scholarly journals Quantitative serum HBV DNA levels during different stages of chronic hepatitis B infection

Hepatology ◽  
2002 ◽  
Vol 36 (6) ◽  
pp. 1408-1415 ◽  
Author(s):  
Chi-Jen Chu ◽  
Munira Hussain ◽  
Anna S. F. Lok
Complexity ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-19
Author(s):  
Bo Wu ◽  
Jianwen Jia

In this paper, a stochastic delayed model is constructed to describe chronic hepatitis B infection with HBV DNA-containing capsids. At first, the existence and uniqueness of the global positive solution are obtained. Secondly, the sufficient conditions are derived that the solution of the stochastic system fluctuates around the disease-free equilibrium E0 and the endemic equilibrium E∗. In the end, some numerical simulations are implemented to support our analytical results.


2010 ◽  
Vol 7 (1) ◽  
pp. 228 ◽  
Author(s):  
Ashraf Mohamadkhani ◽  
Kourosh Sayemiri ◽  
Reza Ghanbari ◽  
Elham Elahi ◽  
Hossein Poustchi ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Raza Malik ◽  
Patrick Kennedy ◽  
Deepak Suri ◽  
Ashley Brown ◽  
Rob Goldin ◽  
...  

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.


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