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However, these relationships in patients with\n                      <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\n                      genotype 2 are not well understood. The aim of this study was to investigate whether the\n                      <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                      of\n                      <jats:styled-content style=\"fixed-case\">IL28B<\/jats:styled-content>\n                      (rs8099917) and amino acid substitutions in the\n                      <jats:styled-content style=\"fixed-case\">NS5A<\/jats:styled-content>\n                      region in patients with\n                      <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\n                      genotype 2 affect the response to\n                      <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                      and ribavirin combination therapy.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      The study enrolled 286 patients with chronic hepatitis\n                      <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\n                      genotype 2. Patients received pegylated\u2010\n                      <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                      \u2010alpha 2b once each week plus oral ribavirin daily for 24 weeks.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Of the 286 patients, 215 (75.2%) achieved sustained virologic response (\n                      <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>\n                      ). Rate of\n                      <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>\n                      was similar in patients with\n                      <jats:styled-content style=\"fixed-case\">IL28B TT<\/jats:styled-content>\n                      allele (76%) and those with\n                      <jats:styled-content style=\"fixed-case\">TG<\/jats:styled-content>\n                      or\n                      <jats:styled-content style=\"fixed-case\">GG<\/jats:styled-content>\n                      alleles (72%). Patients with\n                      <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>\n                      were younger than those without\n                      <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>\n                      (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001).\n                      <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>\n                      was achieved in 65.9% of patients with wild\u2010type\n                      <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                      sensitivity\u2010determining region (\n                      <jats:styled-content style=\"fixed-case\">ISDR<\/jats:styled-content>\n                      ) and 83.5% of patients with mutant type (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001). There were no significant differences in other factors, including sex, alanine aminotransferase, platelet count,\n                      <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\n                      viral load,\n                      <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\n                      genotype, and\n                      <jats:styled-content style=\"fixed-case\">IL28B<\/jats:styled-content>\n                      genotype. The factors related to\n                      <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>\n                      on multivariate analysis were age (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u20090.019) and\n                      <jats:styled-content style=\"fixed-case\">ISDR<\/jats:styled-content>\n                      (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u20090.003).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">ISDR<\/jats:styled-content>\n                      sequence variations are significantly associated with\n                      <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                      responsiveness in patients with\n                      <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\n                      genotype 2. The\n                      <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                      of\n                      <jats:styled-content style=\"fixed-case\">IL28B<\/jats:styled-content>\n                      was not associated with\n                      <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>\n                      in patients with\n                      <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\n                      genotype 2.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jgh.12673","type":"journal-article","created":{"date-parts":[[2014,7,4]],"date-time":"2014-07-04T00:07:51Z","timestamp":1404432471000},"page":"178-183","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Association of interleukin 28\n                    <scp>B<\/scp>\n                    polymorphism and mutations in the\n     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