Association of the TNFRSF1B-rs1061622 variant with nonresponse to infliximab in ulcerative colitis

For severe forms of ulcerative colitis (UC), a chronic inflammatory bowel disease (IBD), biological therapies, including tumor necrosis factor inhibitors (anti-TNF), are often used. However, these drugs have a high variability in treatment response. Multiple factors, such as genetic variants, can affect this variability. The goal of the study was to verify if selected candidate variants could affect response to anti-TNF in UC treatment. This association study included 76 participants suffering from UC and past or current users of anti-TNF. Clinical data for phenotyping was collected through a single visit with the participant and a medical chart review. Blood or saliva samples were collected to extract DNA and to genotype eight selected candidate variants in genes TNF, TNFAIP3, TNFRSF1 A and TNFRSF1B. For anti-TNF users, 30% of individuals were non-responders, 70% suffered from AE and none of the studied variants was associated with the response's phenotype. However, for infliximab users only (n = 44), the TNFRSF1B-rs1061622 variant was associated with nonresponse to infliximab for the first time in a cohort of UC patients (p-value = 0.028). Next steps are to replicate this association in independent cohorts and to perform functional studies to gain more evidence on the variant.

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Publication Details

Journal
Scientific Reports
Published
2025-05-25
DOI
https://doi.org/10.1038/s41598-025-02463-4
Citations
1
Primary Topic
Inflammatory Bowel Disease
Type
article
Field-Weighted Citation Impact
1.82

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article

Association of the TNFRSF1B-rs1061622 variant with nonresponse to infliximab in ulcerative colitis

Karine Tremblay, Catherine Allard, Laurence Tessier, Alexandre Lavoie et al.
1 citations
Scientific Reports
Inflammatory Bowel Disease
1.82
article

Association of the TNFRSF1B-rs1061622 variant with nonresponse to infliximab in ulcerative colitis

Karine Tremblay, Catherine Allard, Laurence Tessier, Alexandre Lavoie, Mathilde Côté, Ann-Lorie Gagnon, Mathieu Durand, A Michaud-Herbst, Danny Bergeron, Sophie St-Amour
article en
1 citations

Abstract

For severe forms of ulcerative colitis (UC), a chronic inflammatory bowel disease (IBD), biological therapies, including tumor necrosis factor inhibitors (anti-TNF), are often used. However, these drugs have a high variability in treatment response. Multiple factors, such as genetic variants, can affect this variability. The goal of the study was to verify if selected candidate variants could affect response to anti-TNF in UC treatment. This association study included 76 participants suffering from UC and past or current users of anti-TNF. Clinical data for phenotyping was collected through a single visit with the participant and a medical chart review. Blood or saliva samples were collected to extract DNA and to genotype eight selected candidate variants in genes TNF, TNFAIP3, TNFRSF1 A and TNFRSF1B. For anti-TNF users, 30% of individuals were non-responders, 70% suffered from AE and none of the studied variants was associated with the response's phenotype. However, for infliximab users only (n = 44), the TNFRSF1B-rs1061622 variant was associated with nonresponse to infliximab for the first time in a cohort of UC patients (p-value = 0.028). Next steps are to replicate this association in independent cohorts and to perform functional studies to gain more evidence on the variant.

Scientific ReportsVol. 15(1)
Université de Sherbrooke (CA), Centre Hospitalier Universitaire de Sherbrooke (CA)
Université de Sherbrooke, Canadian Institutes of Health Research, Fonds de Recherche du Québec - Santé
Good health and well-being
Openalex Percentile: Top 16%
Inflammatory Bowel Disease
1.82
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