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分辨率相关影响的压缩感知在定量 T2 映射的关节软骨。

Resolution-dependent influences of compressed sensing in quantitative T2 mapping of articular cartilage.

机构信息

Center for in vivo Microscopy, Duke University School of Medicine, Durham, North Carolina, USA.

Department of Radiology, Duke University School of Medicine, Durham, North Carolina, USA.

出版信息

NMR Biomed. 2020 Dec;33(12):e4260. doi: 10.1002/nbm.4260. Epub 2020 Feb 10.

Abstract

This study evaluates the resolution-dependent influences of compressed sensing (CS) in MRI quantification of T2 mapping in articular cartilage with osteoarthritis (OA). T2-weighed 2D experiments of healthy and OA cartilage were fully sampled in k-space with five echo times at both 17.6 μm and 195.3 μm in-plane resolutions; termed as microscopic MRI (μMRI) and macroscopic MRI (mMRI) respectively. These fully sampled k-space data were under-sampled at various 2D CS accelerating factors (AF = 4-32). The under-sampled data were reconstructed individually into 2D images using nonlinear reconstruction, which were used to calculate the T2 maps. The bulk and zonal variations of T2 values in cartilage were evaluated at different AFs. The study finds that the T2 images at AFs up to 8 preserved major visual information and produced negligible artifacts for μMRI. The T2 values remained accurate for different sub-tissue zones at various AFs. The absolute difference between the CS (AF up to 32) and the Ground Truth (i.e., using 100% of the k-space data) of the mean T2 values through the whole tissue depth was higher in mMRI versus μMRI. For mMRI (where the resolution mimics the clinical MRI of human cartilage), the quantitative T2 mapping at AFs up to 4 showed negligible variations. This study demonstrates that both clinical MRI and μMRI can benefit from the use of CS in image acquisition, and μMRI benefits more from the use of CS by acquiring much less data, without losing significant accuracy in the quantification of T2 maps in osteoarthritic cartilage.

摘要

本研究评估了压缩感知(CS)在磁共振成像(MRI)定量评估骨关节炎(OA)关节软骨 T2 映射中的分辨率依赖性影响。采用两种不同的空间分辨率(17.6μm 和 195.3μm),对健康和 OA 软骨的 T2 加权二维实验进行了全采样,获得了五个回波时间的 k 空间数据;分别称为微观 MRI(μMRI)和宏观 MRI(mMRI)。对全采样 k 空间数据在各种二维 CS 加速因子(AF=4-32)下进行欠采样。使用非线性重建技术,对欠采样数据进行单独重建,得到二维图像,用于计算 T2 图谱。在不同的 AF 下,评估了软骨的整体和分区 T2 值变化。研究发现,在 AF 高达 8 的情况下,T2 图像保留了主要的视觉信息,并且对于 μMRI 产生的伪影可以忽略不计。在不同的亚组织区域,不同的 AF 下 T2 值仍然保持准确。在整个组织深度上,CS(最高 AF 为 32)和真实数据(即使用 100%的 k 空间数据)之间的平均 T2 值的绝对差异在 mMRI 中比在 μMRI 中更高。对于 mMRI(其分辨率模拟了人类软骨的临床 MRI),在 AF 高达 4 的情况下,定量 T2 映射几乎没有变化。本研究表明,临床 MRI 和 μMRI 都可以从 CS 在图像采集方面的应用中受益,并且 μMRI 通过获取更少的数据,而不会在定量 OA 软骨的 T2 图谱方面损失显著的准确性,从而从 CS 的应用中受益更多。

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