Journal of Korean medical science · 2013
The impact of inosine triphosphatase variants on hemoglobin level and sustained virologic response of chronic hepatitis C in Korean.
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Kim Ju Seung, Ahn Sung-Min, Jung Young Kul, Kwon Oh Sang, Kim Yun Soo, Choi Duck Joo, Kim Ju Hyun
Аннотация
rs1127354, rs7270101) gene cause ITPA deficiency and protect against the hemolytic toxicity of ribavirin. We investigated the clinical significance of ITPA variants in Korean patients treated with pegylated interferon (PEG-IFN) plus ribavirin. Of the 133 patients, 108 were CC and 25 were non-CC at rs1127354 (groups A and B, respectively). On the other hand, at rs7270101 all 133 were AA. The mean values of Hemoglobin (Hgb) after 4, 8, and 12 weeks of treatment in groups A and B were 12.2 and 14.0, 11.8 and 13.2, and 11.5 and 12.9, respectively (P=0.001, 0.036, 0.036). Sustained virologic response (SVR) was achieved in 67.8% (40/59) of genotype 1 patients and in 75% (27/36) of non-genotype 1 patients. Regarding ITPA variants, SVR was achieved by 66% and 80% of genotype 1 (P=0.282), and by 78% and 71% (P=0.726) of non-genotype 1. SVR was not significantly different in groups A and B. In conclusion, non-CC at rs1127354 without involvement of rs7270101 is strongly associated with protection from ribavirin-induced anemia, however, ITPA genotype is not associated with SVR.
Предметные рубрики MeSH
AdultAllelesAntiviral AgentsAsian PeopleCohort StudiesDrug Therapy, CombinationFemaleGenotypeHemoglobinsHemolysisHepacivirusHepatitis C, ChronicHumansInterferon-alphaInterferonsInterleukinsMaleMiddle AgedPolyethylene GlycolsPyrophosphatasesRecombinant ProteinsRepublic of KoreaRetrospective StudiesRibavirinTreatment OutcomeInosine TriphosphataseInterferon Lambda