Evidence map›Paper›PMID 35003109›Full record

SynthesisFrontiers in immunology2021

Endocannabinoid System as a Promising Therapeutic Target in Inflammatory Bowel Disease - A Systematic Review.

Szymon Hryhorowicz, Marta Kaczmarek-Ryś, Aleksandra Zielińska, Rodney J Scott, Ryszard Słomski, Andrzej Pławski

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

38 citing papers in PubMed, 70 citations in OpenAlex.

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  18. A human gutScience (New York, N.Y.) · 2024
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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

6 authors at 3 institutions in 2 countries.

Szymon HryhorowiczInstitute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.
Marta Kaczmarek-RyśInstitute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.
Aleksandra ZielińskaInstitute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.
Rodney J ScottDiscipline of Medical Genetics and Centre for Information-Based Medicine, The University of Newcastle and Hunter Medical Research Institute, Newcastle, NSW, Australia.
Ryszard SłomskiInstitute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.
Andrzej PławskiInstitute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.
Institute of Human Genetics · PLNew South Wales Department of Health · AUPolish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a general term used to describe a group of chronic inflammatory conditions of the gastrointestinal tract of unknown etiology, including two primary forms: Crohn's disease (CD) and ulcerative colitis (UC). The endocannabinoid system (ECS) plays an important role in modulating many physiological processes including intestinal homeostasis, modulation of gastrointestinal motility, visceral sensation, or immunomodulation of inflammation in IBD. It consists of cannabinoid receptors (CB1 and CB2), transporters for cellular uptake of endocannabinoid ligands, endogenous bioactive lipids (Anandamide and 2-arachidonoylglycerol), and the enzymes responsible for their synthesis and degradation (fatty acid amide hydrolase and monoacylglycerol lipase), the manipulation of which through agonists and antagonists of the system, shows a potential therapeutic role for ECS in inflammatory bowel disease. This review summarizes the role of ECS components on intestinal inflammation, suggesting the advantages of cannabinoid-based therapies in inflammatory bowel disease.

Indexed as

AnimalsAnti-Inflammatory AgentsCannabinoid Receptor AgonistsCannabinoid Receptor AntagonistsColitis, UlcerativeCrohn DiseaseDisease Models, AnimalDrug Evaluation, PreclinicalEndocannabinoidsGastrointestinal MotilityHumansIntestinal MucosaRandomized Controlled Trials as TopicReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Signal TransductionAnti-Inflammatory AgentsCannabinoid Receptor AgonistsCannabinoid Receptor AntagonistsEndocannabinoidsReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2cannabinoid receptorcannabisCrohn's diseaseinflammatory bowel diseasethe endocannabinoid systemulcerative colitis

Identifiers

PMID35003109
PMCPMC8727741
OpenAlexW4200150594

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.