P. Colombatto et al., HEPATITIS-G VIRUS-RNA IN THE SERUM OF PATIENTS WITH ELEVATED GAMMA-GLUTAMYL-TRANSPEPTIDASE AND ALKALINE-PHOSPHATASE - A SPECIFIC LIVER-DISEASE, Journal of viral hepatitis, 3(6), 1996, pp. 301-306
We tested the sera of 67 consecutive patients for hepatitis G virus (H
GV) RNA by reverse transcriptase-polymerase chain reaction (RT-PCR). T
hese patients (42 males and 25 females, median age 35 years, range 13-
64 years) had liver disease of unknown aetiology and were without mark
ers of hepatitis (A-E) viruses or signs of genetically determined, aut
oimmune, alcoholic or drug-induced liver disease. The controls in this
study were 110 patients (50 females and 60 males, median age 45 years
, range 9-65 years) with chronic hepatitis E virus (HBV) infection (19
patients) or hepatitis C virus (HCV) infection (91 patients). Ten of
67 (14.9%) patients with cryptogenic disease were positive for HGV RNA
by at least three separate tests; HGV RNA was also detected in one of
19 (5.3%) hepatitis B surface antigen (HBsAg) carriers and in nine of
91 (16.6%) patients with antibody to HCV. These data suggest that HGV
occurs as frequently in HCV-infected patients as in those with crypto
genic disease. Elevated serum gamma glutamyl transpeptidase (gamma-GT)
(higher than twice the normal value) and alkaline phosphatase levels
were found in eight of 10 (80%) HGV RNA positive patients and in six o
f 57 (10.5%) HGV RNA negative patients (P < 0.0001). five (50%) HGV RN
A positive patients had non-specific inflammatory bile duct lesions. A
statistically significant difference was observed between HGV RNA pos
itive and negative patients with chronic HBV or HCV infections (P < 0.
029). Therefore, the spectrum of liver disease associated with HGV is
wide, but a characteristic lesion of the bile duct leading to elevatio
n of cholestatic enzymes might be specific for this virus.