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No association between C-reactive protein gene polymorphisms and decrease of C-reactive protein serum concentration
Stéphanie Willot1, Severine Vermeire, Marc Ohresser
1François-Rabelais University, Immuno-Pharmaco-Genetics of Therapeutic Antibodies Research Group (UPRES EA 3853), Tours, France.
Genetic variations in the C-reactive protein (CRP) gene do not influence infliximab treatment response in Crohn's disease patients. This study found no linkage disequilibrium between CRP and FCGR3A genes, and CRP polymorphisms did not affect treatment outcomes.
Area of Science:
- Genetics
- Immunology
- Gastroenterology
Background:
- Previous research indicated an association between FCGR3A V/F polymorphism and infliximab response in Crohn's disease.
- The C-reactive protein (CRP) and FCGR3A genes are located on the same chromosomal locus (1q23).
Purpose of the Study:
- To investigate potential linkage disequilibrium (LD) between CRP and FCGR3A genes.
- To determine if CRP gene polymorphisms are associated with infliximab treatment response in Crohn's disease patients, specifically focusing on CRP level reduction.
Main Methods:
- Genotyping of FCGR3A (V/F) and three CRP polymorphisms (-717G/A, 1444C/T, CRP 4A/G) in 206 healthy donors and 189 Crohn's disease patients.
- Assessment of clinical and biological (CRP decrease) response to infliximab treatment.
- Statistical analysis to evaluate LD and associations between CRP genotypes and treatment response.
Main Results:
- No evidence of linkage disequilibrium (LD) was found between CRP and FCGR3A genes in either healthy donors or Crohn's disease patients.
- CRP polymorphisms did not significantly impact the decrease in CRP levels following infliximab treatment.
- No statistically significant differences in clinical or biological response rates were observed among different CRP genotypes.
Conclusions:
- CRP gene polymorphisms are not associated with infliximab treatment response in Crohn's disease.
- The findings exclude a role for CRP polymorphisms in predicting or influencing the efficacy of infliximab therapy in this patient cohort.
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