Flakus Mattison J, Wuschner Antonia E, Wallat Eric M, Shao Wei, Shanmuganayagam Dhanansayan, Christensen Gary E, Reinhardt Joseph M, Li Ke, Bayouth John E
Department of Medical Physics, University of Wisconsin-Madison, Madison, WI, United States.
Department of Medicine, University of Florida, Gainesville, FL, United States.
Front Physiol. 2023 Feb 14;14:1040028. doi: 10.3389/fphys.2023.1040028. eCollection 2023.
To quantify the impact of image noise on CT-based lung ventilation biomarkers calculated using Jacobian determinant techniques. Five mechanically ventilated swine were imaged on a multi-row CT scanner with acquisition parameters of 120 kVp and 0.6 mm slice thickness in static and 4-dimensional CT (4DCT) modes with respective pitches of 1 and 0.09. A range of tube current time product (mAs) values were used to vary image dose. On two dates, subjects received two 4DCTs: one with 10 mAs/rotation (low-dose, high-noise) and one with CT simulation standard of care 100 mAs/rotation (high-dose, low-noise). Additionally, 10 intermediate noise level breath-hold (BHCT) scans were acquired with inspiratory and expiratory lung volumes. Images were reconstructed with and without iterative reconstruction (IR) using 1 mm slice thickness. The Jacobian determinant of an estimated transformation from a B-spline deformable image registration was used to create CT-ventilation biomarkers estimating lung tissue expansion. 24 CT-ventilation maps were generated per subject per scan date: four 4DCT ventilation maps (two noise levels each with and without IR) and 20 BHCT ventilation maps (10 noise levels each with and without IR). Biomarkers derived from reduced dose scans were registered to the reference full dose scan for comparison. Evaluation metrics were gamma pass rate (Γ) with 2 mm distance-to-agreement and 6% intensity criterion, voxel-wise Spearman correlation () and Jacobian ratio coefficient of variation ( ). Comparing biomarkers derived from low (CTDI = 6.07 mGy) and high (CTDI = 60.7 mGy) dose 4DCT scans, mean Γ, and values were 93% ± 3%, 0.88 ± 0.03 and 0.04 ± 0.009, respectively. With IR applied, those values were 93% ± 4%, 0.90 ± 0.04 and 0.03 ± 0.003. Similarly, comparisons between BHCT-based biomarkers with variable dose (CTDI = 1.35-7.95 mGy) had mean Γ, and of 93% ± 4%, 0.97 ± 0.02 and 0.03 ± 0.006 without IR and 93% ± 4%, 0.97 ± 0.03 and 0.03 ± 0.007 with IR. Applying IR did not significantly change any metrics ( 0.05). This work demonstrated that CT-ventilation, calculated using the Jacobian determinant of an estimated transformation from a B-spline deformable image registration, is invariant to Hounsfield Unit (HU) variation caused by image noise. This advantageous finding may be leveraged clinically with potential applications including dose reduction and/or acquiring repeated low-dose acquisitions for improved ventilation characterization.
为了量化图像噪声对使用雅可比行列式技术计算的基于CT的肺通气生物标志物的影响。对5只机械通气的猪在多排CT扫描仪上进行成像,在静态和四维CT(4DCT)模式下,采集参数为120 kVp和0.6 mm层厚,各自的螺距为1和0.09。使用一系列管电流时间积(mAs)值来改变图像剂量。在两个日期,受试者接受两次4DCT扫描:一次为10 mAs/旋转(低剂量,高噪声),一次为CT模拟标准护理的100 mAs/旋转(高剂量,低噪声)。此外,采集10次中间噪声水平的屏气(BHCT)扫描,包括吸气和呼气肺容积。使用1 mm层厚,在有和没有迭代重建(IR)的情况下对图像进行重建。使用从B样条可变形图像配准估计的变换的雅可比行列式来创建估计肺组织扩张的CT通气生物标志物。每个受试者每个扫描日期生成24个CT通气图:四个4DCT通气图(两种噪声水平,每种有和没有IR)和20个BHCT通气图(10种噪声水平,每种有和没有IR)。将低剂量扫描得出的生物标志物配准到参考全剂量扫描进行比较。评估指标为伽马通过率(Γ),一致性距离为2 mm,强度标准为6%,体素级斯皮尔曼相关性()和雅可比比率变异系数()。比较低剂量(CTDI = 6.07 mGy)和高剂量(CTDI = 60.7 mGy)4DCT扫描得出的生物标志物,平均Γ、和值分别为93%±3%、0.88±0.03和0.04±0.009。应用IR后,这些值分别为93%±4%、0.90±0.04和0.03±0.003。同样,比较基于BHCT的不同剂量(CTDI = 1.35 - 7.95 mGy)生物标志物,没有IR时平均Γ、和分别为93%±4%、0.97±0.02和0.03±0.006,有IR时为93%±4%、0.97±0.03和0.03±0.007。应用IR没有显著改变任何指标(P>0.05)。这项工作表明,使用从B样条可变形图像配准估计的变换的雅可比行列式计算的CT通气对图像噪声引起的亨氏单位(HU)变化具有不变性。这一有利发现可在临床上加以利用,潜在应用包括降低剂量和/或获取重复的低剂量采集以改善通气特征描述。