Evidence map›Paper›PMID 33950224›Full record

ReviewRheumatology (Oxford, England)2021

JAK1 selective inhibitors for the treatment of spondyloarthropathies.

Jonathan P E White, Laura C Coates

Open access · hybridAbstract readReview
In one paragraph

Review in Rheumatology (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. Review
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

2 authors at 1 institution in 1 country.

Jonathan P E WhiteRheumatology SHO, Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Trust.
Laura C CoatesNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science, University of Oxford, Oxford, UK.ORCID 0000-0002-4756-663X
Nuffield Orthopaedic Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As our understanding of the pathogenesis of SpA improves, focus has turned to the role janus kinase (JAK)-mediated signal transduction and inhibiting its actions as a therapeutic mechanism. Small molecule inhibitors of JAK exist, with variable selectivity for the different JAK isoforms. Less selective JAK inhibitors have variable efficacy and safety profiles, prompting the investigation of selective JAK1 inhibition. In this review, we summarize the current phase 2 and 3 clinical trial data, evaluating the use of JAK1 selective inhibitors in the treatment of SpA, particularly AS and PsA. Selective JAK1 inhibition offers a promising therapeutic approach, however further longer-term trials are needed to fully establish their efficacy and safety at higher doses, and their use in the greater continuum of SpA.

Indexed as

Arthritis, PsoriaticClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicHeterocyclic Compounds, 3-RingHumansJanus Kinase 1Janus Kinase InhibitorsPyridinesSpondylarthropathiesSpondylitis, AnkylosingTriazolesGLPG0634Heterocyclic Compounds, 3-RingJanus Kinase 1Janus Kinase InhibitorsPyridinesTriazolesupadacitinibankylosing spondylitisaxial spondyloarthritismanagementpsoriatic arthritisselective janus kinase inhibitorsspondyloarthropathiestreatment

Identifiers

PMID33950224
PMCPMC8098108
OpenAlexW3096255598

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.