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a Second
Department of Internal Medicine, Faculty of Medicine, Tokyo Medical and
Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, Japan, 113-8519, b Department of Gastroenterology
and Hepatology, Musashino Red Cross Hospital, 1-26-1 Kyonan-cho,
Musashino city, Tokyo, Japan, 180-8610, c Department of Internal Medicine, Tsuchiura Kyodo
General Hospital, 14-7 Manabe-shinmachi, Tsuchiura city, Ibaraki,
Japan, 300-0053, d Second
Department of Internal Medicine, Yokosuka Kyosai General Hospital, 22-7 Yonegahama-dori, Yokosuka city, Kanagawa, Japan, 238-0011, e Department of Health
Science, Faculty of Medicine, Tokyo Medical and Dental University,
1-5-45 Yushima, Bunkyo-ku, Tokyo, Japan, 113-8519
Correspondence to: Dr N Enomoto. nenomoto.med2{at}med.tmd.ac.jp
Accepted for publication 12 December 2000
BACKGROUND AND
AIMS
Chronic hepatitis C is a slowly progressive
disease and eventually causes hepatocellular carcinoma in many
patients. Although interferon (IFN) therapy has been used for viral
eradication, its success rate is only about 30%. In patients in whom
it has failed (non-responders), there are several patterns of serum
alanine aminotransferase (ALT) values, and detection of serum HCV-RNA during and after IFN therapy and improved long term prognosis were
reported in patients whose serum ALT values were normalised by IFN
therapy even if HCV viraemia persisted. The present study sought to
clarify the virological characteristics contributing to these differences.
METHODS
Complete or
partial length dominant sequences of hepatitis C virus genotype 1b
(HCV-1b) were determined by direct sequencing. Firstly, the complete
sequences of HCV-1b genomes were determined in six non-responders;
three showed normalisation of serum ALT values during IFN-
therapy
and the other three did not. Subsequently, the amino acid residues that
were different in the two groups were further analysed retrospectively
in another 82 patients.
RESULTS
Comparison of
the sequences suggested an association between amino acids 2154-2172
of HCV-1b and serum ALT normalisation. A retrospective analysis of 82 patients revealed that the number of amino acid substitutions in this
region was the only statistically significant variable associated with
ALT normalisation (odds ratio 31.0; 95% confidence interval 5.0-286)
in multivariate analyses.
CONCLUSIONS
A HCV
genomic region that correlates with the ALT response to IFN therapy
appears to be present in virologically IFN ineffective patients.
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