Evidence map›Paper›PMID 26423313›Full record

ArticleAlimentary pharmacology & therapeutics2015

Immunopathogenesis of olmesartan-associated enteropathy.

E V Marietta, A M Nadeau, A K Cartee, I Singh, A Rishi, R S Choung, T-T Wu, A Rubio-Tapia, J A Murray

Open access · bronzeAbstract read
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.6field-weighted citation impact, top 5% 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.

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

29 citing papers in PubMed, 68 citations in OpenAlex.

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  14. Olmesartan-Induced Enteropathy: A Case of Recurrent Diarrhoea.European journal of case reports in internal medicine · 2020
    Article
  15. Review
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  19. Autoimmune enteropathies.Virchows Archiv : an international journal of pathology · 2018
    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

9 authors at 2 institutions in 1 country.

E V MariettaDepartment of Immunology, Mayo Clinic, Rochester, MN, USA.
A M NadeauDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
A K CarteeDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
I SinghDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
A RishiDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
R S ChoungDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
T-T WuDepartment of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
A Rubio-TapiaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
J A MurrayDepartment of Immunology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · USWinnMed · US

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
EPIDEMIOLOGY OF CELIAC DISEASE--A POPULATION BASED STUDYR01DK057892 · NIDDK · MAYO CLINIC ROCHESTER · PI MURRAY, JOSEPH A · 2000 to 2010
$3.9M
NIDDK NIH HHS P30 DK084567NIDDK NIH HHS R01 DK057892
6 · The paper itself

Abstract

backgroundOlmesartan-associated enteropathy (OAE) is characterised by diarrhoea, nausea, vomiting, abdominal pain, weight loss and severe sprue-like enteropathy, all of which are resolved after discontinuation of olmesartan medoximil.

aimTo determine the mechanistic similarities of OAE with coeliac sprue.

methodsDuodenal biopsies were extracted from OAE patients before (n = 11) or after (n = 17) discontinuation of olmesartan medoxomil (on or off olmesartan medoxomil). There were seven 'on/off' paired samples. Formalin-fixed biopsies were stained for CD8, CD4, FoxP3, IL-15R and psmad 2/3. Caco2 cells (human colonic epithelial line) were treated with olmesartan medoxomil and stained for IL-15, IL-15R and ZO-1.

resultsIn the 'on olmesartan medoxomil' duodenal biopsies, a significant increase in the numbers of CD8+ cells and the number of cells that are FoxP3+ (a regulatory T-cell marker) are present in the duodenum as compared to the duodenal biopsies from patients who discontinued olmesartan medoxomil. IL15R expression is also increased with olmesartan medoxomil use. Evaluation of the effect of olmesartan medoxomil upon Caco-2 cells demonstrated that IL15 expression is increased in response to olmesartan medoxomil treatment. Further, ZO-1, a tight junction protein, is disrupted in olmesartan medoxomil-treated Caco-2 cells.

conclusionsOlmesartan-associated enteropathy shares many features with coeliac disease, including symptoms and immunopathogenic pathways, such as increased numbers of CD8+ cells and corresponding overexpression of IL15 by epithelial cells. Taken together, the treatment of epithelial cells with olmesartan medoxomil induces a response by intestinal epithelial cells that is similar to the innate effects of gluten upon the epithelium of coeliac patients.

Indexed as

Abdominal PainBiopsyCaco-2 CellsCeliac DiseaseDiarrheaDuodenumFemaleHumansMaleNauseaOlmesartan MedoxomilT-Lymphocytes, RegulatoryVomitingOlmesartan Medoxomil

Identifiers

PMID26423313
PMCPMC4626300
OpenAlexW2111024402

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.