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Accelerating the 3D T 1ρ mapping of cartilage using a signal-compensated robust tensor principal component analysis model

机译:使用信号补偿的鲁棒张量主体分析模型加速软骨3D T1ρ映射

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Background: Magnetic resonance (MR) quantitative T 1ρ imaging has been increasingly used to detect the early stages of osteoarthritis. The small volume and curved surface of articular cartilage necessitate imaging with high in-plane resolution and thin slices for accurate T 1ρ measurement. Compared with 2D T 1ρ mapping, 3D T 1ρ mapping is free from artifacts caused by slice cross-talk and has a thinner slice thickness and full volume coverage. However, this technique needs to acquire multiple T 1ρ -weighted images with different spin-lock times, which results in a very long scan duration. It is highly expected that the scan time can be reduced in 3D T 1ρ mapping without compromising the T 1ρ quantification accuracy and precision. Methods: To accelerate the acquisition of 3D T 1ρ mapping without compromising the T 1ρ quantification accuracy and precision, a signal-compensated robust tensor principal component analysis method was proposed in this paper. The 3D T 1ρ -weighted images compensated at different spin-lock times were decomposed as a low-rank high-order tensor plus a sparse component. Poisson-disk random undersampling patterns were applied to k-space data in the phase- and partition-encoding directions in both retrospective and prospective experiments. Five volunteers were involved in this study. The fully sampled k-space data acquired from 3 volunteers were retrospectively undersampled at R=5.2, 7.7, and 9.7, respectively. Reference values were obtained from the fully sampled data. Prospectively undersampled data for R=5 and R=7 were acquired from 2 volunteers. Bland-Altman analyses were used to assess the agreement between the accelerated and reference T 1ρ measurements. The reconstruction performance was evaluated using the normalized root mean square error and the median of the normalized absolute deviation (MNAD) of the reconstructed T 1ρ -weighted images and the corresponding T 1ρ maps. Results: T 1ρ parameter maps were successfully estimated from T 1ρ -weighted images reconstructed using the proposed method for all accelerations. The accelerated T 1ρ measurements and reference values were in good agreement for R=5.2 (T 1ρ : 40.4±1.4 ms), R=7.7 (T 1ρ : 40.4±2.1 ms), and R=9.7 (T 1ρ : 40.9±2.2 ms) in the Bland-Altman analyses. The T 1ρ parameter maps reconstructed from the prospectively undersampled data also showed promising image quality using the proposed method. Conclusions: The proposed method achieves the 3D T 1ρ mapping of in vivo knee cartilage in eight minutes using a signal-compensated robust tensor principal component analysis method in image reconstruction.
机译:背景:磁共振(MR)定量T1ρ成像越来越多地用于检测骨关节炎的早期阶段。关节软骨的小体积和弯曲表面需要具有高面内分辨率和薄切片的成像,用于精确T1ρ测量。与2D T1ρ映射相比,3D T1ρ映射不受切片串扰引起的伪影,并且具有更薄的切片厚度和全容积覆盖。然而,该技术需要使用不同的旋转锁定时间获取多个T1ρ-重量的图像,这导致非常长的扫描持续时间。高度预期,扫描时间可以在3D t1ρ映射中减少,而不会影响T1ρ定量精度和精度。方法:为了加速3DT1ρ的测绘采集而不影响T1ρ定量精度和精度,本文提出了一种信号补偿的鲁棒张量主成分分析方法。在不同的旋转锁定时间内补偿的3D T1ρ-重量的图像被分解为低级高阶张量加稀疏部件。在回顾性和预期实验中,将泊松盘随机下采样模式应用于相位和分区编码方向的K空间数据。这项研究参与了五名志愿者。从3个志愿者获取的完全采样的k空间数据分别回顾性地向r = 5.2,7.7和9.7处回顾性。从完全采样数据获得参考值。从2个志愿者获取r = 5和r = 7的前瞻性下采样数据。 Bland-Altman分析用于评估加速和参考T1ρ测量之间的协议。使用归一化的根均方误差和重建的T1ρ-重量的图像的归一化的根均线误差和标准化绝对偏差(Mnad)的中值来评估重建性能和相应的T1ρ的映射。结果:使用所提出的所有加速度,成功地从重建的T1ρ-重复的图像成功估计了T1ρ参数映射。加速的T 1ρ测量和参考值符合R = 5.2(T1ρ:40.4±1.4ms),r = 7.7(t1ρ:40.4±2.1ms),r = 9.7(t1ρ:40.9±2.2 MS)在Bland-Altman分析中。从前瞻性下采样的数据重建的T1ρ参数映射也使用所提出的方法显示有前途的图像质量。结论:所提出的方法在图像重建中使用信号补偿的鲁棒张量主成分分析方法在八分钟内实现了体内膝关节软骨的3DT1ρ。

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