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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
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.
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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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