿者的体内,以准确测量脑实质和 CSF 像元位移。模拟结果表明,三维 q-aMRI 可以精确量化体素大小为 0.01 的亚体素运动。对算法超参数进行了优化,并在活体数据上进行了测试。在六名健康志愿者身上显示了三维 q-aMRI 的可重复性和再现性。三维 q-aMRI 提取的体素位移场与相位对比(PC)磁共振成像估计的位移测量值高度相关。此外,通过大脑导水管的体素位移曲线与之前文献报道的 CSF 流曲线相似。与年龄匹配的健康对照组相比,痴呆症患者的大脑运动存在差异。总之,三维 q-aMRI 是一种很有前途的新技术,它既能可视化又能量化脑脉冲运动。三维 q-aMRI 能够以物理单位准确量化亚体素运动,因此具有评估脑脉冲运动和间接评估脑脊液平衡的潜力。虽然还需要进一步研究,但三维 q-aMRI 可为阿尔茨海默病等神经系统疾病提供重要的诊断信息。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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