Noninvasive assessment of clinically significant portal hypertension using ΔT1 of the liver and spleen and ECV of the spleen on routine Gd-EOB-DTPA liver MRI

被引:9
|
作者
Catucci, Damiano [1 ]
Obmann, Verena Carola [1 ]
Berzigotti, Annalisa [2 ]
Graeni, Christoph [3 ]
Guensch, Dominik Paul [1 ,4 ]
Fischer, Kady [4 ]
Ebner, Lukas [1 ]
Heverhagen, Johannes Thomas [1 ]
Christe, Andreas [1 ]
Huber, Adrian Thomas [1 ]
机构
[1] Univ Bern, Bern Univ Hosp, Inselspital, Dept Diagnost Intervent & Pediat Radiol, Bern, Switzerland
[2] Univ Bern, Bern Univ Hosp, Inselspital, Hepatol,Dept Visceral Surg & Med, Bern, Switzerland
[3] Univ Bern, Bern Univ Hosp, Inselspital, Dept Cardiol, Bern, Switzerland
[4] Univ Bern, Bern Univ Hosp, Inselspital, Dept Anaesthesiol & Pain Med, Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Liver diseases; Portal hypertension; Magnetic resonance imaging; Venous congestion; Splenomegaly; T1; mapping; CIRRHOSIS; DIAGNOSIS; RISK;
D O I
10.1016/j.ejrad.2021.109958
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To analyze the predictive value of Delta T1 of the liver and spleen as well as the extracellular volume fraction (ECV) of the spleen as noninvasive biomarkers for the determination of clinically significant portal hypertension (CSPH) on routine Gd-EOB-DTPA liver MRI. Method: 195 consecutive patients with known or suspected chronic liver disease from 9/2018 to 7/2019 with GdEOB-DTPA liver MRI and abdominal T1 mapping were retrospectively included. Based on the presence of splenomegaly with thrombocytopenia, ascites and portosystemic collaterals, the patients were divided into noCSPH (n = 113), compensated CSPH (cCSPH, >= 1 finding without ascites; n = 55) and decompensated CSPH (dCSPH, ascites +/- other findings; n = 27). T1 times were measured in the liver, spleen and abdominal aorta in the unenhanced and contrast-enhanced T1 maps. Native T1 times and Delta T1 of the liver and spleen as well as ECV of the spleen were compared between groups using the Kruskal-Wallis test with Dunn's post hoc test. Furthermore, cutoff values for group differentiation were calculated using ROC analysis with Youden's index. Results: Delta T1 of the liver was significantly lower in patients with cCSPH and dCSPH (p < 0.001) compared to patients with noCSPH. In the ROC analyses for differentiation between noCSPH and CSPH (cCSPH + dCSPH), a cutoff of < 0.67 for Delta T1 of the liver (AUC = 0.79) performed better than Delta T1 (AUC = 0.69) and ECV (AUC = 0.63) of the spleen with cutoffs of > 0.29 and > 41.9, respectively. Conclusion: Delta T1 of the liver and spleen in addition to ECV of the spleen allow for determination of CSPH on routine Gd-EOB-DTPA liver MRI.
引用
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页数:10
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