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Prostaglandin and Cannabinoid Receptors in EoE

M

Medical University of Graz

Status

Completed

Conditions

Eosinophilic Esophagitis (EoE)

Treatments

Other: Biopsy samples
Other: Blood samples

Study type

Observational

Funder types

Other

Identifiers

NCT04626609
KLI 887-B

Details and patient eligibility

About

The purpose of this study is to investigate prostaglandin and cannabinoid receptors and their endogenous ligands in eosinophilic esophagitis (EoE). A prostaglandin D2 receptor antagonist has been shown to improve disease symptoms suggesting a regulatory role for bioactive lipids in EoE. Prostaglandin D2 and E2, and endocannabinoids are lipid mediators that govern the functional and inflammatory behavior of immune cells critical for EoE development. The prostaglandin D2 and E2 receptor axis, and the components of the endocannabinoid may be involved in the pathogenesis of EoE.

Full description

Prostaglandin D2 and E2 receptors, and components of the endocannabinoid system (cannabinoid receptors and endocannabinoid-metabolizing enzymes) are examined in mucosal esophageal biopsies and blood leukocytes from EoE patients (acute and in remission), individuals with gastroesophageal reflux and from individuals with no esophageal disease. Expression of these components are compared between all cohorts by polymerase chain reaction, Western blots, flow cytometry and immunohistochemical methods. EoE disease activity is evaluated by determining a symptom score and the number of eosinophils per high-power field (hpf) in histologic sections of mucosal biopsies. Additionally, an Endoscopic Reference Score (EREFS) is used. Disease activity is correlated with cannabinoid/prostaglandin D2 and E2 receptor expression. Blood is collected and immediately processed for flow cytometric experiments. Prostaglandins and endocannabinoids are measured in plasma and esophageal mucosal biopsy samples of all cohorts by mass spectrometry.

Enrollment

45 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • diagnosed or suspected EoE or GERD
  • without esophageal diseases
  • with signed informed consent

Exclusion criteria

  • viral or parasitic diseases (e.g. herpes, candidiasis)
  • eosinophilic gastroenteritis, hypereosinophilic syndrome, Crohn's disease
  • autoimmune diseases
  • unable to give informed consent
  • immunosuppressive therapy

Trial design

45 participants in 3 patient groups

EoE group
Description:
Patients with confirmed eosinophilic esophagitis
Treatment:
Other: Blood samples
Other: Biopsy samples
GERD group
Description:
Patients with gastro-esophageal reflux disease
Treatment:
Other: Blood samples
Other: Biopsy samples
Control group
Description:
Individuals with no esophageal disease
Treatment:
Other: Blood samples
Other: Biopsy samples

Trial contacts and locations

1

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Central trial contact

Franziska Durchschein, MD; Rudolf Schicho, PhD

Data sourced from clinicaltrials.gov

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