Fibrosis Progression in Chronic Hepatitis C: Morphometric Image Analysis in the HALT-C Trial

被引:55
作者
Goodman, Zachary D. [1 ,2 ]
Stoddard, Anne M. [3 ]
Bonkovsky, Herbert L. [4 ,5 ,6 ]
Fontana, Robert J. [7 ]
Ghany, Marc G. [8 ]
Morgan, Timothy R. [10 ,11 ]
Wright, Elizabeth C. [9 ]
Brunt, Elizabeth M. [12 ]
Kleiner, David E. [13 ]
Shiffmann, Mitchell L. [14 ]
Everson, Gregory T. [15 ]
Lindsay, Karen L. [16 ]
Dienstag, Jules L. [17 ,18 ]
Morishima, Chihiro [19 ]
机构
[1] Armed Forces Inst Pathol, Div Hepat Pathol, Washington, DC 20306 USA
[2] Vet Adm Special Reference Lab Pathol, Washington, DC USA
[3] New England Res Inst, Watertown, MA 02172 USA
[4] Univ Connecticut, Ctr Hlth, Dept Med, Farmington, CT USA
[5] Univ Connecticut, Ctr Hlth, Dept Mol & Struct Biol, Farmington, CT USA
[6] Univ Connecticut, Ctr Hlth, Liver Biliary Pancreat Ctr, Farmington, CT USA
[7] Univ Michigan, Med Ctr, Dept Internal Med, Ann Arbor, MI 48109 USA
[8] NIDDK, Liver Dis Branch, NIH, Dept Hlth & Human Serv, Bethesda, MD USA
[9] NIDDK, Off Director, NIH, Dept Hlth & Human Serv, Bethesda, MD USA
[10] Univ Calif Irvine, Div Gastroenterol, Irvine, CA USA
[11] VA Long Beach Healthcare Syst, Gastroenterol Serv, Long Beach, CA USA
[12] Washington Univ, Dept Pathol & Immunol, St Louis, MO USA
[13] NCI, Pathol Lab, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[14] Virginia Commonwealth Univ, Med Ctr, Hepatol Sect, Richmond, VA USA
[15] Univ Colorado Denver, Dept Internal Med, Div Gastroenterol & Hepatol, Sect Hepatol, Aurora, CO USA
[16] Univ So Calif, Keck Sch Med, Div Gastrointestinal & Liver Dis, Los Angeles, CA 90033 USA
[17] Massachusetts Gen Hosp, Med Serv, Gastrointestinal Unit, Boston, MA USA
[18] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[19] Univ Washington, Dept Lab Med, Div Virol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
LIVER-BIOPSY; INTERFERON; THERAPY; CIRRHOSIS;
D O I
10.1002/hep.23211
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Computer-assisted morphometry can provide precise measurement of hepatic fibrosis on a continuous scale. Previous morphometric studies of large cohorts of patients with treatment refractory chronic hepatitis C have shown a mean increase in fibrosis of 30% to 58% in 1 year. The aim of the present study was to quantify fibrosis progression in biopsy specimens obtained over 1.5 to 44 5 years from three groups of patients with baseline bridging fibrosis or cirrhosis (Ishak stages 3-6) enrolled in the Hepatitis C Antiviral Long-term Treatment Against Cirrhosis Trial. The main group of 346 lead-in nonresponders (viremic after 24 weeks of peginterferon-ribavirin therapy) had a mean fibrosis increase of 61% over pretreatment baseline after 2 years and 80% after 4 years. In contrast, the 78 breakthrough/relapse patients (undetectable serum hepatitis C virus RNA after 24 weeks of peginterferon-ribavirin and receiving antiviral therapy for 48 weeks) showed a mean increase in fibrosis of 48% when biopsied 36 months from pretreatment baseline but no further increase at 60 months. Finally, the 111 express patients with baseline biopsies following unsuccessful peginterferon-ribavirin outside the trial had significantly more baseline fibrosis than the others but an increase of only 21% after 21 months and a slight decrease at 45 months. Maintenance therapy with low-dose peginterferon had no effect on fibrosis changes in any of the groups. Conclusion: Morphometry demonstrated complex, nonlinear changes in fibrosis over time in this heterogeneous cohort of patients with interferon-refractory chronic hepatitis C. (HEPATOLOGY 2009;50:1738-1749.)
引用
收藏
页码:1738 / 1749
页数:12
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