Lack of association of the G22A polymorphism of the ADA gene in patients with ankylosing spondylitis

1Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

Abstract

Genes located outside the HLA region (6p21) have been considered as candidates for susceptibility to ankylosing spondylitis. We tested the hypothesis that the G22A polymorphism of the adenosine deaminase gene (ADA; 20q13.11) is associated with ankylosing spondylitis in 166 Brazilian subjects genotyped for the HLA*27 gene (47 patients and 119 controls matched for gender, age and geographic origin). The HLA-B*27 gene and the G22A ADA polymorphism were identified by PCR with sequence-specific oligonucleotide probes and PCR-RFLP, respectively. There were no significant differences in frequencies of ADA genotypes [odds ratio (OR) = 1.200, 95% confidence interval (CI) = 0.3102-4.643, P > 0.8] and ADA*01 and ADA*02 alleles (OR = 1.192, 95%CI = 0.3155-4.505, P > 0.8) in patients versus controls. We conclude that the G22A polymorphism is not associated with ankylosing spondylitis. © FUNPEC-RP.

Cite

CITATION STYLE

APA

Camargo, U., Toledo, R. A., Cintra, J. R., Nunes, D. P. T., Acayaba de Toledo, R., Brandão de Mattos, C. C., & Mattos, L. C. (2012). Lack of association of the G22A polymorphism of the ADA gene in patients with ankylosing spondylitis. Genetics and Molecular Research, 11(2), 1178–1184. https://doi.org/10.4238/2012.May.7.3

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free