Evidence map›Paper›PMID 41640876›Full record

ArticleWorld journal of gastroenterology2026

Can bile salts affect the contractile oesophageal activity associated with gastroesophageal reflux disease?

Kalinne Kelly Lima Gadelha, Armênio Aguiar Santos, Paulo Correia-de-Sá, Pedro Jorge Caldas Magalhães, Moisés Tolentino Bento da Silva

Abstract readEditorial
In one paragraph

Article in World journal of gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Kalinne Kelly Lima GadelhaDepartment of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza 60020-181, Ceará, Brazil.
Armênio Aguiar SantosDepartment of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza 60020-181, Ceará, Brazil.
Paulo Correia-de-SáLaboratory of Pharmacology and Neurobiology, Department of Immuno-Physiology and Pharmacology, School of Medicine and Biomedical Science, Center for Drug Discovery and Innovative Medicines/RISE-Health: Health Research Network, University of Porto, Porto 4050-313, Portugal.
Pedro Jorge Caldas MagalhãesDepartment of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza 60020-181, Ceará, Brazil.
Moisés Tolentino Bento da SilvaLaboratory of Physiology, Department of Immuno-Physiology and Pharmacology, School of Medicine and Biomedical Science, Center for Drug Discovery and Innovative Medicines/RISE-Health: Health Research Network, University of Porto, Porto 4050-313, Portugal. mtsilva@icbas.up.pt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bile salts are essential molecules that have evolved beyond their digestive surfactant properties to act as relevant pathophysiological signalling modulators. In the gastroesophageal reflux disease (GERD), recurrent exposure of the oesophagus to harmful agents of gastric and duodenal origin, including bile salts, results in chronic inflammation and damage to the oesophageal mucosa, ultimately promoting the progression of the normal oesophageal epithelium to pre-malignant or malignant lesions, such as Barrett's oesophagus and adenocarcinoma. Although the acidity of the refluxed material has long been considered the leading cause of pathological features in GERD, some patients do not respond adequately to conventional therapy with proton pump inhibitors, implicating non-acidic components of the gastroesophageal reflux originating in the stomach and/or duodenum. Oesophageal motor activity is an essential protection against GERD symptoms, as it directly determines the contact time of the refluxed material inside the oesophagus. Oesophageal dysmotility profiles are documented in GERD, and bile salts appear to contribute to this dysfunction. In this work, we highlight the involvement of bile salts in the pathogenesis of GERD, particularly their effect on oesophageal motility and their potential signalling pathways.

Indexed as

Bile Acids and SaltsEsophagusGastroesophageal RefluxAdenocarcinomaAnimalsBarrett EsophagusEsophageal MucosaEsophageal NeoplasmsGastrointestinal MotilityHumansMuscle ContractionProton Pump InhibitorsSignal TransductionBile Acids and SaltsProton Pump InhibitorsBarrett’s oesophagusBile acids and saltsGastroesophageal reflux diseaseG-protein-coupled bile acid receptorOesophageal motility

Identifiers

PMID41640876
PMCPMC12865383

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.