Literature DB >> 27552545

Beneficial Effects of GH in Young Adults With Prader-Willi Syndrome: A 2-Year Crossover Trial.

Renske J Kuppens1, Nienke E Bakker1, Elbrich P C Siemensma1, Roderick F A Tummers-de Lind van Wijngaarden1, Stephany H Donze1, Dederieke A M Festen1, Janielle A E M van Alfen-van der Velden1, Theo Stijnen1, Anita C S Hokken-Koelega1.   

Abstract

CONTEXT: Patients with Prader-Willi syndrome (PWS) are severely at risk to develop morbid obesity, diabetes mellitus type 2, and cardiovascular disease, leading to high mortality. They have an increased fat mass (FM) and decreased lean body mass (LBM). During childhood, GH treatment counteracts the natural course of increasing obesity. Discontinuation of GH treatment at attainment of adult height (AH) might deteriorate their improved clinical condition, whereas continuation might benefit them.
OBJECTIVE: To investigate the effects of GH versus placebo on body composition in young adults with PWS who were GH treated for many years during childhood and had attained AH.
DESIGN: Two-year, randomized, double-blind, placebo-controlled crossover study with stratification for gender and body mass index in 27 young adults with PWS.
SETTING: PWS Reference Center in The Netherlands. INTERVENTION: Crossover intervention with GH (0.67 mg/m2 · d) and placebo, both during 1 year. MAIN OUTCOME MEASURES: Body composition, measured by dual-energy x-ray absorptiometry.
RESULTS: During placebo, FM increased (relative change +21.5%; P < .001). Compared with placebo, GH treatment resulted in lower FM (-2.9 kg; P = .004) and higher LBM (+1.5 kg; P = .005), representing relative changes of -17.3% FM and +3.5% LBM. Both limb and trunk FM percentage were lower during GH versus placebo (relative change +17.3% and +15.6%; P < .001 and P = .007, respectively). No GH-related adverse events occurred.
CONCLUSIONS: GH-treated young adults with PWS who have attained AH benefit from continuation of GH treatment. FM increases during placebo, whereas GH versus placebo results in lower FM and higher LBM. Thus, GH treatment maintains the improved body composition without safety concerns.

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Year:  2016        PMID: 27552545     DOI: 10.1210/jc.2016-2594

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  8 in total

1.  The associations between diet and physical activity with body composition and walking a timed distance in adults with Prader-Willi syndrome.

Authors:  Susan G Woods; Allen Knehans; Sandra Arnold; Carol Dionne; Leah Hoffman; Peggy Turner; Jonathan Baldwin
Journal:  Food Nutr Res       Date:  2018-06-18       Impact factor: 3.894

2.  Three years of growth hormone treatment in young adults with Prader-Willi syndrome: sustained positive effects on body composition.

Authors:  Layla Damen; Stephany H Donze; Renske J Kuppens; Nienke E Bakker; Laura C G de Graaff; Janielle A E M van der Velden; Anita C S Hokken-Koelega
Journal:  Orphanet J Rare Dis       Date:  2020-06-24       Impact factor: 4.123

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

4.  Prevalence of growth hormone (GH) deficiency in previously GH-treated young adults with Prader-Willi syndrome.

Authors:  Stephany H Donze; Layla Damen; Janiëlle A E M van Alfen-van der Velden; Gianni Bocca; Martijn J J Finken; Gera J G Hoorweg-Nijman; Petr E Jira; Mariëtte van Leeuwen; Anita C S Hokken-Koelega
Journal:  Clin Endocrinol (Oxf)       Date:  2019-04-30       Impact factor: 3.478

5.  Evidence for Accelerated Biological Aging in Young Adults with Prader-Willi Syndrome.

Authors:  Stephany H Donze; Veryan Codd; Layla Damen; Wesley J Goedegebuure; Matthew Denniff; Nilesh J Samani; Janiëlle A E M van der Velden; Anita C S Hokken-Koelega
Journal:  J Clin Endocrinol Metab       Date:  2020-06-01       Impact factor: 5.958

6.  Time for a general approval of growth hormone treatment in adults with Prader-Willi syndrome.

Authors:  Charlotte Höybye; Anthony J Holland; Daniel J Driscoll
Journal:  Orphanet J Rare Dis       Date:  2021-02-08       Impact factor: 4.123

7.  An Adapted Model for Transition to Adult Care in Young Adults with Prader-Willi Syndrome.

Authors:  Maria Pedersen; Charlotte Höybye
Journal:  J Clin Med       Date:  2021-05-06       Impact factor: 4.241

Review 8.  PRADER-WILLI SYNDROME: WHAT IS THE GENERAL PEDIATRICIAN SUPPOSED TO DO? - A REVIEW.

Authors:  Caroline Buff Gouveia Passone; Paula Lage Pasqualucci; Ruth Rocha Franco; Simone Sakura Ito; Larissa Baldini Farjalla Mattar; Celia Priszkulnik Koiffmann; Leticia Azevedo Soster; Jorge David Aivazoglou Carneiro; Hamilton Cabral Menezes-Filho; Durval Damiani
Journal:  Rev Paul Pediatr       Date:  2018 Jul-Sep
  8 in total

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