4.7 Article

Diagnostic merits of the Eosinophilic Esophagitis Diagnostic Panel from a single esophageal biopsy

Journal

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
Volume 149, Issue 2, Pages 782-+

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2021.07.032

Keywords

Eosinophilic esophagitis; eosinophilic gastrointestinal diseases; diagnostic panel; EoE transcriptome; eosinophil; molecular diagnostics; predictive medicine

Funding

  1. Consortium of Eosinophilic Gastrointestinal Disease Researchers (CEGIR) [U54 AI117804]
  2. National Institute of Allergy and Infectious Diseases
  3. National Institute of Diabetes and Digestive and Kidney Diseases
  4. National Center for Advancing Translational Sciences
  5. American Partnership for Eosinophilic Disorders, Campaign Urging Research for Eosinophilic Disease, and Eosinophilic Family Coalition
  6. National Institutes of Health [T35DK060444, R37A1045898, U19AI070235]

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This study investigated whether molecular mRNA profiling of a distal esophageal biopsy sample predicts eosinophilia in the proximal esophagus. The results showed a negative correlation between the distal molecular profile score and proximal eosinophil levels. Analysis of histologically negative distal biopsy samples predicted the presence of proximal esophagitis with high sensitivity.
Background: Eosinophilic esophagitis (EoE) is a histologically patchy disease with uneven eosinophil distribution along the esophagus, posing a dilemma for histologically analyzing endoscopic biopsy samples, especially when biopsy samples are limited to only the distal esophagus. Objective: We investigated whether molecular mRNA profiling of a distal esophageal biopsy sample predicts eosinophilia in the proximal esophagus. Methods: Esophageal biopsy samples (n = 507) from subjects with EoE were collected from multiple institutions, spanning adults and pediatric patients. Subjects were grouped on the basis of distinct distal (D) and proximal (P) eosinophil counts (D+P+, D+P-, D-P+, and D-P-, with + and - defined as >= 15 or <15 eosinophils/hpf, respectively). Molecular profiles were assessed by using the EoE Diagnostic Panel (EDP), a set of 96 esophageal transcripts used to derive the EDP score. Results: The distal EDP score was correlated with proximal eosinophil levels (r = -0.73; P < .0001). EDP analysis of a histologically negative distal biopsy sample predicted the presence of proximal esophagitis with high sensitivity (85%). In a 2-year follow-up focusing on the cases with discordant histologic and EDP results, histologically negative patients (D-P-) had higher rates of EoE relapse when the EDP was positive than when the EDP was negative (odds ratio = 11; P = .003), indicating predictive medicine capacity. Conclusion: EDP analysis of a single distal esophageal biopsy sample predicts remote inflammation in patients with spatially heterogeneous eosinophilia and disease relapse in patients with histologic remission, providing diagnostic merit and predictive medicine capacity for molecular diagnosis of EoE.

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