BMC Research Notes | |
Polymorphisms of the cytokine genes TGFB1 and IL10 in a mixed-race population with Crohn’s disease | |
André Castro Lyra1  Mauricio Cardeal1  Denise Carneiro Lemaire1  Maria Teresita Bendicho1  Tamara Celi Almeida1  Genoile Oliveira Santana3  Neogelia Pereira Almeida2  | |
[1] Federal University of Bahia, Salvador, Brazil;Alameda dos Jasmins, n-220, Apt-1902, Cidade Jardim/Candeal, CEP 40296200, Salvador, Bahia, Brazil;Gastroenterology Unit, Roberto Santos General Hospital, Salvador, Bahia, Brazil | |
关键词: IL10; TGFB1; Polymorphism; Crohn’s disease; | |
Others : 1141534 DOI : 10.1186/1756-0500-6-387 |
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received in 2012-11-04, accepted in 2013-09-25, 发布年份 2013 | |
【 摘 要 】
Background
Most Crohn’s disease (CD) genes discovered in recent years are associated with biological systems critical to the development of this disease. TGFB1 and IL10 are cytokines with important roles in CD. The aim of this study was to evaluate the association between CD, its clinical features and TGFB1 and IL10 gene polymorphisms.
Methods
This case–control study enrolled 91 patients and 91 controls from the state of Bahia, Brazil. Five single nucleotide polymorphisms (SNPs) were studied in the TGFB1 gene (codon 10 T > C - rs1800470; codon 25 G > C - rs1800471) and IL10 gene (−1082 A > G - rs1800896; -819 T > C - rs1800871; -592 A > C - rs1800872). An analysis of the genetic polymorphisms was performed using a commercial kit. A comparison of allele frequencies and genotypes was estimated by calculating the odds ratio (OR) with a confidence interval adjusted via the Bonferroni test for a local alpha of 1%. A stratified analysis was applied for gender, race and smoking history. Patients with CD were characterized according to the Montreal classification.
Results
The C allele and CC genotype of the TGFB1 gene rs1800470 were both significantly associated with CD. The stratified analysis showed no confounding factors for the co-variables of gender, race and smoking history. The IL10 gene rs1800896 G allele was significantly associated with age at diagnosis of CD, while the T allele of the IL10 gene rs1800871 was significantly associated with perianal disease. The SNPs rs1800871 and rs1800872 were in 100% linkage disequilibrium.
Conclusions
TGFB1 gene polymorphisms may be associated with susceptibility to the development of CD, and IL10 gene polymorphisms appear to influence the CD phenotype in this admixed population.
【 授权许可】
2013 Almeida et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
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20150327075009663.pdf | 210KB | download |
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