Volume 38, Issue 2 pp. 518-526
Original Article
Free Access

A simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis C

Chun-Tao Wai

Chun-Tao Wai

Division of Gastroenterology, University of Michigan Medical School, Ann Arbor, MI

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Joel K. Greenson

Joel K. Greenson

Department of Pathology, University of Michigan Medical School, Ann Arbor, MI

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Robert J. Fontana

Robert J. Fontana

Division of Gastroenterology, University of Michigan Medical School, Ann Arbor, MI

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John D. Kalbfleisch

John D. Kalbfleisch

Department of Biostatistics, University of Michigan Medical School, Ann Arbor, MI

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Jorge A. Marrero

Jorge A. Marrero

Division of Gastroenterology, University of Michigan Medical School, Ann Arbor, MI

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Hari S. Conjeevaram

Hari S. Conjeevaram

Division of Gastroenterology, University of Michigan Medical School, Ann Arbor, MI

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Anna S.-F. Lok M.D.

Corresponding Author

Anna S.-F. Lok M.D.

Division of Gastroenterology, University of Michigan Medical School, Ann Arbor, MI

Division of Gastroenterology, University of Michigan Medical Center, 3912 Taubman Center, Box 0362, Ann Arbor, MI 48109-0362. fax: 734-936-7392===Search for more papers by this author
First published: 30 December 2003
Citations: 3,307

Abstract

Information on the stage of liver fibrosis is essential in managing chronic hepatitis C (CHC) patients. However, most models for predicting liver fibrosis are complicated and separate formulas are needed to predict significant fibrosis and cirrhosis. The aim of our study was to construct one simple model consisting of routine laboratory data to predict both significant fibrosis and cirrhosis among patients with CHC. Consecutive treatment-naive CHC patients who underwent liver biopsy over a 25-month period were divided into 2 sequential cohorts: training set (n = 192) and validation set (n = 78). The best model for predicting both significant fibrosis (Ishak score ≥ 3) and cirrhosis in the training set included platelets, aspartate aminotransferase (AST), and alkaline phosphatase with an area under ROC curves (AUC) of 0.82 and 0.92, respectively. A novel index, AST to platelet ratio index (APRI), was developed to amplify the opposing effects of liver fibrosis on AST and platelet count. The AUC of APRI for predicting significant fibrosis and cirrhosis were 0.80 and 0.89, respectively, in the training set. Using optimized cut-off values, significant fibrosis could be predicted accurately in 51% and cirrhosis in 81% of patients. The AUC of APRI for predicting significant fibrosis and cirrhosis in the validation set were 0.88 and 0.94, respectively. In conclusion, our study showed that a simple index using readily available laboratory results can identify CHC patients with significant fibrosis and cirrhosis with a high degree of accuracy. Application of this index may decrease the need for staging liver biopsy specimens among CHC patients.

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