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Growth hormone treatment for adults with Prader-Willi syndrome: another point of view
Growth hormone treatment for children with Prader Willi syndrome (PWS) has shown proven benefits not only in increasing final height but also with positive effects on body composition and motor development. In a recent letter to the editor, Hoybye and colleagues recommend growth hormone treatment fo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330048/ https://www.ncbi.nlm.nih.gov/pubmed/34344408 http://dx.doi.org/10.1186/s13023-021-01952-9 |
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author | Hirsch, Harry J. Gross-Tsur, Varda |
author_facet | Hirsch, Harry J. Gross-Tsur, Varda |
author_sort | Hirsch, Harry J. |
collection | PubMed |
description | Growth hormone treatment for children with Prader Willi syndrome (PWS) has shown proven benefits not only in increasing final height but also with positive effects on body composition and motor development. In a recent letter to the editor, Hoybye and colleagues recommend growth hormone treatment for adults with PWS based exclusively on the genetic diagnosis and without regard for growth hormone secretory status. We question whether the benefits of growth hormone treatment in PWS adults, mainly improvement in body composition, are significant enough to justify the as yet unkown consequences of long-term treatment in an adult population. Morbidity and mortality in PWS are mainly due to complications of obesity, and growth hormone treatment does not result in a decrease in BMI or waist circumference. Increases in insulin-like factor-1 as a result of growth hormone treatment over the course of several decades in PWS adults raises concern over possible increase risk of cancer. Compliance with daily injections is likely to be poor. We suggest that efforts to provide appropriate dietary and exercise regimens may be more beneficial and cost-effective than advocating for growth hormone treatment for adults with PWS. |
format | Online Article Text |
id | pubmed-8330048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83300482021-08-04 Growth hormone treatment for adults with Prader-Willi syndrome: another point of view Hirsch, Harry J. Gross-Tsur, Varda Orphanet J Rare Dis Letter to the Editor Growth hormone treatment for children with Prader Willi syndrome (PWS) has shown proven benefits not only in increasing final height but also with positive effects on body composition and motor development. In a recent letter to the editor, Hoybye and colleagues recommend growth hormone treatment for adults with PWS based exclusively on the genetic diagnosis and without regard for growth hormone secretory status. We question whether the benefits of growth hormone treatment in PWS adults, mainly improvement in body composition, are significant enough to justify the as yet unkown consequences of long-term treatment in an adult population. Morbidity and mortality in PWS are mainly due to complications of obesity, and growth hormone treatment does not result in a decrease in BMI or waist circumference. Increases in insulin-like factor-1 as a result of growth hormone treatment over the course of several decades in PWS adults raises concern over possible increase risk of cancer. Compliance with daily injections is likely to be poor. We suggest that efforts to provide appropriate dietary and exercise regimens may be more beneficial and cost-effective than advocating for growth hormone treatment for adults with PWS. BioMed Central 2021-08-03 /pmc/articles/PMC8330048/ /pubmed/34344408 http://dx.doi.org/10.1186/s13023-021-01952-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Letter to the Editor Hirsch, Harry J. Gross-Tsur, Varda Growth hormone treatment for adults with Prader-Willi syndrome: another point of view |
title | Growth hormone treatment for adults with Prader-Willi syndrome: another point of view |
title_full | Growth hormone treatment for adults with Prader-Willi syndrome: another point of view |
title_fullStr | Growth hormone treatment for adults with Prader-Willi syndrome: another point of view |
title_full_unstemmed | Growth hormone treatment for adults with Prader-Willi syndrome: another point of view |
title_short | Growth hormone treatment for adults with Prader-Willi syndrome: another point of view |
title_sort | growth hormone treatment for adults with prader-willi syndrome: another point of view |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330048/ https://www.ncbi.nlm.nih.gov/pubmed/34344408 http://dx.doi.org/10.1186/s13023-021-01952-9 |
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