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  4. Clinical aspects and outcomes of volunteer blood donors testing positive for hepatitis-C virus infection in Taiwan: A prospective study
 
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Clinical aspects and outcomes of volunteer blood donors testing positive for hepatitis-C virus infection in Taiwan: A prospective study

Journal
Liver International
Journal Volume
23
Journal Issue
3
Pages
148-155
Date Issued
2003
Author(s)
CHUN-JEN LIU  
PEI-JER CHEN  
Shau W.-Y.
JIA-HORNG KAO  
Lai M.-Y.
DING-SHINN CHEN  
DOI
10.1034/j.1600-0676.2003.00820.x
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84984575691&doi=10.1034%2fj.1600-0676.2003.00820.x&partnerID=40&md5=9150fbacd145601e0789103869d1c014
https://scholars.lib.ntu.edu.tw/handle/123456789/568756
Abstract
Background/Aim: The natural history of hepatitis-C virus (HCV) infection has been explored in volunteer blood donors, but not yet in hepatitis-B endemic areas. Whether previous or concurrent hepatitis-B virus (HBV) infection influences the natural history of HCV infection remains unknown. Thus, we followed the anti-HCV-positive blood donors who had past or concurrent HBV infection in Taiwan. Methods: From 1992 to 1993, 1588 anti-HCV reactive volunteer blood donors were referred to us from the Taipei Blood Center and 879 (55%) repeatedly reactive for anti-HCV were enrolled. Two hundred and forty-three donors (HCV RNA seropositive rate 49% by polymerase chain reaction (PCR)) received regular follow-ups (mean period: 4.9 years) with their liver disease status determined mainly by clinical and biochemical parameters, serum alpha-fetoprotein level and imaging studies. Hepatitis-C virus genotype and occult HBV infection were determined by PCR-based assays. Results: Of the initial 879 subjects, 250 (28%) had chronic hepatitis, nine (1%) had liver cirrhosis (LC) and two (0.2%) had hepatocellular carcinoma (HCC) already. In the 243 regularly followed donors, 30% had repeatedly normal serum alanine aminotransferase (ALT) and 70% had more than once elevated ALT. Cirrhosis developed in four (1.6%; follow-up period range: 2-6 years) and HCC in two (0.8%; follow-up period: 3 and 4 years, respectively). Distribution of HCV genotype and hepatitis-B surface antigen (HBsAg) did not differ between those with and those without elevation of ALT. Of the 15 donors with LC and/or HCC, only 1(7%) was positive for both HBsAg and HBV DNA and the other 14 were negative for both HBsAg and serum HBV DNA. Conclusions: Incidentally detected hepatitis-C was progressive in a small proportion of anti-HCV-positive volunteer blood donors in Taiwan. Occult HBV infection played a minimal role in the development of LC in this donor population.
SDGs

[SDGs]SDG3

Other Subjects
alanine aminotransferase; alpha fetoprotein; hepatitis B surface antigen; virus antibody; virus DNA; virus RNA; adolescent; adult; alanine aminotransferase blood level; article; biochemistry; blood donor; chronic hepatitis; clinical study; controlled study; diagnostic imaging; disease activity; female; follow up; genotype; hepatitis B; Hepatitis B virus; hepatitis C; Hepatitis C virus; human; immunoreactivity; liver carcinogenesis; liver cell carcinoma; liver cirrhosis; major clinical study; male; nonhuman; outcomes research; polymerase chain reaction; prospective study; protein blood level; school child; serodiagnosis; superinfection; Taiwan; virus pathogenesis; volunteer
Publisher
Blackwell Publishing Ltd
Type
journal article

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