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本帖最后由 StephenW 于 2011-9-2 16:47 编辑
<http://cebp.aacrjournals.org/content/early/2011/08/26/1055-9965.EPI-11-0464.abstract>
Prediction of hepatocellular carcinoma development by plasma ADAMTS13 in
chronic hepatitis B and C.
Hitoshi Ikeda1,*,
Ryosuke Tateishi2,
Kenichiro Enooku3,
Haruhiko Yoshida2,
Hayato Nakagawa4,
Ryota Masuzaki5,
Yuji Kondo6,
Tadashi Goto6,
Shuichiro Shiina7,
Yukio Kume8,
Tomoaki Tomiya2,
Yukiko Inoue6,
Takako Nishikawa6,
Natsuko Ohtomo7,
Yasushi Tanoue7,
Tomoko Ono9,
Kazuhiko Koike10, and
Yutaka Yatomi8
+ Author Affiliations
1Department of Clinical Laboratory Medicine, The University of Tokyo
2Department of Gastroenterology, The University of Tokyo
3Department of Gastroenterology, Graduate School of Medicine, the
University of Tokyo
4Department of Gastroenterology, University of Tokyo
5University of Tokyo
6The University of Tokyo
7Gastroenterology, University of Tokyo
8Department of Laboratory Medicine, The University of Tokyo
9Mitsubishi Chemical Medicine Corporation
10Department of Gatroenterology, The University of Tokyo
↵*Corresponding Author:
Hitoshi Ikeda, Department of Clinical Laboratory Medicine, The University
of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan
[email protected]
Abstract
Background:
Chronic liver injury evokes a wound healing response promoting
fibrosis and finally hepatocellular carcinoma (HCC), in which hepatic
stellate cells play an important role. Although a blood marker of hepatic
stellate cells is not known, those cells importantly contribute to the
regulation of plasma ADAMTS13 activity, a defect of which causes thrombotic
thrombocytopenic purpura.
Methods:
Plasma ADAMTS13 was evaluated in chronic hepatitis B or C patients with or without HCC.
Results:
Plasma ADAMTS13 activity significantly correlated with serum AST and ALT, liver stiffness value and aspartate aminotransferase-to-platelet ratio index, irrespective
of the presence of HCC, suggesting that it may reflect hepatocellular
damage and subsequent wound healing, and fibrosis as a result of hepatic
stellate cell action. During the three-year follow-up period for patients
without HCC, HCC developed in 10 among 81 patients. Plasma ADAMTS13
activity was significantly higher in patients with HCC development than in
those without, and was a significant risk for HCC development by univariate
and multivariate analyses. Furthermore, during the one-year follow-up
period for patients with HCC treated with radiofrequency ablation, HCC
recurred in 55 among 107 patients. Plasma ADAMTS13 activity or antigen
level was significantly higher in patients with HCC recurrence than in
those without, and was retained as a significant risk for HCC recurrence by
multivariate analysis.
Conclusions:
Higher plasma ADAMTS13 activity and
antigen level was a risk of HCC development in chronic liver disease.
Impact:
Plasma ADAMTS13 as a potential marker of hepatic stellate cells may
be useful in the prediction of hepatocarcinogenesis. Received May 18, 2011.
Revision received August 19, 2011. Accepted August 20, 2011. Copyright ©
2011, American Association for Cancer Research. |
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