Gastrointestinal endoscopy biopsy derived proteomic patterns predict indeterminate colitis into ulcerative colitis

Billy Ray Ballard1, Amosy Ephreim M'Koma1

  • 1Billy Ray Ballard, Department of Pathology, Meharry Medical College School of Medicine, Nashville, TN 37208-3599, United States.

Insights

Diagnosing indeterminate colitis (IC) is challenging, often requiring advanced proteomic analysis of endoscopic biopsies. This new method aims for a single, accurate test to differentiate ulcerative colitis (UC) or Crohn

Area of Science:

  • Gastroenterology and Inflammatory Bowel Disease (IBD) research.
  • Proteomics and Biomarker Discovery.
  • Diagnostic Innovation in Colitis.

Background:

  • Indeterminate colitis (IC) presents significant diagnostic challenges, particularly in pediatric patients, with current classification systems failing to definitively diagnose ulcerative colitis (UC) or Crohn's colitis (CC) in 15-30% of inflammatory bowel disease (IBD) cases.
  • The inability to accurately differentiate IC into UC or CC leads to suboptimal patient outcomes, especially following restorative proctocolectomy and ileal pouch-anal anastomosis.
  • Diagnostic accuracy for IC has remained stagnant for decades despite advancements in clinical, endoscopic, radiologic, and histologic examinations.

Purpose of the Study:

  • To develop a single, highly sensitive, and accurate diagnostic test for indeterminate colitis (IC) during the initial patient visit.
  • To utilize endoscopic biopsy-derived proteomic patterns for precise differentiation of IC into ulcerative colitis (UC), Crohn's colitis (CC), or non-IBD conditions.
  • To provide a novel diagnostic tool that assists clinicians in the early and accurate management of IBD patients with IC.

Main Methods:

  • Employing Matrix-assisted-laser desorption/ionization mass spectrometry (MS) and/or imaging MS technologies.
  • Performing a histology-directed cellular test on endoscopic biopsy samples.
  • Identifying phenotype-specific proteins as biomarkers for accurate IC subtyping.

Main Results:

  • The proteomic approach using MS technologies has the potential to identify phenotype-specific proteins.
  • These identified proteins serve as biomarkers to accurately delineate IC as UC, CC, or a non-IBD condition.
  • Ongoing studies on larger cohorts are expected to validate the high accuracy and sensitivity of this novel diagnostic method.

Conclusions:

  • A novel diagnostic approach using proteomic patterns from endoscopic biopsies shows promise for accurately differentiating UC from CC in IC patients.
  • This innovative method could significantly improve patient management and outcomes by enabling precise diagnosis during the first clinical encounter.
  • Further research on larger cohorts is crucial to validate these findings and explore potential mechanistic insights into IBD pathogenesis.

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