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Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency

CONTEXT: Patients with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) therapy. Daily GC doses are often above the physiological cortisol production rate and can cause long-term morbidities such as osteoporosis. No prospective trial h...

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Autores principales: Frey, Kathrin R, Kienitz, Tina, Schulz, Julia, Ventz, Manfred, Zopf, Kathrin, Quinkler, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987359/
https://www.ncbi.nlm.nih.gov/pubmed/29720511
http://dx.doi.org/10.1530/EC-18-0160
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author Frey, Kathrin R
Kienitz, Tina
Schulz, Julia
Ventz, Manfred
Zopf, Kathrin
Quinkler, Marcus
author_facet Frey, Kathrin R
Kienitz, Tina
Schulz, Julia
Ventz, Manfred
Zopf, Kathrin
Quinkler, Marcus
author_sort Frey, Kathrin R
collection PubMed
description CONTEXT: Patients with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) therapy. Daily GC doses are often above the physiological cortisol production rate and can cause long-term morbidities such as osteoporosis. No prospective trial has investigated the long-term effect of different GC therapies on bone mineral density (BMD) in those patients. OBJECTIVES: To determine if patients on hydrocortisone (HC) or prednisolone show changes in BMD after follow-up of 5.5 years. To investigate if BMD is altered after switching from immediate- to modified-release HC. DESIGN AND PATIENTS: Prospective, observational, longitudinal study with evaluation of BMD by DXA at visit1, after 2.2 ± 0.4 (visit2) and after 5.5 ± 0.8 years (visit3) included 36 PAI and 8 CAH patients. Thirteen patients received prednisolone (age 52.5 ± 14.8 years; 8 women) and 31 patients received immediate-release HC (age 48.9 ± 15.8 years; 22 women). Twelve patients on immediate-release switched to modified-release HC at visit2. RESULTS: Prednisolone showed significantly lower Z-scores compared to HC at femoral neck (−0.85 ± 0.80 vs −0.25 ± 1.16, P < 0.05), trochanter (−0.96 ± 0.62 vs 0.51 ± 1.07, P < 0.05) and total hip (−0.78 ± 0.55 vs 0.36 ± 1.04, P < 0.05), but not at lumbar spine, throughout the study. Prednisolone dose decreased by 8% over study time, but no significant effect was seen on BMD. BMD did not change significantly after switching from immediate- to modified-release HC. CONCLUSIONS: The use of prednisolone as hormone replacement therapy results in significantly lower BMD compared to HC. Patients on low-dose HC replacement therapy showed unchanged Z-scores within the normal reference range during the study period.
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spelling pubmed-59873592018-06-08 Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency Frey, Kathrin R Kienitz, Tina Schulz, Julia Ventz, Manfred Zopf, Kathrin Quinkler, Marcus Endocr Connect Research CONTEXT: Patients with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) therapy. Daily GC doses are often above the physiological cortisol production rate and can cause long-term morbidities such as osteoporosis. No prospective trial has investigated the long-term effect of different GC therapies on bone mineral density (BMD) in those patients. OBJECTIVES: To determine if patients on hydrocortisone (HC) or prednisolone show changes in BMD after follow-up of 5.5 years. To investigate if BMD is altered after switching from immediate- to modified-release HC. DESIGN AND PATIENTS: Prospective, observational, longitudinal study with evaluation of BMD by DXA at visit1, after 2.2 ± 0.4 (visit2) and after 5.5 ± 0.8 years (visit3) included 36 PAI and 8 CAH patients. Thirteen patients received prednisolone (age 52.5 ± 14.8 years; 8 women) and 31 patients received immediate-release HC (age 48.9 ± 15.8 years; 22 women). Twelve patients on immediate-release switched to modified-release HC at visit2. RESULTS: Prednisolone showed significantly lower Z-scores compared to HC at femoral neck (−0.85 ± 0.80 vs −0.25 ± 1.16, P < 0.05), trochanter (−0.96 ± 0.62 vs 0.51 ± 1.07, P < 0.05) and total hip (−0.78 ± 0.55 vs 0.36 ± 1.04, P < 0.05), but not at lumbar spine, throughout the study. Prednisolone dose decreased by 8% over study time, but no significant effect was seen on BMD. BMD did not change significantly after switching from immediate- to modified-release HC. CONCLUSIONS: The use of prednisolone as hormone replacement therapy results in significantly lower BMD compared to HC. Patients on low-dose HC replacement therapy showed unchanged Z-scores within the normal reference range during the study period. Bioscientifica Ltd 2018-05-02 /pmc/articles/PMC5987359/ /pubmed/29720511 http://dx.doi.org/10.1530/EC-18-0160 Text en © 2018 The authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Research
Frey, Kathrin R
Kienitz, Tina
Schulz, Julia
Ventz, Manfred
Zopf, Kathrin
Quinkler, Marcus
Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency
title Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency
title_full Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency
title_fullStr Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency
title_full_unstemmed Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency
title_short Prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency
title_sort prednisolone is associated with a worse bone mineral density in primary adrenal insufficiency
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987359/
https://www.ncbi.nlm.nih.gov/pubmed/29720511
http://dx.doi.org/10.1530/EC-18-0160
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