利用多反转自旋和梯度回波磁共振成像技术在一次屏气或呼吸触发采集中同时绘制肝脏多参数图谱

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Mary Kate Manhard, Anandh Kilpattu Ramaniharan, Jean A Tkach, Andrew T Trout, Jonathan R Dillman, Amol S Pednekar
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引用次数: 0

摘要

背景:定量参数图谱是一种日益重要的慢性肝病无创评估工具。目的:研究一种同时估算肝脏 T1、T2 和 T2* 的多反转自旋和梯度回波(MI-SAGE)技术:研究对象16名研究参与者,包括成人和儿童(年龄17.5 ± 4.6岁,8名男性),患有和未患有已知肝病(7名无症状健康对照组、2名纤维化肝病患者、5名脂肪肝患者、2名纤维化和脂肪肝患者):1.5 T、单次屏气和呼吸触发 MI-SAGE、屏气改良 Look-Locker 反转恢复(MOLLI,T1 映射)、屏气梯度和自旋回波(GRASE,T2 映射)以及多重梯度回波(mGRE,T2* 映射)序列:评估:评估了使用 MI-SAGE 和传统参数测绘序列估算的肝脏 T1、T2 和 T2* 之间的一致性。使用同一次采集和第二次采集评估了 MI-SAGE 的重复性和再现性:结果:使用 MI-SAGE 技术获得的肝 T1、T2 和 T2* 估计值的平均偏差分别为 72(LOA:-22 至 166)毫秒、-3(LOA:-10 至 5)毫秒和 2(LOA:-5 至 8)毫秒(单次屏气)和 36(LOA:-43 至 120)毫秒(单次屏气):与使用 MOLLI、GRASE 和 mGRE 进行的传统采集相比,MI-SAGE 的估计值分别为-43 至 120 毫秒、-3(LOA:-17 至 11)毫秒和 4(LOA:-3 至 11)毫秒(呼吸触发)。所有 MI-SAGE 估计值都具有很高的重复性和再现性(ICC > 0.72):数据结论:使用 MI-SAGE 技术获得的肝脏 T1、T2 和 T2* 估计值与传统方法相当,但与 MOLLI 相比,屏气/呼吸触发的 T1 值低估了 12%/6%。呼吸触发和屏气 MI-SAGE 参数图均显示出很强的重复性和再现性:1 技术效率:第 2 阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous Multiparameter Mapping of the Liver in a Single Breath-Hold or Respiratory-Triggered Acquisition Using Multi-Inversion Spin and Gradient Echo MRI.

Background: Quantitative parametric mapping is an increasingly important tool for noninvasive assessment of chronic liver disease. Conventional parametric mapping techniques require multiple breath-held acquisitions and provide limited anatomic coverage.

Purpose: To investigate a multi-inversion spin and gradient echo (MI-SAGE) technique for simultaneous estimation of T1, T2, and T2* of the liver.

Study type: Prospective.

Subjects: Sixteen research participants, both adult and pediatric (age 17.5 ± 4.6 years, eight male), with and without known liver disease (seven asymptomatic healthy controls, two fibrotic liver disease, five steatotic liver disease, and two fibrotic and steatotic liver disease).

Field strength/sequence: 1.5 T, single breath-hold and respiratory triggered MI-SAGE, breath-hold modified Look-Locker inversion recovery (MOLLI, T1 mapping), breath-hold gradient and spin echo (GRASE, T2 mapping), and multiple gradient echo (mGRE, T2* mapping) sequences.

Assessment: Agreement between hepatic T1, T2, and T2* estimated using MI-SAGE and conventional parametric mapping sequences was evaluated. Repeatability and reproducibility of MI-SAGE were evaluated using a same-session acquisition and second-session acquisition.

Statistical tests: Bland-Altman analysis with bias assessment and limits of agreement (LOA) and intraclass correlation coefficients (ICC).

Results: Hepatic T1, T2, and T2* estimates obtained using the MI-SAGE technique had mean biases of 72 (LOA: -22 to 166) msec, -3 (LOA: -10 to 5) msec, and 2 (LOA: -5 to 8) msec (single breath-hold) and 36 (LOA: -43 to 120) msec, -3 (LOA: -17 to 11) msec, and 4 (LOA: -3 to 11) msec (respiratory triggered), respectively, in comparison to conventional acquisitions using MOLLI, GRASE, and mGRE. All MI-SAGE estimates had strong repeatability and reproducibility (ICC > 0.72).

Data conclusion: Hepatic T1, T2, and T2* estimates obtained using an MI-SAGE technique were comparable to conventional methods, although there was a 12%/6% for breath-hold/respiratory triggered underestimation of T1 values compared to MOLLI. Both respiratory triggered and breath-hold MI-SAGE parameter maps demonstrated strong repeatability and reproducibility.

Level of evidence: 1 TECHNICAL EFFICACY: Stage 2.

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