Tumour necrosis factor -308 and -238 promoter polymorphisms are predictors of a null virological response in the treatment of Brazilian hepatitis C patients

Bibliographic Details
Title: Tumour necrosis factor -308 and -238 promoter polymorphisms are predictors of a null virological response in the treatment of Brazilian hepatitis C patients
Authors: Tarciana Grandi, Cláudia Maria Dornelles da Silva, Karine Medeiros Amaral, Paulo Dornelles Picon, Cintia Costi, Nicole Nascimento da Fré, Marilu Fiegenbaum, Tatiana Schäffer Gregianini, Christian Niel, Maria Lucia Rosa Rossetti
Source: Memorias do Instituto Oswaldo Cruz, Vol 109, Iss 3, Pp 345-351 (2014)
Publisher Information: Fundação Oswaldo Cruz (FIOCRUZ), 2014.
Publication Year: 2014
Collection: LCC:Microbiology
LCC:Infectious and parasitic diseases
Subject Terms: TNF, polymorphisms, HCV, virological response, Brazil, Microbiology, QR1-502, Infectious and parasitic diseases, RC109-216
More Details: Certain host single nucleotide polymorphisms (SNPs) affect the likelihood of a sustained virological response (SVR) to treatment in subjects infected with hepatitis C virus (HCV). SNPs in the promoters of interleukin (IL)-10 (-1082 A/G, rs1800896), myxovirus resistance protein 1 (-123 C/A, rs17000900 and -88 G/T, rs2071430) and tumour necrosis factor (TNF) (-308 G/A, rs1800629 and -238 G/A, rs361525) genes and the outcome of PEGylated α-interferon plus ribavirin therapy were investigated. This analysis was performed in 114 Brazilian, HCV genotype 1-infected patients who had a SVR and in 85 non-responders and 64 relapsers. A significantly increased risk of having a null virological response was observed in patients carrying at least one A allele at positions -308 [odds ratios (OR) = 2.58, 95% confidence intervals (CI) = 1.44-4.63, p = 0.001] or -238 (OR = 7.33, 95% CI = 3.59-14.93, p < 0.001) in the TNF promoter. The risk of relapsing was also elevated (-308: OR = 2.87, 95% CI = 1.51-5.44, p = 0.001; -238: OR = 4.20, 95% CI = 1.93-9.10, p < 0.001). Multiple logistic regression of TNF diplotypes showed that patients with at least two copies of the A allele had an even higher risk of having a null virological response (OR = 16.43, 95% CI = 5.70-47.34, p < 0.001) or relapsing (OR = 6.71, 95% CI = 2.18-20.66, p = 0.001). No statistically significant association was found between the other SNPs under study and anti-HCV therapy response.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1678-8060
0074-0276
Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762014000300345&lng=en&tlng=en; https://doaj.org/toc/1678-8060
DOI: 10.1590/0074-0276130372
Access URL: https://doaj.org/article/64024f1f51414b7f80329e57114a8358
Accession Number: edsdoj.64024f1f51414b7f80329e57114a8358
Database: Directory of Open Access Journals
More Details
ISSN:16788060
00740276
DOI:10.1590/0074-0276130372
Published in:Memorias do Instituto Oswaldo Cruz
Language:English