Title of article :
The presence of steatosis and elevation of alanine aminotransferase levels are associated with fibrosis progression in chronic hepatitis C with non-response to interferon therapy
Author/Authors :
Masayuki Kurosaki، نويسنده , , Kotaro Matsunaga، نويسنده , , Itsuko Hirayama، نويسنده , , Tomohiro Tanaka، نويسنده , , Mitsuaki Sato، نويسنده , , Nobutoshi Komatsu، نويسنده , , Naoki Umeda، نويسنده , , Takanori Hosokawa، نويسنده , , Ken Ueda، نويسنده , , Kaoru Tsuchiya، نويسنده , , Hiroyuki Nakanishi، نويسنده , , Jun Itakura، نويسنده , , Yasuhiro Asahina، نويسنده , , Shozo Miyake، نويسنده , , Nobuyuki Enomoto، نويسنده , , Namiki Iz، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
7
From page :
736
To page :
742
Abstract :
Background/Aims Interferon (IFN) therapy leads to regression of hepatic fibrosis in chronic hepatitis C patients who achieve a sustained virologic response (SVR), while the beneficial effect is limited in those who fail to do so. The aim of the present study was to define factors associated with progression of fibrosis in patients who do not achieve a SVR. Methods Fibrosis staging scores were compared between paired liver biopsies before and after IFN in 97 chronic hepatitis C patients who failed therapy. The mean interval between biopsies was 5.9 years. Factors associated with progression of fibrosis were analyzed. Results Fibrosis progressed in 23%, remained unchanged in 47% and regressed in 29%. Steatosis and a high average alanine aminotransferase (ALT) between biopsies were independent factors for progression of fibrosis with risk ratios of 5.53 and 4.48, respectively. Incidence and yearly rate of progression of fibrosis was 64% and 0.22 ± 0.29 fibrosis units per year in those with both risk factors compared to 8% and −0.04 ± 0.17 fibrosis units per year in those negative for both factors. Conclusions Hepatic steatosis and elevated ALT levels are risk factors for progression of fibrosis in chronic hepatitis C patients who fail to achieve a SVR to IFN therapy and therefore may be therapeutic targets to halt the potentially progressive disease.
Keywords :
Steatosis , ALT , fibrosis
Journal title :
Journal of Hepatology
Serial Year :
2008
Journal title :
Journal of Hepatology
Record number :
581585
Link To Document :
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