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The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD
Sodium–glucose cotransporter 2 inhibitors (SGLT2i) exhibit renoprotective effect in patients with chronic kidney disease (CKD) and reduce serum uric acid (UA) in patients with diabetes mellitus. However, it is not clarified whether SGLT2i reduce serum UA levels in patients with advanced CKD. This st...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039024/ https://www.ncbi.nlm.nih.gov/pubmed/36964174 http://dx.doi.org/10.1038/s41598-023-32072-y |
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author | Iwata, Yukimasa Notsu, Shoki Kawamura, Yushi Mitani, Waka Tamai, Shinjiro Morimoto, Madoka Yamato, Masafumi |
author_facet | Iwata, Yukimasa Notsu, Shoki Kawamura, Yushi Mitani, Waka Tamai, Shinjiro Morimoto, Madoka Yamato, Masafumi |
author_sort | Iwata, Yukimasa |
collection | PubMed |
description | Sodium–glucose cotransporter 2 inhibitors (SGLT2i) exhibit renoprotective effect in patients with chronic kidney disease (CKD) and reduce serum uric acid (UA) in patients with diabetes mellitus. However, it is not clarified whether SGLT2i reduce serum UA levels in patients with advanced CKD. This study aimed to investigate the impact of SGLT2i on change in serum UA levels in patients with advanced CKD. Data of 121 Japanese patients with CKD who were newly administered 10 mg dapagliflozin in our department between August 2021 and August 2022 were analyzed. Changes in UA and fractional excretion of UA (FEUA) were analyzed using multiple regression analysis. Of 75 patients, 21 (28.0%) patients, 24 (32.0%) patients, 29 (38.7%) patients, and 1 (1.3%) patient were categorized as having CKD stage 3a, 3b, 4, and 5, respectively. The median age was 67 years, and 72.0% were male. 23 (30.7%) of patients had diabetes mellitus. The median estimated glomerular filtration rate, serum UA, and FEUA were 35.7 mL/min/1.73 m(2), 6.4 mg/dL, and 6.76%, respectively, at the time of dapagliflozin administration. After administration, serum UA decreased to 5.6 mg/dL and FEUA increased to 9.22%. Dapagliflozin increases FEUA and reduces serum UA levels in patients with advanced CKD. |
format | Online Article Text |
id | pubmed-10039024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100390242023-03-26 The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD Iwata, Yukimasa Notsu, Shoki Kawamura, Yushi Mitani, Waka Tamai, Shinjiro Morimoto, Madoka Yamato, Masafumi Sci Rep Article Sodium–glucose cotransporter 2 inhibitors (SGLT2i) exhibit renoprotective effect in patients with chronic kidney disease (CKD) and reduce serum uric acid (UA) in patients with diabetes mellitus. However, it is not clarified whether SGLT2i reduce serum UA levels in patients with advanced CKD. This study aimed to investigate the impact of SGLT2i on change in serum UA levels in patients with advanced CKD. Data of 121 Japanese patients with CKD who were newly administered 10 mg dapagliflozin in our department between August 2021 and August 2022 were analyzed. Changes in UA and fractional excretion of UA (FEUA) were analyzed using multiple regression analysis. Of 75 patients, 21 (28.0%) patients, 24 (32.0%) patients, 29 (38.7%) patients, and 1 (1.3%) patient were categorized as having CKD stage 3a, 3b, 4, and 5, respectively. The median age was 67 years, and 72.0% were male. 23 (30.7%) of patients had diabetes mellitus. The median estimated glomerular filtration rate, serum UA, and FEUA were 35.7 mL/min/1.73 m(2), 6.4 mg/dL, and 6.76%, respectively, at the time of dapagliflozin administration. After administration, serum UA decreased to 5.6 mg/dL and FEUA increased to 9.22%. Dapagliflozin increases FEUA and reduces serum UA levels in patients with advanced CKD. Nature Publishing Group UK 2023-03-24 /pmc/articles/PMC10039024/ /pubmed/36964174 http://dx.doi.org/10.1038/s41598-023-32072-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Iwata, Yukimasa Notsu, Shoki Kawamura, Yushi Mitani, Waka Tamai, Shinjiro Morimoto, Madoka Yamato, Masafumi The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD |
title | The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD |
title_full | The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD |
title_fullStr | The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD |
title_full_unstemmed | The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD |
title_short | The effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced CKD |
title_sort | effect of dapagliflozin on uric acid excretion and serum uric acid level in advanced ckd |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039024/ https://www.ncbi.nlm.nih.gov/pubmed/36964174 http://dx.doi.org/10.1038/s41598-023-32072-y |
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