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Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease
Background: Metabolic acidosis is a common complication in patients with chronic kidney disease (CKD). Oral sodium bicarbonate is often used to treat metabolic acidosis and prevent CKD progression. However, there is limited information about the effect of sodium bicarbonate on major adverse cardiova...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213883/ https://www.ncbi.nlm.nih.gov/pubmed/37251318 http://dx.doi.org/10.3389/fphar.2023.1146668 |
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author | Cheng, Ya-Lien Huang, Shu-Chun Ho, Ming-Yun Li, Yan-Rong Yen, Chieh-Li Chen, Kuan-Hsing Sun, Wei-Chiao Fan, Pei-Yi Chen, Jung-Sheng Lin, Chihung Hsiao, Ching-Chung |
author_facet | Cheng, Ya-Lien Huang, Shu-Chun Ho, Ming-Yun Li, Yan-Rong Yen, Chieh-Li Chen, Kuan-Hsing Sun, Wei-Chiao Fan, Pei-Yi Chen, Jung-Sheng Lin, Chihung Hsiao, Ching-Chung |
author_sort | Cheng, Ya-Lien |
collection | PubMed |
description | Background: Metabolic acidosis is a common complication in patients with chronic kidney disease (CKD). Oral sodium bicarbonate is often used to treat metabolic acidosis and prevent CKD progression. However, there is limited information about the effect of sodium bicarbonate on major adverse cardiovascular events (MACE) and mortality in patients with pre-dialysis advanced CKD. Method: 25599 patients with CKD stage V between January 1, 2001 and December 31, 2019 were identified from the Chang Gung Research Database (CGRD), a multi-institutional electronic medical record database in Taiwan. The exposure was defined as receiving sodium bicarbonate or not. Baseline characteristics were balanced using propensity score weighting between two groups. Primary outcomes were dialysis initiation, all-cause mortality, and major adverse cardiovascular events (MACE) (myocardial infarction, heart failure, stroke). The risks of dialysis, MACE, and mortality were compared between two groups using Cox proportional hazards models. In addition, we performed analyzes using Fine and Gray sub-distribution hazard models that considered death as a competing risk. Result: Among 25599 patients with CKD stage V, 5084 patients (19.9%) were sodium bicarbonate users while 20515 (80.1%) were sodium bicarbonate non-users. The groups had similar risk of dialysis initiation (hazard ratio (HR): 0.98, 95% confidence interval (CI): 0.95-1.02, p < 0.379). However, taking sodium bicarbonate was associated with a significantly lower risks of MACE (HR: 0.95, 95% CI 0.92–0.98, p < 0.001) and hospitalizations for acute pulmonary edema (HR: 0.92, 95% CI 0.88–0.96, p < 0.001) compared with non-users. The mortality risks were significantly lower in sodium bicarbonate users compared with sodium bicarbonate non-users (HR: 0.75, 95% CI 0.74–0.77, p < 0.001). Conclusion: This cohort study revealed that in real world practice, use of sodium bicarbonate was associated with similar risk of dialysis compared with non-users among patients with advanced CKD stage V. Nonetheless, use of sodium bicarbonate was associated with significantly lower rate of MACE and mortality. Findings reinforce the benefits of sodium bicarbonate therapy in the expanding CKD population. Further prospective studies are needed to confirm these findings. |
format | Online Article Text |
id | pubmed-10213883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102138832023-05-27 Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease Cheng, Ya-Lien Huang, Shu-Chun Ho, Ming-Yun Li, Yan-Rong Yen, Chieh-Li Chen, Kuan-Hsing Sun, Wei-Chiao Fan, Pei-Yi Chen, Jung-Sheng Lin, Chihung Hsiao, Ching-Chung Front Pharmacol Pharmacology Background: Metabolic acidosis is a common complication in patients with chronic kidney disease (CKD). Oral sodium bicarbonate is often used to treat metabolic acidosis and prevent CKD progression. However, there is limited information about the effect of sodium bicarbonate on major adverse cardiovascular events (MACE) and mortality in patients with pre-dialysis advanced CKD. Method: 25599 patients with CKD stage V between January 1, 2001 and December 31, 2019 were identified from the Chang Gung Research Database (CGRD), a multi-institutional electronic medical record database in Taiwan. The exposure was defined as receiving sodium bicarbonate or not. Baseline characteristics were balanced using propensity score weighting between two groups. Primary outcomes were dialysis initiation, all-cause mortality, and major adverse cardiovascular events (MACE) (myocardial infarction, heart failure, stroke). The risks of dialysis, MACE, and mortality were compared between two groups using Cox proportional hazards models. In addition, we performed analyzes using Fine and Gray sub-distribution hazard models that considered death as a competing risk. Result: Among 25599 patients with CKD stage V, 5084 patients (19.9%) were sodium bicarbonate users while 20515 (80.1%) were sodium bicarbonate non-users. The groups had similar risk of dialysis initiation (hazard ratio (HR): 0.98, 95% confidence interval (CI): 0.95-1.02, p < 0.379). However, taking sodium bicarbonate was associated with a significantly lower risks of MACE (HR: 0.95, 95% CI 0.92–0.98, p < 0.001) and hospitalizations for acute pulmonary edema (HR: 0.92, 95% CI 0.88–0.96, p < 0.001) compared with non-users. The mortality risks were significantly lower in sodium bicarbonate users compared with sodium bicarbonate non-users (HR: 0.75, 95% CI 0.74–0.77, p < 0.001). Conclusion: This cohort study revealed that in real world practice, use of sodium bicarbonate was associated with similar risk of dialysis compared with non-users among patients with advanced CKD stage V. Nonetheless, use of sodium bicarbonate was associated with significantly lower rate of MACE and mortality. Findings reinforce the benefits of sodium bicarbonate therapy in the expanding CKD population. Further prospective studies are needed to confirm these findings. Frontiers Media S.A. 2023-05-11 /pmc/articles/PMC10213883/ /pubmed/37251318 http://dx.doi.org/10.3389/fphar.2023.1146668 Text en Copyright © 2023 Cheng, Huang, Ho, Li, Yen, Chen, Sun, Fan, Chen, Lin and Hsiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Cheng, Ya-Lien Huang, Shu-Chun Ho, Ming-Yun Li, Yan-Rong Yen, Chieh-Li Chen, Kuan-Hsing Sun, Wei-Chiao Fan, Pei-Yi Chen, Jung-Sheng Lin, Chihung Hsiao, Ching-Chung Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease |
title | Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease |
title_full | Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease |
title_fullStr | Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease |
title_full_unstemmed | Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease |
title_short | Effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease |
title_sort | effect of sodium bicarbonate on cardiovascular outcome and mortality in patients with advanced chronic kidney disease |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213883/ https://www.ncbi.nlm.nih.gov/pubmed/37251318 http://dx.doi.org/10.3389/fphar.2023.1146668 |
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