2015
DOI: 10.4103/0255-0857.148827
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The predictive value of early indicators for HBeAg seroconversion in HBeAg-positive chronic hepatitis B patients with Telbivudine treatment for 104 weeks

Abstract: Good efficacy of long-term LDT treatment in biological and virological response and its advantage in serological response was confirmed again in our study. The HBeAg level at week 24 showed significant value in prediction for HBeAg seroconversion at week 104 compared to other serological markers in the early period.

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Cited by 3 publications
(2 citation statements)
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“…In this study, we found that HBeAg titer < 0.8 lg PEIU/mL combined with its declined value > 0.84 lg PEIU/mL at 12-wk predicted VR after 96-wk LAM and ADV optimized therapy with a sensitivity, specificity, PPV, NPV of 71%, 91%, 91% and 71%, respectively, and accompanied with an AUROC of 0.812. In addition, although some studies indicated that the on-treatment HBeAg level or declined value at 24-wk was a predictor for NAs treatment response[9,12], the sample size was small or HBeAg was detected using a semi-quantitative method which cannot accurately quantify HBeAg level, thus limited the validity of the prediction. For example, Zhang et al[12] detected serum HBeAg semi-quantitatively and found that the on-treatment declined value of HBeAg (> 65%) at 24-wk was the best predictor for treatment response (HBeAg seroconversion and accompanied by undetectable serum HBV DNA) after 96-wk ETV therapy, and the PPV, NPV, AUROC was 83.3%, 93.6% and 0.885, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…In this study, we found that HBeAg titer < 0.8 lg PEIU/mL combined with its declined value > 0.84 lg PEIU/mL at 12-wk predicted VR after 96-wk LAM and ADV optimized therapy with a sensitivity, specificity, PPV, NPV of 71%, 91%, 91% and 71%, respectively, and accompanied with an AUROC of 0.812. In addition, although some studies indicated that the on-treatment HBeAg level or declined value at 24-wk was a predictor for NAs treatment response[9,12], the sample size was small or HBeAg was detected using a semi-quantitative method which cannot accurately quantify HBeAg level, thus limited the validity of the prediction. For example, Zhang et al[12] detected serum HBeAg semi-quantitatively and found that the on-treatment declined value of HBeAg (> 65%) at 24-wk was the best predictor for treatment response (HBeAg seroconversion and accompanied by undetectable serum HBV DNA) after 96-wk ETV therapy, and the PPV, NPV, AUROC was 83.3%, 93.6% and 0.885, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies have identified the association between pretreatment alanine aminotransferase (ALT), HBV DNA, hepatitis B surface antigen (HBsAg), quantitative HBeAg (qHBeAg), platelets (PLT), gamma-glutamyl transpeptidase (GGT), and quantitative anti-hepatitis B core antibody (qAnti-HBc) levels with HBeAg seroconversion (Chi et al, 2015;Fan et al, 2016;Fried et al, 2008;Li et al, 2014;Wang et al, 2015a;Hou et al, 2015;Huang et al, 2015). Although several clinically useful models have been established for assessing HBeAg seroconversion, they require complex calculations or concentrate on the response to interferon (Wang et al, 2015b;Lee et al, 2014;Lee et al, 2011;Liu et al, 2015).…”
Section: Introductionmentioning
confidence: 99%