SSFP Cardiovascular MR Imaging on 3.0T Using Unified-Coil Local Shimming
SSFP Cardiovascular MR Imaging on 3.0T Using Unified-Coil Local Shimming
批准号:
10152406
负责人:
Anthony G Christodoulou
金额:
$62.5万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-12-15 至 2024-11-30
关键词:
AbdomenAdoptionAirAngiographyBreathingCardiacCardiovascular DiseasesCardiovascular systemCause of DeathChestClinicalClinical ManagementCoronaryDevelopmentEcho-Planar ImagingFeedbackFrequenciesGoalsHeartImageImaging TechniquesLungMagnetic ResonanceMagnetic Resonance ImagingMagnetismMethodsMorphologic artifactsMotionMyocardial tissueNoiseOrganPenetrationPerformancePredispositionPropertyProtocols documentationRF coilResolutionRespirationSafetyScanningSignal TransductionSourceSystemTechniquesTechnologyTimeTissuesVariantVendorVertebral columnWorkbasehealthy volunteerheart functionhuman subjectimprovedinnovationmultitasknovelpreventrespiratory
中文摘要
摘要
心血管疾病是全球主要的死亡原因。心血管磁共振(CMR)
是心血管疾病临床治疗中的常规方法,也是
心功能和心肌组织特性的评估。今天,大多数临床CMR研究仍然是
在1.5T扫描仪上进行,因为它们在执行CMR协议时的可用性和健壮性。在……里面
一般而言,3.0T提供比1.5T更高的SNR、空间分辨率和更短的扫描时间。然而,
B0场强的增加也给CMR带来了技术挑战。一个主要的挑战是易感性或
由于B0场不均匀性恶化而产生的非共振伪影。
在过去的二十年里,稳态自由进动(SSFP)使1.5T上的CMR发生了革命性的变化,因为它
与基于梯度回波的采集相比,显著提高了SNR和对比噪声比(CNR)。然而,它的
3.0T上的常规使用一直不一致,尽管不断改善B0的均质性和垫片
能力。因此,仍然常规地使用基于梯度回波的采集,例如用于电影成像,
心脏松弛测量和冠状动脉MRA,否定了3.0T用于CMR的主要优势。由于距离的关系
来自目标器官的标准全身垫片线圈,它们仅提供高达
二阶球谐(SH),不能对高阶局域场变化进行匀场
例如出现在心肺界面附近的那些。这仍然是一个未得到满足的挑战。
在这个项目中,我们将应用一种新的统一垫片-射频线圈技术来克服在
3.0T CMR。我们将开发一种统一的垫片-射频线圈,并验证其安全性和高阶垫片能力
(目标1)。我们将基于我们的低排名开发一种呼吸运动分辨的B0场标测技术
多任务框架和实时填补电路,允许自由呼吸CMR的动态填补(目标2)。
然后我们将在3.0T(目标3)上在人体受试者身上验证这项技术。本项目圆满完成
将在3.0T上实现强大的SSFP CMR,这是一项重大的技术挑战,它允许可靠的高分辨率、高
SNR CMR,包括但不限于Cine和冠状动脉MRA。这种新型的心脏垫片系统具有
可能对加速3.0T CMR的临床采用产生重大影响。
英文摘要
Abstract
Cardiovascular disease is the leading cause of death globally. Cardiovascular magnetic resonance (CMR)
is routinely used in the clinical management of cardiovascular disease and is the standard method for the
assessment of cardiac function and myocardial tissue properties. Today, most clinical CMR studies are still
conducted on 1.5T scanners because of their availability and robustness in executing CMR protocols. In
general, 3.0T provides higher SNR, spatial resolution, and reduced scan time than 1.5T. However, the
increased B0 field strength also poses technical challenges for CMR. A major challenge is the susceptibility or
off-resonance artifacts due to worsened B0 field inhomogeneity.
In the last two decades, steady-state free precession (SSFP) has revolutionized CMR on 1.5T because it
boosts SNR and contrast to noise ratio (CNR) markedly over gradient-echo based acquisitions. However, its
routine use on 3.0T has been inconsistent despite continuously improving B0 homogeneity and shimming
capabilities. Therefore, gradient-echo based acquisitions are still routinely used, such as for cine imaging,
cardiac relaxometry, and coronary MRA, negating the major advantages of 3.0T for CMR. Due to the distance
of standard whole-body shimming coils from the target organ, they only provide shimming capabilities up to the
second-order spherical harmonic (SH), and are incapable of shimming higher-order localized field variations
such as those present near the heart-lung interface. This remains an unmet challenge.
In this project, we will apply a novel unified shim-RF coil technique to overcome the primary limitation in
3.0T CMR. We will develop a unified shim-RF coil and validate its safety and high-order shimming capability
(Aim 1). We will develop a respiratory motion-resolved B0 field mapping technique based on our low-rank
Multitasking framework and real-time shim circuits to allow dynamic shimming for free breathing CMR (Aim 2).
We will then validate the technology in human subjects on 3.0T (Aim 3). Successful completion of this project
will enable robust SSFP CMR on 3.0T, a major technical challenge, which allows reliable high-resolution, high-
SNR CMR, including but not limited to cine and coronary MRA. This novel cardiac shimming system has the
potential to have a major impact in accelerating the clinical adoption of 3.0T CMR.
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科研奖励(0)
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海外基金