Metabolism - Clinical and Experimental
Volume 57, Issue 5 , Pages 683-690, May 2008

The association between insulin resistance and cytokines in adolescents: the role of weight status and exercise

  • Daniela A. Rubin

      Affiliations

    • Department of Exercise and Sport Science, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
    • School of Medicine, Department of Allied Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
    • Department of Kinesiology, California State University Fullerton, Fullerton, CA 92834, USA
    • Corresponding Author InformationCorresponding author. Department of Kinesiology, KHS 138, California State University Fullerton, Fullerton, CA, 92834-3599, USA. Tel.: +1 714 278 4704; fax: +1 714 278 5317.
  • ,
  • Robert G. McMurray

      Affiliations

    • Department of Exercise and Sport Science, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
    • School of Medicine, Department of Allied Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
  • ,
  • Joanne S. Harrell

      Affiliations

    • School of Nursing, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
  • ,
  • Anthony C. Hackney

      Affiliations

    • Department of Exercise and Sport Science, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
    • School of Medicine, Department of Allied Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
  • ,
  • Deborah E. Thorpe

      Affiliations

    • School of Medicine, Department of Allied Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
  • ,
  • Andrea M. Haqq

      Affiliations

    • Department of Pediatrics, Duke University Medical Center, Durham, NC 27710, USA

Received 9 April 2007; accepted 7 January 2008.

Abstract 

Increased adiposity is associated with insulin resistance (IR) and an inflammatory response in adults. We tested the hypotheses that cytokines associated with adiposity are also correlated with IR in early adolescents and that these relationships are moderated by weight status, levels of vigorous physical activity (VPA), or maximal aerobic power (pVO2max). Body mass, stature, and a fasting blood sample were obtained from 120 midpubertal adolescents (60 girls and 60 boys). Habitual VPA was obtained by a survey. Predicted VO2max was determined using a cycle ergometer test. Weight status was based on body mass index (BMI) percentiles (normal weight = BMI <75th percentile, overweight = BMI >95th percentile). Glucose, insulin, adiponectin, resistin, tumor necrosis factor–α (TNF-α), and interleukin-6 were measured; and IR index was based on the Homeostatic Model Assessment. Adiponectin, resistin, and TNF-α were associated with IR in all adolescents (R2 = 0.329, P < .001; R2 = 0.152, P = .001; and R2 = 0.141, P = .002; respectively); but interleukin-6 was not (R2 = 0.148, P = .114). The degree of association between adiponectin and IR was stronger in overweight than in normal-weight adolescents (P < .050). When regression models included weight status, neither TNF-α nor resistin was significantly related to IR (P > .050). Exercise did not moderate the association between these cytokines and IR. However, higher levels of VPA and/or pVO2max were associated with higher adiponectin, lower resistin, and lower TNF-α in at least one of the sexes. Our results indicate that the pathophysiology of obesity is already established in early adolescents. Increased adiposity, resulting in reduced adiponectin and increased resistin and TNF-α, may link these cytokines with IR in adolescents.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0026-0495(08)00038-3

doi:10.1016/j.metabol.2008.01.005

Metabolism - Clinical and Experimental
Volume 57, Issue 5 , Pages 683-690, May 2008