Literature DB >> 23782572

Long-term effects of recombinant human growth hormone therapy in children with Prader-Willi syndrome.

Peter M Wolfgram1, Aaron L Carrel, David B Allen.   

Abstract

PURPOSE OF REVIEW: Recombinant human growth hormone (hGH) therapy in children with Prader-Willi syndrome (PWS) improves linear growth, body composition, physical strength and agility, and other metabolic parameters. These benefits must be weighed against potential adverse effects, including rare occurrences of sudden death. This review summarizes recent evidence important to a benefit-risk analysis of hGH use in children with PWS. RECENT
FINDINGS: Studies consistently show that hGH improves stature, body composition, fat percentage and distribution, and other metabolic markers in children with PWS. Preliminary reports of improved cognitive development during hGH have also emerged. Scoliosis progression is influenced by growth rate, but frequency of occurrence and severity are not increased by hGH exposure. PWS genotype does not appear to affect response to hGH. Concerns about hGH-associated sudden death persist, but recent studies show either absence of change in sleep-disordered breathing or improved sleep cardiovascular function during hGH therapy.
SUMMARY: Recent studies confirm and expand reported benefits of hGH therapy in children with PWS, including a possible salutary role in cognitive development. These findings support previous assertions that hGH can reduce morbidity and improve function in children with PWS, and suggest that potential risks of such treatment are favorably balanced by its benefits.

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Year:  2013        PMID: 23782572      PMCID: PMC4396180          DOI: 10.1097/MOP.0b013e328362c7a2

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  24 in total

1.  Growth hormone improves body composition, fat utilization, physical strength and agility, and growth in Prader-Willi syndrome: A controlled study.

Authors:  A L Carrel; S E Myers; B Y Whitman; D B Allen
Journal:  J Pediatr       Date:  1999-02       Impact factor: 4.406

2.  Sustained effects of recombinant GH replacement after 7 years of treatment in adults with GH deficiency.

Authors:  A A van der Klaauw; J A Romijn; N R Biermasz; J W A Smit; J van Doorn; O M Dekkers; F Roelfsema; A M Pereira
Journal:  Eur J Endocrinol       Date:  2006-11       Impact factor: 6.664

3.  Fatal outcome of sleep apnoea in PWS during the initial phase of growth hormone treatment. A case report.

Authors:  Urs Eiholzer; Yves Nordmann; Dagmar L'Allemand
Journal:  Horm Res       Date:  2002

4.  Benefits of long-term GH therapy in Prader-Willi syndrome: a 4-year study.

Authors:  Aaron L Carrel; Susan E Myers; Barbara Y Whitman; David B Allen
Journal:  J Clin Endocrinol Metab       Date:  2002-04       Impact factor: 5.958

5.  Sudden death in Prader-Willi syndrome: brief review of five additional cases. Concerning the article by U. Eiholzer et al.: Deaths in children with Prader-Willi syndrome. A contribution to the debate about the safety of growth hormone treatment in children with PWS (Horm Res 2005;63:33-39).

Authors:  Bert Bakker; Thomas Maneatis; Barbara Lippe
Journal:  Horm Res       Date:  2006-12-12

6.  Treatment with human growth hormone in patients with Prader-Labhart-Willi syndrome reduces body fat and increases muscle mass and physical performance.

Authors:  U Eiholzer; R Gisin; C Weinmann; S Kriemler; H Steinert; T Torresani; M Zachmann; A Prader
Journal:  Eur J Pediatr       Date:  1998-05       Impact factor: 3.183

7.  Mental and motor development before and during growth hormone treatment in infants and toddlers with Prader-Willi syndrome.

Authors:  D A M Festen; M Wevers; A C Lindgren; B Böhm; B J Otten; J M Wit; H J Duivenvoorden; A C S Hokken-Koelega
Journal:  Clin Endocrinol (Oxf)       Date:  2007-11-19       Impact factor: 3.478

8.  Final adult height in children with Prader-Willi syndrome with and without human growth hormone treatment.

Authors:  Moris A Angulo; Mariano Castro-Magana; Michele Lamerson; Raul Arguello; Siham Accacha; Asjad Khan
Journal:  Am J Med Genet A       Date:  2007-07-01       Impact factor: 2.802

9.  Long-term growth hormone therapy changes the natural history of body composition and motor function in children with prader-willi syndrome.

Authors:  Aaron L Carrel; Susan E Myers; Barbara Y Whitman; Jens Eickhoff; David B Allen
Journal:  J Clin Endocrinol Metab       Date:  2010-01-08       Impact factor: 5.958

Review 10.  Review of 64 cases of death in children with Prader-Willi syndrome (PWS).

Authors:  M Tauber; G Diene; C Molinas; M Hébert
Journal:  Am J Med Genet A       Date:  2008-04-01       Impact factor: 2.802

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  13 in total

Review 1.  Growth Hormone Deficiency: Health and Longevity.

Authors:  Manuel H Aguiar-Oliveira; Andrzej Bartke
Journal:  Endocr Rev       Date:  2019-04-01       Impact factor: 19.871

Review 2.  Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.

Authors:  Dai Yang-Li; Luo Fei-Hong; Zhang Hui-Wen; Ma Ming-Sheng; Luo Xiao-Ping; Liu Li; Wang Yi; Zhou Qing; Jiang Yong-Hui; Zou Chao-Chun
Journal:  Orphanet J Rare Dis       Date:  2022-06-13       Impact factor: 4.303

3.  Effects of growth hormone treatment on adult height in severely short children with X-linked hypophosphatemic rickets.

Authors:  Nadine Meyerhoff; Dieter Haffner; Hagen Staude; Elke Wühl; Michaela Marx; Rolf Beetz; Uwe Querfeld; Martin Holder; Heiko Billing; Wolfgang Rabl; Carmen Schröder; Olaf Hiort; Jürgen H Brämswig; Annette Richter-Unruh; Dirk Schnabel; Miroslav Živičnjak
Journal:  Pediatr Nephrol       Date:  2017-10-20       Impact factor: 3.714

4.  Pediatric Obesity-Assessment, Treatment, and Prevention: An Endocrine Society Clinical Practice Guideline.

Authors:  Dennis M Styne; Silva A Arslanian; Ellen L Connor; Ismaa Sadaf Farooqi; M Hassan Murad; Janet H Silverstein; Jack A Yanovski
Journal:  J Clin Endocrinol Metab       Date:  2017-03-01       Impact factor: 5.958

5.  Word-of-Mouth Innovation: Hypothesis Generation for Supplement Repurposing based on Consumer Reviews.

Authors:  Jung-Wei Fan; Yves A Lussier
Journal:  AMIA Annu Symp Proc       Date:  2018-04-16

Review 6.  Syndromic disorders with short stature.

Authors:  Zeynep Şıklar; Merih Berberoğlu
Journal:  J Clin Res Pediatr Endocrinol       Date:  2014

7.  AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome: A randomized placebo-controlled trial.

Authors:  Soraya Allas; Assumpta Caixàs; Christine Poitou; Muriel Coupaye; Denise Thuilleaux; Françoise Lorenzini; Gwenaëlle Diene; Antonino Crinò; Frédéric Illouz; Graziano Grugni; Diane Potvin; Sarah Bocchini; Thomas Delale; Thierry Abribat; Maithé Tauber
Journal:  PLoS One       Date:  2018-01-10       Impact factor: 3.240

8.  Influence of growth hormone treatment on radiographic indices of the spine: propensity-matched analysis.

Authors:  Yeo-Hon Yun; Soon-Sun Kwon; Youngdo Koh; Dong-Jun Kim; Jonghyun Ahn; Seung Yeol Lee
Journal:  J Orthop Surg Res       Date:  2017-09-06       Impact factor: 2.359

Review 9.  Growth Hormone Therapy in Adults with Prader-Willi Syndrome.

Authors:  Karen S Vogt; Jill E Emerick
Journal:  Diseases       Date:  2015-04-16

Review 10.  Growth hormone therapy for Prader-willi syndrome: challenges and solutions.

Authors:  Graziano Grugni; Alessandro Sartorio; Antonino Crinò
Journal:  Ther Clin Risk Manag       Date:  2016-06-02       Impact factor: 2.423

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