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Interleukin 28B Genetic Polymorphisms Play a Minor Role in Identifying Optimal Treatment Duration in HCV Genotype 1 Slow Responders to Pegylated Interferon plus Ribavirin
Author(s) -
ChenHua Liu,
ChengChao Liang,
ChunJen Liu,
TaiChung Tseng,
ChihLin Lin,
ShengShun Yang,
TungHung Su,
JouWei Lin,
Jun-Herng Chen,
PeiJer Chen,
DingShinn Chen,
JiaHorng Kao
Publication year - 2012
Publication title -
antiviral therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.747
H-Index - 87
eISSN - 2040-2058
pISSN - 1359-6535
DOI - 10.3851/imp2322
Subject(s) - ribavirin , pegylated interferon , medicine , interleukin 28b , viral load , gastroenterology , genotype , snp , hepatitis c virus , immunology , single nucleotide polymorphism , biology , virus , biochemistry , gene
Pegylated interferon and ribavirin for 72 weeks improve sustained virological response (SVR) in HCV genotype 1 (HCV-1) slow viral responders. Whether interleukin 28B (IL28B) single nucleotide polymorphism (SNP) genotypes and on-treatment viral responses can identify non-rapid virological response (RVR) patients who benefit from 48 or 72 weeks of therapy remains unclear.

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