Evidence map›Paper›PMID 30833991›Full record

ArticleTherapeutic advances in musculoskeletal disease2019

IL-12/IL-23p40 identified as a downstream target of apremilast in

Tue W Kragstrup, Mary Adams, Søren Lomholt, Morten A Nielsen, Line D Heftdal, Peter Schafer, Bent Deleuran

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in musculoskeletal disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

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  11. Skin manifestations in spondyloarthritis.Therapeutic advances in musculoskeletal disease · 2020
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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

7 authors at 1 institution in 1 country.

Tue W KragstrupDepartment of Biomedicine, Wilhelm Meyers Allé 4, Aarhus University, DK-8000 Aarhus C, Denmark.ORCID https://orcid.org/0000-0002-6439-397X
Mary AdamsDepartment of Translational Development, Celgene Corporation, Summit, NJ, USA.
Søren LomholtDepartment of Biomedicine, Aarhus University, Denmark.
Morten A NielsenDepartment of Biomedicine, Aarhus University, Denmark.
Line D HeftdalDepartment of Biomedicine, Aarhus University, Denmark.
Peter SchaferDepartment of Translational Development, Celgene Corporation, Summit, NJ, USA.
Bent DeleuranDepartment of Biomedicine, Aarhus University, Denmark.
Aarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApremilast (Otezla

methodsSynovial fluid was obtained from patients with active rheumatoid arthritis (RA), PsA or peripheral spondyloarthritis (SpA;

resultsIn SFMCs cultured for 48 h, apremilast decreased the production of interleukin (IL)-12/IL-23p40 (the shared subunit of IL-12 and IL-23), colony-stimulating factor 1, CD6, and CD40 and increased the production of C-X-C motif chemokine 5 dose-dependently. Apremilast had a very different response signature compared with the tumor necrosis factor alpha inhibitor adalimumab with a substantially greater inhibition of IL-12/IL-23p40. In SFMCs cultured for 21 days, apremilast increased the secretion of IL-10. In FLS cultures, apremilast decreased matrix metalloproteinase-3 production. Apremilast decreased osteoclastogenesis but did not affect mineralization by human osteoblasts.

conclusionThis study reveals the downstream effects of apremilast in

Indexed as

apremilastcyclic adenosine monophosphatePALACEphosphodiesterase 4psoriatic arthritisrheumatoid arthritisspondyloarthritis

Identifiers

PMID30833991
PMCPMC6391542
OpenAlexW2917488494

What OpenQuestion holds

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Registered trials

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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.