Insulin-like growth factor-binding protein-2 levels in pediatric patients with growth hormone deficiency, eating disorders and acute lymphoblastic leukemia
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1Division of Pediatric Endocrinology, Hospital Universitario Niño Jesús, Madrid, Spain.
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.
Abstract:
Insulin-like growth factor (IGF)-binding protein-2 (IGFBP-2) is altered in different diseases and might be used as an indication of its severity. The aims of our study were to investigate: (1) the developmental pattern of the serum IGFBP-2 concentration at birth and during childhood and adolescence; (2) whether the serum IGFBP-2 level could be a marker for the diagnosis and evolution of diseases where the growth hormone (GH)-IGF axis is altered, and (3) whether this binding protein shows a relationship with IGF-I, its free fraction, IGFBP-1 and -3. We report reference values for 55 normal full-term newborns and 221 normal children who were divided into 5 groups according to their Tanner stage. Serum levels were higher in newborns when compared with Tanner stages I-V (p < 0.001, ANOVA), with no further changes throughout development. Furthermore, we studied IGFBP-2 levels in 24 children with congenital GH deficiency (GHD), 26 with acute lymphoblastic leukemia (ALL), 75 obese children, and 60 girls with anorexia nervosa (AN) at diagnosis and during a follow-up period. IGFBP-2 at diagnosis was increased in GHD, ALL and AN, and decreased in obesity (p < 0.05, ANOVA). During the follow-up, IGFBP-2 concentrations tended to normalize. IGFBP-2 correlated positively with IGFBP-1 and negatively with IGF-I and IGFBP-3 in normal subjects and at diagnosis of the pathologies studied. Although IGFBP-2 functions are not well understood, these results suggest a possible role for this protein in diseases where the GH-IGF axis is altered.
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