Evidence map›Paper›PMID 21590343›Full record

ArticleJournal of gastroenterology2011

Role of Th-2 cytokines in the development of Barrett's esophagus in rats.

Yukie Kohata, Yasuhiro Fujiwara, Hirohisa Machida, Hirotoshi Okazaki, Hirokazu Yamagami, Tetsuya Tanigawa, Kenji Watanabe, Toshio Watanabe, Kazunari Tominaga, Min Wei and 2 more

Registry-linked trialAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of gastroenterology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02699060 (Experimental Study to Determine the Effects of Human Refluxate), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
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.

NCT02699060 nacompletednot on this mapstarted 2016, after this paper: background citation

Experimental Study to Determine the Effects of Human Refluxate (Biliary, Gastric, Duodenogastric) on Macrophage Phenotype and Its Correlation With Different Forms of GERD: Motility Talent Group Study

TypeinterventionalSponsorIvashkin Vladimir TrofimovichRan2016 to 2019Enrolled68ConditionsGastroesophageal Reflux Disease (GERD)ArmsUpper gastrointestinal endoscopy with biopsy and collection of refluxate, Esophageal high-resolution manometry and 24-h esophageal pH-impedance monitoring
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Molecules involved in the development of Barrett's esophagus phenotype in chronic eosinophilic esophagitis.American journal of physiology. Gastrointestinal and liver physiology · 2022
    Article
  3. Review
  4. Article
  5. Article
  6. Esophageal Tumor Microenvironment.Advances in experimental medicine and biology · 2020
    Review
  7. Barrett's esophagus is negatively associated with eosinophilic esophagitis in Japanese subjects.Esophagus : official journal of the Japan Esophageal Society · 2019
    Observational
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Circulating inflammatory cytokines and adipokines are associated with increased risk of Barrett's esophagus: a case-control study.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2014
    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

12 authors at 1 institution in 1 country.

Yukie KohataDepartment of Gastroenterology, Osaka City University Graduate School of Medicine, 1-4-7 Asahimachi, Abenoku, Osaka, 545-8585, Japan.
Yasuhiro Fujiwara
Hirohisa Machida
Hirotoshi Okazaki
Hirokazu Yamagami
Tetsuya Tanigawa
Kenji Watanabe
Toshio Watanabe
Kazunari Tominaga
Min Wei
Hideki Wanibuchi
Tetsuo Arakawa
Osaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBarrett's esophagus is characterized by a distinct Th-2-predominant cytokine profile, unlike the pro-inflammatory nature of reflux esophagitis. The aim of this study was to examine the role of Th-2 cytokines during the development of Barrett's esophagus, using a rat model.

methodsBarrett's esophagus was induced by Levrat's esophagojejunostomy technique in Brown-Norway (BN) rats. Rats were killed at 8, 15, 30, and 50 weeks after the operation. We studied the incidences of esophagitis and Barrett's esophagus, and the mRNA expression of cytokines and CDX2 by real-time reverse transcriptase-polymerase chain reaction and immunohistochemical staining. Finally, we compared the incidence of Barrett's esophagus in BN rats with that in Sprague-Dawley (SD) rats.

resultsEsophagitis was found in all rats. Barrett's esophagus appeared 8 weeks after the operation, and its incidence and length increased over time. Levels of Th-2 cytokines such as interleukin (IL)-4, IL-10, and IL-13 were significantly increased in Barrett's esophagus as compared to those in non-Barrett's esophagus, while there were no differences in the levels of pro-inflammatory cytokines. The peak of elevated IL-4 mRNA was observed before that of CDX2 mRNA. IL-4 was co-localized in CD4-positive cells and CDX2-positive goblet cells. The incidence of Barrett's esophagus was more common in BN rats (8/10, 80%) than in SD rats (2/7, 28%) at 30 weeks.

conclusionTh-2 cytokines, especially IL-4, may play a crucial role in the development of Barrett's esophagus in an early phase. These results provide understanding of the pathogenesis of Barrett's esophagus from the aspect of the Th-2 immune response.

Indexed as

AnimalsBarrett EsophagusCDX2 Transcription FactorDisease Models, AnimalDisease ProgressionEsophagitis, PepticFluorescent Antibody TechniqueHomeodomain ProteinsImmunohistochemistryInterleukin-10Interleukin-13Interleukin-4MaleRatsRats, Inbred BNRats, Sprague-DawleyCdx2 protein, ratCDX2 Transcription FactorHomeodomain ProteinsInterleukin-10Interleukin-13Interleukin-4RNARNA, MessengerRNA primersTranscription Factors

Identifiers

PMID21590343
OpenAlexW2071745503

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.