Endocrine pancreatic dysfunction in HIV-infected children: association with growth alterations

J Infect Dis. 2004 Sep 1;190(5):908-12. doi: 10.1086/422255. Epub 2004 Jul 23.

Abstract

Background: The pancreatic endocrine system normally guarantees a quick and efficient response to daily metabolic perturbations, but associated data for human immunodeficiency virus (HIV)-infected patients are lacking. A prospective study was performed to evaluate pancreatic endocrine secretion and its possible association with failure to thrive among HIV-infected children.

Methods: Fourteen well-nourished, prepubertal, HIV-infected children (6 boys and 8 girls; age range, 5-11 years), none of whom were receiving protease inhibitors, and 16 clinically healthy sex- and age-matched children formed the patient group and the control group, respectively. At yearly follow-up examinations, insulin, glucagon, C-peptide, and glucose levels were measured; the ratio of insulin to glucose, the ratio of insulin to glucagon, and the homeostasis model assessment (HOMA) index were calculated; the glucagon test was administered; and growth hormone, thyroid-stimulating hormone, adrenocorticotropic hormone, cortisol, and lipid patterns were evaluated.

Results: Insulin, glucagon, C-peptide, glucose, and HOMA measurements were significantly higher among patients, compared with control subjects, at all 3 follow-ups performed to date. The glucagon test revealed a normal glycemic response in all the healthy control subjects and a significantly impaired response in 11 patients. A significant correlation emerged between the ratio of insulin to glucagon and the growth velocity of HIV-infected children.

Conclusion: To our knowledge, the present study provides the first evidence of altered pancreatic endocrine secretion and its association with growth failure among HIV-infected children.

MeSH terms

  • Blood Glucose
  • C-Peptide / blood
  • Child
  • Female
  • Glucagon / blood
  • Growth Disorders / etiology*
  • Growth Disorders / physiopathology*
  • HIV Infections / complications*
  • HIV Infections / physiopathology
  • Homeostasis
  • Hormones / blood
  • Humans
  • Insulin / blood
  • Lipids / blood
  • Male
  • Pancreas / physiopathology*
  • Prospective Studies

Substances

  • Blood Glucose
  • C-Peptide
  • Hormones
  • Insulin
  • Lipids
  • Glucagon