Prediction Model for Adult Height of Small for Gestational Age Children at the Start of Growth Hormone Treatment

Author:

de Ridder Maria A. J.12,Stijnen Theo3,Hokken-Koelega Anita C. S.42

Affiliation:

1. Department of Epidemiology and Biostatistics (M.A.J.d.R.) Erasmus Medical Center-University Medical Center, 3000 CA Rotterdam, The Netherlands

2. Dutch Growth Foundation (M.A.J.d.R., A.C.S.H.-K.), 3001 KB Rotterdam, The Netherlands

3. Department of Medical Statistics (T.S.), Leiden University Medical Center, 2300 RC Leiden, The Netherlands

4. Department of Pediatrics, Division of Endocrinology (A.C.S.H.-K.), Sophia Children’s Hospital, Erasmus Medical Center-University Medical Center Rotterdam, 3000 CB Rotterdam, The Netherlands

Abstract

Abstract Context: GH treatment is approved for short children born small for gestational age (SGA). The optimal dose is not yet established. Objective: Our objective was to develop a model for prediction of height at the onset of puberty and of adult height (AH). Design and Setting: Two GH studies were performed in short SGA children. Patients/Intervention: A total of 150 SGA children with height sd scores (SDS) less than −2, age 3 yr or older, no signs of catch-up growth, available height at the onset of puberty, and at least 1 yr of GH treatment before the onset of puberty were studied. In one study, patients were randomly assigned to either 0.033 or 0.067 mg/kg·d; in the other study all received 0.033 mg/kg·d. In 71 children, AH was reached. Main Outcome Measures: Height SDS at the onset of puberty and AH SDS were calculated. Results: Determinants positively related to height SDS at the onset of puberty were: height SDS at the start; target height SDS; and GH dose, whereas age at the start and female gender were negatively related. Positively related to AH SDS were: height SDS and chronological age − bone age at the start; target height SDS; and GH dose, whereas serum IGF binding protein (IGFBP)-3 SDS at the start was negatively related. There was a significant interaction between GH dose and IGFBP-3 SDS, indicating a smaller GH dose effect for higher levels of IGFBP-3. The final model explained 57% of the variance in height SDS at the onset of puberty and 41% of AH SDS. Conclusions: The prediction model for height SDS at the onset of puberty and AH SDS of short SGA children treated with GH provides useful information about the expected long-term growth. Because GH dosage is one of the determinants, the model aids in determining the optimal GH dose for each child.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference31 articles.

1. Management of the child born small for gestational age through to adulthood: a consensus statement of the International Societies of Pediatric Endocrinology and the Growth Hormone Research Society.;Clayton;J Clin Endocrinol Metab,2007

2. Efficacy and safety of long-term continuous growth hormone treatment of children born small for gestational age;Hokken-Koelega;Horm Res,2004

3. Growth hormone therapy in short children born small for gestational age;de Zegher;Horm Res,2006

4. Adult height after long-term, continuous growth hormone (GH) treatment in short children born small for gestational age: results of a randomized, double-blind, dose-response GH trial.;Van Pareren;J Clin Endocrinol Metab,2003

5. Growth hormone therapy for children born small for gestational age: height gain is less dose dependent over the long term than over the short term;de Zegher;Pediatrics,2005

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