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Quantitative magnetic resonance imaging (MRI) in the evaluation of the degree of steatosis, iron accumulation and fibrosis in chronic liver diseases (MRKER STUDY)
  1. C L Hoad *1,
  2. L Marciani1,
  3. P Kaye2,
  4. I N Guha3,
  5. C Costigan4,
  6. A Austin5,
  7. R C Spiller3,
  8. M W James3,
  9. P A Gowland4,
  10. S Francis4,
  11. G P Aithal3
  1. 1Sir Peter Mansfield Magnetic Resonance Centre, School of Physics and Astronomy, Nottingham University, Nottingham, UK
  2. 2Department of Cellular Pathology, Nottingham University Hospitals NHS Trust, Nottingham, UK
  3. 3Nottingham Digestive Disease Centre, NIRH Biomedical Research Unit, Nottingham, UK
  4. 4Sir Peter Mansfield Magnetic Resonance Centre, School of Physics and Astronomy, University of Nottingham, Nottingham, UK
  5. 5Department of Gastroenterology, Derby Royal Hospital, Derby, UK


Introduction Approximately 12 500 liver biopsies are performed annually in England and Wales. Liver biopsies are associated with sampling errors, observer variability and complications. In contrast, use of ultrasound and MR elastography may be limited by inter-operator variability, cost and access. Fat, iron accumulation and fibrosis are critical contributors to the pathogenesis of major chronic liver disease.

Aim To correlate quantitative multimodal MRI parameters with histological grading of fat, iron accumulation and fibrosis.

Methods MRI relaxation time data (T1, T2 and T2*) were acquired using a novel Echo Planar Imaging technique with a respiratory-triggered (r.t.) rapid acquisition method, repeated multiple times with different contrast to generate accurate voxel-by-voxel (3×3×8 mm3 voxel) relaxation time maps of the liver tissue. 1H MR spectra were acquired (r.t.) using a multiple echo PRESS acquisition which allowed for individual T2 correction to the spectrum for accurate quantification of the fat fraction in a 30×30×30mm3 voxel.

Results Sixty two subjects (range 23–72 years) were included in the study based on the adequacy of liver biopsy. Liver biopsies were (mean ±SD) 28.7±7.3 mm long and 0.96±0.2 mm wide. Histology revealed non-alcoholic fatty liver in 50%, chronic viral hepatitis (HCV and HBV) in 24%, alcoholic liver disease in 11%, normal in 11% and haemochromatosis in 3%. There was significant correlation between MR measures of fat fraction and percentage of fat on histology (r =0.81; p<0.001), T2* with hepatic iron content (r = − 0.65, p<0.001) and T1 with percentage of fibrosis on histology (r=0.48, p<0.001). Performance characteristic of T1 MR parameter in the detection of different histological stages of fibrosis is listed in table 1.

Table 1

OC-110 Performance characteristics of T1 MR parameter compared with histology

Conclusion In chronic liver diseases, MR measures of fat fraction, hepatic iron content and fibrosis correlate well with histological grading. Quantitative MR techniques allow accurate distinction of different stages of fibrosis on liver biopsy. If these are replicated in independent cohorts, these techniques can be translated into clinical applications.

  • fibrosis
  • iron
  • liver
  • MRI

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  • Competing interests None.

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