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Published on: September 12, 2019
Gene Signatures of Early Response to Anti-TNF Drugs in Pediatric Inflammatory Bowel Disease
Sara Salvador-Martín1, Irene Raposo-Gutiérrez1, Víctor Manuel Navas-López2
1Pharmacy Department, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.
Insights
SMAD7 gene expression can predict early response to anti-TNF therapy in pediatric inflammatory bowel disease (IBD) patients. This finding may help personalize treatment for young IBD patients receiving anti-tumor necrosis factor (anti-TNF) drugs.
Area of Science:
- Pediatric Gastroenterology
- Pharmacogenomics
- Inflammatory Bowel Disease Research
Background:
- Pediatric inflammatory bowel disease (IBD) affects 20-30% of patients, often requiring anti-tumor necrosis factor (anti-TNF) therapies.
- While effective, up to 30% of IBD patients exhibit primary non-response to anti-TNF agents, necessitating predictive biomarkers.
Purpose of the Study:
- To identify predictive biomarkers for early response to anti-TNF therapy in pediatric IBD patients.
- To analyze gene expression profiles associated with treatment response in young IBD patients.
Main Methods:
- Analyzed gene expression of 43 pediatric IBD patients (<18 years) starting infliximab or adalimumab.
- Utilized qPCR to assess gene expression in whole-blood samples pre-treatment and at 2 weeks.
- Defined response as >15-point decrease in disease activity index at 10 weeks (infliximab) or 26 weeks (adalimumab).
Main Results:
- Decreased SMAD7 gene expression before and after 2 weeks of anti-TNF treatment was significantly associated with non-response (p < 0.05).
- DEFA5 expression decreased in responders but not non-responders during the initial 2 weeks of anti-TNF therapy.
- TLR2 expression changes were observed but did not reach statistical significance.
Conclusions:
- SMAD7 gene expression serves as a pharmacogenomic biomarker for predicting early response to anti-TNF agents in pediatric IBD.
- TLR2 and DEFA5 warrant further validation in larger cohorts to confirm their utility as predictive markers.
Abstract:
Around a 20-30% of inflammatory bowel disease (IBD) patients are diagnosed before they are 18 years old. Anti-TNF drugs can induce and maintain remission in IBD, however, up to 30% of patients do not respond. The aim of the work was to identify markers that would predict an early response to anti-TNF drugs in pediatric patients with IBD. The study population included 43 patients aged <18 years with IBD who started treatment with infliximab or adalimumab. Patients were classified into primary responders (n = 27) and non-responders to anti-TNF therapy (n = 6). Response to treatment could not be analyzed in 10 patients. Response was defined as a decrease in over 15 points in the disease activity indexes from week 0 to week 10 of infliximab treatment or from week 0 to week 26 of adalimumab treatment. The expression profiles of nine genes in total RNA isolated from the whole-blood of pediatric IBD patients taken before biologic administration and after 2 weeks were analyzed using qPCR and the 2-∆∆Ct method. Before initiation and after 2 weeks of treatment the expression of SMAD7 was decreased in patients who were considered as non-responders (p value < 0.05). Changes in expression were also observed for TLR2 at T0 and T2, although that did not reach the level of statistical significance. In addition, the expression of DEFA5 decreased 1.75-fold during the first 2 weeks of anti-TNF treatment in responders, whereas no changes were observed in non-responders. Expression of the SMAD7 gene is a pharmacogenomic biomarker of early response to anti-TNF agents in pediatric IBD. TLR2 and DEFA5 need to be validated in larger studies.
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