Association of IFNL3 and IFNL4 polymorphisms with hepatitis C virus infection in a population from southeastern Brazil

Carregando...
Imagem de Miniatura
Citações na Scopus
9
Tipo de produção
article
Data de publicação
2016
Título da Revista
ISSN da Revista
Título do Volume
Editora
SPRINGER WIEN
Autores
DINIZ, Marcio Augusto
ABE-SANDES, Kiyoko
SANTOS, Sidney Emanuel Batista dos
LYRA, Andre de Castro
Citação
ARCHIVES OF VIROLOGY, v.161, n.6, p.1477-1484, 2016
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Hepatitis C virus (HCV) infection is a major cause of chronic liver disease and associated complications such as liver cirrhosis and hepatocellular carcinoma (HCC). Viral and host factors are known to be predictors for antiviral therapy. Host factors that are predictors of sustained viral response (SVR) were discovered by genome-wide association studies (GWAS), including single-nucleotide polymorphisms (SNPs) in or near the interferon lambda gene (rs8099917, rs12979860 and rs368234815). The aim of the present study was to verify the genotype frequencies of SNPs rs8099917, rs12979860 and rs368234815 and to evaluate the association between SNPs and the outcome of HCV infection, taking into account the population ancestry. In this study, there was an association of the three polymorphisms with both clinical outcome and response to treatment with PEG-IFN and RBV. The polymorphisms rs12979860 and rs368234815 were associated with increased sensitivity (97.7 %, 95 % CI 87.2-100, and 93.3 %, 95 % CI 81.3-98.3; respectively) and with a greater predictive value of a positive response to treatment. In multivariable analysis adjusted by gender, age and ancestry, the haplotype G/T/Delta G was related to non-response to treatment (OR = 21.09, 95 % CI 5.33-83.51; p < 0.001) and to a higher chance of developing chronic infection (OR = 5.46, 95 % CI 2.06-14.46; p = 0.001) when compared to the haplotype T/C/TT. These findings may help to adjust our treatment policies for HCV infection based on greater certainty in studies with populations with such genetic characteristics, as well as allowing us to get to know the genetic profile of our population for these polymorphisms.
Palavras-chave
Referências
  1. Tanaka Y, 2009, NAT GENET, V41, P1105, DOI 10.1038/ng.449
  2. Manns M, 2011, ANTIVIR THER, V16, P1021, DOI 10.3851/IMP1894
  3. Ge DL, 2009, NATURE, V461, P399, DOI 10.1038/nature08309
  4. Ramos JA, 2012, MEM I OSWALDO CRUZ, V107, P888, DOI 10.1590/S0074-02762012000700008
  5. Lozano R, 2012, LANCET, V380, P2095, DOI 10.1016/S0140-6736(12)61728-0
  6. Hamming OJ, 2013, EMBO J, V32, P3055, DOI 10.1038/emboj.2013.232
  7. O'Brien TR, 2015, J HEPATOL, V63, P1103, DOI [10.1016/j.jhep.2015.06.035, 10.1016/j.jhep.2015.06]
  8. Prokunina-Olsson L, 2013, NAT GENET, V45, P164, DOI 10.1038/ng.2521
  9. Razavi H, 2014, J VIRAL HEPATITIS, V21, P34, DOI 10.1111/jvh.12248
  10. Nelson DR, 2015, HEPATOLOGY, V61, P1127, DOI 10.1002/hep.27726
  11. Thomas DL, 2009, NATURE, V461, P798, DOI 10.1038/nature08463
  12. Esser C, 2005, J INVEST DERMATOL, V124, P1082, DOI 10.1111/j.0022-202X.2005.23709.x
  13. Akamatsu S, 2015, J HEPATOL, V63, P554, DOI 10.1016/j.jhep.2015.03.033
  14. Kowdley KV, 2013, LANCET, V381, P2100, DOI 10.1016/S0140-6736(13)60247-0
  15. Lake SL, 2003, HUM HERED, V55, P56, DOI 10.1159/000071811
  16. HOLM S, 1979, SCAND J STAT, V6, P65
  17. Jouvin-Marche E, 2014, J INFECT DIS, V209, P1907, DOI 10.1093/infdis/jiu016
  18. Olmedo DB, 2015, J MED VIROL, V87, P1702, DOI 10.1002/jmv.24227
  19. Cavalcante LN, 2012, LIVER INT, V32, P476, DOI 10.1111/j.1478-3231.2011.02653.x
  20. Manns MP, 2015, J VIRAL HEPATITIS, V22, P366, DOI 10.1111/jvh.12346
  21. Tian C, 2008, HUM MOL GENET, V17, pR143, DOI 10.1093/hmg/ddn268
  22. Suppiah V, 2009, NAT GENET, V41, P1100, DOI 10.1038/ng.447
  23. Wack A, 2015, NAT IMMUNOL, V16, P802, DOI 10.1038/ni.3212
  24. Gower E, 2014, J HEPATOL, V61, pS45, DOI 10.1016/j.jhep.2014.07.027
  25. Santos NPC, 2010, HUM MUTAT, V31, P184, DOI 10.1002/humu.21159
  26. Lawitz EJ, 2012, J HEPATOL, V57, P24, DOI 10.1016/j.jhep.2011.12.029
  27. Gane EJ, 2013, ANTIMICROB AGENTS CH, V58, P1136
  28. IBGE, 2015, EST POV
  29. O'Brien TR, 2015, OPEN FORUM INFECT DI, V2
  30. Terczynska-Dyla E, 2014, NAT COMMUN, V5