Journal Information
Vol. 15. Issue 2.
Pages 159-162 (March - April 2011)
Share
Share
Download PDF
More article options
Vol. 15. Issue 2.
Pages 159-162 (March - April 2011)
Brief Communication
Open Access
Absence of occult hepatitis B among blood donors in southern Brazil
Visits
2915
Fernando Herz Wolff1,
Corresponding author
fhwolff@gmail.com
fhwolff@terra.com.br

Correspondence to: Rua Dr. Freire Alemão 351 /703, 90450060, Porto Alegre, RS, Brazil. Phone: 55 51 30296136, 55 51 92490979.
, Sandra Costa Fuchs2, Ajacio B.M. Brandão3
1 Researcher of the National Institute of Science and Technology for Health Technology Assessment (IATS) - CNPq/Brazil; Post-graduation Program in Epidemiology, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul - UFRGS, Brazil
2 Associate Professor, Departament of Social Medicine, Faculdade de Medicina, UFRGS; Researcher, Instituto de Avaliação de Tecnologias em Saúde - HCPA/UFRGS/CNPQ; National Institute for Science and Technology for Health Technology Assessment (IATS/CNPq), Porto Alegre, Brazil
3 Director, Faculty of Medicine and Associate Professor, Universidade Federal de Ciências da Saúde de Porto Alegre - UFCSPA; Researcher, Instituto de Avaliação de Tecnologias em Saúde - HCPA/UFRGS/CNPQ; Internal Medicine Department, Faculdade de Medicina, UFCSPA, Brazil
This item has received

Under a Creative Commons license
Article information
Abstract
Background

Occult hepatitis B virus (HBV) infection is characterized by the detection of HBV DNA in serum and/or in liver in the absence of detectable hepatitis B surface antigen (HBsAg). The reported prevalence of occult hepatitis B varies markedly among populations and according to the sensitivity of the HBV DNA assay. The aim of the present study was to describe the prevalence of occult hepatitis B among HCV-infected and non-infected blood donors in Porto Alegre, Southern Brazil, using a highly sensitive real time polymerase chain reaction (PCR) method.

Methodology

Between 1995 and 1997 a sample of 178 blood donors with two positive anti-HCV ELISA tests were consecutively selected as cases, and 356 anti-HCV negative donors were selected as controls. Blood donors were randomly selected from eight blood centers in Porto Alegre, Southern Brazil, representative of the whole blood donor population. Blood samples were kept at 70°C and defrosted for the first time for the analysis of this report. Tests previously performed in the laboratory using the same real time PCR for HBV DNA had sensitivity for detecting as low as 9 copies/mL. Among 158 blood samples from HBsAg-negative blood donors, five were anti-HBc positive, 53 tested positive for anti-HCV and 105 had anti-HCV negative. The samples analysis was performed in duplicate and all blood samples tested negative for HBV DNA.

Conclusion

The result reflects a very low prevalence of occult hepatitis B in our setting.

Keywords:
hepatitis B
hepatitis B virus
blood donors
seroepidemiologic studies
Full text is only aviable in PDF
References
[1.]
M. Torbenson, D.L. Thomas.
Occult hepatitis B.
Lancet Infect Dis, 2 (2002), pp. 479-486
[2.]
S. Bowden, A. Bartholomeusz, S. Locarnini.
Lamivudine resistant occult HBV: implications for public health?.
J Hepatol, 38 (2003), pp. 526-528
[3.]
C. Bréchot, V. Thiers, D. Kremsdorf, et al.
Persistent Hepatitis B Virus Infection in Subjects Without Hepatitis B Surface Antigen: Clinically Significant or Purely “Occult”?.
Hepatology, 34 (2001), pp. 194-203
[4.]
L.O. Souza, J.R. Pinho, F.J. Carrilho, L.C. da Silva.
Absence of hepatitis B virus DNA in patients with hepatitis C and non-A-E hepatitis in the State of São Paulo, Brazil.
Braz J Med Biol Res, 37 (2004), pp. 1665-1668
[5.]
R.S. Alencar, M.M. Gomes, R. Sitnik, et al.
Low occurrence of occult hepatitis B virus infection and high frequency of hepatitis C virus genotype 3 in hepatocellular carcinoma in Brazil.
Braz J Med Biol Res, 41 (2008), pp. 235-240
[6.]
K. Shetty, M. Hussain, L. Nei, K.R. Reddy, A.S. Lok.
Prevalence and significance of occult hepatitis B in a liver transplant population with chronic hepatitis C.
Liver Transpl, 14 (2008), pp. 534-540
[7.]
A.B.M. Brandão, S.C. Fuchs.
Risk Factors for hepatitis C infecton among blood donors in southern Brazil: a case-control study.
BMC Gastroenterol, 2 (2002), pp. 18
[8.]
A. Kramvis, S. Bukofzer, M.C. Kew.
Comparison of Hepatitis B Virus DNA Extractions from Serum by the QIAamp Blood Kit, GeneReleaser, and the Phenol-Chloroform Method J.
Clin. Microbiol, 34 (1996), pp. 2731-2733
[9.]
S.D. Pas, E. Fries, R.A. de Man, A.D.M.E. Osterhaus, H.G.M. Niester.
Development of a Quantitative Real-Time Detection Assay for Hepatitis B Virus DNA and Comparison with Two Commercial Assays.
J. Clin. Microbiol, 38 (2000), pp. 2897-2901
[10.]
F. Branco, A.A. Mattos, G.P. Coral, et al.
Occult hepatitis B virus infection in patients with chronic liver disease due to hepatitis C virus and hepatocellular carcinoma in Brazil.
Arq Gastroenterol, 44 (2007), pp. 58-63
[11.]
M. Krajden, J.M. Minor, O. Rifkin, L. Comanor.
Effect of Multiple Freeze-Thaw Cycles on Hepatitis B Virus DNA and Hepatitis C Virus RNA Quantification as Measured with Branched-DNA Technology.
J Clin Microbiol, 37 (1999), pp. 1683-1686
[12.]
I. Cacciola, T. Pollicino, G. Squadrito, et al.
Occult hepatitis B virus infection in patients with chronic hepatitis C liver disease.
N Engl J Med, 341 (1999), pp. 22-26
[13.]
R. Fukuda, N. Ishimura, M. Niigaki, et al.
Serologically silent hepatitis B virus co-infection in patients with hepatitis C virus-associated chronic liver disease: clinical and virological significance.
J Med Virol, 58 (1999), pp. 201-207
[14.]
S. Mrani, I. Chemin, K. Menouar, et al.
Occult HBV infection may represent a major risk factor of nonresponse to antiviral therapy of chronic hepatitis C.
J Med Virol, 79 (2007), pp. 1075-1081
[15.]
P. Paterlini, F. Driss, B. Nalpas, et al.
Persistence of hepatitis B and hepatitis C viral genomes in primary liver cancers from HBsAg-negative patients: a study of a low-endemic area.
Hepatology, 17 (1993), pp. 20-29
[16.]
M. Takeuchi, J. Fujimoto, H. Niwamoto, Y. Yamamoto, E. Okamoto.
Frequent detection of hepatitis B virus X-gene DNA in hepatocellular carcinoma and adjacent liver tissue in hepatitis B surface antigennegative patients.
Dig Dig Sci, 42 (1997), pp. 2264-2269
[17.]
D.S. Lee, K. Huh, E.H. Lee, et al.
HCV and HBV coexist in HBsAg-negative patients with HCV viraemia: possibility of coinfection in these patients must be considered in HBV-high endemic area.
J Gastroenterol Hepatol, 12 (1997), pp. 855-861
[18.]
K. Koike, T. Tsutsumi, H. Fujie, Y. Shintani, M. Kyoji.
Molecular mechanism of viral hepatocarcinogenesis.
Oncology, 62 (2002), pp. 29-37
[19.]
M. Satake, R. Taira, H. Yugi, et al.
Infectivity of blood components with low hepatitis B virus DNA levels identified in a lookback program.
Transfusion, 47 (2007), pp. 1197-1205
[20.]
D. Candotti, J.P. Allain.
Transfusion-transmitted hepatitis B virus infection.
J Hepatol, 51 (2009), pp. 798-809
[21.]
A.S.F. Lok, R.H.S. Liang, E.K.W. Chiu, et al.
Reactivation of hepatitis B virus replication in patients receiving cytotoxic therapy. Report of a prospective study.
Gastroenterology, 100 (1999), pp. 182-188
[22.]
J.M. Wu, Y.H. Huang, P.C. Lee, H.C. Lin, S.D. Lee.
Fatal reactivation of hepatitis B virus in a patient who was hepatitis B surface antigen negative and core antibody body positive before receiving chemotherapy for non-Hodgkin lymphoma.
J Clin Gastroenterol, 43 (2009), pp. 496-498
[23.]
B. Bloquel, H. Jeulin, C. Burty, et al.
Occult hepatitis B infection in patients infected with HIV: report of two cases of hepatitis B reactivation and prevalence in a hospital cohort.
J Med Virol, 82 (2010), pp. 206-212
Copyright © 2011. Elsevier Editora Ltda.. All rights reserved
Download PDF
The Brazilian Journal of Infectious Diseases
Article options
Tools