Abstract | AIM: METHOD: Total 108 subjects with CHB infection and 102 healthy controls were enrolled in this study. IL-6 (-174G/C) was genotyped using Mutagenically separated Polymerase Chain Reaction (MS-PCR) while sequence specific primers-PCR (SSP-PCR) was used for studying -572G/C and -597G/A. IL-6 plasma level was measured using Enzyme-linked immunosorbent assay (ELISA). RESULTS: A significant increase (P < 0.01, P < 0.01, P < 0.001) in -174GG, -572GC and -597GA; respectively in the CHB group compared to control group, while -572GG genotype was significantly decreased (P < 0.01) in CHB patients. A significant increase (p < 0.01, p < 0.01) in -174 G and -597A alleles was observed in the CHB patient group; respectively. GGA haplotype is significantly increased (P < 0.05) while GCA haplotype is significantly decreased (P < 0.001) in the patient group. A moderate linkage disequilibrium (LD) (D' = 0.719, r2 = 0.474; P < 0.001) between IL-6 (-572G/C and -597G/A) was observed. A significant reduction (P < 0.01) in IL-6 plasma level in CHB patients compared to healthy controls (22.28 ± 1.93 versus 32.08 ± 2.41), which was negatively correlated (r = -0.216; P < 0.01) with HBV infection. CONCLUSIONS: This study pointed to the potential role of IL-6 (-174G/C, -572 G/C and -597G/A) gene polymorphisms in the susceptibility to HBV infection. Our results allow for only preliminary conclusions due to relatively small sample size. There is a need for further larger scale studies to fully examine the possible relationship between these cytokine gene polymorphisms and the development of CHB.
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Authors | Eman A El-Maadawy, Roba M Talaat, Maha M Ahmed, Soha Z El-Shenawy |
Journal | Human immunology
(Hum Immunol)
Vol. 80
Issue 3
Pg. 208-214
(Mar 2019)
ISSN: 1879-1166 [Electronic] United States |
PMID | 30594561
(Publication Type: Journal Article)
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Copyright | Copyright © 2018. Published by Elsevier Inc. |
Chemical References |
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Topics |
- Adult
- Alleles
- Biomarkers
- Egypt
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Genotype
- Haplotypes
- Hepatitis B virus
- Hepatitis B, Chronic
(blood, etiology)
- Humans
- Interleukin-6
(blood, genetics)
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
- Promoter Regions, Genetic
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