Evidence map›Paper›PMID 31043678›Full record

ArticleThe pharmacogenomics journal2019

Genetic association between CD96 locus and immunogenicity to anti-TNF therapy in Crohn's disease.

Adrià Aterido, Núria Palau, Eugeni Domènech, Pilar Nos Mateu, Ana Gutiérrez, Fernando Gomollón, Juan L Mendoza, Esther Garcia-Planella, Manuel Barreiro-de Acosta, Fernando Muñoz and 15 more

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In one paragraph

Article in The pharmacogenomics journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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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

25 authors at 16 institutions in 1 country.

Adrià Aterido *Rheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.
Núria Palau *Rheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.
Eugeni DomènechGastroenterology and Hepatology Department, Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
Pilar Nos MateuCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
Ana GutiérrezCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
Fernando GomollónCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
Juan L MendozaGastroenterology Service, Hospital Clínico San Carlos, Madrid, Spain.
Esther Garcia-PlanellaGastroenterology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Manuel Barreiro-de AcostaGastroenterology Service, Hospital Clínico Universitario, Santiago de Compostela, Spain.
Fernando MuñozGastroenterology Service, Complejo Hospitalario de León, León, Spain.
Maribel VeraGastroenterology Service, Hospital Universitario Puerta de Hierro, Madrid, Spain.
Cristina SaroInternal Medicine Service, Hospital de Cabueñes, Gijón, Spain.
Maria EsteveCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
Montserrat AndreuGastroenterology Department, Institut Hospital del Mar d'Investigacions Mèdiques, Institute of Research Hospital del Mar, Parc de Salut Mar, Pompeu Fabra University, Barcelona, Spain.
María ChaparroCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
Julián PanésCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain.
Valle García-SánchezDigestive System Service, Universidad de Córdoba/Instituto Maimónides de Investigación Biomédica de Córdoba/Hospital Universitario Reina Sofía, Córdoba, Spain.
María López-LasantaRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.
Andrea PlumaRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.
Laia CodóLife Sciences Department, Barcelona Supercomputing Centre, Barcelona, Spain.
Andrés García-MonteroBanco Nacional de ADN Carlos III, University of Salamanca, Salamanca, Spain.
Josep ManyéGastroenterology and Hepatology Department, Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
Javier P GisbertCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain. javier.p.gisbert@gmail.com.
Sara MarsalRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, Spain. sara.marsal@vhir.org.
Antonio JuliàRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.ORCID http://orcid.org/0000-0001-6064-3620
Vall d'Hebron Institut de Recerca · ESCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESHospital Universitario de La Princesa · ESUniversitat Pompeu Fabra · ESBarcelona Supercomputing Center · ESComplejo Hospitalario Universitario de Santiago · ESHospital Clínic de Barcelona · ESHospital Clínico San Carlos · ESHospital de León · ESHospital de Sant Pau · ESHospital Universitari Germans Trias i Pujol · ESHospital Universitario De Cabueñes · ESHospital Universitario Puerta de Hierro Majadahonda · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESMútua Terrassa · ESUniversidad de Salamanca · ES

Funding

FAMILY DEMOGRAPHY OF AGINGK01AG000587 · NIA · DUKE UNIVERSITY · PI PARNELL, ALLAN M · 1993 to 1995
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6 · The paper itself

Abstract

The production of antibodies to anti-tumor necrosis factor alpha (TNF) agents is one of the main causes of treatment failure in Crohn's disease (CD). To date, however, the contribution of genetics to anti-TNF immunogenicity in CD is still unknown. The objective of the present study was to identify genetic variation associated with anti-TNF immunogenicity in CD. We performed a two-stage genome-wide association study in a cohort of 96 and 123 adalimumab-treated patients, respectively. In the discovery stage, we identified a genome-wide significant association between the CD96 locus and the production of antibodies to anti-TNF treatment (P = 1.88e-09). This association was validated in the replication stage (P < 0.05). The risk allele for anti-TNF immunogenicity was found to be also associated with a lack of response to anti-TNF therapy (P = 0.019). These findings represent an important step toward the understanding of the immunogenicity-based mechanisms that underlie anti-TNF response in CD.

Indexed as

AdalimumabAged, 80 and overAntibodies, MonoclonalAntigens, CDAnti-Inflammatory AgentsCrohn DiseaseFemaleGenetic VariationGenome-Wide Association StudyHumansMaleMiddle AgedTumor Necrosis Factor-alphaAdalimumabAntibodies, MonoclonalAntigens, CDAnti-Inflammatory AgentsCD96 antigenTumor Necrosis Factor-alpha

Identifiers

PMID31043678
OpenAlexW2942970137

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.