4.7 Article

Noninvasive diagnosis of portal hypertension using gadoxetate DCE-MRI of the liver and spleen

期刊

EUROPEAN RADIOLOGY
卷 31, 期 7, 页码 4804-4812

出版社

SPRINGER
DOI: 10.1007/s00330-020-07495-0

关键词

Perfusion imaging; Portal hypertension; Portal pressure; Liver diseases; Liver cirrhosis

资金

  1. NIDDK grant [R01DK113272]

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The results of this study demonstrate the potential utility of hepatocyte uptake parameters and spleen interstitial fraction obtained with gadoxetate DCE-MRI for the diagnosis of portal hypertension and clinically significant portal hypertension. Liver uptake rate shows good diagnostic performance for the diagnosis of portal hypertension, while the combination of liver uptake rate with spleen interstitial fraction exhibits excellent diagnostic performance for the diagnosis of clinically significant portal hypertension.
Objectives To assess the performance of gadoxetate dynamic contrast-enhanced (DCE) MRI of the liver and spleen for noninvasive diagnosis of portal hypertension (PH). Methods Thirty-five patients (M/F 22/13, mean age 55 years) with chronic liver disease who underwent hepatic venous pressure gradient (HVPG) measurements were prospectively enrolled in this IRB-approved study. All patients underwent multiparametric MRI including gadoxetate DCE-MRI acquisition. Model-based and model-free DCE-MRI analyses were performed. The correlation between DCE-MRI parameters and HVPG was assessed. ROC analysis was employed to determine the diagnostic performance of DCE-MRI parameters alone and in combination for prediction of PH and clinically significant (CS)PH (HVPG > 5 and >= 10 mmHg, respectively). Results Mean HVPG was 7.0 +/- 5.0 mmHg (range 0-18 mmHg). Twenty-one (60%) patients had PH, of whom 9 had CSPH. Modeled liver uptake fraction f(i) and uptake rate k(i) and model-free parameters liver upslope and uptake were all significantly negatively correlated with HVPG (r range - 0.490 to - 0.398, p value range 0.003-0.018), while spleen interstitial fraction v(e) was significantly positively correlated with HVPG (r = 0.336, p = 0.048). For PH diagnosis, liver k(i) showed the best diagnostic performance with an AUC, sensitivity, and specificity of 0.74 (confidence interval (CI) 0.57-0.91), 71.4%, and 78.6%. The combination of liver k(i) and spleen v(e) was selected as the best classifier for diagnosis of CSPH with an AUC, sensitivity, and specificity of 0.87 (CI 0.75-0.99), 100%, and 73.1%. Conclusions Our results demonstrate the potential utility of hepatocyte uptake parameters and spleen interstitial fraction obtained with gadoxetate DCE-MRI for the diagnosis of PH and CSPH. Key Points Liver uptake and spleen interstitial fraction estimates from gadoxetate DCE-MRI are significantly correlated with portal pressure measurements. Liver uptake rate shows good diagnostic performance for the diagnosis of portal hypertension. The combination of liver uptake rate with spleen interstitial fraction exhibits excellent diagnostic performance for the diagnosis of clinically significant portal hypertension.

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