• Title of article

    Inverse association between serum adiponectin level and transaminase activities in Japanese male workers

  • Author/Authors

    Hirokazu Yokoyama، نويسنده , , Hiroshi Hirose، نويسنده , , Hideki Ohgo، نويسنده , , Ikuo Saito، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2004
  • Pages
    6
  • From page
    19
  • To page
    24
  • Abstract
    Background/Aims Since a novel polypeptide named adiponectin was shown to prevent the development of steatosis and steatohepatitis in animal models, we studied whether it was also possible in a clinical situation. Methods Associations between serum adiponectin levels and serum transaminase activities were studied in 791 Japanese males who were not heavy drinkers, and had no autoimmune or HBV- or HCV-induced liver diseases. Results Various markers of metabolic diseases including levels of body mass index (BMI), serum triglyceride, total cholesterol, and insulin resistance assessed by the homeostasis model were significantly higher in subjects with increased transaminase activities when compared to those with normal activities. Single regression analyses demonstrated that the logarithmic serum adiponectin level was inversely correlated with the levels of logarithmic serum AST (r=−0.229, P<0.0001), ALT (r=−0.305, P<0.0001), and γGTP (r=−0.278, P<0.0001). Even in multiple regression analyses in which subjectsʹ age and levels of BMI, serum triglyceride, total cholesterol, and insulin resistance were adjusted, the inverse correlations were significant (P=0.0426, 0.0332, and 0.0011, respectively). Conclusions Hypoadiponectinemia may worsen liver diseases associated with metabolic diseases in clinical cases. In addition to aggravation of insulin resistance and hyperlipidemia, some hypoadiponectinemia specific mechanisms may stand behind the association.
  • Keywords
    Adiponectin , fatty liver , insulin resistance
  • Journal title
    Journal of Hepatology
  • Serial Year
    2004
  • Journal title
    Journal of Hepatology
  • Record number

    586152