Superficial oesophageal mucosal innervation may contribute to severity of symptoms in oesophageal motility disorders.

achalasia chest pain dysphagia oesophageal motility disorders oesophageal mucosal afferent nerves

Journal

Alimentary pharmacology & therapeutics
ISSN: 1365-2036
Titre abrégé: Aliment Pharmacol Ther
Pays: England
ID NLM: 8707234

Informations de publication

Date de publication:
Jan 2024
Historique:
revised: 31 08 2023
received: 09 08 2023
accepted: 07 10 2023
pubmed: 17 10 2023
medline: 17 10 2023
entrez: 17 10 2023
Statut: ppublish

Résumé

Mechanisms underlying perception of dysphagia and chest pain have not been completely elucidated, although oesophageal mucosal afferent nerves might play an important role. To evaluate the relationship between oesophageal mucosal afferent nerves and the severity of dysphagia and chest pain in oesophageal motility disorders. We prospectively recruited patients with oesophageal motility disorders having dysphagia and/or chest pain from whom oesophageal biopsies were obtained. High-resolution manometry classified patients into disorders of oesophagogastric junction (OGJ) outflow and disorders of peristalsis. Symptom severity was assessed using validated questionnaires including Brief Oesophageal Dysphagia Questionnaire (BEDQ). Immunohistochemistry was performed on oesophageal biopsies to evaluate the location of calcitonin gene-related peptide (CGRP)-immunoreactive mucosal afferent nerves. Findings were compared to existing data from 10 asymptomatic healthy volunteers. Of 79 patients, 61 patients had disorders of OGJ outflow and 18 had disorders of peristalsis. CGRP-immunoreactive mucosal nerves were more superficially located in the mucosa of patients with oesophageal motility disorders compared to healthy volunteers. Within disorders of OGJ outflow, the location of CGRP-immunoreactive nerves negatively correlated with BEDQ score both in the proximal (ρ = -0.567, p < 0.001) and distal oesophagus (ρ = -0.396, p = 0.003). In the proximal oesophagus, strong chest pain was associated with more superficially located mucosal nerves than weak chest pain (p = 0.04). Multivariate analysis showed superficial nerves in the proximal oesophagus was independently associated with severe dysphagia in disorders of OGJ outflow (p = 0.008). Superficial location of mucosal nerves in the proximal oesophagus might contribute to symptoms, especially severe dysphagia, in disorders of OGJ outflow.

Sections du résumé

BACKGROUND BACKGROUND
Mechanisms underlying perception of dysphagia and chest pain have not been completely elucidated, although oesophageal mucosal afferent nerves might play an important role.
AIMS OBJECTIVE
To evaluate the relationship between oesophageal mucosal afferent nerves and the severity of dysphagia and chest pain in oesophageal motility disorders.
METHODS METHODS
We prospectively recruited patients with oesophageal motility disorders having dysphagia and/or chest pain from whom oesophageal biopsies were obtained. High-resolution manometry classified patients into disorders of oesophagogastric junction (OGJ) outflow and disorders of peristalsis. Symptom severity was assessed using validated questionnaires including Brief Oesophageal Dysphagia Questionnaire (BEDQ). Immunohistochemistry was performed on oesophageal biopsies to evaluate the location of calcitonin gene-related peptide (CGRP)-immunoreactive mucosal afferent nerves. Findings were compared to existing data from 10 asymptomatic healthy volunteers.
RESULTS RESULTS
Of 79 patients, 61 patients had disorders of OGJ outflow and 18 had disorders of peristalsis. CGRP-immunoreactive mucosal nerves were more superficially located in the mucosa of patients with oesophageal motility disorders compared to healthy volunteers. Within disorders of OGJ outflow, the location of CGRP-immunoreactive nerves negatively correlated with BEDQ score both in the proximal (ρ = -0.567, p < 0.001) and distal oesophagus (ρ = -0.396, p = 0.003). In the proximal oesophagus, strong chest pain was associated with more superficially located mucosal nerves than weak chest pain (p = 0.04). Multivariate analysis showed superficial nerves in the proximal oesophagus was independently associated with severe dysphagia in disorders of OGJ outflow (p = 0.008).
CONCLUSIONS CONCLUSIONS
Superficial location of mucosal nerves in the proximal oesophagus might contribute to symptoms, especially severe dysphagia, in disorders of OGJ outflow.

Identifiants

pubmed: 37845817
doi: 10.1111/apt.17773
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100-112

Informations de copyright

© 2023 John Wiley & Sons Ltd.

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Auteurs

Akinari Sawada (A)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.
Department of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.

Mengyu Zhang (M)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.

Ahsen Ustaoglu (A)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.

Kornilia Nikaki (K)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.

Chung Lee (C)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.

Philip Woodland (P)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.

Etsuro Yazaki (E)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.

Shingo Takashima (S)

Department of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.

Masaki Ominami (M)

Department of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.

Fumio Tanaka (F)

Department of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.

Clorinda Ciafardini (C)

Gastroenterology and Endoscopy Unit, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.

Fabio Nachman (F)

Fundacion Favaloro Hospital, Buenos Aires, Argentina.

Andrés Ditaranto (A)

Fundacion Favaloro Hospital, Buenos Aires, Argentina.

Joaquín Agotegaray (J)

Fundacion Favaloro Hospital, Buenos Aires, Argentina.

Claudio Bilder (C)

Fundacion Favaloro Hospital, Buenos Aires, Argentina.

Edoardo Savarino (E)

Gastroenterology Unit, Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy.

C Prakash Gyawali (CP)

Division of Gastroenterology, Washington University School of Medicine, St. Louis, Missouri, USA.

Roberto Penagini (R)

Gastroenterology and Endoscopy Unit, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.
Department of Pathophysiology and Transplantation, University of Milan, Italy.

Yasuhiro Fujiwara (Y)

Department of Gastroenterology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.

Daniel Sifrim (D)

Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.

Classifications MeSH