深度学习去噪算法对不同空间分辨率下生长板扩散张量成像的影响

IF 2.2 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Tomography Pub Date : 2024-04-02 DOI:10.3390/tomography10040039
Laura Santos, H. Hsu, Ronald R. Nelson, Brendan Sullivan, Jaemin Shin, Maggie Fung, M. Lebel, Sachin Jambawalikar, Diego Jaramillo
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引用次数: 0

摘要

为了评估深度学习(DL)去噪重建算法对以两种不同体素维度(代表不同的空间分辨率)获取的相同患者扫描的影响,这项经 IRB 批准的前瞻性研究在一家三级儿科中心进行,符合《健康保险可携性与责任法案》(Health Insurance Portability and Accountability Act)。研究人员使用通用电气公司的 Signa Premier 设备(GE 医疗系统公司,威斯康星州密尔沃基市)在 3T 下采集了每名儿童左膝的两个 DTI(弥散张量成像)序列:平面内 2.0 × 2.0 mm2、切片厚度为 3.0 mm 和 2 mm3 等体积体素;两者均无交叉间隙。在图像采集时,使用了脂肪抑制单发自旋回波回声平面序列(20 个非共线方向;b 值为 0 和 600 s/mm2)的多波段 DTI。磁共振供应商提供的商用 DL 模型在 75% 降噪设置下应用于不同空间分辨率的同一受试者 DTI 序列。我们比较了股骨和胫骨在每个空间分辨率下的 DL 重建扫描和非变性扫描的 DTI 道指标。我们使用 Wilcoxon-signed 秩序检验和 Bland-Altman 图对差异进行了评估。在使用 2 mm × 2 mm × 3 mm 象素维度比较股骨和胫骨的 DL 与非变色扩散指标时,束计数(p = 0.1,p = 0.14)、束体积(p = 0.1,p = 0.29)或胫骨束长度(p = 0.16)之间没有显著差异;股骨束长度则表现出显著差异(p < 0.01)。在股骨和胫骨椎体中,使用 2 mm3 像元大小的 DL 重建扫描得出的所有扩散指标(束数、体积、长度和分数各向异性 (FA))都与非变性扫描的 DTI 指标有显著差异(p < 0.001)。DL重建导致两种体素尺寸的股骨胫骨FA显著下降(p < 0.01)。利用去噪算法可以解决与较小体素体积相关的较低信噪比(SNR)的缺点,并利用其更好的空间分辨率,从而更准确地量化弥散指标。
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Impact of Deep Learning Denoising Algorithm on Diffusion Tensor Imaging of the Growth Plate on Different Spatial Resolutions.
To assess the impact of a deep learning (DL) denoising reconstruction algorithm applied to identical patient scans acquired with two different voxel dimensions, representing distinct spatial resolutions, this IRB-approved prospective study was conducted at a tertiary pediatric center in compliance with the Health Insurance Portability and Accountability Act. A General Electric Signa Premier unit (GE Medical Systems, Milwaukee, WI) was employed to acquire two DTI (diffusion tensor imaging) sequences of the left knee on each child at 3T: an in-plane 2.0 × 2.0 mm2 with section thickness of 3.0 mm and a 2 mm3 isovolumetric voxel; neither had an intersection gap. For image acquisition, a multi-band DTI with a fat-suppressed single-shot spin-echo echo-planar sequence (20 non-collinear directions; b-values of 0 and 600 s/mm2) was utilized. The MR vendor-provided a commercially available DL model which was applied with 75% noise reduction settings to the same subject DTI sequences at different spatial resolutions. We compared DTI tract metrics from both DL-reconstructed scans and non-denoised scans for the femur and tibia at each spatial resolution. Differences were evaluated using Wilcoxon-signed ranked test and Bland-Altman plots. When comparing DL versus non-denoised diffusion metrics in femur and tibia using the 2 mm × 2 mm × 3 mm voxel dimension, there were no significant differences between tract count (p = 0.1, p = 0.14) tract volume (p = 0.1, p = 0.29) or tibial tract length (p = 0.16); femur tract length exhibited a significant difference (p < 0.01). All diffusion metrics (tract count, volume, length, and fractional anisotropy (FA)) derived from the DL-reconstructed scans, were significantly different from the non-denoised scan DTI metrics in both the femur and tibial physes using the 2 mm3 voxel size (p < 0.001). DL reconstruction resulted in a significant decrease in femorotibial FA for both voxel dimensions (p < 0.01). Leveraging denoising algorithms could address the drawbacks of lower signal-to-noise ratios (SNRs) associated with smaller voxel volumes and capitalize on their better spatial resolutions, allowing for more accurate quantification of diffusion metrics.
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来源期刊
Tomography
Tomography Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
2.70
自引率
10.50%
发文量
222
期刊介绍: TomographyTM publishes basic (technical and pre-clinical) and clinical scientific articles which involve the advancement of imaging technologies. Tomography encompasses studies that use single or multiple imaging modalities including for example CT, US, PET, SPECT, MR and hyperpolarization technologies, as well as optical modalities (i.e. bioluminescence, photoacoustic, endomicroscopy, fiber optic imaging and optical computed tomography) in basic sciences, engineering, preclinical and clinical medicine. Tomography also welcomes studies involving exploration and refinement of contrast mechanisms and image-derived metrics within and across modalities toward the development of novel imaging probes for image-based feedback and intervention. The use of imaging in biology and medicine provides unparalleled opportunities to noninvasively interrogate tissues to obtain real-time dynamic and quantitative information required for diagnosis and response to interventions and to follow evolving pathological conditions. As multi-modal studies and the complexities of imaging technologies themselves are ever increasing to provide advanced information to scientists and clinicians. Tomography provides a unique publication venue allowing investigators the opportunity to more precisely communicate integrated findings related to the diverse and heterogeneous features associated with underlying anatomical, physiological, functional, metabolic and molecular genetic activities of normal and diseased tissue. Thus Tomography publishes peer-reviewed articles which involve the broad use of imaging of any tissue and disease type including both preclinical and clinical investigations. In addition, hardware/software along with chemical and molecular probe advances are welcome as they are deemed to significantly contribute towards the long-term goal of improving the overall impact of imaging on scientific and clinical discovery.
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