Evidence map›Paper›PMID 28981629›Full record

ArticleJournal of Crohn's & colitis2017

Usefulness of Transcriptional Blood Biomarkers as a Non-invasive Surrogate Marker of Mucosal Healing and Endoscopic Response in Ulcerative Colitis.

Núria Planell, M Carme Masamunt, Raquel Franco Leal, Lorena Rodríguez, Miriam Esteller, Juan J Lozano, Anna Ramírez, Maria de Lourdes Setsuko Ayrizono, Claudio Saddy Rodrigues Coy, Ignacio Alfaro and 6 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03885713 (Identification of Predictive Biomarkers for Response to Biologic Therapies and Tofacitinib in Inflammatory Bowel Disease by Proteomic and Mass Cytometry Approaches), which is not on this map. Cited by 50 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 4 pooled it
5.9field-weighted citation impact, top 4% 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.

NCT03885713 phase4completednot on this mapstarted 2019, after this paper: background citation

Identification of Predictive Biomarkers for Response to Biologic Therapies and Tofacitinib in Inflammatory Bowel Disease by Proteomic and Mass Cytometry Approaches

TypeinterventionalSponsorFundación de Investigación Biomédica - Hospital Universitario de La PrincesaRan2019 to 2024Enrolled180ConditionsInflammatory Bowel Diseases, Crohn Disease, Ulcerative ColitisArmsInfliximab or adalimumab or golimumab or vedolizumab or ustekinumab or tofacitinib
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 4 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. A Treat-to-Target Update in Ulcerative Colitis: A Systematic Review.The American journal of gastroenterology · 2019
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  20. Gene Expression Dysregulation in Whole Blood of Patients withInternational journal of molecular sciences · 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

16 authors at 7 institutions in 3 countries.

Núria PlanellDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
M Carme MasamuntDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Raquel Franco LealDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Lorena RodríguezDepartment of Gastroenterology, Hospital Universitari de Bellvitge-Institut d'Investigació Biomèdica de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.
Miriam EstellerDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Juan J LozanoBioinformatics Platform, CIBER-EHD, Barcelona, Spain.
Anna RamírezDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Maria de Lourdes Setsuko AyrizonoIBD Research Laboratory, Surgery Department, University of Campinas, Sao Paulo, Brazil.
Claudio Saddy Rodrigues CoyIBD Research Laboratory, Surgery Department, University of Campinas, Sao Paulo, Brazil.
Ignacio AlfaroDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Ingrid OrdásDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Sudha VisvanathanBoehringer-Ingelheim Pharmaceuticals, Ridgefield, CT, USA.
Elena RicartDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Jordi GuardiolaDepartment of Gastroenterology, Hospital Universitari de Bellvitge-Institut d'Investigació Biomèdica de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.
Julián PanésDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Azucena SalasDepartment of Gastroenterology, IDIBAPS, Hospital Clínic, CIBER-EHD, Barcelona, Spain.
Centro de Investigación Biomédica en Red · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital Clínic de Barcelona · ESUniversidade Estadual de Campinas (UNICAMP) · BRBellvitge University Hospital · ESBoehringer Ingelheim (United States) · USInstitut d'Investigació Biomédica de Bellvitge · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsUlcerative colitis [UC] is a chronic inflammatory disease of the colon. Colonoscopy remains the gold standard for evaluating disease activity, as clinical symptoms are not sufficiently accurate. The aim of this study is to identify new accurate non-invasive biomarkers based on whole-blood transcriptomics that can predict mucosal lesions and response to treatment in UC patients.

methodsWhole-blood samples were collected for a total of 152 UC patients at endoscopy. Blood RNA from 25 UC individuals and 20 controls was analysed using microarrays. Genes that correlated with endoscopic activity were validated using real-time polymerase chain reaction in an independent group of 111 UC patients, and a prediction model for mucosal lesions was evaluated. Responsiveness to treatment was assessed in a longitudinal cohort of 16 UC patients who started anti-tumour necrosis factor [TNF] therapy and were followed up for 14 weeks.

resultsMicroarray analysis identified 122 genes significantly altered in the blood of endoscopically active UC patients. A significant correlation with the degree of endoscopic activity was observed in several genes, including HP, CD177, GPR84, and S100A12. Using HP as a predictor of endoscopic disease activity, an accuracy of 67.3% was observed, compared with 52.4%, 45.2%, and 30.3% for C-reactive protein, erythrocyte sedimentation rate, and platelet count, respectively. Finally, at 14 weeks of treatment, response to anti-TNF therapy induced alterations in blood HP, CD177, GPR84, and S100A12 transcripts that correlated with changes in endoscopic activity.

conclusionsTranscriptional changes in UC patients are sensitive to endoscopic improvement and appear to be an effective tool to monitor patients over time.

Indexed as

AdultBiomarkersColitis, UlcerativeColonColonoscopyFemaleHumansIntestinal MucosaMaleMiddle AgedOligonucleotide Array Sequence AnalysisReal-Time Polymerase Chain ReactionTreatment OutcomeBiomarkersanti-TNF-αblood biomarkersGene expressionulcerative colitis

Identifiers

PMID28981629
PMCPMC5881703
OpenAlexW2587201313

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.