Evidence map›Paper›PMID 24386448›Full record

Trial reportPloS one2013

Endocannabinoid and cannabinoid-like fatty acid amide levels correlate with pain-related symptoms in patients with IBS-D and IBS-C: a pilot study.

Jakub Fichna, Jodianne T Wood, Malvina Papanastasiou, Subramanian K Vadivel, Piotr Oprocha, Maciej Sałaga, Marta Sobczak, Anna Mokrowiecka, Adam I Cygankiewicz, Piotr K Zakrzewski and 5 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
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  5. Article
  6. Review
  7. The Endocannabinoid System and Physical Exercise.International journal of molecular sciences · 2023
    Review
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  19. Endocannabinoid-related compounds in gastrointestinal diseases.Journal of cellular and molecular medicine · 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

15 authors at 6 institutions in 4 countries.

Jakub FichnaSnyder Institute for Chronic Diseases, University of Calgary, Calgary, Alberta, Canada ; Department of Medicine, Division of Gastroenterology, University of Calgary, Calgary, Alberta, Canada ; Department of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Jodianne T WoodCenter for Drug Discovery, Northeastern University, Boston, Massachusetts, United States of America.
Malvina PapanastasiouCenter for Drug Discovery, Northeastern University, Boston, Massachusetts, United States of America.
Subramanian K VadivelCenter for Drug Discovery, Northeastern University, Boston, Massachusetts, United States of America.
Piotr OprochaFaculty of Applied Mathematics, AGH University of Science and Technology, Cracow, Poland.
Maciej SałagaDepartment of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Marta SobczakDepartment of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Anna MokrowieckaDepartment of Digestive Tract Diseases, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Adam I CygankiewiczDepartment of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Piotr K ZakrzewskiDepartment of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Ewa Małecka-PanasDepartment of Digestive Tract Diseases, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Wanda M KrajewskaDepartment of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Piotr KościelniakFaculty of Mathematics and Computer Science, Jagiellonian University, Cracow, Poland.
Alexandros MakriyannisCenter for Drug Discovery, Northeastern University, Boston, Massachusetts, United States of America.
Martin A StorrSnyder Institute for Chronic Diseases, University of Calgary, Calgary, Alberta, Canada ; Department of Medicine, Division of Gastroenterology, University of Calgary, Calgary, Alberta, Canada ; Department of Medicine, Division of Gastroenterology, Ludwig Maximilians University of Munich, Munich, Germany.
Medical University of Lodz · PLNortheastern University · USUniversity of Łódź · PLAGH University of Krakow · PLJagiellonian University · PLUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsIrritable bowel syndrome (IBS) is a functional gastrointestinal (GI) disorder, associated with alterations of bowel function, abdominal pain and other symptoms related to the GI tract. Recently the endogenous cannabinoid system (ECS) was shown to be involved in the physiological and pathophysiological control of the GI function. The aim of this pilot study was to investigate whether IBS defining symptoms correlate with changes in endocannabinoids or cannabinoid like fatty acid levels in IBS patients.

methodsAEA, 2-AG, OEA and PEA plasma levels were determined in diarrhoea-predominant (IBS-D) and constipation-predominant (IBS-C) patients and were compared to healthy subjects, following the establishment of correlations between biolipid contents and disease symptoms. FAAH mRNA levels were evaluated in colonic biopsies from IBS-D and IBS-C patients and matched controls.

resultsPatients with IBS-D had higher levels of 2AG and lower levels of OEA and PEA. In contrast, patients with IBS-C had higher levels of OEA. Multivariate analysis found that lower PEA levels are associated with cramping abdominal pain. FAAH mRNA levels were lower in patients with IBS-C.

conclusionIBS subtypes and their symptoms show distinct alterations of endocannabinoid and endocannabinoid-like fatty acid levels. These changes may partially result from reduced FAAH expression. The here reported changes support the notion that the ECS is involved in the pathophysiology of IBS and the development of IBS symptoms.

Indexed as

AdultAmidesConstipationDiarrheaEndocannabinoidsFatty AcidsFemaleHumansIrritable Bowel SyndromeAmidesEndocannabinoidsFatty Acids

Identifiers

PMID24386448
PMCPMC3874007
OpenAlexW1978855692

What OpenQuestion holds

Textmetadata
LicenceCC0
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 OpenQuestion graph.