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The influence of gene-chronic hepatitis C virus infection on hepatic fibrosis and steatosis.
- Source :
-
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2020 Jun; Vol. 97 (2), pp. 115025. Date of Electronic Publication: 2020 Feb 19. - Publication Year :
- 2020
-
Abstract
- Host single nucleotide polymorphisms (SNPs) in different genes can play a role in chronic hepatitis C virus (HCV) infection and influence the presence of hepatic fibrosis and comorbidities such as hepatic steatosis. We assessed the combined effect of SNPs in the PNPLA3, MTTP, TM6SF2, and IFNL3/IFNL4 genes in 288 Brazilian patients who were chronically infected with HCV. Hepatic fibrosis was observed in 246 (85.4%) patients and hepatic steatosis in 141 (49.0%) patients. PNPLA3 rs738409 (CG/GG) (P = 0.044) and TM6SF2 rs58542926 (CT) (P = 0.004) were alone associated with fibrosis, and PNPLA3 rs738409 (P < 0.05, in distinct genetic models) was associated with steatosis. Multiple logistic regression of each SNP combined with HCV genotype 3 infection showed that MTTP rs1800591 (GT/TT) combined with HCV genotype 3 was associated with a 6.72-fold increased chance of hepatic steatosis (P = 0.013). In the analysis of SNPs combined 2 by 2, no influence on hepatic fibrosis or steatosis was observed.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Subjects :
- Adult
Aged
Brazil
Carrier Proteins genetics
Fatty Liver virology
Female
Genetic Association Studies
Genotype
Hepacivirus genetics
Hepacivirus pathogenicity
Hepatitis C, Chronic virology
Humans
Interferons genetics
Lipase genetics
Liver Cirrhosis virology
Male
Membrane Proteins genetics
Middle Aged
Fatty Liver genetics
Hepatitis C, Chronic genetics
Liver Cirrhosis genetics
Polymorphism, Single Nucleotide
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0070
- Volume :
- 97
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Diagnostic microbiology and infectious disease
- Publication Type :
- Academic Journal
- Accession number :
- 32147132
- Full Text :
- https://doi.org/10.1016/j.diagmicrobio.2020.115025