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IGF-1 Levels, Complex Formation, and IGF Bioactivity in Growth Hormone-Treated Children With Prader-Willi Syndrome.
Bakker, N E; van Doorn, J; Renes, J S; Donker, G H; Hokken-Koelega, A C S.
Afiliação
  • Bakker NE; Dutch Growth Research Foundation (N.E.B., A.C.S.H.-K.), 3016 AH Rotterdam, The Netherlands; Department of Pediatrics (N.E.B., J.S.R., A.C.S.H.-K.), Subdivision of Endocrinology, Erasmus Medical Center/Sophia Children's Hospital, 3000 DR Rotterdam, The Netherlands; and Department of Clinical Chemistr
  • van Doorn J; Dutch Growth Research Foundation (N.E.B., A.C.S.H.-K.), 3016 AH Rotterdam, The Netherlands; Department of Pediatrics (N.E.B., J.S.R., A.C.S.H.-K.), Subdivision of Endocrinology, Erasmus Medical Center/Sophia Children's Hospital, 3000 DR Rotterdam, The Netherlands; and Department of Clinical Chemistr
  • Renes JS; Dutch Growth Research Foundation (N.E.B., A.C.S.H.-K.), 3016 AH Rotterdam, The Netherlands; Department of Pediatrics (N.E.B., J.S.R., A.C.S.H.-K.), Subdivision of Endocrinology, Erasmus Medical Center/Sophia Children's Hospital, 3000 DR Rotterdam, The Netherlands; and Department of Clinical Chemistr
  • Donker GH; Dutch Growth Research Foundation (N.E.B., A.C.S.H.-K.), 3016 AH Rotterdam, The Netherlands; Department of Pediatrics (N.E.B., J.S.R., A.C.S.H.-K.), Subdivision of Endocrinology, Erasmus Medical Center/Sophia Children's Hospital, 3000 DR Rotterdam, The Netherlands; and Department of Clinical Chemistr
  • Hokken-Koelega AC; Dutch Growth Research Foundation (N.E.B., A.C.S.H.-K.), 3016 AH Rotterdam, The Netherlands; Department of Pediatrics (N.E.B., J.S.R., A.C.S.H.-K.), Subdivision of Endocrinology, Erasmus Medical Center/Sophia Children's Hospital, 3000 DR Rotterdam, The Netherlands; and Department of Clinical Chemistr
J Clin Endocrinol Metab ; 100(8): 3041-9, 2015 Aug.
Article em En | MEDLINE | ID: mdl-26050733
ABSTRACT
CONTEXT Children with Prader-Willi syndrome (PWS) attain high-serum immunoreactive IGF-1 levels during a standard-dose GH treatment, which leads to concern, but lowering the dose deteriorates their body composition.

OBJECTIVE:

The objective of the study was to evaluate serum IGF-1, IGF binding protein (IGFBP)-3, and acid-labile subunit (ALS) levels, complex formation, and IGF bioactivity in GH-treated PWS children.

DESIGN:

This was a cross-sectional study.

SETTING:

The setting of the study was a Dutch PWS cohort.

PARTICIPANTS:

Forty GH-treated PWS children compared with 41 age- and sex-matched healthy controls participated in the study.

INTERVENTIONS:

Interventions included GH treatment (1.0 mg/m(2) · d = ∼0.035 mg/kg · d). MAIN OUTCOME

MEASURES:

Serum IGF-1, IGFBP-3, and ALS levels, complex formation, and IGF bioactivity by IGF-1 receptor kinase activation assay were measured.

RESULTS:

Serum IGF-1, IGFBP-3, and ALS levels and IGF-1 to IGFBP-3 ratio were significantly higher in GH-treated PWS children than in healthy controls. The 150-kDa ternary complex formation was, however, also significantly higher than in controls, indicating that most of serum IGF-1 is sequestered in the ternary 150-kDa complex with ALS and IGFBP-3. Young GH-treated PWS children [median (interquartile range) aged 5.2 (4.3-7.2) y] exhibited higher serum IGF bioactivity than controls, but no difference was observed in IGF bioactivity between older GH-treated PWS children, aged 14.9 (13.8-16.2) years, and controls. The proportion of IGF bioactivity of total serum IGF-1 was, however, lower in GH-treated PWS children than in controls. Serum immunoreactive IGF-1 levels did not correlate with IGF bioactivity in GH-treated children with PWS, in contrast to a strong positive correlation in healthy controls.

CONCLUSIONS:

In GH-treated PWS children, most serum IGF-1 is sequestered in the 150-kDa complex. Higher IGF bioactivity was found only in young GH-treated PWS children and not in the older ones. IGF bioactivity during GH showed a wide variation, and there was a disrupted correlation with immunoreactive IGF-1 levels, which makes immunoreactive IGF-1 levels an inappropriate indicator for GH dosing in PWS children.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Fator de Crescimento Insulin-Like I / Hormônio do Crescimento Humano Tipo de estudo: Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Fator de Crescimento Insulin-Like I / Hormônio do Crescimento Humano Tipo de estudo: Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2015 Tipo de documento: Article