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GWAS Study

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

Aterido A, Palau N, Domènech E et al.

31043678 PubMed ID
GWAS Study Type
150 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AA
Aterido A
PN
Palau N
DE
Domènech E
NM
Nos Mateu P
GA
Gutiérrez A
GF
Gomollón F
MJ
Mendoza JL
GE
Garcia-Planella E
BA
Barreiro-de Acosta M
MF
Muñoz F
VM
Vera M
SC
Saro C
EM
Esteve M
AM
Andreu M
CM
Chaparro M
PJ
Panés J
GV
García-Sánchez V
LM
López-Lasanta M
PA
Pluma A
CL
Codó L
GA
García-Montero A
MJ
Manyé J
GJ
Gisbert JP
MS
Marsal S
JA
Julià A
Chapter II

Abstract

Summary of the research findings

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.

9 European ancestry cases, 53 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

150
Total Participants
GWAS
Study Type
Yes
Replicated
3 European ancestry cases, 85 European ancestry controls
Replication Participants
European
Ancestry
Spain
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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