Evidence map›Paper›PMID 32203403›Full record

ReviewNature reviews. Gastroenterology & hepatology2020

JAK-STAT pathway targeting for the treatment of inflammatory bowel disease.

Azucena Salas, Cristian Hernandez-Rocha, Marjolijn Duijvestein, William Faubion, Dermot McGovern, Severine Vermeire, Stefania Vetrano, Niels Vande Casteele

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Gastroenterology & hepatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04576000 (PhaRmacOkinetics and PHarmacodynamic BiomarkErs of Janus Kinase Inhibitor Therapy in PatIents With Ulcerative Colitis), which is not on this map. Cited by 342 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
342citing papers in PubMed, 4 pooled it
27.5field-weighted citation impact, top 1% 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.

NCT04576000 terminatednot on this map

PhaRmacOkinetics and PHarmacodynamic BiomarkErs of Janus Kinase Inhibitor Therapy in PatIents With Ulcerative Colitis (PROPHETIC)

TypeobservationalSponsorAlimentiv Inc.Ran2020 to 2021Enrolled3ConditionsUlcerative ColitisArmsJanus Kinase Inhibitor
3 · Its place in the literature

Who cites it

342 citing papers in PubMed, 4 syntheses or guidelines pooled it, 608 citations in OpenAlex.

  1. Pooled it
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  12. Identification of Pyrrolo [2,3-Molecules (Basel, Switzerland) · 2026
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  19. A deeper quiet: Tofacitinib and the potential of endo-histologic remission.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2026
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282 more citing papers are in PubMed but not listed here.

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

8 authors at 8 institutions in 6 countries.

Azucena SalasDepartment of Gastroenterology, IDIBAPS, Barcelona, Spain.ORCID http://orcid.org/0000-0003-4572-2907
Cristian Hernandez-RochaZane Cohen Center for Digestive Diseases, Mount Sinai Hospital Inflammatory Bowel Disease Group, Toronto, Ontario, Canada.
Marjolijn DuijvesteinGastroenterology and Hepatology, Amsterdam Gastroenterology and Metabolism, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.ORCID http://orcid.org/0000-0003-4814-9376
William FaubionGastroenterology and Hepatology, Mayo Clinic, Rochester, MI, USA.
Dermot McGovernF. Widjaja Foundation Inflammatory Bowel and Immunobiology Research Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Severine VermeireDepartment of Gastroenterology, University Hospitals Leuven, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0001-9942-3019
Stefania VetranoDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Niels Vande CasteeleRobarts Clinical Trials, London, ON, Canada. nvandecasteele@health.ucsd.edu.ORCID http://orcid.org/0000-0003-0854-0274
Amsterdam University Medical Centers · NLCedars-Sinai Medical Center · USCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESHumanitas University · ITKU Leuven · BEMayo Clinic in Arizona · USMount Sinai Hospital · CAUC San Diego Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokines are involved in intestinal homeostasis and pathological processes associated with inflammatory bowel disease (IBD). The biological effects of cytokines, including several involved in the pathology of Crohn's disease and ulcerative colitis, occur as a result of receptor-mediated signalling through the Janus kinase (JAK) and signal transducer and activator of transcription (STAT) DNA-binding families of proteins. Although therapies targeting cytokines have revolutionized IBD therapy, they have historically targeted individual cytokines, and an unmet medical need exists for patients who do not respond to or lose response to these treatments. Several small-molecule inhibitors of JAKs that have the potential to affect multiple pro-inflammatory cytokine-dependent pathways are in clinical development for the treatment of IBD, with one agent, tofacitinib, already approved for ulcerative colitis and several other agents with demonstrated efficacy in early phase trials. This Review describes the current understanding of JAK-STAT signalling in intestinal homeostasis and disease and the rationale for targeting this pathway as a treatment for IBD. The available evidence for the efficacy, safety and pharmacokinetics of JAK inhibitors in IBD as well as the potential approaches to optimize treatment with these agents, such as localized delivery or combination therapy, are also discussed.

Indexed as

Colitis, UlcerativeCrohn DiseaseCytokinesHumansInflammatory Bowel DiseasesIntestinesJanus Kinase InhibitorsJanus KinasesSignal TransductionSTAT Transcription FactorsCytokinesJanus Kinase InhibitorsJanus KinasesSTAT Transcription Factors

Identifiers

PMID32203403
OpenAlexW3012377065

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.