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Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4
BACKGROUND: Disordered bone and mineral metabolism are a common complication of chronic kidney disease (CKD). Phosphate binders are often prescribed in advanced CKD, when hyperphosphataemia develops. Little is known about the role of these drugs in earlier stages, when serum phosphorus levels are ke...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886574/ https://www.ncbi.nlm.nih.gov/pubmed/33623678 http://dx.doi.org/10.1093/ckj/sfz181 |
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author | Neto, Ricardo Frazão, João |
author_facet | Neto, Ricardo Frazão, João |
author_sort | Neto, Ricardo |
collection | PubMed |
description | BACKGROUND: Disordered bone and mineral metabolism are a common complication of chronic kidney disease (CKD). Phosphate binders are often prescribed in advanced CKD, when hyperphosphataemia develops. Little is known about the role of these drugs in earlier stages, when serum phosphorus levels are kept in the normal range by increased urinary excretion. METHODS: A retrospective, controlled observational study was conducted on a cohort of 78 pre-dialysis patients. Subjects had CKD Stage 3 or 4, normal serum phosphorus levels and increased urinary fractional excretion of phosphate. Thirty-eight patients receiving calcium carbonate for 24 months were compared with 40 patients under no phosphate binders, regarding mineral metabolism parameters and vascular calcification scores. RESULTS: Calcium carbonate decreased mean urinary fractional excretion of phosphate and median 24-h urine phosphorus, whereas no significant change was seen in the control group. Mean serum phosphorus and median serum intact parathyroid hormone (iPTH) remained stable in treated patients but increased in the control group. Vascular calcification, assessed by Kauppila and Adragão scores, worsened under calcium carbonate with no significant change in the control group. CONCLUSIONS: Calcium carbonate reduced urinary phosphate excretion and prevented the rise in phosphorus and iPTH serum levels in a cohort of normophosphataemic pre-dialysis patients. However, treatment was associated with increased vascular calcification, suggesting that calcium-based phosphate binders are not a safe option for CKD patients. |
format | Online Article Text |
id | pubmed-7886574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78865742021-02-22 Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4 Neto, Ricardo Frazão, João Clin Kidney J Original Articles BACKGROUND: Disordered bone and mineral metabolism are a common complication of chronic kidney disease (CKD). Phosphate binders are often prescribed in advanced CKD, when hyperphosphataemia develops. Little is known about the role of these drugs in earlier stages, when serum phosphorus levels are kept in the normal range by increased urinary excretion. METHODS: A retrospective, controlled observational study was conducted on a cohort of 78 pre-dialysis patients. Subjects had CKD Stage 3 or 4, normal serum phosphorus levels and increased urinary fractional excretion of phosphate. Thirty-eight patients receiving calcium carbonate for 24 months were compared with 40 patients under no phosphate binders, regarding mineral metabolism parameters and vascular calcification scores. RESULTS: Calcium carbonate decreased mean urinary fractional excretion of phosphate and median 24-h urine phosphorus, whereas no significant change was seen in the control group. Mean serum phosphorus and median serum intact parathyroid hormone (iPTH) remained stable in treated patients but increased in the control group. Vascular calcification, assessed by Kauppila and Adragão scores, worsened under calcium carbonate with no significant change in the control group. CONCLUSIONS: Calcium carbonate reduced urinary phosphate excretion and prevented the rise in phosphorus and iPTH serum levels in a cohort of normophosphataemic pre-dialysis patients. However, treatment was associated with increased vascular calcification, suggesting that calcium-based phosphate binders are not a safe option for CKD patients. Oxford University Press 2019-12-22 /pmc/articles/PMC7886574/ /pubmed/33623678 http://dx.doi.org/10.1093/ckj/sfz181 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Neto, Ricardo Frazão, João Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4 |
title | Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4 |
title_full | Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4 |
title_fullStr | Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4 |
title_full_unstemmed | Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4 |
title_short | Efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease Stages 3 and 4 |
title_sort | efficacy and safety of calcium carbonate in normophosphataemic patients with chronic kidney disease stages 3 and 4 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886574/ https://www.ncbi.nlm.nih.gov/pubmed/33623678 http://dx.doi.org/10.1093/ckj/sfz181 |
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