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ResearchIn-Press PreviewGastroenterologyNeuroscience Open Access | 10.1172/jci.insight.199820

Proximal ganglionic intestine in Hirschsprung disease is fibrotic and stiff

Prisca C. Obidike,1 Britney A. Hsu,2 Chioma Moneme,1 Oluyinka O. Olutoye II,2 Walker D. Short,2 Mary Hui Li,2 Swathi Balaji,2 Yuwen Zhang,1 Sundeep G. Keswani,3 and Lily S. Cheng1

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Obidike, P. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Hsu, B. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Moneme, C. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Olutoye II, O. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Short, W. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Li, M. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Balaji, S. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Zhang, Y. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Keswani, S. in: PubMed | Google Scholar

1Division of Pediatric Surgery, Department of Surgery, University of Virginia, Charlottesville, United States of America

2Department of Surgery, Baylor College of Medicine, Houston, United States of America

3Division of Pediatric Surgery, Department of Surgery, Texas Children's Hospital, Houston, United States of America

Find articles by Cheng, L. in: PubMed | Google Scholar

Published February 10, 2026 - More info

JCI Insight. https://doi.org/10.1172/jci.insight.199820.
Copyright © 2026, Obidike et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Published February 10, 2026 - Version history
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Abstract

Hirschsprung disease (HSCR) is a congenital intestinal disorder characterized by the absence of ganglia in the distal intestine. Despite surgical resection of the aganglionic intestine and pull-through surgery, HSCR patients still experience bowel dysfunction, indicating that latent abnormalities may also exist in the proximal ganglionic intestine. To elucidate possible causes of postoperative bowel dysfunction in HSCR, we investigated differences in the proximal ganglionic intestine using an animal model of HSCR (Ednrb-null mice) and validated our findings in tissue from human HSCR patients. We found that the proximal ganglionic colon of HSCR mice exhibited greater stiffness and fibrosis than their wild-type littermates. Similarly, submucosal fibrosis was significantly greater in the proximal ganglionic intestine of HSCR patients than in intestinal tissue from age and site-matched controls. Furthermore, we observed dysregulated expression of extracellular matrix (ECM)-related genes in the proximal ganglionic intestine of HSCR mice compared to controls. We conclude that increased fibrosis, stiffness, and alterations in ECM composition may contribute to persistent dysfunction of the ganglionic intestine in HSCR. These findings add to the growing body of literature that describe abnormalities in the proximal ganglionic intestine of HSCR and suggest that HSCR is not limited to the aganglionic intestine alone.

Supplemental material

View Supplemental Table 1: List of all differentially expressed genes in the proximal colon of wildtype and HSCR littermates.

View Supplemental Table 2: Genes involved in fibrosis, ECM-receptor interaction, focal adhesion, and neuroactive-receptor ligand pathways in Mus musculus (house mouse) that were queried for heat map shown in Figure 4.

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  • Version 1 (February 10, 2026): In-Press Preview

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