Literature DB >> 10626558

Five years of growth hormone treatment in children with Prader-Willi syndrome. Swedish National Growth Hormone Advisory Group.

A C Lindgren1, E M Ritzén.   

Abstract

The authors have followed 18 prepubertal children (3-12 years of age) with Prader-Willi syndrome during 5 years of growth hormone (GH) treatment. Initially, all the children participated in a randomized, controlled GH trial, conducted to assess the effects of GH treatment on growth, body composition and behaviour. GH was administered to group A (n = 9) at a dose of 0.1 IU/kg/day (0.033 mg/kg/day) for 2 years. Group B (n = 9) was untreated for the first year, but the children were given GH at a dose of 0.2 IU/kg/day (0.066 mg/kg/day) during the second year. Thereafter, all children stopped GH treatment for 6 months and were then restarted with GH at a dose of 0.1 IU/kg/day (0.033 mg/kg/day). During the first year of GH treatment, there was a dramatic increase in height SDS in both groups. The attained height percentile was maintained during the continued GH treatment. Five years after the start of GH treatment, mean height SDS is still above average for age. Four children have reached final height, all within 2 SD of target height. During the first year of GH treatment, body mass index (BMI) SDS decreased significantly from 3.0 to 1.5 SDS in group A and from 2.8 to 1.2 SDS in group B, but it increased again during the 6-month period without treatment. Following the restart of GH treatment, BMI SDS has stabilized at 1.7 SDS for group A and 2.5 SDS for group B. In 16 of 18 patients, fasting insulin, glucose and the A1c fraction of glycosylated haemoglobin remained within normal ranges during 5 years of GH treatment. Following a period of rapid weight gain, two children have developed non-insulin-dependent diabetes mellitus. Glucose homeostasis returned to normal when GH treatment was withdrawn. In conclusion, GH treatment has a proven favourable effect on growth and body composition in patients with Prader-Willi syndrome. Treatment should be individualized, and close surveillance of glucose homeostasis is needed, especially if the patient is severely obese.

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Year:  1999        PMID: 10626558     DOI: 10.1111/j.1651-2227.1999.tb14416.x

Source DB:  PubMed          Journal:  Acta Paediatr Suppl        ISSN: 0803-5326


  16 in total

Review 1.  Growth hormone therapy in the Prader-Willi syndrome.

Authors:  W F Paterson; M D C Donaldson
Journal:  Arch Dis Child       Date:  2003-04       Impact factor: 3.791

2.  Growth hormone receptor (GHR) gene polymorphism and scoliosis in Prader-Willi syndrome.

Authors:  Merlin G Butler; Waheeda Hossain; Maaz Hassan; Ann M Manzardo
Journal:  Growth Horm IGF Res       Date:  2017-12-06       Impact factor: 2.372

3.  Growth hormone treatment in a girl with Prader Willi syndrome.

Authors:  S N Pandey; R A Vaidya; A Irani
Journal:  Indian J Pediatr       Date:  2003-04       Impact factor: 1.967

4.  Clinical management of behavioral characteristics of Prader-Willi syndrome.

Authors:  Alan Y Ho; Anastasia Dimitropoulos
Journal:  Neuropsychiatr Dis Treat       Date:  2010-05-06       Impact factor: 2.570

5.  The impact of real practice inappropriateness and devices' inefficiency to variability in growth hormone consumption.

Authors:  F Spandonaro; M Cappa; R Castello; F Chiarelli; E Ghigo; L Mancusi
Journal:  J Endocrinol Invest       Date:  2014-08-08       Impact factor: 4.256

6.  Growth hormone receptor (GHR) gene polymorphism and Prader-Willi syndrome.

Authors:  Merlin G Butler; Jennifer Roberts; Jena Hayes; Xiaoyu Tan; Ann M Manzardo
Journal:  Am J Med Genet A       Date:  2013-05-21       Impact factor: 2.802

Review 7.  Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.

Authors:  Krystal A Irizarry; Mark Miller; Michael Freemark; Andrea M Haqq
Journal:  Adv Pediatr       Date:  2016-08

Review 8.  Growth hormone treatment in children: review of safety and efficacy.

Authors:  Mark Harris; Paul L Hofman; Wayne S Cutfield
Journal:  Paediatr Drugs       Date:  2004       Impact factor: 3.022

9.  [Changes in carbohydrate metabolism and insulin resistance in patients with Prader-Willi Syndrome (PWS) under growth hormone therapy].

Authors:  Constanze Lämmer; Edda Weimann
Journal:  Wien Med Wochenschr       Date:  2007-02

10.  Treatment of short stature and growth hormone deficiency in children with somatotropin (rDNA origin).

Authors:  Dana S Hardin
Journal:  Biologics       Date:  2008-12
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