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Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up

BACKGROUND AND PURPOSE: — Osteogenesis imperfecta (OI) is a heritable disorder of connective tissue caused by a defect in collagen type I synthesis. For bone, this includes fragility, low bone mass, and progressive skeletal deformities, which can result in various degrees of short stature. The purpo...

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Autores principales: Kok, Dieke H J, Sakkers, Ralph J B, Pruijs, Hans E H, Joosse, Pieter, Castelein, René M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768047/
https://www.ncbi.nlm.nih.gov/pubmed/23992144
http://dx.doi.org/10.3109/17453674.2013.831321
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author Kok, Dieke H J
Sakkers, Ralph J B
Pruijs, Hans E H
Joosse, Pieter
Castelein, René M
author_facet Kok, Dieke H J
Sakkers, Ralph J B
Pruijs, Hans E H
Joosse, Pieter
Castelein, René M
author_sort Kok, Dieke H J
collection PubMed
description BACKGROUND AND PURPOSE: — Osteogenesis imperfecta (OI) is a heritable disorder of connective tissue caused by a defect in collagen type I synthesis. For bone, this includes fragility, low bone mass, and progressive skeletal deformities, which can result in various degrees of short stature. The purpose of this study was to investigate development of bone mineral density in children with OI. PATIENTS AND METHODS: — Development of lumbar bone mineral density was studied retrospectively in a cohort of 74 children with OI. Mean age was 16.3 years (SD 4.3). In 52 children, repeated measurements were available. Mean age at the start of measurement was 8.8 years (SD 4.1), and mean follow-up was 9 years (SD 2.7). A longitudinal data analysis was performed. In the total cohort (74 children), a cross-sectional analysis was performed with the latest-measured BMD. Age at the latest BMD measurement was almost equal for girls and boys: 17.4 and 17.7 years respectively. RESULT: — Mean annual increase in BMD in the 52 children was 0.038 g/cm(2)/year (SD 0.024). Annual increase in BMD was statistically significantly higher in girls, in both the unadjusted and adjusted analysis. In cross-sectional analysis, in the whole cohort the latest-measured lumbar BMD was significantly higher in girls, in the children with OI of type I, in walkers, and in those who were older, in both unadjusted and adjusted analysis. INTERPRETATION: — During 9 years of follow-up, there appeared to be an increase in bone mineral density, which was most pronounced in girls. One possible explanation might be a later growth spurt and older age at peak bone mass in boys.
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spelling pubmed-37680472013-09-16 Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up Kok, Dieke H J Sakkers, Ralph J B Pruijs, Hans E H Joosse, Pieter Castelein, René M Acta Orthop Child BACKGROUND AND PURPOSE: — Osteogenesis imperfecta (OI) is a heritable disorder of connective tissue caused by a defect in collagen type I synthesis. For bone, this includes fragility, low bone mass, and progressive skeletal deformities, which can result in various degrees of short stature. The purpose of this study was to investigate development of bone mineral density in children with OI. PATIENTS AND METHODS: — Development of lumbar bone mineral density was studied retrospectively in a cohort of 74 children with OI. Mean age was 16.3 years (SD 4.3). In 52 children, repeated measurements were available. Mean age at the start of measurement was 8.8 years (SD 4.1), and mean follow-up was 9 years (SD 2.7). A longitudinal data analysis was performed. In the total cohort (74 children), a cross-sectional analysis was performed with the latest-measured BMD. Age at the latest BMD measurement was almost equal for girls and boys: 17.4 and 17.7 years respectively. RESULT: — Mean annual increase in BMD in the 52 children was 0.038 g/cm(2)/year (SD 0.024). Annual increase in BMD was statistically significantly higher in girls, in both the unadjusted and adjusted analysis. In cross-sectional analysis, in the whole cohort the latest-measured lumbar BMD was significantly higher in girls, in the children with OI of type I, in walkers, and in those who were older, in both unadjusted and adjusted analysis. INTERPRETATION: — During 9 years of follow-up, there appeared to be an increase in bone mineral density, which was most pronounced in girls. One possible explanation might be a later growth spurt and older age at peak bone mass in boys. Informa Healthcare 2013-08 2013-09-02 /pmc/articles/PMC3768047/ /pubmed/23992144 http://dx.doi.org/10.3109/17453674.2013.831321 Text en Copyright: © Nordic Orthopaedic Federation http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.
spellingShingle Child
Kok, Dieke H J
Sakkers, Ralph J B
Pruijs, Hans E H
Joosse, Pieter
Castelein, René M
Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up
title Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up
title_full Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up
title_fullStr Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up
title_full_unstemmed Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up
title_short Bone mineral density in developing children with osteogenesis imperfecta: A longitudinal study with 9 years of follow-up
title_sort bone mineral density in developing children with osteogenesis imperfecta: a longitudinal study with 9 years of follow-up
topic Child
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768047/
https://www.ncbi.nlm.nih.gov/pubmed/23992144
http://dx.doi.org/10.3109/17453674.2013.831321
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