Literature DB >> 20333875

Benefit of early commencement of growth hormone therapy in children with Prader-Willi syndrome.

O Nyunt1, M Harris, I Hughes, T Huynh, P S W Davies, A M Cotterill.   

Abstract

Prader-Willi syndrome (PWS) is a chromosomal disorder and growth failure is a common presentation. Growth hormone (GH) treatment is beneficial in PWS although the optimal age for starting GH is unknown. We investigated whether GH response in PWS was associated with the age of GH commencement by comparing 16 children who commenced GH before 3 years of age (early group) with 40 children who commenced GH after 3 years of age (late group) from the Ozgrow database. Height SDS, body mass index (BMI) SDS, bone age (BA)-chronological age (CA) ratio, change in height (delta Ht) SDS and change in BMI during 4 years of GH treatment were compared between the groups. The early group had better height SDS and delta Ht SDS. BA delay was more pronounced in the early group but BA did not mature beyond CA with GH therapy in either group. Although the initial GH dose for the early group was lower than that of the late group, the former had better height outcome. The starting GH dose seen in the database is lower than the dose used by international centres.

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Year:  2009        PMID: 20333875     DOI: 10.1515/jpem.2009.22.12.1151

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  4 in total

1.  Contributing factors of mortality in Prader-Willi syndrome.

Authors:  Jennifer Proffitt; Kathryn Osann; Barbara McManus; Virginia E Kimonis; Janalee Heinemann; Merlin G Butler; David A Stevenson; June-Anne Gold
Journal:  Am J Med Genet A       Date:  2018-12-19       Impact factor: 2.802

Review 2.  GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome.

Authors:  Cheri L Deal; Michèle Tony; Charlotte Höybye; David B Allen; Maïthé Tauber; Jens Sandahl Christiansen
Journal:  J Clin Endocrinol Metab       Date:  2013-03-29       Impact factor: 5.958

3.  Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial.

Authors:  Aram Yang; Jin-Ho Choi; Young Bae Sohn; Yunae Eom; Jiyoon Lee; Han-Wook Yoo; Dong-Kyu Jin
Journal:  Orphanet J Rare Dis       Date:  2019-09-11       Impact factor: 4.123

4.  Growth hormone treatment in Prader-Willi syndrome patients: systematic review and meta-analysis.

Authors:  Caroline de Gouveia Buff Passone; Ruth Rocha Franco; Simone Sakura Ito; Evelinda Trindade; Michel Polak; Durval Damiani; Wanderley Marques Bernardo
Journal:  BMJ Paediatr Open       Date:  2020-04-29
  4 in total

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