Evidence map›Paper›PMID 29618084›Full record

ReviewRheumatology (Oxford, England)2019

The rationale for Janus kinase inhibitors for the treatment of spondyloarthritis.

Douglas J Veale, Dennis McGonagle, Iain B McInnes, James G Krueger, Christopher T Ritchlin, Dirk Elewaut, Keith S Kanik, Thijs Hendrikx, Gabriel Berstein, Jennifer Hodge and 1 more

Registry-linked trialOpen access · hybridAbstract readReview
In one paragraph

Review in Rheumatology (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06114407 (Baricitinib in the Treatment of Refractory Axial Spondyloarthritis Patients), which is not on this map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
8.9field-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.

NCT06114407 phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

Baricitinib in the Treatment of Refractory Axial Spondyloarthritis Patients: A Comparison With Tofacitinib

TypeinterventionalSponsorBangabandhu Sheikh Mujib Medical University, Dhaka, BangladeshRan2023 to 2024Enrolled184ConditionsSpondyloarthritis, AxialArmsBaricitinib 2mg, Tofacitinib 5 mg
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  6. Trial
  7. Article
  8. Population pharmacokinetics of tofacitinib in patients with active ankylosing spondylitis.International journal of clinical pharmacology and therapeutics · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
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  16. Article
  17. Article
  18. Osteoimmunology of Spondyloarthritis.International journal of molecular sciences · 2023
    Review
  19. 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

11 authors at 7 institutions in 4 countries.

Douglas J VealeThe Centre for Arthritis and Rheumatic Diseases, St Vincent's University Hospital, Dublin, Ireland.
Dennis McGonagleLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, UK.
Iain B McInnesInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
James G KruegerLaboratory of Investigative Dermatology, The Rockefeller University, New York, USA.
Christopher T RitchlinAllergy, Immunology & Rheumatology Division, University of Rochester Medical Center, Rochester, NY, USA.
Dirk ElewautUnit for Molecular Immunology and Inflammation, VIB Inflammation Research Center, Ghent University and Department of Rheumatology, Ghent University Hospital, Ghent, Belgium.
Keith S KanikPfizer Inc, Groton, CT, USA.
Thijs HendrikxPfizer Inc, Collegeville, PA, USA.
Gabriel BersteinPfizer Inc, Cambridge, MA, USA.
Jennifer HodgePfizer Inc, New York, NY, USA.
Jean-Baptiste TelliezPfizer Inc, Cambridge, MA, USA.
Pfizer (United States) · USChapel Allerton Hospital · GBRockefeller University · USUniversity College Dublin · IEUniversity of Glasgow · GBUniversity of Rochester Medical Center · USVIB-UGent Center for Inflammation Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pathogenesis of SpA is multifactorial and involves a range of immune cell types and cytokines, many of which utilize Janus kinase (JAK) pathways for signaling. In this review, we summarize the animal and pre-clinical data that have demonstrated the effects of JAK blockade on the underlying molecular mechanisms of SpA and provide a rationale for JAK inhibition for the treatment of SpA. We also review the available clinical trial data evaluating JAK inhibitors tofacitinib, baricitinib, peficitinib, filgotinib and upadacitinib in PsA, AS and related inflammatory diseases, which have demonstrated the efficacy of these agents across a range of SpA-associated disease manifestations. The available clinical trial data, supported by pre-clinical animal model studies demonstrate that JAK inhibition is a promising therapeutic strategy for the treatment of SpA and may offer the potential for improvements in multiple articular and extra-articular disease manifestations of PsA and AS.

Indexed as

Antirheumatic AgentsArthritis, PsoriaticCytokinesHumansJanus Kinase InhibitorsJanus KinasesSignal TransductionSpondylarthritisSTAT Transcription FactorsAntirheumatic AgentsCytokinesJanus Kinase InhibitorsJanus KinasesSTAT Transcription Factors

Identifiers

PMID29618084
PMCPMC6343466
OpenAlexW2796283304

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.