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1 Laboratory of Molecular Microbiology, St Petersburg Pasteur Institute, St Petersburg 197101, Russia
2 Research Institute of Phthisiopulmonology, St Petersburg 193063, Russia
Correspondence
Igor Mokrousov
imokrousov{at}mail.ru
or
igormokrousov{at}yahoo.com
Received 18 June 2007
Accepted 11 January 2008
2=3.2, 1 d.f., P=0.2). The –762C allele was highly and almost equally represented in both groups in this study (68.2 % in patients and 69.3 % in controls). This result differs strikingly from a Gambian study where this allele was found in only 7 and 12 % of pulmonary TB patients and controls, respectively [Li, C. M., Campbell, S. J., Kumararatne, D. S., Bellamy, R., Ruwende, C., McAdam, K. P. W. J., Hill, A. V. S. & Lammas, D. A. (2002). J Infect Dis 186, 1458–1462]. In contrast, the frequency of the C allele at position 1513 in exon 13, resulting in a loss of P2X7 function, was significantly higher among pulmonary TB patients in this study (P=0.02). Thus, analysis of the P2X7 receptor gene in the Russian Slavic population showed that the 1513C allele, acting dominantly, is a possible risk factor for clinical TB, whereas the –762 P2RX7 polymorphism did not appear to be associated with human susceptibility to TB.
Abbreviations: CI, confidence interval; HIV, human immunodeficiency virus; HWE, Hardy–Weinberg equilibrium; LD, linkage disequilibrium; OR, odds ratio; SNP, single-nucleotide polymorphism; TB, tuberculosis.
A table showing the results of stratification analysis for the –762 and 1513 genotypes and alleles is available as supplementary material with the online version of this paper.
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