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Hepatitis C virus infection in patients with chronic liver disease or chronic renal failure and blood donors in Thailand

dc.contributor.authorPairoj Luengrojanakulen_US
dc.contributor.authorKriengsak Vareesangthipen_US
dc.contributor.authorTermchai Chainuvatien_US
dc.contributor.authorKazumoto Murataen_US
dc.contributor.authorFumio Tsudaen_US
dc.contributor.authorHajime Tokitaen_US
dc.contributor.authorHiroaki Okamotoen_US
dc.contributor.authorYuzo Miyakawaen_US
dc.contributor.authorMakoto Mayumien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherMie Universityen_US
dc.contributor.otherViral Hepatitis Research Foundation of Japanen_US
dc.contributor.otherMita Instituteen_US
dc.contributor.otherJichi Medical Universityen_US
dc.date.accessioned2018-02-27T04:27:01Z
dc.date.available2018-02-27T04:27:01Z
dc.date.issued1994-01-01en_US
dc.description.abstractHepatitis C virus (HCV) RNA and genotypes, as well as markers of hepatitis B virus infection, were surveyed in 171 patients with chronic liver disease, 276 patients with chronic renal failure, and 961 blood donors in Thailand. HCV RNA was detected in 30 (23%) of 128 patients with nonalcoholic chronic liver disease and hepatitis B surface antigen (HBsAg) in 60 (47%), and both HCV RNA and HBsAg in 3; the cause of liver disease was not established in 41 (32%) patients. HCV RNA was detected in 44 (20%) of 221 patients on maintenance hemodialysis or with kidney transplantation, but in none of 55 patients on peritoneal dialysis. Antibodies to synthetic HCV core peptides were detected in 39 (4.1%) of sera from 961 blood donors, and HCV RNA was detected in 8 (0.8%). Of the 90 HCV RNA samples from patients and donors, genotype V prevailed (46%) followed by II (22%), I (14%), III (3%), and VI (2%); genotypes were not classifiable into any of I‐VI in the remaining 10%. There were six sera which contained HCV RNA, but were without antibody to HCV detectable by the second‐generation enzyme immunoassay. HCV RNA titers were high in four patients with kidney transplantation, but low in one patient with chronic liver disease and one patient on maintenance hemodialysis. HCV RNA at high titer (≥10 4 /ml) was not classifiable in one patient. These results indicate HCV of novel genotypes in Thailand, seronegative HCV infection in patie nts with kidney transplantation, and a low risk of HCV infection in patients treated by peritoneal dialysis. © 1994 wiiey‐Liss, Inc. Copyright © 1994 Wiley‐Liss, Inc., A Wiley Companyen_US
dc.identifier.citationJournal of Medical Virology. Vol.44, No.3 (1994), 287-292en_US
dc.identifier.doi10.1002/jmv.1890440313en_US
dc.identifier.issn10969071en_US
dc.identifier.issn01466615en_US
dc.identifier.other2-s2.0-0028125056en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/9607
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028125056&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleHepatitis C virus infection in patients with chronic liver disease or chronic renal failure and blood donors in Thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028125056&origin=inwarden_US

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