The Role of Liver Fibrosis Assessment in the Management of Patients with Chronic Hepatitis B Infection: Lessons Learned from a Single Centre Experience

Author:

Malik Raza1ORCID,Kennedy Patrick2,Suri Deepak3,Brown Ashley4,Goldin Rob4,Main Janice4,Thomas Howard4,Thursz Mark4

Affiliation:

1. Liver Center, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, 110 Francis Street, Suite 4A, Boston, MA 02215, USA

2. Institute of Cell and Molecular Science, Barts and The London School of Medicine, 4 Newark Sreet, London E1 4AT, UK

3. Hepatology Unit, Division of Gastroenterology, University College London Hospital, 235 Euston Road, London NW1 2BU, UK

4. Hepatology Unit, Department of Medicine, 10th Floor, St Mary's Hospital, Imperial College London, Praed Street, London, W2 1NY, UK

Abstract

Background & Aims. Assess the clinical utility of the Prati criteria and normal ALT (<40 IU/L) in a cohort of patients with chronic hepatitis B infection (CHB). Methods. Serology, radiology, and histology were obtained in 140 patients with CHB. Results. HBeAg+ group: 7 patients (7/56−12% HBeAg+ group) misclassified as “immunotolerant”, with HBV DNA > 6 log copies/ml and normal ALT, who in fact had moderate/severe fibrosis on liver biopsy. HBeAg group: 10 patients with normal ALT and moderate/severe fibrosis on liver biopsy; 4 of these patients had >3 log copies/ml HBV DNA levels and 6 patients misclassified as “inactive carriers” with negative HBV DNA levels normal ALT and moderate/severe fibrosis (6/84−7% HBeAg group). Two male HBeAg+ and three male HBeAg- patients with ALT between 20 and 30 IU/L and moderate/severe fibrosis on liver biopsy would have been further mischaracterised using the Prati criteria for normal ALT. Age and ethnic group were more important predictors of moderate/severe fibrosis in multivariate analysis. Conclusion. HBeAg status, age, ethnic origin with longitudinal assessment of LFTs and viral load should be studied in patients with “normal ALT” at the upper end of normal range (ALT 20–40 IU/L) to appropriately classify patients and identify patients for liver fibrosis assessment to inform treatment decisions.

Publisher

Hindawi Limited

Subject

Hepatology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The TNF-α -308 Promoter Gene Polymorphism and Chronic HBV Infection;Hepatitis Research and Treatment;2012-10-24

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