Clinicopathological features and genotype distribution in patients with hepatitis C virus chronic liver disease
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  • 作者:Rachel Abraham (1)
    Banumathi Ramakrishna (1)
    Avinash Balekuduru (2)
    Hubert Darius J. Daniel (3)
    Priya Abraham (3)
    C. Eapen Eapen (2)
    George Kurian (2)
  • 关键词:Fibrosis ; Genotype ; Hepatitis C ; Histological activity ; Steatosis
  • 刊名:Indian Journal of Gastroenterology
  • 出版年:2009
  • 出版时间:March 2009
  • 年:2009
  • 卷:28
  • 期:2
  • 页码:53-58
  • 全文大小:581KB
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  • 作者单位:Rachel Abraham (1)
    Banumathi Ramakrishna (1)
    Avinash Balekuduru (2)
    Hubert Darius J. Daniel (3)
    Priya Abraham (3)
    C. Eapen Eapen (2)
    George Kurian (2)

    1. Department of Pathology, Christian Medical College, Vellore, India
    2. Department of Gastrointestinal Sciences, Christian Medical College, Vellore, India
    3. Department of Clinical Virology, Christian Medical College, Vellore, India
文摘
Background and Objective Hepatitis C virus (HCV) genotype influences the severity of disease and response to therapy. This retrospective study examined the clinical and histological features and the genotype distribution in biopsied patients with HCV related chronic liver disease. Methods Of 105 biopsies from patients with HCV infection, 96 from patients with chronic liver disease were reviewed. The Ishak scoring system was used for histological analysis. Results Genotype 3 was most common accounting for 77.1%, and genotype 1 for 9.4% of cases. There was no significant association of transaminase levels, viral load or necro-inflammatory activity score with genotype. A severe degree of fibrosis was seen in 77.8% cases of genotype 1 and in 63.5% of genotype 3 (p=0.76). Variable degrees of steatosis were noted in 68.8% of cases. However, severe steatosis was noted only in genotype 3 (7 cases). Serum transaminase levels did not correlate with either histological activity (p=0.43) or degree of fibrosis (p=0.72). Severe fibrosis / cirrhosis was seen in 74.24% of patients above 40 years of age as compared to 33.3% of patients below 40 years (p=0.001). The frequency of Mallory hyaline was significantly different between genotypes 1 and 3 infection (P<0.001). Conclusions This study confirms the preponderance of genotype 3 in Indian patients with HCV related chronic liver disease. Severe steatosis was seen only in genotype 3 and Mallory hyaline was very common in genotype 1. The small numbers of patients in non genotype 3 could be a reason for the apparent lack of histological differences between different HCV genotypes. Severe fibrosis seen in older age groups confirms that HCV infection is progressive and major acceleration of the disease process occurs after 40 years of age.

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