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   <subfield code="a">10.1007/s00535-011-0381-2</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s00535-011-0381-2</subfield>
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   <subfield code="a">Post-challenge hyperglycemia is a significant risk factor for the development of hepatocellular carcinoma in patients with chronic hepatitis C</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Hirokazu Takahashi, Toshihiko Mizuta, Yuichiro Eguchi, Yasunori Kawaguchi, Takuya Kuwashiro, Satoshi Oeda, Hiroshi Isoda, Noriko Oza, Shinji Iwane, Kenichi Izumi, Keizou Anzai, Iwata Ozaki, Kazuma Fujimoto]</subfield>
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   <subfield code="a">Background: Several epidemiological studies have reported that diabetes mellitus is a risk factor for hepatocellular carcinoma (HCC) in hepatitis C virus (HCV)-positive patients. However, it is unclear whether or not post-challenge hyperglycemia is a risk factor. The purpose of this study was to determine the association between post-challenge hyperglycemia and hepatocarcinogenesis in HCV-positive patients. Methods: A total of 203 HCV-RNA-positive subjects (108 males, mean age 54.3±10.8years; 95 females, mean age 56.6±10.3years; genotype 1b/2a/2b/3a: 152/38/12/1) who underwent liver biopsy and a 75-g oral glucose tolerance test, and who were treated with interferon (IFN) were enrolled in this study. None of the subjects had been treated with antidiabetic drugs. The subjects underwent ultrasonography and/or computed tomography every 6months after the end of the IFN therapy. Results: Thirteen patients, including one patient who achieved a sustained viral response (SVR) with IFN, developed HCC. On multivariate analysis, male sex, age &gt;65years, excessive alcohol consumption, non-SVR, liver steatosis area &gt;5% in liver specimens, and 120-min post-challenge hyperglycemia were risk factors for the development of HCC. After matching subjects for sex, age, alcohol intake, and response to the IFN therapy, advanced fibrosis stages [hazard ratio (HR) 2.8], liver steatosis (HR 5.4), and 120-min post-challenge hyperglycemia (HR 4.9) were significant risk factors for the development of HCC. Furthermore, after matching for the fibrosis stage, liver steatosis (HR 5.7) and 120-min post-challenge hyperglycemia (HR 6.9) remained as significant factors for HCC development. Conclusion: Post-challenge hyperglycemia is an independent risk factor for HCC in HCV-positive patients.</subfield>
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   <subfield code="a">Springer, 2011</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Hyperglycemia</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Oral glucose tolerance test</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Hepatocellular carcinoma</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Hepatitis C</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">HCV : Hepatitis C virus</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HBV : Hepatitis B virus</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HCC : Hepatocellular carcinoma</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DM : Diabetes mellitus</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HR : Hazard ratio</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BMI : Body mass index</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">ALT : Alanine aminotransferase</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HbA1c : Hemoglobin A1c</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">IFN : Interferon</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">OGTT : Oral glucose tolerance test</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PCR : Polymerase chain reaction</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HOMA-IR : Homeostasis model assessment for insulin resistance</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SVR : Sustained viral response</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Takahashi</subfield>
   <subfield code="D">Hirokazu</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Mizuta</subfield>
   <subfield code="D">Toshihiko</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Eguchi</subfield>
   <subfield code="D">Yuichiro</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Kawaguchi</subfield>
   <subfield code="D">Yasunori</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Kuwashiro</subfield>
   <subfield code="D">Takuya</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Oeda</subfield>
   <subfield code="D">Satoshi</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Isoda</subfield>
   <subfield code="D">Hiroshi</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Oza</subfield>
   <subfield code="D">Noriko</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Iwane</subfield>
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   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Izumi</subfield>
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   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Anzai</subfield>
   <subfield code="D">Keizou</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Ozaki</subfield>
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   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
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   <subfield code="a">Fujimoto</subfield>
   <subfield code="D">Kazuma</subfield>
   <subfield code="u">Department of Internal Medicine, Saga Medical School, Nabeshima, Saga, Japan</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Journal of Gastroenterology</subfield>
   <subfield code="d">Springer Japan</subfield>
   <subfield code="g">46/6(2011-06-01), 790-798</subfield>
   <subfield code="x">0944-1174</subfield>
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