Periportal thickening on magnetic resonance imaging for hepatic fibrosis in infantile cholestasis

World J Gastroenterol. 2020 Jun 7;26(21):2821-2830. doi: 10.3748/wjg.v26.i21.2821.

Abstract

Background: Untreated neonatal cholestasis can progress to liver cirrhosis and end stage liver disease in infancy due to prolonged hepatocyte and biliary tree injury and may require liver transplantation. Therefore, non-invasive evaluation of hepatic fibrosis is important in infants with cholestasis.

Aim: To investigate the usefulness of periportal thickening (PT) measured on liver magnetic resonance imaging (MRI) for the assessment of hepatic fibrosis in infants with cholestasis including biliary atresia (BA).

Methods: This retrospective study included infants less than 6 mo who underwent liver MRI and biopsy for the evaluation of infantile cholestasis. PT and spleen size were measured on MRI. Serologic assessment was based on aspartate transaminase to platelet ratio index (APRI). The grade of histopathologic fibrosis was assessed by the METAVIR grading system. Correlation and diagnostic performance of PT, normalized spleen size ratio (SR, using the upper normal size limit), and APRI for diagnosing hepatic fibrosis were obtained by receiver-operating characteristic (ROC) curve analysis.

Results: A total of 155 patients were included, 110 of which were diagnosed with BA. Mean age at the time of MRI was 57.6 ± 34.4 d. There were positive correlations between fibrosis grade and PT and SR, even after adjusting age (all, P < 0.001). For the diagnosis of significant fibrosis (METAVIR grade F2-F4), the area under the ROC curve was 0.899 (95%CI: 0.840-0.941) for PT (cutoff, 4.2 mm), which was higher than 0.741 (95%CI: 0.664-0.808) for SR and 0.712 (95%CI: 0.634-0.782) for APRI (both, P < 0.001). For the diagnosis of cirrhosis (F4), the area under the ROC curve was the highest with SR as 0.790 (95%CI: 0.718-0.852).

Conclusion: Liver MRI findings of PT and SR are useful to assess clinically significant hepatic fibrosis (F2 and higher) in infants with cholestasis including BA.

Keywords: Biliary atresia; Cholestasis; Fibrosis; Infants; Liver; Magnetic resonance imaging.

Publication types

  • Evaluation Study

MeSH terms

  • Aspartate Aminotransferases / blood
  • Biliary Atresia / blood
  • Biliary Atresia / complications*
  • Biliary Atresia / diagnosis
  • Biliary Atresia / pathology
  • Biopsy
  • Cholestasis / blood
  • Cholestasis / etiology*
  • Cholestasis / pathology
  • Female
  • Humans
  • Hyperbilirubinemia / blood
  • Hyperbilirubinemia / etiology*
  • Hyperbilirubinemia / pathology
  • Infant
  • Infant, Newborn
  • Liver / blood supply
  • Liver / diagnostic imaging*
  • Liver / pathology
  • Liver Cirrhosis / blood
  • Liver Cirrhosis / diagnosis*
  • Liver Cirrhosis / etiology
  • Liver Cirrhosis / pathology
  • Magnetic Resonance Imaging
  • Male
  • Platelet Count
  • Portal Vein / diagnostic imaging
  • ROC Curve
  • Retrospective Studies
  • Severity of Illness Index

Substances

  • Aspartate Aminotransferases