Metabolism - Clinical and Experimental
Volume 59, Issue 1 , Pages 20-24, January 2010

Metabolically healthy but obese individuals: relationship with hepatic enzymes

  • Virginie Messier

      Affiliations

    • Department of Nutrition, Université de Montréal, Montreal, Canada H3T 1A8
    • Institut de recherches cliniques de Montréal (IRCM), Montreal, Canada H2W 1R7
    • Equal authorship.
  • ,
  • Antony D. Karelis

      Affiliations

    • Department of Kinanthropology, Université du Québec à Montréal, Montreal, Canada H3C 3P8
    • Corresponding Author InformationCorresponding author. Tel.: +1 514 987 3000x5082; fax: +1 514 987 6616.
    • Equal authorship.
  • ,
  • Marie-Ève Robillard

      Affiliations

    • Department of Kinanthropology, Université du Québec à Montréal, Montreal, Canada H3C 3P8
  • ,
  • Philippe Bellefeuille

      Affiliations

    • Department of Kinanthropology, Université du Québec à Montréal, Montreal, Canada H3C 3P8
  • ,
  • Martin Brochu

      Affiliations

    • Faculty of Physical Education and Sports, Université de Sherbrooke, Sherbrooke, Canada J1K 2R1
    • Research Center on Aging, Health and Social Services Centre, University Institute of Geriatrics of Sherbrooke, Sherbrooke, Canada J1H 4C4
  • ,
  • Jean-Marc Lavoie

      Affiliations

    • Department of kinesiology, Université de Montréal, Montreal, Canada H3C 3J7
  • ,
  • Rémi Rabasa-Lhoret

      Affiliations

    • Department of Nutrition, Université de Montréal, Montreal, Canada H3T 1A8
    • Institut de recherches cliniques de Montréal (IRCM), Montreal, Canada H2W 1R7
    • Montreal Diabetes Research Center, Montreal, Canada H1W 4A4
    • Research Center of the Centre Hospitalier de l’Université de Montréal, Montreal, Canada H2W 1T8

Received 17 May 2009; accepted 30 June 2009. published online 26 August 2009.

Abstract 

The purpose of this study was to investigate the level of plasma hepatic enzymes in obese women displaying the metabolically healthy but obese (MHO) phenotype. We studied 104 obese, sedentary, postmenopausal women. Subjects were classified as MHO or at risk based on insulin sensitivity as assessed with the oral glucose tolerance test–derived Matsuda index. Subjects were divided into quartiles according to insulin sensitivity values. Subjects in the upper quartile were categorized as MHO, whereas subjects in the lower 3 quartiles represented at-risk subjects. Outcome measures were hepatic enzymes (aspartate aminotransferase [AST], alanine aminotransferase [ALT], alkaline phosphatase, and γ-glutamyltransferase [GGT]], high-density lipoprotein cholesterol, triglycerides, triglycerides to high-density lipoprotein cholesterol ratio, apolipoprotein B, fatty liver index, body composition (dual-energy x-ray absorptiometry), and visceral adipose tissue (computed tomography). The MHO individuals had significantly lower concentrations of ALT, AST, and GGT as well as a lower fatty liver index compared with at-risk subjects (P < .05). In addition, lean body mass index and visceral adipose tissue were significantly lower in MHO individuals (P < .05). Moreover, stepwise regression analysis showed that ALT explained 17.9% of the variation in insulin sensitivity in our cohort, which accounted for the greatest source of unique variance. Results of the present study indicate that postmenopausal women displaying the MHO phenotype present favorable levels of ALT, AST, and GGT. Lower concentrations of hepatic enzymes, in particular, lower circulating ALT levels, in MHO individuals may reflect lower hepatic insulin resistance and lower liver fat content; and this could be involved, at least in part, in the protective profile of MHO individuals.

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 The work was carried out at the Department of Nutrition of the Université de Montréal.

PII: S0026-0495(09)00265-0

doi:10.1016/j.metabol.2009.06.020

Metabolism - Clinical and Experimental
Volume 59, Issue 1 , Pages 20-24, January 2010