Evidence map›Paper›PMID 28811704›Full record

ReviewWorld journal of gastroenterology2017

Gastrointestinal neuroendocrine peptides/amines in inflammatory bowel disease.

Magdy El-Salhy, Tefera Solomon, Trygve Hausken, Odd Helge Gilja, Jan Gunnar Hatlebakk

Abstract readReview
In one paragraph

Review in World journal of gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Mechanisms and clinical implications of gut-brain interactions.The Journal of clinical investigation · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Engineered spermidine-secretingFrontiers in neuroscience · 2025
    Article
  9. The Potential of the Probiotic IsolateFood science & nutrition · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Role of the Ghrelin System in Colorectal Cancer.International journal of molecular sciences · 2022
    Review
  19. Review
  20. Article
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.

Magdy El-SalhyMagdy El-Salhy, Division of Gastroenterology, Department of Medicine, Stord Hospital, Box 4000, 5409 Stord, Norway.
Tefera SolomonMagdy El-Salhy, Division of Gastroenterology, Department of Medicine, Stord Hospital, Box 4000, 5409 Stord, Norway.
Trygve HauskenMagdy El-Salhy, Division of Gastroenterology, Department of Medicine, Stord Hospital, Box 4000, 5409 Stord, Norway.
Odd Helge GiljaMagdy El-Salhy, Division of Gastroenterology, Department of Medicine, Stord Hospital, Box 4000, 5409 Stord, Norway.
Jan Gunnar HatlebakkMagdy El-Salhy, Division of Gastroenterology, Department of Medicine, Stord Hospital, Box 4000, 5409 Stord, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a chronic recurrent condition whose etiology is unknown, and it includes ulcerative colitis, Crohn's disease, and microscopic colitis. These three diseases differ in clinical manifestations, courses, and prognoses. IBD reduces the patients' quality of life and is an economic burden to both the patients and society. Interactions between the gastrointestinal (GI) neuroendocrine peptides/amines (NEPA) and the immune system are believed to play an important role in the pathophysiology of IBD. Moreover, the interaction between GI NEPA and intestinal microbiota appears to play also a pivotal role in the pathophysiology of IBD. This review summarizes the available data on GI NEPA in IBD, and speculates on their possible role in the pathophysiology and the potential use of this information when developing treatments. GI NEPA serotonin, the neuropeptide Y family, and substance P are proinflammatory, while the chromogranin/secretogranin family, vasoactive intestinal peptide, somatostatin, and ghrelin are anti-inflammatory. Several innate and adaptive immune cells express these NEPA and/or have receptors to them. The GI NEPA are affected in patients with IBD and in animal models of human IBD. The GI NEPA are potentially useful for the diagnosis and follow-up of the activity of IBD, and are candidate targets for treatments of this disease.

Indexed as

Gastrointestinal MicrobiomeAminesAnimalsChromograninsDisease Models, AnimalGastrointestinal TractGhrelinHumansInflammatory Bowel DiseasesNeuroendocrine CellsNeuropeptide YNeurosecretory SystemsPrevalenceQuality of LifeRecurrenceSerotoninAminesChromograninsGhrelinNeuropeptide YSerotoninSerotonin AntagonistsSomatostatinSubstance PVasoactive Intestinal PeptideEnteric nervous systemEnteroendocrine cellsImmune cellsInflammatory bowel diseaseMusashi-1Neurogenin 3Stem cells

Identifiers

PMID28811704
PMCPMC5537176

What OpenQuestion holds

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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 OpenQuestion graph.