HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Clinical presentation of GB-C virus infection in drug abusers with chronic hepatitis C.

AbstractBACKGROUND/AIMS:
Recently, the hepatitis GB-C virus (GBV-C) has been identified as another virus potentially causing chronic hepatitis. Although high rates of coinfection are emerging in drug addicts with chronic hepatitis C virus infection, no detailed data on clinical presentation are available. Therefore, co-infection was sought in hepatitis C virus patients to determine the impact of GB-C virus on clinical presentation.
METHODS:
GBV-C was determined by nested reverse transcriptase-polymerase chain reaction in serum of 70 HIV negative intravenous drug abusers with chronic hepatitis C. Biochemical, histological and virological parameters were compared between patients with or without GBV-C coinfection.
RESULTS:
Hepatitis C virus and GBV-C coinfection was found in 18 of 70 (25.7%) patients. Cases with coinfection were younger and had shorter duration of disease (31.4+/-6.2 vs. 35.3+/-7.3 (p=0.09) and 9.9+/-6.8 vs. 12.9+/-7.7 (p=0.17) years) than those without coinfection. Neither hepatitis C virus genotype distribution and HCV RNA levels nor serum liver function tests, titers of immunoglobulins or autoantibodies differed between the two groups. Histologically, chronic active hepatitis (16.7 vs. 46.4%, p=0.07), fibrosis (8.3% vs. 21.4%, p=0.3), and cirrhosis (0% vs. 8.2%, p=0.31) were less prevalent in coinfected patients. After interferon treatment, 5/6 coinfected and 11/19 patients with hepatitis C virus infection alone had cleared HCV RNA and 4/6 lost GBV-C RNA from serum. The two patients with GBV-C/HCV infection who persistently cleared hepatitis C virus but not GBV-C from serum had normal transaminases during follow-up despite persistence of GBV-C.
CONCLUSIONS:
Coinfection of chronic hepatitis C patients with GBV-C does not lead to a significant change in clinical presentation, severity of liver disease, hepatitis C viremia, or response to interferon treatment.
AuthorsT Goeser, S Seipp, R Wahl, H M Müller, W Stremmel, L Theilmann
JournalJournal of hepatology (J Hepatol) Vol. 26 Issue 3 Pg. 498-502 (Mar 1997) ISSN: 0168-8278 [Print] Netherlands
PMID9075655 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Antinuclear
  • Antiviral Agents
  • DNA Primers
  • Hepatitis C Antibodies
  • Interferon-alpha
  • RNA, Viral
  • Alanine Transaminase
Topics
  • Adult
  • Alanine Transaminase (blood)
  • Antibodies, Antinuclear (analysis)
  • Antiviral Agents (therapeutic use)
  • Chronic Disease
  • DNA Primers (chemistry)
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Flaviviridae (genetics, immunology)
  • Follow-Up Studies
  • Genotype
  • Hepacivirus (genetics, immunology)
  • Hepatitis C (complications, pathology, therapy)
  • Hepatitis C Antibodies (analysis)
  • Hepatitis, Viral, Human (complications, pathology, therapy)
  • Humans
  • Interferon-alpha (therapeutic use)
  • Male
  • Polymerase Chain Reaction
  • RNA, Viral (analysis)
  • Retrospective Studies
  • Substance Abuse, Intravenous (blood, complications, virology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: