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Association of cytokine genetic polymorphism with hepatites B infection evolution in adult patients
The infection by the hepatitis B virus (HBV) has different forms of evolution, ranging from self-limited infection to chronic hepatic disease. The objective of this study was to evaluate the influence of cytokine genetic polymorphisms in the disease evolution. The patients were divided into two grou...
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Published in: | Memórias do Instituto Oswaldo Cruz 2007-06, Vol.102 (4), p.435-440 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The infection by the hepatitis B virus (HBV) has different forms of
evolution, ranging from self-limited infection to chronic hepatic
disease. The objective of this study was to evaluate the influence of
cytokine genetic polymorphisms in the disease evolution. The patients
were divided into two groups, one with chronic HBV (n = 30), and the
other with self-limited infection (n = 41). The genotyping for TNF
(-308), TGFB1 (+869, +915), IL- 10 (1082, -819, and
-592), IL-6 (-174), and IFNG (+874) was accomplished by the
PCR-SSP (polymerase chain reaction with sequence specific primers
technique using the One Lambda kit. Although no statistically
significant differences were found between the groups, the combination
of TNF -308GG and IFNG +874TA was found in a lower frequency in
chronic patients than in individuals with self-limited infection (26.7
versus 46.3%; P = 0.079; OR = 0.40; IC95% = 0.14-1.11). In chronic
patients with histological alterations it was not observed the genotype
TGFB1+869 C/C, against 24.4% in the self limited infection group (100
versus 75.6%; P = 0.096; OR = 7.67; IC95% = 0.42-141.63). Further
studies in other populations, and evaluation of a greater number of
individuals could contribute for a better understanding of the cytokine
genetic polymorphism influence in HBV infection evolution. |
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ISSN: | 1678-8060 0074-0276 1678-8060 |
DOI: | 10.1590/S0074-02762007005000043 |