Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Metwalley, Kotb Abbass, El-Saied, Abdel-Rahman Abbdel-Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
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
_version_ 1782335968390414336
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
work_keys_str_mv AT metwalleykotbabbass bonemineralstatusinegyptianchildrenwithclassiccongenitaladrenalhyperplasiaasinglecenterstudyfromupperegypt
AT elsaiedabdelrahmanabbdelhamed bonemineralstatusinegyptianchildrenwithclassiccongenitaladrenalhyperplasiaasinglecenterstudyfromupperegypt