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dc.creatorAnagnostou, O.en
dc.creatorManolakopoulos, S.en
dc.creatorBakoyannis, G.en
dc.creatorPapatheodoridis, G.en
dc.creatorZisouli, A.en
dc.creatorRaptopoulou-Gigi, M.en
dc.creatorManesis, E.en
dc.creatorKetikoglou, I.en
dc.creatorDalekos, G.en
dc.creatorGogos, C.en
dc.creatorVassiliadis, T.en
dc.creatorTzourmakliotis, D.en
dc.creatorKaratapanis, S.en
dc.creatorKanatakis, S.en
dc.creatorZoumpoulis-Vafiadis, I.en
dc.creatorHounta, A.en
dc.creatorKoutsounas, S.en
dc.creatorGiannoulis, G.en
dc.creatorTassopoulos, N.en
dc.creatorTouloumi, G.en
dc.date.accessioned2015-11-23T10:22:10Z
dc.date.available2015-11-23T10:22:10Z
dc.date.issued2014
dc.identifier.issn1108-4189
dc.identifier.urihttp://hdl.handle.net/11615/25530
dc.description.abstractBackground and aim: Patients with genotype 4 (G4) chronic hepatitis C (CHC) are considered a difficult to treat population, although current data on G4 treatment responsiveness and duration are controversial. Greece represents a country with an intermediate prevalence of G4 infections, offering an opportunity to compare treatment outcomes by genotype and to identify potential prognostic factors for sustained virologic response (SVR). Methods: All CHC patients from the HepNet. Greece, an ongoing nationwide cohort study on viral hepatitis, with known hepatitis C virus (HCV) genotype who received treatment with Peg-IFNa and ribavirin were analyzed. Results: From 4443 patients, 951 (61.7% males, 78.4% Greeks, median age 40.6 years, 10% cirrhosis) fulfilled the inclusion criteria. G4 was found in 125 (13.1%) patients. Genotype distribution was not significantly different between Greeks and immigrants. Patients with G4 had similar odds of SVR compared to G1 but significantly lower compared to G2/G3. Age, treatment discontinuation, presence of cirrhosis and previous history of HCV-treatment were associated with lower probabilities of SVR. Ethnicity did not affect SVR for all genotypes while response to treatment was similar between Greek and Egyptian patients groups (35.7% vs 40.9%, p= 0.660%) with G4 infection. The relation between SVR and genotype did not substantially change after adjustment for age, gender, cirrhosis, treatment interruption and history of HCV-treatment. Conclusions: The findings of this large cohort of CHC patients with a well balanced genotype distribution further supports the idea of considering G4 as a difficult to treat genotype. Further investigation is needed to identify genotype specific prognostic factors.en
dc.sourceHippokratiaen
dc.source.uri<Go to ISI>://WOS:000335442400012
dc.subjectViral hepatitisen
dc.subjectHCV treatmenten
dc.subjectinterferonen
dc.subjectpegylated-interferonen
dc.subjectCHRONIC HEPATITIS-Cen
dc.subjectALPHA-2B PLUS RIBAVIRINen
dc.subjectSUSTAINED VIROLOGICALen
dc.subjectRESPONSEen
dc.subjectPEGINTERFERON ALPHA-2Ben
dc.subjectVIRUS-INFECTIONen
dc.subjectMOLECULARen
dc.subjectEPIDEMIOLOGYen
dc.subjectTREATMENT DURATIONen
dc.subjectLIVER FIBROSISen
dc.subjectCIRRHOSISen
dc.subjectPOLYMORPHISMen
dc.subjectMedicine, General & Internalen
dc.titleGenotype 4 HCV infection is difficult to cure with pegylated interferon and ribavirin. Results from a Greek Nationwide Cohort Studyen
dc.typejournalArticleen


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