Publication:
Hepatitis G infection and therapeutic response to interferon in HCV-related chronic liver disease

dc.contributor.authorChutima Pramoolsinsapen_US
dc.contributor.authorYong Poovorawanen_US
dc.contributor.authorThanyachai Suraen_US
dc.contributor.authorApiradee Theamboonlersen_US
dc.contributor.authorNunta Busagornen_US
dc.contributor.authorSucha Kurathongen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherMed. Genetics and Molecular Medicineen_US
dc.date.accessioned2018-07-04T08:12:00Z
dc.date.available2018-07-04T08:12:00Z
dc.date.issued1998-09-01en_US
dc.description.abstractCirculating HGV-RNA was determined in 117 patients with HCV-related chronic liver disease and in 200 healthy blood donors. The patients, aged 50.8±13.8 years, were classified as chronic hepatitis (CH; n = 82), liver cirrhosis (n = 25) and hepatocellular carcinoma (HCC; n = 10). HGV-RNA was detected in 5 (4.3%) patients, all with CH and in 10 (5%) of blood donors The majority of all groups (52% to70%) were infected with HCV genotype II/1b, including 4/5 patients with HGV co-infection. Of 5 patients with HGV co-infection, 4 were positive for anti-HBs and anti-HBc and none exhibited jaundice. A 24-week course of interferon treatment with 12-month follow-up was achieved in 27 patients with chronic active hepatitis, including 3 with HGV co-infection. Of these, 55.6% responded to the therapy, but only 6/27 (22.2%) patients were sustained responders. The majority of sustained responders were HCV genotype III/ 2a (4/6) while genotype II/1b was found in the majority of patients with relapse (7/9) and non-responders (9/12). At the 48- month follow up, 2/6 sustained responders (one with HGV co-infection) became HCV RNA positive. These results show that the prevalence of HGV infection in HCV-related chronic liver disease is low, as in the general population, and is found in younger patients with chronic hepatitis. HGV coinfection does not interfere with clinical severity, disease progression or response to interferon in patients with HCV-related chronic liver disease. The favorable factors of interferon treatment for HCV infection are young age, low HCV-RNA levels and HCV genotype III/2a.en_US
dc.identifier.citationSoutheast Asian Journal of Tropical Medicine and Public Health. Vol.29, No.3 (1998), 480-490en_US
dc.identifier.issn01251562en_US
dc.identifier.other2-s2.0-0032149482en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/18494
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032149482&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleHepatitis G infection and therapeutic response to interferon in HCV-related chronic liver diseaseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032149482&origin=inwarden_US

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