Key result
Recombinant human IGF-I therapy did not significantly increase serum IGFBPs in children with GH insensitivity, whereas GH therapy significantly increased them in GH-deficient children (p<0.0001).
Why the study?
Does recombinant human IGF-I therapy increase serum levels of IGFBPs and ALS in children with growth hormone insensitivity compared to GH therapy in GH-deficient children?
Cohort (n=82)
Does recombinant human IGF-I therapy increase serum levels of IGFBPs and ALS in children with growth hormone insensitivity compared to GH therapy in GH-deficient children?
p-value: p=<0.0001
Growth hormone, rather than IGF-I, directly regulates the serum concentrations of IGFBP-3, -4, -5, and ALS in vivo.
Supports GH as primary regulator of IGFBPs; leaves open effects on growth outcomes in insensitivity syndromes.
Burren CP, Wanek D, Mohan S, Cohen P, Guevara‐Aguirre J, Rosenfeld RG. Serum levels of insulin‐like growth factor binding proteins in Ecuadorean children with growth hormone insensitivity. Acta Pædiatr 1999; Suppl 428: 185–91. Stockholm. ISSN 0803–5326 Although insulin‐like growth factor binding proteins (IGFBPs) are known to be important modulators of the action of insulin‐like growth factors (IGFs), regulation of their production in vivo is not completely understood. Serum concentrations of IGFBP‐3, ‐4 and ‐5 and acid‐labile subunit (ALS) were therefore examined in 20 children with growth hormone (GH) insensitivity before and after 6 months of therapy with recombinant human IGF‐I (80 or 120 ug/kg twice daily). The IGFBP concentrations in these children were compared with those in 62 GH‐deficient children receiving GH therapy for 3 months. Serum levels of IGFBP‐3, ‐4 and ‐5 and ALS all increased significantly (p < 0.0001) in GH‐deficient children in response to GH therapy, whereas no significant increases occurred in the children with GH insensitivity. These findings indicate that GH is responsible for the regulation of serum levels of IGFBP‐3, ‐4 and ‐5 and ALS, and that IGF‐I does not directly regulate the concentrations of these circulating IGFBPs. □Growth hormone, growth hormone insensitivity, insulin‐like growth factor I, insulin‐like growth factor binding protein
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Burren et al. (1999) conducted a cohort in Growth hormone insensitivity (n=82). Recombinant human IGF-I vs. Growth hormone therapy was evaluated on Serum concentrations of IGFBP-3, -4 and -5 and acid-labile subunit (ALS) (p=<0.0001). Recombinant human IGF-I therapy did not significantly increase serum IGFBPs in children with GH insensitivity, whereas GH therapy significantly increased them in GH-deficient children (p<0.0001).
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