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Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome
BACKGROUND: Recombinant human growth hormone (rhGH) therapy has shown to improve height and body composition in children with Prader–Willi syndrome (PWS), the evidence of early rhGH treatment on motor and mental development is still accumulating. This study explored the time effect on psychomotor de...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Nature Singapore
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149441/ https://www.ncbi.nlm.nih.gov/pubmed/36564648 http://dx.doi.org/10.1007/s12519-022-00653-y |
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author | Cheng, Ruo-Qian Ying, Yan-Qin Qiu, Zheng-Qing Fu, Jun-Fen Gong, Chun-Xiu Yang, Yan-Ling Shi, Wei Li, Hui Ma, Ming-Sheng Wang, Chang-Yan Liu, Min Chen, Jia-Jia Su, Chang Luo, Xiao-Ping Luo, Fei-Hong Lu, Wei |
author_facet | Cheng, Ruo-Qian Ying, Yan-Qin Qiu, Zheng-Qing Fu, Jun-Fen Gong, Chun-Xiu Yang, Yan-Ling Shi, Wei Li, Hui Ma, Ming-Sheng Wang, Chang-Yan Liu, Min Chen, Jia-Jia Su, Chang Luo, Xiao-Ping Luo, Fei-Hong Lu, Wei |
author_sort | Cheng, Ruo-Qian |
collection | PubMed |
description | BACKGROUND: Recombinant human growth hormone (rhGH) therapy has shown to improve height and body composition in children with Prader–Willi syndrome (PWS), the evidence of early rhGH treatment on motor and mental development is still accumulating. This study explored the time effect on psychomotor development, anthropometric indexes, and safety for infants and young children with PWS. METHODS: A phase 3, single-arm, multicenter, self-controlled study was conducted in six sites. Patients received rhGH at 0.5 mg/m(2)/day for first four weeks, and 1 mg/m(2)/day thereafter for up to 52 weeks. Motor development was measured using Peabody Developmental Motor Scales-second edition, mental development using Griffiths Development Scales-Chinese (GDS-C). Height standard deviation score (SDS), body weight SDS, and body mass index (BMI) SDS were also assessed. RESULTS: Thirty-five patients were enrolled totally. Significant improvements were observed in height, body weight, and BMI SDS at week 52; GDS-C score showed significant improvement in general quotient (GQ) and sub-quotients. In a linear regression analysis, total motor quotient (TMQ), gross motor quotient (GMQ), and fine motor quotient were negatively correlated with age; however, treatment may attenuate deterioration of TMQ and GMQ. Changes in GQ and locomotor sub-quotient in < 9-month group were significantly higher than ≥ 9-month group. Mild to moderate severity adverse drug reactions were reported in six patients. CONCLUSION: Fifty-two-week treatment with rhGH improved growth, BMI, mental development, and lessened the deterioration of motor function in infants and young children with PWS. Improved mental development was more pronounced when instituted in patients < 9 months old. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-022-00653-y. |
format | Online Article Text |
id | pubmed-10149441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-101494412023-05-02 Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome Cheng, Ruo-Qian Ying, Yan-Qin Qiu, Zheng-Qing Fu, Jun-Fen Gong, Chun-Xiu Yang, Yan-Ling Shi, Wei Li, Hui Ma, Ming-Sheng Wang, Chang-Yan Liu, Min Chen, Jia-Jia Su, Chang Luo, Xiao-Ping Luo, Fei-Hong Lu, Wei World J Pediatr Original Article BACKGROUND: Recombinant human growth hormone (rhGH) therapy has shown to improve height and body composition in children with Prader–Willi syndrome (PWS), the evidence of early rhGH treatment on motor and mental development is still accumulating. This study explored the time effect on psychomotor development, anthropometric indexes, and safety for infants and young children with PWS. METHODS: A phase 3, single-arm, multicenter, self-controlled study was conducted in six sites. Patients received rhGH at 0.5 mg/m(2)/day for first four weeks, and 1 mg/m(2)/day thereafter for up to 52 weeks. Motor development was measured using Peabody Developmental Motor Scales-second edition, mental development using Griffiths Development Scales-Chinese (GDS-C). Height standard deviation score (SDS), body weight SDS, and body mass index (BMI) SDS were also assessed. RESULTS: Thirty-five patients were enrolled totally. Significant improvements were observed in height, body weight, and BMI SDS at week 52; GDS-C score showed significant improvement in general quotient (GQ) and sub-quotients. In a linear regression analysis, total motor quotient (TMQ), gross motor quotient (GMQ), and fine motor quotient were negatively correlated with age; however, treatment may attenuate deterioration of TMQ and GMQ. Changes in GQ and locomotor sub-quotient in < 9-month group were significantly higher than ≥ 9-month group. Mild to moderate severity adverse drug reactions were reported in six patients. CONCLUSION: Fifty-two-week treatment with rhGH improved growth, BMI, mental development, and lessened the deterioration of motor function in infants and young children with PWS. Improved mental development was more pronounced when instituted in patients < 9 months old. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-022-00653-y. Springer Nature Singapore 2022-12-24 2023 /pmc/articles/PMC10149441/ /pubmed/36564648 http://dx.doi.org/10.1007/s12519-022-00653-y Text en © The Author(s) 2022 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/) . |
spellingShingle | Original Article Cheng, Ruo-Qian Ying, Yan-Qin Qiu, Zheng-Qing Fu, Jun-Fen Gong, Chun-Xiu Yang, Yan-Ling Shi, Wei Li, Hui Ma, Ming-Sheng Wang, Chang-Yan Liu, Min Chen, Jia-Jia Su, Chang Luo, Xiao-Ping Luo, Fei-Hong Lu, Wei Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome |
title | Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome |
title_full | Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome |
title_fullStr | Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome |
title_full_unstemmed | Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome |
title_short | Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome |
title_sort | early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with prader–willi syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149441/ https://www.ncbi.nlm.nih.gov/pubmed/36564648 http://dx.doi.org/10.1007/s12519-022-00653-y |
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