Jl. Lozano et al., CORRELATION BETWEEN HEPATITIS-B VIREMIA AND THE CLINICAL AND HISTOLOGICAL ACTIVITY OF CHRONIC DELTA-HEPATITIS, Medical microbiology and immunology, 183(3), 1994, pp. 159-167
To analyze the serological, clinical and histological significance of
hepatitis B virus (HBV) replication among a group of patients with chr
onic delta hepatitis (CDH), wt have studied the clinical and the histo
logical activity in 49 patients with CDH. The HBV-DNA was analyzed by
dot-blot and polymerase chain reaction (PCR). Concomitant infection wi
th hepatitis C virus (HCV) was analyzed by reverse transcriptase (RT)-
PCR, HDV replication by dot-blot, and human immunodeficiency virus (HI
V) infection by enzyme-linked immunosorbent assay. The subjects were d
ivided into three groups according to HBV-DNA status: group I: 14 pati
ents HBV-DNA dot-blot positive; group II: 29 patients HBV-DNA positive
only by PCR, and group III: 6 patients HBV-DNA negative by dot-blot a
nd PCR. We have found HBV-DNA by dot-blot in 28.5% of patients, and by
PCR in 87.7%. Also 22 patients were anti-HCV positive (86.3% had HCV-
RNA by RT-PCR). The first group (HBV-DNA dot-blot positive) had signif
icantly higher serum alanine aminotransferase (ALT) and aspartate amin
otransferase (AST) than those in the second and third groups. Likewise
, serum ALT and AST were significantly higher in the second group (HBV
-DNA positive by PCR) than in those of the third group. Histological i
nflammatory activity was significantly higher in the group of patients
with HBV-DNA detectable by dot-blot. The prevalence of serum HDV-RNA
and IgM anti-HDV were similar in the three groups. These results were
similar in the anti-HCV-positive and -negative patients. In conclusion
, these data suggest that: (1) persistence of HBV replication is a maj
or determinant of severe liver damage in chronic delta hepatitis, and
(2) HCV and HIV infections do not influence the natural history of CDH
.