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GENE POLYMORPHISMS IN PATIENTS WITH PULMONARY TUBERCULOSIS FROM MOZAMBIQUE
Author
Affilliation
Instituto Nacional de Saúde. Laboratório de Virologia Molecular. Maputo, Mozambique.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
Instituto Nacional de Saúde. Laboratório de Virologia Molecular. Maputo, Mozambique.
Instituto Nacional de Saúde. Laboratório de Virologia Molecular. Maputo, Mozambique.
Fundação Oswaldo Cruz. Programa de Computação Científica. Rio de Janeiro, RJ, Brasil.
Instituto Nacional de Saúde. Laboratório de Virologia Molecular. Maputo, Mozambique.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
Instituto Nacional de Saúde. Laboratório de Virologia Molecular. Maputo, Mozambique.
Instituto Nacional de Saúde. Laboratório de Virologia Molecular. Maputo, Mozambique.
Fundação Oswaldo Cruz. Programa de Computação Científica. Rio de Janeiro, RJ, Brasil.
Instituto Nacional de Saúde. Laboratório de Virologia Molecular. Maputo, Mozambique.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
Abstract
Several host and environmental factors contribute
to tuberculosis outcome, interestingly single nucleotide polymorphisms
(SNPs) in candidate genes have been evaluated in
populations with different ethnicities and TB infection. In the
present study we focused on SNPs in cytokine and inflammatory
mediator genes: tumor necrosis factor (TNF) -308G[A
(rs1800629), interleukin-10 (IL10) -819C[T (rs1800871),
interferon-gamma (IFNG) ?874T[A (rs2430561), and leukotriene
A4 hydrolase (LTA4H) rs1978331, rs17525495 and
rs2660898 in a case–control study involving 102 pulmonary
tuberculosis patients and 456 controls from Mozambique.
LTA4H, IL10 and IFNG SNPs showed no associations with
pulmonary tuberculosis. However, distribution of the TNF
-308A allele, genotype and carrier frequencies showed a significant
risk association with tuberculosis that was maintained
after adjustment for non-genetic variables and Bonferroni
correction (AAgenotype,OR= 1.9, pBonf\0.001;AalleleOR
= 2.9, pBonf = 0.005 and GA/AA carrier OR = 2.6,
pBonf = 0.035). Interestingly, this association has not been
reported in a sub-Saharan African population before. Our
results suggest a role of -308 TNF polymorphism and tuberculosis
susceptibility.
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