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Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt
AIM OF THE STUDY: To evaluate bone mineral density (BMD) and levels of bone turnover markers in Egyptian children with classic congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency and its relationship with disease-related variables. PATIENTS AND METHODS: The study population cons...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171895/ https://www.ncbi.nlm.nih.gov/pubmed/25285289 http://dx.doi.org/10.4103/2230-8210.139236 |
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author | Metwalley, Kotb Abbass El-Saied, Abdel-Rahman Abbdel-Hamed |
author_facet | Metwalley, Kotb Abbass El-Saied, Abdel-Rahman Abbdel-Hamed |
author_sort | Metwalley, Kotb Abbass |
collection | PubMed |
description | AIM OF THE STUDY: To evaluate bone mineral density (BMD) and levels of bone turnover markers in Egyptian children with classic congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency and its relationship with disease-related variables. PATIENTS AND METHODS: The study population consisted of 28 children from Upper Egypt with classic CAH, their mean age 8.3 ± 2.4 years and 28 age and sex matched healthy control. They were subjected to measurement of BMD of lumbar spines (L1-L4) and femoral neck using dual-energy-X-ray absorptiometry (DXA) and laboratory evaluation of bone turnover markers including Osteocalcin and serum receptor activator of nuclear factor κB-ligand (RANKL). RESULT: Children with CAH had significantly lower bone-mineral density (BMD) for both, vertebrae and femoral neck than controls. This difference is more obvious in children with poor control and in those receiving prednisone therapy. There was a significantly lower serum osteocalcin, and significantly higher serum RANKL levels in patients with CAH than the healthy controls. This differences is more obvious in children with poor control and in those receiving prednisone therapy. Total bone mineral content (BMC [gm]) have significant negative correlations to age (r = −0.81, P < 0.001), disease duration (r = −0.881, P < 0.001), 17 OH Progesterone level (r = −0.543, P < 0.05), RANKL level (r = −0.635, P < 0.05), and significant positive correlation with osteocalcin (r = 0.576, P < 0.001). CONCLUSIONS: Children from Upper Egypt with classic CAH may have reduced BMD and increase bone turnover compared with controls. This difference is more obvious in children with poor control and in those receiving prednisone therapy. RECOMMENDATIONS: Active monitoring of BMD in CAH children using Dual-energy X-ray absorptiometry (DEXA) scanning. Furthermore, effort should be done to bring hydrocortisone to Upper Egypt to replace prednisone in children with classic congenital adrenal hyperplasia. |
format | Online Article Text |
id | pubmed-4171895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41718952014-10-03 Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt Metwalley, Kotb Abbass El-Saied, Abdel-Rahman Abbdel-Hamed Indian J Endocrinol Metab Original Article AIM OF THE STUDY: To evaluate bone mineral density (BMD) and levels of bone turnover markers in Egyptian children with classic congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency and its relationship with disease-related variables. PATIENTS AND METHODS: The study population consisted of 28 children from Upper Egypt with classic CAH, their mean age 8.3 ± 2.4 years and 28 age and sex matched healthy control. They were subjected to measurement of BMD of lumbar spines (L1-L4) and femoral neck using dual-energy-X-ray absorptiometry (DXA) and laboratory evaluation of bone turnover markers including Osteocalcin and serum receptor activator of nuclear factor κB-ligand (RANKL). RESULT: Children with CAH had significantly lower bone-mineral density (BMD) for both, vertebrae and femoral neck than controls. This difference is more obvious in children with poor control and in those receiving prednisone therapy. There was a significantly lower serum osteocalcin, and significantly higher serum RANKL levels in patients with CAH than the healthy controls. This differences is more obvious in children with poor control and in those receiving prednisone therapy. Total bone mineral content (BMC [gm]) have significant negative correlations to age (r = −0.81, P < 0.001), disease duration (r = −0.881, P < 0.001), 17 OH Progesterone level (r = −0.543, P < 0.05), RANKL level (r = −0.635, P < 0.05), and significant positive correlation with osteocalcin (r = 0.576, P < 0.001). CONCLUSIONS: Children from Upper Egypt with classic CAH may have reduced BMD and increase bone turnover compared with controls. This difference is more obvious in children with poor control and in those receiving prednisone therapy. RECOMMENDATIONS: Active monitoring of BMD in CAH children using Dual-energy X-ray absorptiometry (DEXA) scanning. Furthermore, effort should be done to bring hydrocortisone to Upper Egypt to replace prednisone in children with classic congenital adrenal hyperplasia. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4171895/ /pubmed/25285289 http://dx.doi.org/10.4103/2230-8210.139236 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Metwalley, Kotb Abbass El-Saied, Abdel-Rahman Abbdel-Hamed Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt |
title | Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt |
title_full | Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt |
title_fullStr | Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt |
title_full_unstemmed | Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt |
title_short | Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper Egypt |
title_sort | bone mineral status in egyptian children with classic congenital adrenal hyperplasia. a single-center study from upper egypt |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171895/ https://www.ncbi.nlm.nih.gov/pubmed/25285289 http://dx.doi.org/10.4103/2230-8210.139236 |
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