Evaluation of liver fibrosis with T2 relaxation time in infants with cholestasis: comparison with normal controls

Mi-Jung Lee1, Myung-Joon Kim, Choon-Sik Yoon

  • 1Department of Radiology and Research Institute of Radiological Science, Severance Children's Hospital, Yonsei University, College of Medicine, 250 Seongsanno (134 Sinchon-dong), Seodaemun-gu, Seoul, 120-752, South Korea.

Pediatric Radiology
|October 21, 2010
PubMed

Insights

T2 relaxation time measurements in infants did not effectively quantify liver fibrosis in biliary atresia. This noninvasive method showed no significant difference between healthy infants and those with biliary atresia or varying fibrosis stages.

Area of Science:

  • Pediatric Radiology
  • Hepatology
  • Medical Imaging

Background:

  • Early diagnosis of liver fibrosis in biliary atresia (BA) is crucial for prognosis.
  • Liver biopsy, the current gold standard, is invasive and requires sedation in infants.
  • Noninvasive methods for assessing liver fibrosis are highly desirable.

Purpose of the Study:

  • To evaluate the potential of T2 relaxation time measurements for quantifying liver fibrosis in infants.
  • To determine if T2 relaxation time can serve as a noninvasive biomarker for liver fibrosis in BA.

Main Methods:

  • Prospective study involving infants with neonatal cholestasis and healthy controls.
  • T2 relaxation time of the liver measured using 1.5-T MRI with spin-echo sequences.
  • Correlation analysis between T2 relaxation times and histopathological fibrosis stages from liver biopsies.

Main Results:

  • No statistically significant difference in T2 relaxation times was found between normal controls and infants with BA (57.8 ms vs 56.8 ms, P=0.811).
  • T2 relaxation times did not differ significantly between low-stage (≤F1) and high-stage (≥F2) fibrosis.
  • Mean T2 relaxation time in normal infants (57.8 ms) was comparable to adult values.

Conclusions:

  • T2 relaxation time measurement at 1.5-T MRI is not a suitable method for quantifying liver fibrosis in infants with biliary atresia.
  • The technique did not differentiate between varying stages of liver fibrosis in the study population.
Abstract