Claudin-3, lipopolysaccharide binding protein, and jaundice clearance in infants with biliary atresia

Jain, Vandana, Nulty, Jessica, Alexander, Emma C., Burford, Charlotte, Davenport, Mark, Chokshi, Shilpa, Riva, Antonio, Dalby, Matthew J., Verma, Anita, Hall, Lindsay J., Yuksel, Muhammed and Dhawan, Anil (2025) Claudin-3, lipopolysaccharide binding protein, and jaundice clearance in infants with biliary atresia. Journal of Pediatrics, 286. ISSN 0022-3476

[thumbnail of Jain_etal_2025_JPediatrics]
Preview
PDF (Jain_etal_2025_JPediatrics) - Published Version
Available under License Creative Commons Attribution.

Download (2MB) | Preview

Abstract

Objective: To explore the relationship among bacterial translocation, intestinal barrier integrity, and systemic inflammation in early biliary atresia (BA). Study design: Newly diagnosed infants with BA were assessed longitudinally before as well as 6, 12, and 24 weeks after undergoing Kasai portoenterostomy. Plasma immune marker measurement included interleukin (IL)-2, interferon-gamma (IFNγ), IL-4, IL-10, tumor necrosis factor alpha, IL-6, IL-8, IL-1β, IL-17, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1). Bacterial translocation (lipopolysaccharide binding protein [LBP]; D-lactate), intestinal barrier (claudin-3; intestinal fatty acid binding protein [IFABP], fecal calprotectin) biomarkers, and fecal microbiota genus abundance were analyzed. Results: Fifty-five infants were included, of whom 60% cleared their jaundice. Early post-Kasai, upregulation of plasma adhesion molecules and pro-inflammatory cytokines were associated with poorer jaundice clearance and liver fibrosis and correlated with jaundice severity. Elevated claudin-3 early post-Kasai was associated with poor jaundice clearance [OR 1.02 (1.00, 1.04); P = .02] and jaundice severity [P < .01]. On multivariable analysis, early ICAM-1 elevation (OR 1.008 [1.002, 1.014]; P = .01) and claudin-3 (OR 1.038 [1.009, 1.068]; P = .02), represented independent prognostic markers for persistent jaundice. Increased longitudinal trends of LBP (OR 0.79 [0.71, 0.89]; P < .01) and IFABP (OR <0.01 [2.4E-43, 0.24]; P = .04) were associated with poor jaundice clearance. LBP positively correlated with pro-inflammatory-cytokines (IL-6, P < .01: TNFα, P < .01) and ICAM-1 (P < .01) early post-Kasai. Fecal calprotectin positively correlated with jaundice severity (P < .01) by 24 weeks post-Kasai. No correlation between fecal microbiota abundance and bacterial translocation/intestinal integrity markers was demonstrated. Conclusions: Bacterial translocation may be linked to post-Kasai BA-immune pathways. Claudin-3 could represent a novel biomarker of early intestinal permeability in BA; links to the gut microbiota need further exploration.

Item Type: Article
Additional Information: Publisher Copyright: © 2025
Uncontrolled Keywords: claudin-3,cytokine,gut microbiota,intercellular adhesion molecule 1,lipopolysaccaride-binding protein,pediatrics, perinatology, and child health ,/dk/atira/pure/subjectarea/asjc/2700/2735
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
UEA Research Groups: Faculty of Medicine and Health Sciences > Research Centres > Metabolic Health
Related URLs:
Depositing User: LivePure Connector
Date Deposited: 20 Aug 2025 09:30
Last Modified: 27 Aug 2025 08:28
URI: https://ueaeprints.uea.ac.uk/id/eprint/100157
DOI: 10.1016/j.jpeds.2025.114703

Downloads

Downloads per month over past year

Actions (login required)

View Item View Item