Gastroenterology
Volume 134, Issue 5 , Pages 1369-1375, May 2008

Liver, Muscle, and Adipose Tissue Insulin Action Is Directly Related to Intrahepatic Triglyceride Content in Obese Subjects

  • Kevin M. Korenblat

      Affiliations

    • Center for Human Nutrition, Washington University School of Medicine, St Louis, Missouri
    • Division of Gastroenterology, Washington University School of Medicine, St Louis, Missouri
  • ,
  • Elisa Fabbrini

      Affiliations

    • Center for Human Nutrition, Washington University School of Medicine, St Louis, Missouri
    • Department of Medical Pathophysiology, University of Rome “La Sapienza,” Rome, Italy
  • ,
  • B. Selma Mohammed

      Affiliations

    • Center for Human Nutrition, Washington University School of Medicine, St Louis, Missouri
  • ,
  • Samuel Klein

      Affiliations

    • Center for Human Nutrition, Washington University School of Medicine, St Louis, Missouri
    • Corresponding Author InformationAddress requests for reprints to: Samuel Klein, MD, Center for Human Nutrition, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8031, St Louis, Missouri 63110. fax: (314) 362-8230.

Received 9 September 2007; accepted 18 January 2008. published online 31 January 2008.

Background & Aims: Nonalcoholic fatty liver disease is associated with insulin resistance and diabetes. The purpose of this study was to determine the relationship between intrahepatic triglyceride (IHTG) content and insulin action in liver (suppression of glucose production), skeletal muscle (stimulation of glucose uptake), and adipose tissue (suppression of lipolysis) in nondiabetic obese subjects. Methods: A euglycemic-hyperinsulinemic clamp procedure and stable isotopically labeled tracer infusions were used to assess insulin action, and magnetic resonance spectroscopy was used to determine IHTG content, in 42 nondiabetic obese subjects (body mass index, 36 ± 4 kg/m2) who had a wide range of IHTG content (1%–46%). Results: Hepatic insulin sensitivity, assessed as a function of glucose production rate and plasma insulin concentration, was inversely correlated with IHTG content (r = −0.599; P < .001). The ability of insulin to suppress fatty acid release from adipose tissue and to stimulate glucose uptake by skeletal muscle were also inversely correlated with IHTG content (adipose tissue: r = −0.590, P < .001; skeletal muscle: r = −0.656, P < .001). Multivariate linear regression analyses found that IHTG content was the best predictor of insulin action in liver, skeletal muscle, and adipose tissue, independent of body mass index and percent body fat, and accounted for 34%, 42%, and 44% of the variability in these tissues, respectively (P < .001 for each model). Conclusions: These results show that progressive increases in IHTG content are associated with progressive impairment of insulin action in liver, skeletal muscle, and adipose tissue in nondiabetic obese subjects. Therefore, nonalcoholic fatty liver disease should be considered part of a multiorgan system derangement in insulin sensitivity.

Abbreviations used in this paper: BMI, body mass index, BSA, body surface area, FFM, fat-free mass, IAAT, intra-abdominal adipose tissue, IHTG, intrahepatic triglyceride, NAFLD, nonalcoholic fatty liver disease, Ra, rate of appearance, Rd, rate of disappearance

 

 The authors report that no conflicts of interests exist.

 Supported by National Institutes of Health grants DK 37948, DK 56341 (Clinical Nutrition Research Unit), RR-00036 (General Clinical Research Center), and RR-00954 (Biomedical Mass Spectrometry Resource) and by DK 52574 (Washington University Digestive Diseases Research Core Center) and an American Gastroenterological Association Roche Junior Faculty Clinical Research Award in Hepatology (to K.M.K.).

PII: S0016-5085(08)00181-9

doi:10.1053/j.gastro.2008.01.075

Gastroenterology
Volume 134, Issue 5 , Pages 1369-1375, May 2008