Serum concentrations of fibrosis markers in children with inflammatory bowel disease

Stanisław Pieczarkowski1, Kinga Kowalska-Deptuch2, Przemko Kwinta3

  • 1Department of Pediatrics, Gastroenterology and Nutrition, Jagiellonian University Medical College Kraków, Poland.

Insights

N-terminal propeptide of type III procollagen (PIIINP) and YKL-40/CHI3L1 serum levels help monitor fibrosis in pediatric inflammatory bowel disease (IBD). PIIINP is a more accurate marker for fibrosis severity in Crohn

Area of Science:

  • Pediatric Gastroenterology
  • Biomarker Research
  • Inflammatory Bowel Disease (IBD) Pathogenesis

Background:

  • Inflammatory bowel disease (IBD) encompasses Crohn's disease (CD) and ulcerative colitis (UC), affecting children.
  • Monitoring disease activity and fibrosis progression is crucial in pediatric IBD.
  • Non-invasive biomarkers for fibrosis assessment are needed.

Purpose of the Study:

  • To evaluate the utility of serum YKL-40/CHI3L1 and N-terminal propeptide of type III procollagen (PIIINP) in monitoring inflammation and fibrosis in pediatric IBD.
  • To compare the fibrosis markers between CD and UC patients.

Main Methods:

  • Serum concentrations of YKL-40/CHI3L1 and PIIINP were measured in 60 children with IBD (41 CD, 19 UC) at baseline and after 6-8 weeks of treatment.
  • Statistical analysis, including the Kruskal-Wallis test, was used to compare marker levels.

Main Results:

  • PIIINP concentrations were significantly higher in CD patients compared to UC patients at baseline and follow-up.
  • Fibrosis severity, indicated by both YKL-40/CHI3L1 and PIIINP, increased in CD patients over 6-8 weeks.
  • In UC patients, YKL-40/CHI3L1 and PIIINP levels decreased over the follow-up period.

Conclusions:

  • Fibrosis is more severe in pediatric CD than in UC.
  • PIIINP is a more accurate serum marker for differentiating fibrosis severity between CD and UC in children.
  • YKL-40/CHI3L1 and PIIINP show potential for monitoring fibrosis in pediatric IBD.
Abstract

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