Super High Contrast USPIO-Enhanced Cerebrovascular Angiography Using Ultrashort Time-to-Echo MRI

IF 3.3 Q2 ENGINEERING, BIOMEDICAL
Liam Timms, Tianyi Zhou, J. Qiao, Codi A. Gharagouzloo, Vishala Mishra, R. Lahoud, John W. Chen, Mukesh Harisinghani, Srinivas Sridhar
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引用次数: 0

Abstract

Background Ferumoxytol (Ferahame, AMAG Pharmaceuticals, Waltham, MA) is increasingly used off-label as an MR contrast agent due to its relaxivity and safety profiles. However, its potent T2∗ relaxivity limits achievable T1-weighted positive contrast and leads to artifacts in standard MRI protocols. Optimization of protocols for ferumoxytol deployment is necessary to realize its potential. Methods We present first-in-human clinical results of the Quantitative Ultrashort Time-to-Echo Contrast Enhanced (QUTE-CE) MRA technique using the superparamagnetic iron oxide nanoparticle agent ferumoxytol for vascular imaging of the head/brain in 15 subjects at 3.0T. The QUTE-CE MRA method was implemented on a 3T scanner using a stack-of-spirals 3D Ultrashort Time-to-Echo sequence. Time-of-flight MRA and standard TE T1-weighted (T1w) images were also collected. For comparison, gadolinium-enhanced blood pool phase images were obtained retrospectively from clinical practice. Signal-to-noise ratio (SNR), contrast-to-noise ratio (CNR), and intraluminal signal heterogeneity (ISH) were assessed and compared across approaches with Welch's two-sided t-test. Results Fifteen volunteers (54 ± 17 years old, 9 women) participated. QUTE-CE MRA provided high-contrast snapshots of the arterial and venous networks with lower intraluminal heterogeneity. QUTE-CE demonstrated significantly higher SNR (1707 ± 226), blood-tissue CNR (1447 ± 189), and lower ISH (0.091 ± 0.031) compared to ferumoxytol T1-weighted (551 ± 171; 319 ± 144; 0.186 ± 0.066, respectively) and time-of-flight (343 ± 104; 269 ± 82; 0.190 ± 0.016, respectively), with p < 0.001 in each comparison. The high CNR increased the depth of vessel visualization. Vessel lumina were captured with lower heterogeneity. Conclusion Quantitative Ultrashort Time-to-Echo Contrast-Enhanced MR angiography provides approximately 5-fold superior contrast with fewer artifacts compared to other contrast-enhanced vascular imaging techniques using ferumoxytol or gadolinium, and to noncontrast time-of-flight MR angiography, for clinical vascular imaging. This trial is registered with NCT03266848.
利用超短回波时间磁共振成像进行超高对比度 USPIO 增强脑血管血管造影术
背景 Ferumoxytol(Ferahame,AMAG 制药公司,马萨诸塞州沃尔瑟姆)因其弛豫性和安全性,越来越多地被用作非标签 MR 造影剂。然而,其强大的 T2∗弛豫性限制了可实现的 T1 加权正向对比,并导致标准 MRI 方案中出现伪影。因此,有必要优化铁氧体部署方案,以发挥其潜力。方法 我们首次展示了在 3.0T 下使用超顺磁性氧化铁纳米粒子制剂铁氧体对 15 名受试者的头部/脑部血管成像进行定量超短时间到回波对比度增强(QUTE-CE)MRA 技术的人体临床结果。QUTE-CE MRA 方法是在 3T 扫描仪上使用螺旋堆叠三维超短时间回波序列实现的。同时还采集了飞行时间 MRA 和标准 TE T1 加权(T1w)图像。为了进行比较,还从临床实践中回顾性地获得了钆增强血池相位图像。评估信噪比(SNR)、对比度-信噪比(CNR)和管腔内信号异质性(ISH),并通过韦尔奇双侧 t 检验对不同方法进行比较。结果 15 名志愿者(54 ± 17 岁,9 名女性)参与了研究。QUTE-CE MRA 可提供高对比度的动脉和静脉网络快照,且管腔内异质性较低。与铁氧体 T1 加权(分别为 551 ± 171;319 ± 144;0.186 ± 0.066)和飞行时间(分别为 343 ± 104;269 ± 82;0.190 ± 0.016)相比,QUTE-CE 的信噪比(1707 ± 226)、血液-组织 CNR(1447 ± 189)和 ISH(0.091 ± 0.031)均明显更高,各项比较的 p 均小于 0.001。高 CNR 增加了血管可视化的深度。捕捉到的血管管腔异质性较低。结论 与其他使用铁氧体或钆的对比度增强血管成像技术以及非对比度飞行时间磁共振血管成像技术相比,定量超短回波对比度增强磁共振血管成像技术在临床血管成像中的对比度高出约 5 倍,伪影更少。该试验已注册为 NCT03266848。
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来源期刊
CiteScore
12.00
自引率
0.00%
发文量
11
审稿时长
20 weeks
期刊介绍: The International Journal of Biomedical Imaging is managed by a board of editors comprising internationally renowned active researchers. The journal is freely accessible online and also offered for purchase in print format. It employs a web-based review system to ensure swift turnaround times while maintaining high standards. In addition to regular issues, special issues are organized by guest editors. The subject areas covered include (but are not limited to): Digital radiography and tomosynthesis X-ray computed tomography (CT) Magnetic resonance imaging (MRI) Single photon emission computed tomography (SPECT) Positron emission tomography (PET) Ultrasound imaging Diffuse optical tomography, coherence, fluorescence, bioluminescence tomography, impedance tomography Neutron imaging for biomedical applications Magnetic and optical spectroscopy, and optical biopsy Optical, electron, scanning tunneling/atomic force microscopy Small animal imaging Functional, cellular, and molecular imaging Imaging assays for screening and molecular analysis Microarray image analysis and bioinformatics Emerging biomedical imaging techniques Imaging modality fusion Biomedical imaging instrumentation Biomedical image processing, pattern recognition, and analysis Biomedical image visualization, compression, transmission, and storage Imaging and modeling related to systems biology and systems biomedicine Applied mathematics, applied physics, and chemistry related to biomedical imaging Grid-enabling technology for biomedical imaging and informatics
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