Steatosis
and Long-term Liver Disease Progression after Antiviral Therapy Steatosis
(fatty liver) is recognized as a cofactor influencing the presence and progression
of fibrosis in patients with
chronic hepatitis C. Studies have shown that antiviral therapy can reduce fibrosis
progression, especially in patients who achieve sustained
virological response (SVR); treatment also appears to provide some histological
benefit for nonresponders and relapsers. To
assess whether steatosis might affect long-term histological outcomes of antiviral
therapy, researchers looked at paired liver
biopsy results from 161 consecutive patients in Taiwan treated with conventional
interferon alfa-2b plus ribavirin. Biopsies samples were taken an average
of 29 months apart; about half the participants had genotype 1 HCV, and about
half had genotype 2. Results
Variables associated with baseline steatosis were:
-
higher body mass index (25 or higher; P = 0.002); - higher fibrosis stage
(2 or higher; P = 0.019).
Evaluation of paired biopsies showed no difference in the distribution of steatosis
evolution between patients with and without SVR (P = 0.374).
Neither the presence nor the severity of steatosis were associated with SVR.
Among patients achieving SVR, there was a significant difference in fibrosis progression
between those with grade 0 or 1 steatosis and those with grade 2 or 3 steatosis
at the post-treatment biopsy (P = 0.041).
Changes in histological activity index scores did not differ based on steatosis
grade (P = 0.740).
Stepwise logistic regression analysis showed that SVR and grade 0 or 1 post-treatment
steatosis were independently associated with fibrosis regression.
Conclusion The
authors concluded that, "In patients with chronic hepatitis C, steatosis
not only correlates with advanced fibrosis at baseline but also affects fibrosis
regression after antiviral therapy." 7/28/06 Reference C-H
Hung, F-Y Kuo, J-H Wang, and others. Impact of steatosis on long-term histological
outcome in chronic hepatitis C after antiviral therapy. Antiviral Therapy
11(4): 483-489. 2006.
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