Abstract

BackgroundPediatric patients with liver disease require noninvasive monitoring to evaluate the risk of fibrosis progression. This study aimed to identify the significant factors affecting liver stiffness values using two-dimensional shear-wave elastography (2D-SWE), and determine whether liver stiffness can predict the fibrosis stage of various childhood liver diseases.MethodsThis study included 30 children (22 boys and 8 girls; mean age, 5.1 ± 6.1 years; range, 7 days–17.9 years) who had undergone biochemical evaluation, 2D-SWE examination, histopathologic analysis of fibrosis grade (F0 to F3), assessment of necroinflammatory activity, and steatosis grading between August 2016 and March 2020. The liver stiffness from 2D-SWE was compared between fibrosis stages using Kruskal–Wallis analysis. Factors that significantly affected liver stiffness were evaluated using univariate and multivariate linear regression analyses. The diagnostic performance was determined from the area under the receiver operating curve (AUC) values of 2D-SWE liver stiffness.ResultsLiver stiffness at the F0-1, F2, and F3 stages were 7.9, 13.2, and 21.7 kPa, respectively (P < 0.001). Both fibrosis stage and necroinflammatory grade were significantly associated with liver stiffness (P < 0.001 and P = 0.021, respectively). However, in patients with alanine aminotransferase (ALT) levels below 200 IU/L, the only factor affecting liver stiffness was fibrosis stage (P = 0.030). The liver stiffness value could distinguish significant fibrosis (≥ F2) with an AUC of 0.950 (cutoff value, 11.3 kPa) and severe fibrosis (F3 stage) with an AUC of 0.924 (cutoff value, 18.1 kPa). The 2D-SWE values for differentiating significant fibrosis were 10.5 kPa (≥ F2) and 18.1 kPa (F3) in patients with ALT levels below 200 IU/L.ConclusionThe liver stiffness values on 2D-SWE can be affected by both fibrosis and necroinflammatory grade and can provide excellent diagnostic performance in evaluating the fibrosis stage in various pediatric liver diseases. However, clinicians should be mindful of potential confounders, such as necroinflammatory activity or transaminase level, when performing 2D-SWE measurements for liver fibrosis staging.

Highlights

  • Pediatric patients with liver disease require noninvasive monitoring to evaluate the risk of fibrosis progression

  • Previous studies have shown that various serum biochemical indicators, such as aspartate aminotransferase (AST), alanine aminotransferase (ALT), Aspartate aminotransferase (AST) to platelet ratio index (APRI), AST and Alanine aminotransferase (ALT) ratio (AAR), and fibrosis index based on the 4 factor (FIB-4) score, could be candidate markers in adult chronic liver patients [3,4,5]

  • We have shown that both necroinflammatory and fibrotic stages based on histopathologic analysis can influence 2D-Shear-wave elastography (SWE) liver stiffness values despite various liver diseases

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Summary

Introduction

Pediatric patients with liver disease require noninvasive monitoring to evaluate the risk of fibrosis progression. Pediatric patients with liver disease require monitoring for the likelihood of liver fibrosis progression similar to adult patients. Both liver function biochemical assessment and ultrasound (US) examination are used for liver fibrosis monitoring, but liver biopsy, which is performed only if necessary, is considered the gold standard despite its invasiveness and potential for sampling errors [1]. Previous studies have shown that various serum biochemical indicators, such as aspartate aminotransferase (AST), alanine aminotransferase (ALT), AST to platelet ratio index (APRI), AST and ALT ratio (AAR), and fibrosis index based on the 4 factor (FIB-4) score, could be candidate markers in adult chronic liver patients [3,4,5]. Further evaluation of their clinical utility for liver fibrosis is needed in pediatric patients because of their different etiologies [6, 7]

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