N. Campo et al., Hepatitis G virus infection in intravenous drug users with or without human immunodeficiency virus infection, HEP-GASTRO, 47(35), 2000, pp. 1385-1388
Background/Aims: To evaluate the HGV infection prevalence in a group of int
ravenous drug users with or without human immunodeficiency virus coinfectio
n.
Methodology: We studied 57 patients (48 males and 9 females) who were eithe
r previous or still ongoing intravenous drug users. Thirty-seven patients w
ere HTV+ve, 55 patients were anti-HCV+ve and 3 patients were HBsAg chronic
carriers. Patient sera were tested for HGV-RNA, anti-E2, qualitative and qu
antitative HCV-RNA as well as for HCV genotypes. Moreover, the ALT level wa
s checked in the serum sample of each patient.
Results:We found a high prevalence (35/57; 61.4%) of HGV infection in our p
atients. HGV-RNA was detected in 16 out of the 57 intravenous drug users (2
8%). In particular HGV-RNA was positive in 12 out of the 37 HIV+ve patients
(32.4%) and in 4 out of the 20 HIV-ve patients (20%). Anti-E2 were detecte
d in 19 out of the 57 patients (33.3%) with greater prevalence among HIV-ve
subjects (12/20; 60%) compared to HIV+ve group (7/37; 18.9%). This resulti
ng difference was statistically significant (P<0.05). All HGV-RNA+ve/anti-E
2+ve patients were anti-HCV/HCV-RNA+ve and none of our patients were anti-E
2+ve/HGV-RNA+ve at the same time. Significant differences were not found be
tween HGV-RNA+ve and HGV-RNA-ve patients as far as clinical and virological
data are concerned.
Conclusions: The prevalence of HGV infection in intravenous drug users prov
ed to be high especially in the HIV+ve group. Moreover HGV was associated w
ith HCV in all our cases. The actual clinical impact of HGV infection remai
ns unclear since HGV does not seems to influence the biochemical, virologic
al or histological alterations caused by HCV infection.