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   <subfield code="a">Defining Virologic Relapse in Chronic Hepatitis B</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kyung Kim, Dong Sinn, Won Yun, Hyun Cho, Yun Lee, Geum-Youn Gwak, Moon Choi, Joon Lee, Kwang Koh, Byung Yoo, Seung Paik]</subfield>
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   <subfield code="a">Background and Aims: Different definitions of virologic relapse (VR) are being used. One way of defining VR is &quot;reappearance of HBV DNA in the serum,” while another definition is an &quot;increase in HBV DNA level greater than 1 log in two determinations at least 4 weeks apart.” The aim of this study was to see the effectiveness of these two definitions Methods: Forty-five HBeAg-positive chronic hepatitis B patients with a virologic response [negative PCR (&lt;12IU/ml)] who had discontinued therapy were analyzed retrospectively for VR, HBeAg reversion and biochemical flare. Results: HBV DNA reappeared in the serum (≥12IU/ml) of all 45 patients (100%). An increase in HBV DNA level greater than 1 log in two determinations at least 4weeks apart was identified in 20 of 25 patients (80%). Biochemical flare and HBeAg reversion were observed in 18 (40%) and 14 (31%) patients, respectively. Peak off-therapy HBV DNA level was significantly associated with biochemical flare (r=0.758, P&lt;0.001) and HBeAg reversion (r=0.645, P&lt;0.001). Two patients with high initial off-therapy HBV DNA levels (≥4.0 log10 IU/ml) were reassessed at 4weeks, and both experienced a biochemical flare and HBeAg reversion. Two patients had an increase in HBV DNA level greater than 1 log at a very low level (1 log to 2 or 3 log), but did not experience biochemical flare or HBeAg reversion during follow-up. Conclusions: Reappearance of HBV DNA was universal when sensitive HBV DNA assay was used. Waiting 4weeks to confirm VR may be harmful for patients with a high HBV DNA level, and was ineffective to indicate re-therapy for patients with increase in HBV DNA at a very low level. There is a need for improved and standardized definitions of VR.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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   <subfield code="a">Chronic hepatitis B</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Polymerase chain reaction</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Virologic relapse</subfield>
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   <subfield code="a">Cutoff values</subfield>
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   <subfield code="a">Biochemical flare</subfield>
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   <subfield code="a">CHB : Chronic hepatitis B</subfield>
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   <subfield code="a">NA : Nucleoside/nucleotide analogues</subfield>
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   <subfield code="a">HBV : Hepatitis B virus</subfield>
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   <subfield code="a">PCR : Polymerase chain reaction</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">ALT : Alanine aminotransferase</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HBeAg : Hepatitis B e-antigen</subfield>
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   <subfield code="a">VR : Virologic relapse</subfield>
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   <subfield code="a">Kim</subfield>
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   <subfield code="u">Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Gangnam-gu, 135-710, Seoul, Korea</subfield>
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   <subfield code="a">Yun</subfield>
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   <subfield code="u">Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Gangnam-gu, 135-710, Seoul, Korea</subfield>
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   <subfield code="t">Digestive Diseases and Sciences</subfield>
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