Evidence map›Paper›PMID 34741617›Full record

ArticleInflammatory bowel diseases2022

Effects of JAK1-Preferential Inhibitor Filgotinib on Circulating Biomarkers and Whole Blood Genes/Pathways of Patients With Moderately to Severely Active Crohn's Disease.

Xavier Roblin, Adrian Serone, Oh Kyu Yoon, Luting Zhuo, Ethan Grant, Jacky Woo, Jinfeng Liu, René Galien, Geert D'Haens

Open access · hybridAbstract read
In one paragraph

Article in Inflammatory bowel diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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  7. IL-22, a vital cytokine in autoimmune diseases.Clinical and experimental immunology · 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

9 authors at 4 institutions in 3 countries.

Xavier RoblinGastroenterology Unit, University Hospital of Saint Etienne, Saint-Priest-en-Jarez, France.
Adrian SeroneGilead Sciences, Inc., Foster City, CA, USA.
Oh Kyu YoonGilead Sciences, Inc., Foster City, CA, USA.
Luting ZhuoGilead Sciences, Inc., Foster City, CA, USA.
Ethan GrantGilead Sciences, Inc., Foster City, CA, USA.
Jacky WooGilead Sciences, Inc., Foster City, CA, USA.
Jinfeng LiuGilead Sciences, Inc., Foster City, CA, USA.
René GalienGalapagos SASU, Romainville, France.
Geert D'HaensInflammatory Bowel Disease Centre, Academic Medical Centre, 1105 AZ Amsterdam, Netherlands.ORCID 0000-0003-2784-4046
Gilead Sciences (United States) · USAmsterdam UMC Location University of Amsterdam · NLGalapagos (France) · FRInstitute Cancer De La Loire Lucien Neuwirth · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPro-inflammatory cytokines are dysregulated in Crohn's disease (CD) and could serve as surrogate markers to improve diagnostic and therapeutic approaches, potentially addressing an unmet need. We profiled circulating biomarkers and whole blood transcriptional pathway activity to identify those associated with CD using data from the phase 2 FITZROY study with filgotinib, an oral preferential janus kinase-1 inhibitor.

methodsPatients with serum and whole blood samples taken from the induction period were included. Serum cytokines were measured (ELISA), whole blood RNA sequenced, and stool samples taken to measure fecal calprotectin (FC). Spearman's Rank correlations were assessed between biomarkers and baseline disease activity; post-treatment endoscopic improvement was measured by the Simplified Endoscopy Score for CD (SES-CD), FC and the Crohn's Disease Activity Index. Effect of filgotinib on circulating biomarkers was also evaluated.

resultsSerum biomarkers (n = 168) and whole blood RNA sequencing (n = 104) were assessed. Moderate correlation between serum analytes with SES-CD and FC was noted; most highly correlated were acute phase proteins CRP (rho = 0.35 [SES-CD] and 0.47 [FC]), serum amyloid A (rho = 0.40 and 0.39, respectively) and pro-inflammatory cytokines interleukin (IL)-6 (rho = 0.31 and 0.30, respectively), IL-22 (rho = 0.36 and 0.35, respectively), and oncostatin M (rho = 0.35 and 0.33, respectively). Filgotinib treatment was associated with reduction of many candidate biomarkers, particularly in patients with treatment response. Early changes in IL-6 and IL-10 may be prognostic for endoscopic response.

conclusionsSeveral circulating factors with potential as CD activity biomarkers were identified. Larger studies are necessary to investigate the best utility of these markers for CD.

Indexed as

Crohn DiseaseJanus Kinase InhibitorsBiomarkersC-Reactive ProteinCytokinesFecesHumansInterleukin-6Janus Kinase 1Leukocyte L1 Antigen ComplexPyridinesSeverity of Illness IndexTriazolesBiomarkersC-Reactive ProteinCytokinesGLPG0634Interleukin-6JAK1 protein, humanJanus Kinase 1Janus Kinase InhibitorsLeukocyte L1 Antigen ComplexPyridinesTriazolesbloodCrohn’s diseasefilgotinibIBDJAK1

Identifiers

PMID34741617
PMCPMC9340524
OpenAlexW3214461995

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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.