We studied the prevalence of the hepatitis C virus (HCV), human immuno
deficiency virus (HIV) and GB virus C or hepatitis G virus (GBV-C/HGV)
, and characteristics of infections in Japanese haemophilia patients.
Haemophilia patients were highly infected with HCV (88.2%) because of
frequent use of unheated blood concentrates. Analysis for HCV genotype
s revealed characteristics of HCV infection in haemophilia patients. J
apanese haemophilia patients were highly infected with rare genotypes
in Japan: genotype la (26.5%), genotype 3 (14.5%) and genotype 4 (2.4%
). HIV infection was observed in 32.3% of haemophilia patients. HCV qu
asispecies (clones) and direct sequencing were investigated in patient
s with a single HCV genotype in the hypervariable region 1 of HCV, whi
ch resulted in a high degree of diversity. This indicates that even a
single genotype of HCV might have multiple origins. GBV-C/HGV infectio
n was noted in 20.9% of Japanese haemophilia patients. Over 40 haemoph
ilia patients with chronic hepatitis C have been treated with interfer
on alpha for 6 months at total doses of 480-720 million units. About 3
8% showed clearance of HCV RNA from serum. Six patients with HIV infec
tion were included in the study and they did not show eradication of H
CV from the serum. This might derive from that they had high serum HCV
RNA titers and genotype la or Ib. Histologic assessment was performed
in 36 haemophilia patients with HCV. No case showed a histologically
normal liver. Hepatic fibrosis in the biopsy specimens was classified
into five stages of fibrosis and compared with serum hepatic fibrosis
markers. Serum hyaluronic acid mostly correlated with hepatic fibrosis
(r = 0.78, P < 0.0001) followed by type IV collagen (r = 0.38, P < 0.
05). This suggests that estimation of serum fibrosis markers might be
substituted for liver biopsy in haemophilia patients.