Greater age and hepatocellular aging are independent risk factors for hepatocellular carcinoma arising from non-B non-C non-alcoholic chronic liver disease

We previously reported that hepatocellular aging can be assessed by measuring the nuclear size of hepatocytes. We attempted to elucidate whether this method is useful to identify the high risk group of hepatocellular carcinoma (HCC) in the patients with non‐B non‐C non‐alcoholic liver injury. Fourte...

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Published inPathology international Vol. 61; no. 10; pp. 572 - 576
Main Authors Nakajima, Tomoki, Nakashima, Toshiaki, Yamaoka, Junko, Shibuya, Akiko, Konishi, Eiichi, Okada, Yoshihisa, Jo, Masayasu, Nishikawa, Taichirou, Itoh, Yoshihito, Yoshikawa, Toshikazu
Format Journal Article
LanguageEnglish
Published Melbourne, Australia Blackwell Publishing Asia 01.10.2011
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Summary:We previously reported that hepatocellular aging can be assessed by measuring the nuclear size of hepatocytes. We attempted to elucidate whether this method is useful to identify the high risk group of hepatocellular carcinoma (HCC) in the patients with non‐B non‐C non‐alcoholic liver injury. Fourteen patients with HCC and 78 without HCC, both of whom presented with non‐B non‐C non‐alcoholic chronic liver injury and underwent liver biopsy, were selected. Twelve histologically normal liver tissues were selected as controls. The relative nuclear size (RNS) was calculated as the average nuclear size of the hepatocytes divided by that of lymphocytes. Multiple clinicopathological parameters were studied. The RNS values of normal livers ranged from 1.32 to 2.10, showing a gradual increase in an age‐dependent manner. The RNS values of the injured livers without HCC increased after middle age. Univariate analysis identified greater age, existence of diabetes and RNS, as significantly positive contributors and ALT value and the degree of steatosis as negative contributors for the occurrence of HCC. Only age and RNS retained significance in multivariate analysis. All of the HCC patients were older than 50 and showed RNS values higher than 2.00. Therefore, such patients are classified as a high risk group of HCC.
Bibliography:istex:2118B0AFAA0250F19E2177A861EE5AC4059C80B5
ark:/67375/WNG-4VX1WTXV-9
ArticleID:PIN2743
Correction added on 19 December 2016, after first online publication: The author name has been corrected to Taichiro Nishikawa
Received 12 February 2011. Accepted for publication 12 June 2011.
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ISSN:1320-5463
1440-1827
DOI:10.1111/j.1440-1827.2011.02743.x