Insulin-like growth factor-binding protein-2 levels in pediatric patients with growth hormone deficiency, eating

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V Barrios1, M Buño, J Pozo

  • 1Division of Pediatric Endocrinology, Hospital Universitario Niño Jesús, Madrid, Spain.

Hormone Research
|January 11, 2001
PubMed

Insights

Serum Insulin-like Growth Factor (IGF)-binding protein-2 (IGFBP-2) levels vary by age and disease state. IGFBP-2 may serve as a diagnostic marker for conditions affecting the growth hormone-IGF axis.

Area of Science:

  • Endocrinology
  • Pediatrics
  • Biochemistry

Background:

  • Insulin-like Growth Factor (IGF)-binding protein-2 (IGFBP-2) levels are altered in various diseases, potentially indicating disease severity.
  • The precise role and developmental pattern of IGFBP-2 require further investigation, particularly concerning its relationship with the growth hormone (GH)-IGF axis.

Purpose of the Study:

  • To establish reference values for serum IGFBP-2 during development from birth through adolescence.
  • To evaluate IGFBP-2 as a potential diagnostic and prognostic marker in conditions involving the GH-IGF axis, including congenital GH deficiency (GHD), acute lymphoblastic leukemia (ALL), obesity, and anorexia nervosa (AN).
  • To explore the correlation between IGFBP-2 and other key components of the GH-IGF axis, such as IGF-I, its free fraction, IGFBP-1, and IGFBP-3.

Main Methods:

  • Serum IGFBP-2 concentrations were measured in 55 healthy newborns and 221 healthy children across different Tanner stages.
  • IGFBP-2 levels were analyzed at diagnosis and during follow-up in children with GHD, ALL, obesity, and AN.
  • Statistical analysis, including ANOVA, was employed to compare IGFBP-2 levels between groups and assess correlations.

Main Results:

  • Serum IGFBP-2 levels were significantly higher in newborns compared to children in Tanner stages I-V, with no further developmental changes observed.
  • At diagnosis, IGFBP-2 levels were elevated in GHD, ALL, and AN, but decreased in obesity (p < 0.05).
  • During follow-up, IGFBP-2 concentrations showed a trend toward normalization. Positive correlations were found between IGFBP-2 and IGFBP-1, while negative correlations existed with IGF-I and IGFBP-3.

Conclusions:

  • IGFBP-2 exhibits distinct concentration patterns during early development and in specific pediatric diseases.
  • Altered IGFBP-2 levels in GHD, ALL, AN, and obesity suggest its involvement in the GH-IGF axis dysregulation characteristic of these conditions.
  • IGFBP-2 may serve as a valuable biomarker for diagnosing and monitoring diseases impacting the GH-IGF axis, despite its exact functions remaining unclear.