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Vol. 64, Suppl. 3, 2005   

Free Abstract     Article (Fulltext)     Article (PDF 133 KB)     

Methods to Determine Insulin Sensitivity in Clinical Practice. Growth Hormone and Cognition.
Editor(s): Ranke, M.B. (Tübingen), Vance, M.L. (Charlottesville, Va.)


Insulin Sensitivity: Clinical Impact

Turner Syndrome, Insulin Sensitivity and Growth Hormone Treatment
Laura Mazzanti, Rosalba Bergamaschi, Laura Castiglioni, Franco Zappulla, Piero Pirazzoli, Alessandro Cicognani

Department of Pediatrics, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy

Address of Corresponding Author

Horm Res 2005;64 (Suppl. 3):51-57 (DOI: 10.1159/000089318)


 goto top of page Key Words

  • Turner syndrome
  • Children
  • Growth hormone
  • Insulin sensitivity
  • Insulin resistance

 goto top of page Abstract

Mild insulin resistance appears to be an early metabolic defect in girls with Turner syndrome (TS). Impaired glucose tolerance has been reported in 10-34% of patients with TS, and type 2 diabetes mellitus is 2-4 times more common and occurs at a younger age in girls with TS than in the general population. In a mixed longitudinal and cross-sectional study, we analysed carbohydrate tolerance and insulin sensitivity in 46 children and adolescents with TS who reached their final height after long-term treatment (mean 6.3 ± 2.5 years) with growth hormone (GH: 0.33 mg/kg/week [0.05 mg/kg/day]), and in 36 of these patients who were followed-up after the cessation of GH therapy (mean follow-up, 2.6 ± 2.5 years; range, 1-9.5 years). Patients with TS were compared with an age-matched female control group. Insulin sensitivity appeared to be lower in patients with TS than in controls, even before the start of GH therapy. As in controls, insulin sensitivity decreased with age in patients with TS, and levels were lower in those aged >12 years than in those aged <12 years. GH therapy resulted in good catch-up growth in patients with TS, with final height significantly higher than projected height evaluated before the initiation of GH therapy. Insulin sensitivity increased after 7-8 years of therapy and, on the cessation of GH therapy, returned to pre-treatment levels. The increase in insulin sensitivity seen on the cessation of GH therapy appeared to be influenced negatively by body mass index and triglyceride levels, and correlated positively with the number of years since cessation of GH therapy. As in the general population, excess weight and an abnormal lipid profile, in particular excess triglyceride levels, worsened insulin sensitivity. In conclusion, our study confirms that GH therapy reduces insulin sensitivity, but at its cessation there is a return to pre-therapy values. We therefore report a progressive improvement in carbohydrate tolerance and insulin function in patients with TS, despite an increase in age.

Copyright © 2005 S. Karger AG, Basel


 goto top of page Author Contacts

Dr. L. Mazzanti
Pediatric Clinic, Auxology and Syndromology Surgery, S. Orsola-Malpighi Hospital
Via Massarenti 11
IT-40138 Bologna (Italy)
Tel. +39 051 636 3723, Fax +39 051 636 4440, E-Mail laura.mazzanti@unibo.it


 goto top of page Article Information

Published online: January 20, 2006
Number of Print Pages : 7
Number of Figures : 2, Number of Tables : 1, Number of References : 26

 
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Medline Abstract (ID 16439845)
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