Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years

Abstract Background Prader-Willi syndrome (PWS) is a multisystem genetic disorder, which has a typical eating behavior and growth pattern. In the infancy period, children with PWS have low body weight followed by hyperphagia in later childhood. Disease-specific growth charts have been recommended fo...

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Main Authors: Nantiya Mongkollarp, Thipwimol Tim-Aroon, Chusak Okascharoen, Khunton Wichajarn, Jeeraparn Phosuwattanakul, Nalinee Chongviriyaphan, Duangrurdee Wattanasirichaigoon
Format: Article
Language:English
Published: BMC 2020-05-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13023-020-01388-7
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spelling doaj-0822a97fde054ffd9275efae1ec55e1c2020-11-25T02:18:33ZengBMCOrphanet Journal of Rare Diseases1750-11722020-05-011511910.1186/s13023-020-01388-7Growth charts for Thai children with Prader-Willi syndrome aged 0–18 yearsNantiya Mongkollarp0Thipwimol Tim-Aroon1Chusak Okascharoen2Khunton Wichajarn3Jeeraparn Phosuwattanakul4Nalinee Chongviriyaphan5Duangrurdee Wattanasirichaigoon6Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol UniversityDivision of Medical Genetics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol UniversityDivision of Evidence-based Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol UniversityDivision of Medical Genetics, Department of Pediatrics, Faculty of Medicine, Khon Kaen UniversityDivision of Nutrition, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol UniversityDivision of Nutrition, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol UniversityDivision of Medical Genetics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol UniversityAbstract Background Prader-Willi syndrome (PWS) is a multisystem genetic disorder, which has a typical eating behavior and growth pattern. In the infancy period, children with PWS have low body weight followed by hyperphagia in later childhood. Disease-specific growth charts have been recommended for monitoring PWS patients. Previous literature demonstrated growth differences among individuals with PWS of different ethnicity. Methods A retrospective multicenter study was performed in PWS patients from different areas of Thailand included collaboration with the Thai PWS support group during 2000–2017. Baseline characteristics and anthropometric data were reviewed. Both growth hormone and non-growth hormone received patients were included, but the data after receiving GH were excluded before curve construction. Growth charts for Thai PWS compared to the 50th normative centile were constructed using Generalized Least Squares (GLS) methods. Curve smoothing was performed by Fractional Polynomials and Exponential Transformation. Result One hundred and thirteen patients with genetically confirmed PWS (55 males and 58 females) were enrolled. Fifty percent of patients were diagnosed less than 6 months of age. We developed growth charts for non-growth hormone treated Thai children with PWS aged between 0 and 18 years. A growth pattern was similar to other ethnicities while there were some differences. Mean birth weight of PWS patients was less than that of typical newborns. Mean adult height at 18 years of age in Thai children with PWS was lower than that in American children, but taller than Japanese. Mean weight of Thai PWS males at 18 years of age was more than those from other countries. Conclusion This study is the first to document PWS-specific growth charts in Southeast Asian population. These growth charts will be useful in improving the quality of patient care and in evaluating the impact of growth hormone treatment in the future.http://link.springer.com/article/10.1186/s13023-020-01388-7Prader-Willi syndromeGrowth chartBody heightBody weightHead circumferenceSoutheast Asian
collection DOAJ
language English
format Article
sources DOAJ
author Nantiya Mongkollarp
Thipwimol Tim-Aroon
Chusak Okascharoen
Khunton Wichajarn
Jeeraparn Phosuwattanakul
Nalinee Chongviriyaphan
Duangrurdee Wattanasirichaigoon
spellingShingle Nantiya Mongkollarp
Thipwimol Tim-Aroon
Chusak Okascharoen
Khunton Wichajarn
Jeeraparn Phosuwattanakul
Nalinee Chongviriyaphan
Duangrurdee Wattanasirichaigoon
Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years
Orphanet Journal of Rare Diseases
Prader-Willi syndrome
Growth chart
Body height
Body weight
Head circumference
Southeast Asian
author_facet Nantiya Mongkollarp
Thipwimol Tim-Aroon
Chusak Okascharoen
Khunton Wichajarn
Jeeraparn Phosuwattanakul
Nalinee Chongviriyaphan
Duangrurdee Wattanasirichaigoon
author_sort Nantiya Mongkollarp
title Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years
title_short Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years
title_full Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years
title_fullStr Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years
title_full_unstemmed Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years
title_sort growth charts for thai children with prader-willi syndrome aged 0–18 years
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2020-05-01
description Abstract Background Prader-Willi syndrome (PWS) is a multisystem genetic disorder, which has a typical eating behavior and growth pattern. In the infancy period, children with PWS have low body weight followed by hyperphagia in later childhood. Disease-specific growth charts have been recommended for monitoring PWS patients. Previous literature demonstrated growth differences among individuals with PWS of different ethnicity. Methods A retrospective multicenter study was performed in PWS patients from different areas of Thailand included collaboration with the Thai PWS support group during 2000–2017. Baseline characteristics and anthropometric data were reviewed. Both growth hormone and non-growth hormone received patients were included, but the data after receiving GH were excluded before curve construction. Growth charts for Thai PWS compared to the 50th normative centile were constructed using Generalized Least Squares (GLS) methods. Curve smoothing was performed by Fractional Polynomials and Exponential Transformation. Result One hundred and thirteen patients with genetically confirmed PWS (55 males and 58 females) were enrolled. Fifty percent of patients were diagnosed less than 6 months of age. We developed growth charts for non-growth hormone treated Thai children with PWS aged between 0 and 18 years. A growth pattern was similar to other ethnicities while there were some differences. Mean birth weight of PWS patients was less than that of typical newborns. Mean adult height at 18 years of age in Thai children with PWS was lower than that in American children, but taller than Japanese. Mean weight of Thai PWS males at 18 years of age was more than those from other countries. Conclusion This study is the first to document PWS-specific growth charts in Southeast Asian population. These growth charts will be useful in improving the quality of patient care and in evaluating the impact of growth hormone treatment in the future.
topic Prader-Willi syndrome
Growth chart
Body height
Body weight
Head circumference
Southeast Asian
url http://link.springer.com/article/10.1186/s13023-020-01388-7
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