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Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality
KEY POINTS: An increase in serum phosphate variability is an independent risk factor of mortality. The effects of a positive directional range (DR) is most pronounced in patients with high serum phosphate levels whereas the effects of a negative DR is most pronounced in patients with low serum phosp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Nephrology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103252/ https://www.ncbi.nlm.nih.gov/pubmed/36918167 http://dx.doi.org/10.34067/KID.0000000000000062 |
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author | ter Meulen, Karlien J. Ye, Xiaoling Wang, Yuedong Usvyat, Len A. van der Sande, Frank M. Konings, Constantijn J. Kotanko, Peter Kooman, Jeroen P. Maddux, Franklin W. |
author_facet | ter Meulen, Karlien J. Ye, Xiaoling Wang, Yuedong Usvyat, Len A. van der Sande, Frank M. Konings, Constantijn J. Kotanko, Peter Kooman, Jeroen P. Maddux, Franklin W. |
author_sort | ter Meulen, Karlien J. |
collection | PubMed |
description | KEY POINTS: An increase in serum phosphate variability is an independent risk factor of mortality. The effects of a positive directional range (DR) is most pronounced in patients with high serum phosphate levels whereas the effects of a negative DR is most pronounced in patients with low serum phosphate and/or serum albumin. BACKGROUND: In maintenance hemodialysis (HD) patients, previous studies have shown that serum phosphate levels have a bidirectional relation to outcome. Less is known about the relation between temporal dynamics of serum phosphate in relation to outcome. We aimed to further explore the relation between serum phosphate variability and all-cause mortality. METHODS: All adult incident HD patients treated in US Fresenius Kidney Care clinics between January 2010 and October 2018 were included. Baseline period was defined as 6 months after initiation of HD and months 7–18 as follow-up period. All-cause mortality was recorded during the follow-up period. The primary metric of variability used was directional range (DR) that is the difference between the largest and smallest values within a time period; DR was positive when the smallest value preceded the largest and negative otherwise. Cox proportional hazards models with spline terms were applied to explore the association between phosphate, DR, and all-cause mortality. In addition, tensor product smoothing splines were computed to further elucidate the interactions of phosphate, DR, and all-cause mortality. RESULTS: We included 302,613 patients. Baseline phosphate was 5.1±1.2 mg/dl, and mean DR was +0.6±3.3 mg/dl. Across different levels of phosphate, higher levels of DR of phosphate were associated with higher risk of all-cause mortality. In patients with lower levels of phosphate and serum albumin, the effect of a negative DR was most pronounced, whereas in patients with higher phosphate levels, a positive DR was related to increased mortality. CONCLUSIONS: Higher variability of serum phosphate is related to mortality at all levels of phosphate, especially in lower levels with a negative DR and in low serum albumin levels. This could possibly reflect dietary intake in patients who are already inflamed or malnourished, where a further reduction in serum phosphate should prompt for nutritional evaluation. |
format | Online Article Text |
id | pubmed-10103252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society of Nephrology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101032522023-08-03 Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality ter Meulen, Karlien J. Ye, Xiaoling Wang, Yuedong Usvyat, Len A. van der Sande, Frank M. Konings, Constantijn J. Kotanko, Peter Kooman, Jeroen P. Maddux, Franklin W. Kidney360 Original Investigation KEY POINTS: An increase in serum phosphate variability is an independent risk factor of mortality. The effects of a positive directional range (DR) is most pronounced in patients with high serum phosphate levels whereas the effects of a negative DR is most pronounced in patients with low serum phosphate and/or serum albumin. BACKGROUND: In maintenance hemodialysis (HD) patients, previous studies have shown that serum phosphate levels have a bidirectional relation to outcome. Less is known about the relation between temporal dynamics of serum phosphate in relation to outcome. We aimed to further explore the relation between serum phosphate variability and all-cause mortality. METHODS: All adult incident HD patients treated in US Fresenius Kidney Care clinics between January 2010 and October 2018 were included. Baseline period was defined as 6 months after initiation of HD and months 7–18 as follow-up period. All-cause mortality was recorded during the follow-up period. The primary metric of variability used was directional range (DR) that is the difference between the largest and smallest values within a time period; DR was positive when the smallest value preceded the largest and negative otherwise. Cox proportional hazards models with spline terms were applied to explore the association between phosphate, DR, and all-cause mortality. In addition, tensor product smoothing splines were computed to further elucidate the interactions of phosphate, DR, and all-cause mortality. RESULTS: We included 302,613 patients. Baseline phosphate was 5.1±1.2 mg/dl, and mean DR was +0.6±3.3 mg/dl. Across different levels of phosphate, higher levels of DR of phosphate were associated with higher risk of all-cause mortality. In patients with lower levels of phosphate and serum albumin, the effect of a negative DR was most pronounced, whereas in patients with higher phosphate levels, a positive DR was related to increased mortality. CONCLUSIONS: Higher variability of serum phosphate is related to mortality at all levels of phosphate, especially in lower levels with a negative DR and in low serum albumin levels. This could possibly reflect dietary intake in patients who are already inflamed or malnourished, where a further reduction in serum phosphate should prompt for nutritional evaluation. American Society of Nephrology 2023-03-14 /pmc/articles/PMC10103252/ /pubmed/36918167 http://dx.doi.org/10.34067/KID.0000000000000062 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Investigation ter Meulen, Karlien J. Ye, Xiaoling Wang, Yuedong Usvyat, Len A. van der Sande, Frank M. Konings, Constantijn J. Kotanko, Peter Kooman, Jeroen P. Maddux, Franklin W. Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality |
title | Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality |
title_full | Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality |
title_fullStr | Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality |
title_full_unstemmed | Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality |
title_short | Variability of Serum Phosphate in Incident Hemodialysis Patients: Association with All-Cause Mortality |
title_sort | variability of serum phosphate in incident hemodialysis patients: association with all-cause mortality |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103252/ https://www.ncbi.nlm.nih.gov/pubmed/36918167 http://dx.doi.org/10.34067/KID.0000000000000062 |
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