Quantitative hepatic perfusion modeling using DCE-MRI with sequential breathholds

J Magn Reson Imaging. 2014 Apr;39(4):853-65. doi: 10.1002/jmri.24238. Epub 2013 Nov 4.

Abstract

Purpose: To develop and demonstrate the feasibility of a new formulation for quantitative perfusion modeling in the liver using interrupted DCE-MRI data acquired during multiple sequential breathholds.

Materials and methods: A new mathematical formulation to estimate quantitative perfusion parameters using interrupted data was developed. Using this method, we investigated whether a second degree-of-freedom in the tissue residue function (TRF) improves quality-of-fit criteria when applied to a dual-input single-compartment perfusion model. We subsequently estimated hepatic perfusion parameters using DCE-MRI data from 12 healthy volunteers and 9 cirrhotic patients with a history of hepatocellular carcinoma (HCC); and examined the utility of these estimates in differentiating between healthy liver, cirrhotic liver, and HCC.

Results: Quality-of-fit criteria in all groups were improved using a Weibull TRF (2 degrees-of-freedom) versus an exponential TRF (1 degree-of-freedom), indicating nearer concordance of source DCE-MRI data with the Weibull model. Using the Weibull TRF, arterial fraction was greater in cirrhotic versus normal liver (39 ± 23% versus 15 ± 14%, P = 0.07). Mean transit time (20.6 ± 4.1 s versus 9.8 ± 3.5 s, P = 0.01) and arterial fraction (39 ± 23% versus 73 ± 14%, P = 0.04) were both significantly different between cirrhotic liver and HCC, while differences in total perfusion approached significance.

Conclusion: This work demonstrates the feasibility of estimating hepatic perfusion parameters using interrupted data acquired during sequential breathholds.

Keywords: DCE-MRI; hepatic perfusion modeling; hepatocellular carcinoma; quantitative perfusion MRI; tumor perfusion modeling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Blood Flow Velocity
  • Breath Holding
  • Carcinoma, Hepatocellular / diagnosis*
  • Carcinoma, Hepatocellular / physiopathology*
  • Computer Simulation
  • Diagnosis, Differential
  • Feasibility Studies
  • Female
  • Humans
  • Image Enhancement / methods
  • Image Interpretation, Computer-Assisted / methods
  • Liver Circulation
  • Liver Cirrhosis / diagnosis*
  • Liver Cirrhosis / physiopathology*
  • Liver Neoplasms / diagnosis*
  • Liver Neoplasms / physiopathology*
  • Magnetic Resonance Angiography / methods*
  • Male
  • Middle Aged
  • Models, Biological
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Young Adult