Department of Radiology and Diagnostic Imaging, University of Alberta, Edmonton, Alberta, Canada.
Department of Biomedical Engineering, University of Alberta, Edmonton, Alberta, Canada.
J Magn Reson Imaging. 2024 Nov;60(5):2063-2075. doi: 10.1002/jmri.29262. Epub 2024 Feb 2.
T1 mapping of the liver is confounded by the presence of fat. Multiparametric T1 mapping combines fat-water separation with T1-weighting to enable imaging of water-specific T1 (T1), proton density fat fraction (PDFF), and T2* values. However, normative T1 values in the liver and its dependence on age/sex is unknown.
Determine normative values for T1 in the liver with comparison to MOLLI and evaluate a T2*-compensation approach to reduce T1 variability.
Prospective observational; phantoms.
One hundred twenty-four controls (56 male, 18-75 years), 50 patients at-risk for liver disease (18 male, 30-76 years).
FIELD STRENGTH/SEQUENCE: 2.89 T; Saturation-recovery chemical-shift encoded T1 Mapping (SR-CSE); MOLLI.
SR-CSE provided T1 measurements, PDFF and T2* values in the liver across three slices in 6 seconds. These were compared with MOLLI T1 values. A new T2*-compensation approach to reduce T1 variability was evaluated test/re-test reproducibility.
Linear regression, ANCOVA, t-test, Bland and Altman, intraclass correlation coefficient (ICC). P < 0.05 was considered statistically significant.
Liver T1 values were significantly higher in healthy females (F) than males (M) for both SR-CSE (F-973 ± 78 msec, M-930 ± 72 msec) and MOLLI (F-802 ± 55 msec, M-759 ± 69 msec). T1 values were negatively correlated with age, with similar sex- and age-dependencies observed in T2*. The T2*-compensation model reduced the variability of T1 values by half and removed sex- and age-differences (SR-CSE: F-946 ± 36 msec, M-941 ± 43 msec; MOLLI: F-775 ± 35 msec, M-770 ± 35 msec). At-risk participants had elevated PDFF and T1 values, which became more distinct from the healthy cohort after T2*-compensation. MOLLI systematically underestimated liver T1 values by 170 msec with an additional positive T1-bias from fat content (11 msec/1% in PDFF). Reproducibility ICC values were ≥0.96 for all parameters.
Liver T1 values were lower in males and decreased with age, as observed for SR-CSE and MOLLI acquisitions. MOLLI underestimated liver T1 with an additional large positive fat-modulated T1 bias. T2*-compensation removed sex- and age-dependence in liver T1, reduced the range of healthy values and increased T1 group differences between healthy and at-risk groups.
2 TECHNICAL EFFICACY: Stage 1.
肝脏的 T1 映射受到脂肪的影响。多参数 T1 映射将脂肪-水分离与 T1 加权相结合,从而能够对水特异性 T1(T1)、质子密度脂肪分数(PDFF)和 T2* 值进行成像。然而,肝脏的 T1 的正常数值及其对年龄/性别的依赖性尚不清楚。
确定肝脏 T1 的正常数值,并与 MOLLI 进行比较,并评估一种 T2*-补偿方法来减少 T1 变异性。
前瞻性观察;体模。
124 名对照者(56 名男性,18-75 岁),50 名患有肝病风险的患者(18 名男性,30-76 岁)。
场强/序列:2.89T;饱和恢复化学位移编码 T1 映射(SR-CSE);MOLLI。
SR-CSE 在 6 秒内提供了肝脏三个切片的 T1 测量值、PDFF 和 T2* 值。将这些与 MOLLI T1 值进行比较。评估了一种新的 T2*-补偿方法来减少 T1 变异性,并测试了其重复性。
线性回归、ANCOVA、t 检验、Bland 和 Altman、组内相关系数(ICC)。P<0.05 被认为具有统计学意义。
与 MOLLI 相比,健康女性(F)的肝脏 T1 值明显高于男性(M)(SR-CSE:F-973±78msec,M-930±72msec;MOLLI:F-802±55msec,M-759±69msec)。T1 值与年龄呈负相关,T2也表现出相似的性别和年龄依赖性。T2-补偿模型将 T1 值的变异性降低了一半,并消除了性别和年龄差异(SR-CSE:F-946±36msec,M-941±43msec;MOLLI:F-775±35msec,M-770±35msec)。高危组的 PDFF 和 T1 值升高,经过 T2*-补偿后,与健康组的差异更加明显。MOLLI 系统地低估了肝脏 T1 值约 170msec,并且脂肪含量还存在一个额外的正 T1 偏差(约 11msec/1%在 PDFF 中)。所有参数的重复性 ICC 值均≥0.96。
与 MOLLI 采集一样,男性的肝脏 T1 值较低,且随年龄增长而降低。MOLLI 低估了肝脏 T1 值,且脂肪调节的 T1 偏差较大。T2*-补偿消除了肝脏 T1 的性别和年龄依赖性,减少了健康值的范围,并增加了健康组和高危组之间的 T1 组差异。
2 技术功效:第 1 阶段。