Assessment of liver fibrosis using pharmacokinetic parameters of dynamic contrast-enhanced magnetic resonance imaging

Zhiming Li1, Jihong Sun1, Lumin Chen1

  • 1Department of Radiology, Sir Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

Abstract

Insights

Dynamic contrast-enhanced MRI (DCE-MRI) pharmacokinetic parameters, particularly K(trans), effectively diagnose and stage liver fibrosis in rabbits. This imaging technique shows promise for non-invasively assessing liver disease progression.

Area of Science:

  • Radiology
  • Medical Imaging
  • Pharmacokinetics

Background:

  • Liver fibrosis is a significant health concern.
  • Accurate staging of liver fibrosis is crucial for patient management.
  • Non-invasive diagnostic methods are highly desirable.

Purpose of the Study:

  • To evaluate dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) pharmacokinetic parameters for diagnosing and staging liver fibrosis in rabbits.
  • To assess the diagnostic performance of DCE-MRI parameters in differentiating fibrosis stages.

Main Methods:

  • DCE-MRI was performed on rabbits with CCl4-induced liver fibrosis and a control group.
  • Fibrosis was staged using the METAVIR system (F0, F1-2, F3-4).
  • Pharmacokinetic parameters (K(trans), kep, Ve, vp) were measured using a dual-input extended Tofts model.

Main Results:

  • K(trans) and Ve decreased with increasing fibrosis stage.
  • K(trans) showed significant differences between control and all fibrosis groups (P < 0.001).
  • K(trans) demonstrated high diagnostic performance (AUROCs > 0.887) for differentiating fibrosis stages.

Conclusions:

  • K(trans) is an excellent DCE-MRI pharmacokinetic parameter for differentiating normal livers from fibrotic livers.
  • DCE-MRI parameters, especially K(trans), can effectively stage liver fibrosis in rabbits.
  • This study highlights the potential of DCE-MRI for non-invasive liver fibrosis assessment.

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