基于压缩svd的L + S模型并行重构欠采样动态MRI数据。

IF 2 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Muhammad Shafique, Sohaib Ayaz Qazi, Hammad Omer
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引用次数: 0

摘要

背景:磁共振成像(MRI)是一种高分辨率、大容量覆盖、能够捕捉身体器官动态和功能信息的医学成像系统,如心脏MRI被用来评估心脏结构和评估心脏瓣膜的血流动力学。MRI的主要缺点是扫描时间长,使得患者在扫描过程中难以保持静止。目的:通过采集更少的测量值,可以缩短MRI扫描时间,但这种欠采样会导致重建图像中的混叠伪影。先进的图像重建算法已在文献中使用,以克服这些欠采样的工件。这些算法在计算上很昂贵,并且需要很长的重建时间,这使得它们不适合实时临床应用,例如心脏MRI。然而,利用这些算法中固有的并行性可以帮助减少它们的计算时间。方法:低秩加稀疏(L+S)矩阵分解模型是文献中采用的一种以较长重建时间为代价重建高度欠采样动态MRI (dMRI)数据的技术。本文在L+S分解模型中采用压缩奇异值分解(cSVD)模型来代替传统的奇异值分解(SVD),以减少重构时间。结果提高了重建图像的质量。此外,还观察到cSVD和L+S模型的其他部分具有高度并行的操作;为此,提出了一种基于定制GPU的改进L+S模型并行架构,进一步缩短了重构时间。结果:本文使用4组心脏MRI数据集(3组不同患者的不同心脏灌注数据和1组心脏影像数据)进行实验,每组数据的加速因子分别为2、6和8。实验结果表明,在不影响图像质量的情况下,与传统的CPU重构方法相比,使用所提出的并行架构进行心脏灌注数据重构的加速系数高达19.15倍(有内存延迟)和70.55倍(无内存延迟)。结论:该方法适合于实时临床应用,可大大缩短重建时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Compressed SVD-based L + S model to reconstruct undersampled dynamic MRI data using parallel architecture.

Compressed SVD-based L + S model to reconstruct undersampled dynamic MRI data using parallel architecture.

Background: Magnetic Resonance Imaging (MRI) is a highly demanded medical imaging system due to high resolution, large volumetric coverage, and ability to capture the dynamic and functional information of body organs e.g. cardiac MRI is employed to assess cardiac structure and evaluate blood flow dynamics through the cardiac valves. Long scan time is the main drawback of MRI, which makes it difficult for the patients to remain still during the scanning process.

Objective: By collecting fewer measurements, MRI scan time can be shortened, but this undersampling causes aliasing artifacts in the reconstructed images. Advanced image reconstruction algorithms have been used in literature to overcome these undersampling artifacts. These algorithms are computationally expensive and require a long time for reconstruction which makes them infeasible for real-time clinical applications e.g. cardiac MRI. However, exploiting the inherent parallelism in these algorithms can help to reduce their computation time.

Methods: Low-rank plus sparse (L+S) matrix decomposition model is a technique used in literature to reconstruct the highly undersampled dynamic MRI (dMRI) data at the expense of long reconstruction time. In this paper, Compressed Singular Value Decomposition (cSVD) model is used in L+S decomposition model (instead of conventional SVD) to reduce the reconstruction time. The results provide improved quality of the reconstructed images. Furthermore, it has been observed that cSVD and other parts of the L+S model possess highly parallel operations; therefore, a customized GPU based parallel architecture of the modified L+S model has been presented to further reduce the reconstruction time.

Results: Four cardiac MRI datasets (three different cardiac perfusion acquired from different patients and one cardiac cine data), each with different acceleration factors of 2, 6 and 8 are used for experiments in this paper. Experimental results demonstrate that using the proposed parallel architecture for the reconstruction of cardiac perfusion data provides a speed-up factor up to 19.15× (with memory latency) and 70.55× (without memory latency) in comparison to the conventional CPU reconstruction with no compromise on image quality.

Conclusion: The proposed method is well-suited for real-time clinical applications, offering a substantial reduction in reconstruction time.

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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
58
审稿时长
>12 weeks
期刊介绍: MAGMA is a multidisciplinary international journal devoted to the publication of articles on all aspects of magnetic resonance techniques and their applications in medicine and biology. MAGMA currently publishes research papers, reviews, letters to the editor, and commentaries, six times a year. The subject areas covered by MAGMA include: advances in materials, hardware and software in magnetic resonance technology, new developments and results in research and practical applications of magnetic resonance imaging and spectroscopy related to biology and medicine, study of animal models and intact cells using magnetic resonance, reports of clinical trials on humans and clinical validation of magnetic resonance protocols.
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