Poster Session II - A256  <i>IL1B</i> -RS1143634 ASSOCIATED TO NONRESPONSE TO INFLIXIMAB IN ULCERATIVE COLITIS TREATMENT

Abstract Background Molecular targeted therapies (MTT), such as anti-TNFs (infliximab, adalimumab and golimumab), are used to achieve remission in moderate to severe ulcerative colitis (UC) patients. We observe a high variability in treatment response to these therapies which is influenced by multiple factors such as genetics. Indeed, 102 variants are associated with response phenotype in inflammatory bowel disease (IBD) in the literature, but none has strong enough evidence to be used to predict response. Aims Therefore, the aim of this study is to perform a genetic association study of these candidate pharmacogenetic variants. Methods A cohort of 101 people using MTT for UC in Saguenay–Lac-St-Jean was recruited. The treatment response was evaluated retrospectively and patient’s whole genome was genotyped. The variants list obtained by literature review was validated by a burden test comparing responders and non-responders. Once the list was validated, the association of the variants was evaluated in the recruited cohort. Results from the significantly associated variants were compared with other IBD studies in literature. Results The variants list was validated only for the infliximab group (n = 40, p = 0.029) and not for the anti-TNF combined group (n = 67, p = 0.770). For the infliximab group, the variant IL1B-rs1143634 was associated with nonresponse (p = 0.01). Additionally, a literature review revealed two other studies had verified the associated variant in IBD and the association was maintained after the combination of these three studies (OR = 1.97 [1.29-3.01], p = 0.002). Conclusions The association of IL1B-rs1143634 increases its interest to better understand nonresponse to infliximab. Further replication and functional studies are necessary for this variant to become a potential clinical marker. Funding Agencies CCC, CIHRFRQS, Fondation de ma vie, Faculté de médecine et des sciences de la santé de Université de Sherbrooke

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Journal
Journal of the Canadian Association of Gastroenterology
Published
2026-02-01
DOI
https://doi.org/10.1093/jcag/gwaf042.255
Primary Topic
Inflammatory Bowel Disease
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article
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article

Poster Session II - A256  IL1B -RS1143634 ASSOCIATED TO NONRESPONSE TO INFLIXIMAB IN ULCERATIVE COLITIS TREATMENT

Karine Tremblay, Alexandre Lavoie, A Michaud-Herbst, L Tessier et al.
Journal of the Canadian Association of Gastroenterology
Inflammatory Bowel Disease
article

Poster Session II - A256  IL1B -RS1143634 ASSOCIATED TO NONRESPONSE TO INFLIXIMAB IN ULCERATIVE COLITIS TREATMENT

Karine Tremblay, Alexandre Lavoie, A Michaud-Herbst, L Tessier, J D Rioux
article en

Abstract

Abstract Background Molecular targeted therapies (MTT), such as anti-TNFs (infliximab, adalimumab and golimumab), are used to achieve remission in moderate to severe ulcerative colitis (UC) patients. We observe a high variability in treatment response to these therapies which is influenced by multiple factors such as genetics. Indeed, 102 variants are associated with response phenotype in inflammatory bowel disease (IBD) in the literature, but none has strong enough evidence to be used to predict response. Aims Therefore, the aim of this study is to perform a genetic association study of these candidate pharmacogenetic variants. Methods A cohort of 101 people using MTT for UC in Saguenay–Lac-St-Jean was recruited. The treatment response was evaluated retrospectively and patient’s whole genome was genotyped. The variants list obtained by literature review was validated by a burden test comparing responders and non-responders. Once the list was validated, the association of the variants was evaluated in the recruited cohort. Results from the significantly associated variants were compared with other IBD studies in literature. Results The variants list was validated only for the infliximab group (n = 40, p = 0.029) and not for the anti-TNF combined group (n = 67, p = 0.770). For the infliximab group, the variant IL1B-rs1143634 was associated with nonresponse (p = 0.01). Additionally, a literature review revealed two other studies had verified the associated variant in IBD and the association was maintained after the combination of these three studies (OR = 1.97 [1.29-3.01], p = 0.002). Conclusions The association of IL1B-rs1143634 increases its interest to better understand nonresponse to infliximab. Further replication and functional studies are necessary for this variant to become a potential clinical marker. Funding Agencies CCC, CIHRFRQS, Fondation de ma vie, Faculté de médecine et des sciences de la santé de Université de Sherbrooke

Journal of the Canadian Association of GastroenterologyVol. 9(Supplement_1)
Université de Sherbrooke (CA), Montreal Heart Institute (CA), Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean (CA), Université de Montréal (CA)
Good health and well-being
Openalex Percentile: Top 55%
Inflammatory Bowel Disease
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