4.3 Article

Low liver stiffness among cirrhotic patients with hepatitis B after prolonged treatment with nucleoside analogs

期刊

SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
卷 46, 期 6, 页码 760-766

出版社

INFORMA HEALTHCARE
DOI: 10.3109/00365521.2011.565068

关键词

Cirrhosis; hepatitis B; nucleoside analogs; transient elastography

资金

  1. A.P. Moeller Foundation for the Advancement of Medical Science
  2. Anna and Preben Simonsens Foundation
  3. Roche A/S
  4. MSD Pharmaceuticals
  5. Gilead Science
  6. Bristol-Myers Squibb
  7. Swedish Orphan A/S
  8. Schering-Plough A/S

向作者/读者索取更多资源

Objective. Case reports and short-term clinical trials have suggested that treatment for chronic hepatitis B (CHB) may lead to improvement of cirrhosis. The aim of the present study was to measure liver stiffness in patients diagnosed with advanced fibrosis or cirrhosis prior to prolonged treatment with nucleoside or nucleotide analogs (NUCs) for CHB. Materials and methods. Patients with CHB and advanced fibrosis or cirrhosis prior to treatment with NUCs for at least 1 year were offered inclusion in the study. We measured liver stiffness using transient elastography (TE) at follow-up. TE cut-off levels to Metavir classification for fibrosis stage F2, F3 and F4 were >= a parts per thousand yen7.2 kPa, >= a parts per thousand yen8.1, and >= a parts per thousand yen11.0 kPa, respectively. Results. Among 66 patients with a successful TE examination at follow-up, 53 patients (80%) had cirrhosis and 13 had (20%) advanced fibrosis (F3) prior to treatment. Median treatment duration was 50.5 months. Among patients with cirrhosis prior to treatment, 26 (49%) had liver stiffness below 11.0 kPa at follow-up, suggesting regression of cirrhosis. Among patients with advanced fibrosis (F3) prior to treatment, 10 (77%) had liver stiffness below 8.1 kPa after treatment, suggesting improvement of fibrosis. Conclusion. Transient elastography examinations demonstrate that prolonged treatment with NUCs in patients with CHB results in low liver stiffness, suggesting regression of fibrosis in a majority of patients with advanced fibrosis or cirrhosis.

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