Liver iron overload assessment by MRI R2* relaxometry in highly transfused pediatric patients: an agreement and reproducibility study

Diagn Interv Imaging. 2015 Mar;96(3):259-64. doi: 10.1016/j.diii.2014.11.021. Epub 2014 Dec 19.

Abstract

Aims: Perform an agreement and reproducibility study of the estimation of iron overload in highly transfused pediatric patients comparing R2* relaxometry (R2*=1000/T2*) to the reference technique liver/muscle signal intensity ratio (SIR).

Patients and methods: Ninety-two MRI were performed in 68 children who were mainly transfused for sickle cell disease, mean age 9.9 years old. The examination included six sequences for the SIR protocol and a single multiecho T2* sequence. R2* relaxometry was measured by two radiologists independently, either by a region of interest (ROI) in the right liver, or an outline of the whole liver. Hepatic iron load was determined by the Wood formula (Fe mg/g=R2*×0.0254+0.202). The validity of R2* relaxometry compared to SIR was evaluated by the coefficient of variation and the quadratic weighted Kappa value.

Results: The correlation between R2* relaxometry and SIR was very good with a Pearson coefficient of 0.89 and a coefficient of variation of 17.3%. The inter- and intraobserver reproducibility of the measurement of R2* relaxometry by ROI and whole liver mapping was excellent. However, we observed a common positive variation of one class between SIR and R2* relaxometry, with higher hepatic iron content values with SIR than with R2* relaxometry.

Conclusion: Hepatic iron content can be rapidly and precisely estimated on MRI by multiecho gradient-echo sequences.

Keywords: Iron overload; Liver MRI; Sickle cell disease.

MeSH terms

  • Adolescent
  • Anemia, Sickle Cell / therapy
  • Blood Transfusion*
  • Child
  • Child, Preschool
  • Humans
  • Iron Overload / complications
  • Iron Overload / diagnosis*
  • Liver / pathology
  • Liver Diseases / complications
  • Liver Diseases / diagnosis*
  • Magnetic Resonance Imaging / methods*
  • Muscle, Skeletal / pathology
  • Reproducibility of Results
  • Young Adult