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Factors associated with Advanced Bone Age in Overweight and Obese Children
PURPOSE: Obese children may often present with advanced bone age. We aimed to evaluate the correlation between factors associated with childhood obesity and advanced bone age. METHODS: We enrolled 232 overweight or obese children. Anthropometric and laboratory data, and the degree of nonalcoholic fa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966218/ https://www.ncbi.nlm.nih.gov/pubmed/31988879 http://dx.doi.org/10.5223/pghn.2020.23.1.89 |
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author | Oh, Min-Su Kim, Sorina Lee, Juyeon Lee, Mu Sook Kim, Yoon-Joo Kang, Ki-Soo |
author_facet | Oh, Min-Su Kim, Sorina Lee, Juyeon Lee, Mu Sook Kim, Yoon-Joo Kang, Ki-Soo |
author_sort | Oh, Min-Su |
collection | PubMed |
description | PURPOSE: Obese children may often present with advanced bone age. We aimed to evaluate the correlation between factors associated with childhood obesity and advanced bone age. METHODS: We enrolled 232 overweight or obese children. Anthropometric and laboratory data, and the degree of nonalcoholic fatty liver disease (NAFLD) were measured. We analyzed factors associated with advanced bone age by measuring the differences between bone and chronological ages. RESULTS: The normal and advanced bone age groups were comprised of 183 (78.9%) and 49 (21.1%) children, respectively. The prevalence of advanced bone age significantly increased as the percentiles of height, weight, waist circumference, and body mass index (BMI) increased. BMI z-score was higher in the advanced bone age group than in the normal bone age group (2.43±0.52 vs. 2.10±0.46; p<0.001). The levels of insulin (27.80±26.13 μU/mL vs. 18.65±12.33 μU/mL; p=0.034) and homeostatic model assessment–insulin resistance (6.56±6.18 vs. 4.43±2.93; p=0.037) were significantly higher, while high density lipoprotein-cholesterol levels were lower (43.88±9.98 mg/dL vs. 48.95±10.50 mg/dL; p=0.005) in the advanced bone age group compared to those in the normal bone age group, respectively. The prevalence of advanced bone age was higher in obese children with metabolic syndrome than in those without (28.2% vs. 14.7%; p=0.016). The prevalence of advanced bone age was higher in obese children with a more severe degree of NAFLD. CONCLUSION: Advanced bone age is associated with a severe degree of obesity and its complications. |
format | Online Article Text |
id | pubmed-6966218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-69662182020-01-27 Factors associated with Advanced Bone Age in Overweight and Obese Children Oh, Min-Su Kim, Sorina Lee, Juyeon Lee, Mu Sook Kim, Yoon-Joo Kang, Ki-Soo Pediatr Gastroenterol Hepatol Nutr Original Article PURPOSE: Obese children may often present with advanced bone age. We aimed to evaluate the correlation between factors associated with childhood obesity and advanced bone age. METHODS: We enrolled 232 overweight or obese children. Anthropometric and laboratory data, and the degree of nonalcoholic fatty liver disease (NAFLD) were measured. We analyzed factors associated with advanced bone age by measuring the differences between bone and chronological ages. RESULTS: The normal and advanced bone age groups were comprised of 183 (78.9%) and 49 (21.1%) children, respectively. The prevalence of advanced bone age significantly increased as the percentiles of height, weight, waist circumference, and body mass index (BMI) increased. BMI z-score was higher in the advanced bone age group than in the normal bone age group (2.43±0.52 vs. 2.10±0.46; p<0.001). The levels of insulin (27.80±26.13 μU/mL vs. 18.65±12.33 μU/mL; p=0.034) and homeostatic model assessment–insulin resistance (6.56±6.18 vs. 4.43±2.93; p=0.037) were significantly higher, while high density lipoprotein-cholesterol levels were lower (43.88±9.98 mg/dL vs. 48.95±10.50 mg/dL; p=0.005) in the advanced bone age group compared to those in the normal bone age group, respectively. The prevalence of advanced bone age was higher in obese children with metabolic syndrome than in those without (28.2% vs. 14.7%; p=0.016). The prevalence of advanced bone age was higher in obese children with a more severe degree of NAFLD. CONCLUSION: Advanced bone age is associated with a severe degree of obesity and its complications. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2020-01 2020-01-08 /pmc/articles/PMC6966218/ /pubmed/31988879 http://dx.doi.org/10.5223/pghn.2020.23.1.89 Text en Copyright © 2020 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition https://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Oh, Min-Su Kim, Sorina Lee, Juyeon Lee, Mu Sook Kim, Yoon-Joo Kang, Ki-Soo Factors associated with Advanced Bone Age in Overweight and Obese Children |
title | Factors associated with Advanced Bone Age in Overweight and Obese Children |
title_full | Factors associated with Advanced Bone Age in Overweight and Obese Children |
title_fullStr | Factors associated with Advanced Bone Age in Overweight and Obese Children |
title_full_unstemmed | Factors associated with Advanced Bone Age in Overweight and Obese Children |
title_short | Factors associated with Advanced Bone Age in Overweight and Obese Children |
title_sort | factors associated with advanced bone age in overweight and obese children |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966218/ https://www.ncbi.nlm.nih.gov/pubmed/31988879 http://dx.doi.org/10.5223/pghn.2020.23.1.89 |
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