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Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s
The situation of secondary hyperparathyroidism (SHPT) in chronic kidney disease patients not on dialysis (ND-CKD) is probably best characterised by the Kidney Disease: Improving Global Outcomes Chronic Kidney Disease–Mineral and Bone Disorder Update 2017 guideline 4.2.1 stating that the optimal para...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229290/ https://www.ncbi.nlm.nih.gov/pubmed/35977397 http://dx.doi.org/10.1093/ndt/gfac236 |
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author | Ketteler, Markus Bover, Jordi Mazzaferro, Sandro |
author_facet | Ketteler, Markus Bover, Jordi Mazzaferro, Sandro |
author_sort | Ketteler, Markus |
collection | PubMed |
description | The situation of secondary hyperparathyroidism (SHPT) in chronic kidney disease patients not on dialysis (ND-CKD) is probably best characterised by the Kidney Disease: Improving Global Outcomes Chronic Kidney Disease–Mineral and Bone Disorder Update 2017 guideline 4.2.1 stating that the optimal parathyroid hormone levels are not known in these stages. Furthermore, new caution became recommended with regard to the routine use of active vitamin D analogues in early CKD stages and moderate SHPT phenotypes, due to their potential risks for hypercalcaemia and hyperphosphataemia aggravation. Nevertheless, there is still a substantial clinical need to prevent the development of parathyroid gland autonomy, with its associated consequences of bone and vascular damage, including fracture risks and cardiovascular events. Therefore we now attempt to review the current guideline-based and clinical practice management of SHPT in ND-CKD, including their strengths and weaknesses, favouring individualised approaches respecting calcium and phosphate homeostasis. We further comment on extended-release calcifediol (ERC) as a new differential therapeutic option now also available in Europe and on a potentially novel understanding of a required vitamin D saturation in more advanced CKD stages. There is no doubt, however, that knowledge gaps will remain unless powerful randomised controlled trials with hard and meaningful endpoints are performed. |
format | Online Article Text |
id | pubmed-10229290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102292902023-05-31 Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s Ketteler, Markus Bover, Jordi Mazzaferro, Sandro Nephrol Dial Transplant Review The situation of secondary hyperparathyroidism (SHPT) in chronic kidney disease patients not on dialysis (ND-CKD) is probably best characterised by the Kidney Disease: Improving Global Outcomes Chronic Kidney Disease–Mineral and Bone Disorder Update 2017 guideline 4.2.1 stating that the optimal parathyroid hormone levels are not known in these stages. Furthermore, new caution became recommended with regard to the routine use of active vitamin D analogues in early CKD stages and moderate SHPT phenotypes, due to their potential risks for hypercalcaemia and hyperphosphataemia aggravation. Nevertheless, there is still a substantial clinical need to prevent the development of parathyroid gland autonomy, with its associated consequences of bone and vascular damage, including fracture risks and cardiovascular events. Therefore we now attempt to review the current guideline-based and clinical practice management of SHPT in ND-CKD, including their strengths and weaknesses, favouring individualised approaches respecting calcium and phosphate homeostasis. We further comment on extended-release calcifediol (ERC) as a new differential therapeutic option now also available in Europe and on a potentially novel understanding of a required vitamin D saturation in more advanced CKD stages. There is no doubt, however, that knowledge gaps will remain unless powerful randomised controlled trials with hard and meaningful endpoints are performed. Oxford University Press 2022-08-17 /pmc/articles/PMC10229290/ /pubmed/35977397 http://dx.doi.org/10.1093/ndt/gfac236 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the ERA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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 | Review Ketteler, Markus Bover, Jordi Mazzaferro, Sandro Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s |
title | Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s |
title_full | Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s |
title_fullStr | Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s |
title_full_unstemmed | Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s |
title_short | Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s |
title_sort | treatment of secondary hyperparathyroidism in non-dialysis ckd: an appraisal 2022s |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229290/ https://www.ncbi.nlm.nih.gov/pubmed/35977397 http://dx.doi.org/10.1093/ndt/gfac236 |
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