Usefulness of quantitative HBsAg in outcome prediction of acute hepatitis B
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- Takahashi Hideaki
- Department of Internal Medicine, Division of Gastroenterology and Hepatology, St. Marianna University, School of Medicine
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- Okuse Chiaki
- Department of Internal Medicine, Division of Gastroenterology and Hepatology, St. Marianna University, School of Medicine
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- Yotsuyanagi Hiroshi
- Department of Internal Medicine, Division of Infectious Diseases, Faculty of Medicine, University of Tokyo
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- Yamada Norie
- Department of Internal Medicine, Division of Gastroenterology and Hepatology, St. Marianna University, School of Medicine Department of Internal Medicine, Center for Liver Disease, Seizankai Kiyokawa Hospital
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- Yasuda Kiyomi
- Department of Internal Medicine, Center for Liver Disease, Seizankai Kiyokawa Hospital
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- Nagase Yoshihiko
- Department of Internal Medicine, Division of Gastroenterology and Hepatology, St. Marianna University, School of Medicine
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- Suzuki Michihiro
- Department of Internal Medicine, Division of Gastroenterology and Hepatology, St. Marianna University, School of Medicine
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- Koike Kazuhiko
- Department of Internal Medicine, Division of Gastroenterology, Faculty of Medicine, University of Tokyo
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- Itoh Fumio
- Department of Internal Medicine, Division of Gastroenterology and Hepatology, St. Marianna University, School of Medicine
Bibliographic Information
- Other Title
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- B型急性肝炎の経過予測におけるHBs抗原定量の有用性
- Bガタ キュウセイ カンエン ノ ケイカ ヨソク ニ オケル HBs コウゲン テイリョウ ノ ユウヨウセイ
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Abstract
We evaluated the usefulness of quantitative evaluation of HBsAg in outcome prediction among 133 patients with acute hepatitis B (AH-B). Patients were classified into 4 groups according to duration of HBsAg positivity as follows: less than 3 months (Group I); less than 6 months (Group II); over 6 months (Group III); and over 12 months (Group IV). An abrupt decrease in HBsAg levels was observed and HBsAg levels at 2 weeks were significantly lower than those at the initial visit in Group I (p<0.001). On the other hand, levels of HBsAg remained high at 4 weeks and 8 weeks in Groups III and IV. Furthermore, HBsAg levels showed an increase from 2 weeks to 4 weeks in Group IV. These results suggest that quantitation of HBsAg at 4 or 8 weeks after initial visit may be useful in the prediction of clinical outcome in AH-B.<br>
Journal
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- Kanzo
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Kanzo 52 (6), 380-382, 2011
The Japan Society of Hepatology
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Details 詳細情報について
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- CRID
- 1390282679771190016
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- NII Article ID
- 10029285612
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- NII Book ID
- AN00047770
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- ISSN
- 18813593
- 04514203
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- NDL BIB ID
- 11133917
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed