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Factors affecting bone mineral density in children and adolescents with secondary osteoporosis

PURPOSE: This study aimed to investigate the clinical factors associated with bone mineral density (BMD) among children and adolescents with osteoporosis secondary to treatment for underlying clinical conditions. METHODS: We retrospectively reviewed the medical records of patients aged 10–18 years a...

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Autores principales: Jang, Min Jeong, Shin, Chungwoo, Kim, Seongkoo, Lee, Jae Wook, Chung, Nack-Gyun, Cho, Bin, Jung, Min Ho, Suh, Byung-Kyu, Ahn, Moon Bae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073031/
https://www.ncbi.nlm.nih.gov/pubmed/35798303
http://dx.doi.org/10.6065/apem.2244026.013
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author Jang, Min Jeong
Shin, Chungwoo
Kim, Seongkoo
Lee, Jae Wook
Chung, Nack-Gyun
Cho, Bin
Jung, Min Ho
Suh, Byung-Kyu
Ahn, Moon Bae
author_facet Jang, Min Jeong
Shin, Chungwoo
Kim, Seongkoo
Lee, Jae Wook
Chung, Nack-Gyun
Cho, Bin
Jung, Min Ho
Suh, Byung-Kyu
Ahn, Moon Bae
author_sort Jang, Min Jeong
collection PubMed
description PURPOSE: This study aimed to investigate the clinical factors associated with bone mineral density (BMD) among children and adolescents with osteoporosis secondary to treatment for underlying clinical conditions. METHODS: We retrospectively reviewed the medical records of patients aged 10–18 years and evaluated them for lumbar spine BMD (LSBMD) after treatment for underlying diseases, including hemato-oncologic, rheumatologic system, and inflammatory bowel diseases. LSBMD measured by dual-energy x-ray absorptiometry (DXA) performed from March 2019 to March 2021 was evaluated. We analyzed 117 patients who underwent initial DXA after treatment for underlying diseases. RESULTS: Subjects in this study had multiple underlying diseases: hemato-oncologic (78.6%), rheumatologic (11.1%), and inflammatory bowel diseases (10.3%). There was no significant association between the z-score and bone metabolic markers (P>0.05). However, higher cumulative glucocorticoid (GC) dose significantly reduced LSBMD z-score (P=0.029). Moreover, the association between cumulative dose of GC and initial z-score of LSBMD was significant in logarithmic regression analysis (P=0.003, R(2)=0.149). GC accumulation was a significant risk factor for vertebral fracture when the initial BMD was evaluated after treatment (P=0.043). Bone metabolic markers did not significantly influence the risk of vertebral fracture. CONCLUSIONS: Initial bone mass density of the lumbar spine evaluated after long-term GC use for underlying diseases is a predictor of further vertebral fractures.
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spelling pubmed-100730312023-04-06 Factors affecting bone mineral density in children and adolescents with secondary osteoporosis Jang, Min Jeong Shin, Chungwoo Kim, Seongkoo Lee, Jae Wook Chung, Nack-Gyun Cho, Bin Jung, Min Ho Suh, Byung-Kyu Ahn, Moon Bae Ann Pediatr Endocrinol Metab Original Article PURPOSE: This study aimed to investigate the clinical factors associated with bone mineral density (BMD) among children and adolescents with osteoporosis secondary to treatment for underlying clinical conditions. METHODS: We retrospectively reviewed the medical records of patients aged 10–18 years and evaluated them for lumbar spine BMD (LSBMD) after treatment for underlying diseases, including hemato-oncologic, rheumatologic system, and inflammatory bowel diseases. LSBMD measured by dual-energy x-ray absorptiometry (DXA) performed from March 2019 to March 2021 was evaluated. We analyzed 117 patients who underwent initial DXA after treatment for underlying diseases. RESULTS: Subjects in this study had multiple underlying diseases: hemato-oncologic (78.6%), rheumatologic (11.1%), and inflammatory bowel diseases (10.3%). There was no significant association between the z-score and bone metabolic markers (P>0.05). However, higher cumulative glucocorticoid (GC) dose significantly reduced LSBMD z-score (P=0.029). Moreover, the association between cumulative dose of GC and initial z-score of LSBMD was significant in logarithmic regression analysis (P=0.003, R(2)=0.149). GC accumulation was a significant risk factor for vertebral fracture when the initial BMD was evaluated after treatment (P=0.043). Bone metabolic markers did not significantly influence the risk of vertebral fracture. CONCLUSIONS: Initial bone mass density of the lumbar spine evaluated after long-term GC use for underlying diseases is a predictor of further vertebral fractures. Korean Society of Pediatric Endocrinology 2023-03 2022-06-28 /pmc/articles/PMC10073031/ /pubmed/35798303 http://dx.doi.org/10.6065/apem.2244026.013 Text en © 2023 Annals of Pediatric Endocrinology & Metabolism 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 (http://creativecommons.org/licenses/by-nc/4.0/ (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
Jang, Min Jeong
Shin, Chungwoo
Kim, Seongkoo
Lee, Jae Wook
Chung, Nack-Gyun
Cho, Bin
Jung, Min Ho
Suh, Byung-Kyu
Ahn, Moon Bae
Factors affecting bone mineral density in children and adolescents with secondary osteoporosis
title Factors affecting bone mineral density in children and adolescents with secondary osteoporosis
title_full Factors affecting bone mineral density in children and adolescents with secondary osteoporosis
title_fullStr Factors affecting bone mineral density in children and adolescents with secondary osteoporosis
title_full_unstemmed Factors affecting bone mineral density in children and adolescents with secondary osteoporosis
title_short Factors affecting bone mineral density in children and adolescents with secondary osteoporosis
title_sort factors affecting bone mineral density in children and adolescents with secondary osteoporosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073031/
https://www.ncbi.nlm.nih.gov/pubmed/35798303
http://dx.doi.org/10.6065/apem.2244026.013
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