Literature DB >> 23781979

Response to growth hormone treatment in Prader-Willi syndrome: auxological criteria versus genetic diagnosis.

Elly Scheermeyer1, Ian Hughes, Mark Harris, Geoff Ambler, Patricia Crock, Charles F Verge, Maria E Craig, Phil Bergman, George Werther, Mieke van Driel, Peter Sw Davies, Catherine S Y Choong.   

Abstract

AIM: The Australian Prader-Willi Syndrome (PWS) database was established to monitor the efficacy and safety of growth hormone (GH) treatment in PWS. This study aims to compare response to GH based on eligibility criteria.
METHODS: Comparative study: 72 children received GH on the basis of short stature or evidence of GH deficiency (pre-2009: PWS-SS) and 94 on a genetic diagnosis (post-2009: PWS-Dx). We report on mandatory patient data for GH prescription: median and standard deviation score (SDS) for height and body mass index (BMI), waist/height ratio, bone age/chronological age ratio and adverse events. Comparisons were made using non-parametric tests.
RESULTS: At baseline, the PWS-SS cohort was shorter (height SDS: -2.6 vs. -1.1, P < 0.001), had a lower BMI (0.6 vs. 1.5 SDS, P < 0.05) and greater bone age delay (bone age/chronological age: 0.7 vs. 0.9, P < 0.05) than the PWS-Dx cohort. PWS-SS parents were shorter (mid-parental height SDS: -0.13 vs. 0.28, P < 0.005). Mean change in height over 2 years was 0.9 SDS and in BMI using PWS reference standards -0.3 SDSPWS (n = 106) (year 2, height SDS: PWS-SS = -1.7, PWS-Dx = 0.1; BMI SDSPWS : PWS-SS = -1.0, PWS-Dx = -0.6). The waist/height ratio reduced (PWS-Dx: 0.60 vs. 0.56, P < 0.05) and bone age delay was unchanged over this period. No serious adverse events were reported.
CONCLUSIONS: The PWS-SS cohort represents a subgroup of the wider PWS-Dx population; however both cohorts improved height SDS with normalisation of height in the PWS-Dx cohort and lowering of BMI relative to PWS standards supporting the efficacy of treatment under the current Australian GH programme.
© 2013 The Authors. Journal of Paediatrics and Child Health © 2013 Paediatrics and Child Health Division (Royal Australasian College of Physicians).

Entities:  

Keywords:  Prader-Willi syndrome; disability; growth hormone; metabolic; obesity

Mesh:

Substances:

Year:  2013        PMID: 23781979     DOI: 10.1111/jpc.12294

Source DB:  PubMed          Journal:  J Paediatr Child Health        ISSN: 1034-4810            Impact factor:   1.954


  3 in total

1.  Sleep-disordered breathing in Australian children with Prader-Willi syndrome following initiation of growth hormone therapy.

Authors:  Daan Caudri; Gillian M Nixon; Aleisha Nielsen; Linda Mai; Claire R Hafekost; Nitin Kapur; Chris Seton; Andrew Tai; Greg Blecher; Geoff Ambler; Philip B Bergman; Komal A Vora; Patricia Crock; Charles F Verge; Elaine Tham; Yassmin Musthaffa; Antony R Lafferty; Peter Jacoby; Andrew C Wilson; Jenny Downs; Catherine S Choong
Journal:  J Paediatr Child Health       Date:  2021-08-16       Impact factor: 1.929

2.  Growth Trajectories in Genetic Subtypes of Prader-Willi Syndrome.

Authors:  Daisy A Shepherd; Niels Vos; Susan M Reid; David E Godler; Angela Guzys; Margarita Moreno-Betancur; David J Amor
Journal:  Genes (Basel)       Date:  2020-07-02       Impact factor: 4.096

Review 3.  Requirements for improving health and well-being of children with Prader-Willi syndrome and their families.

Authors:  Jessica Mackay; Zoe McCallum; Geoffrey R Ambler; Komal Vora; Gillian Nixon; Philip Bergman; Nora Shields; Kate Milner; Nitin Kapur; Patricia Crock; Daan Caudri; Jaqueline Curran; Charles Verge; Chris Seton; Andrew Tai; Elaine Tham; Yassmin Musthaffa; Antony R Lafferty; Greg Blecher; Jessica Harper; Cara Schofield; Aleisha Nielsen; Andrew Wilson; Helen Leonard; Catherine S Choong; Jenny Downs
Journal:  J Paediatr Child Health       Date:  2019-06-30       Impact factor: 1.954

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.