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Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease

The elderly chronic kidney disease (CKD) population is growing. Both aging and CKD can disrupt calcium (Ca(2+)) homeostasis and cause alterations of multiple Ca(2+)-regulatory mechanisms, including parathyroid hormone, vitamin D, fibroblast growth factor-23/Klotho, calcium-sensing receptor and Ca(2+...

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Autores principales: Tejwani, Vickram, Qian, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725483/
https://www.ncbi.nlm.nih.gov/pubmed/23760058
http://dx.doi.org/10.3390/nu5061913
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author Tejwani, Vickram
Qian, Qi
author_facet Tejwani, Vickram
Qian, Qi
author_sort Tejwani, Vickram
collection PubMed
description The elderly chronic kidney disease (CKD) population is growing. Both aging and CKD can disrupt calcium (Ca(2+)) homeostasis and cause alterations of multiple Ca(2+)-regulatory mechanisms, including parathyroid hormone, vitamin D, fibroblast growth factor-23/Klotho, calcium-sensing receptor and Ca(2+)-phosphate product. These alterations can be deleterious to bone mineral metabolism and soft tissue health, leading to metabolic bone disease and vascular calcification and aging, termed CKD-mineral and bone disorder (MBD). CKD-MBD is associated with morbid clinical outcomes, including fracture, cardiovascular events and all-cause mortality. In this paper, we comprehensively review Ca(2+) regulation and bone mineral metabolism, with a special emphasis on elderly CKD patients. We also present the current treatment-guidelines and management options for CKD-MBD.
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spelling pubmed-37254832013-07-29 Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease Tejwani, Vickram Qian, Qi Nutrients Review The elderly chronic kidney disease (CKD) population is growing. Both aging and CKD can disrupt calcium (Ca(2+)) homeostasis and cause alterations of multiple Ca(2+)-regulatory mechanisms, including parathyroid hormone, vitamin D, fibroblast growth factor-23/Klotho, calcium-sensing receptor and Ca(2+)-phosphate product. These alterations can be deleterious to bone mineral metabolism and soft tissue health, leading to metabolic bone disease and vascular calcification and aging, termed CKD-mineral and bone disorder (MBD). CKD-MBD is associated with morbid clinical outcomes, including fracture, cardiovascular events and all-cause mortality. In this paper, we comprehensively review Ca(2+) regulation and bone mineral metabolism, with a special emphasis on elderly CKD patients. We also present the current treatment-guidelines and management options for CKD-MBD. MDPI 2013-05-29 /pmc/articles/PMC3725483/ /pubmed/23760058 http://dx.doi.org/10.3390/nu5061913 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Tejwani, Vickram
Qian, Qi
Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease
title Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease
title_full Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease
title_fullStr Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease
title_full_unstemmed Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease
title_short Calcium Regulation and Bone Mineral Metabolism in Elderly Patients with Chronic Kidney Disease
title_sort calcium regulation and bone mineral metabolism in elderly patients with chronic kidney disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725483/
https://www.ncbi.nlm.nih.gov/pubmed/23760058
http://dx.doi.org/10.3390/nu5061913
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