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Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients
BACKGROUND: Many of the existing research studies have shown that serum uric acid (SUA) is a predictor of renal disease progression. More recently, studies have suggested an association between renal function-normalized SUA and all-cause mortality in adults. This study aims to examine the associatio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067315/ https://www.ncbi.nlm.nih.gov/pubmed/37004085 http://dx.doi.org/10.1186/s40885-023-00235-8 |
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author | Kawamoto, Ryuichi Kikuchi, Asuka Ninomiya, Daisuke Tokumoto, Yoshio Kumagi, Teru |
author_facet | Kawamoto, Ryuichi Kikuchi, Asuka Ninomiya, Daisuke Tokumoto, Yoshio Kumagi, Teru |
author_sort | Kawamoto, Ryuichi |
collection | PubMed |
description | BACKGROUND: Many of the existing research studies have shown that serum uric acid (SUA) is a predictor of renal disease progression. More recently, studies have suggested an association between renal function-normalized SUA and all-cause mortality in adults. This study aims to examine the association between the ratio of SUA to creatinine (SUA/Cr) and all-cause mortality with a focus on hypertensive patients. METHODS: This study is based on 2,017 participants, of whom 916 were male (mean age, 67 ± 11 years) and 1,101 were female (mean age, 69 ± 9 years). All participants were part of the Nomura Cohort Study in 2002 (cohort 1) and 2014 (cohort 2), as well as the follow-up period (2002 follow-up rate, 94.8%; 2014 follow-up rate, 98.0%). We obtained adjusted relative risk estimates for all-cause mortality from a basic resident register. In addition, we employed a Cox proportional hazards model and adjusted it for possible confounders to determine the hazard ratio (HR) and 95% confidence interval (CI). RESULTS: Of the total participants, 639 (31.7%) were deceased; of these, 327 (35.7%) were male and 312 (28.3%) were female. We found an independent association between a higher ratio of SUA/Cr and a higher risk of all-cause mortality in female participants only (HR, 1.10; 95% CI, 1.02–1.18). The multivariable-adjusted HRs (95% CI) for all-cause mortality across quintiles of baseline SUA/Cr were 1.28 (0.91–1.80), 1.00, 1.38 (0.95–1.98), 1.37 (0.94–2.00), and 1.57 (1.03–2.40) for male participants, and 0.92 (0.64–1.33), 1.00, 1.04 (0.72–1.50), 1.56 (1.06–2.30), and 1.59 (1.06–2.38) for female participants. When the data were further stratified on the basis of age (< 65 or ≥ 65 years), body mass index (< 22.0 or ≥ 22.0 kg/m(2)), estimated glomerular filtration rate (< 60 or ≥ 60 mL/min/1.73 m(2)), and presence of SUA-lowering medication, trends similar to those of the full population were found in all groups. CONCLUSION: Baseline SUA/Cr is independently and significantly associated with future all-cause mortality among hypertensive patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40885-023-00235-8. |
format | Online Article Text |
id | pubmed-10067315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100673152023-04-03 Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients Kawamoto, Ryuichi Kikuchi, Asuka Ninomiya, Daisuke Tokumoto, Yoshio Kumagi, Teru Clin Hypertens Research BACKGROUND: Many of the existing research studies have shown that serum uric acid (SUA) is a predictor of renal disease progression. More recently, studies have suggested an association between renal function-normalized SUA and all-cause mortality in adults. This study aims to examine the association between the ratio of SUA to creatinine (SUA/Cr) and all-cause mortality with a focus on hypertensive patients. METHODS: This study is based on 2,017 participants, of whom 916 were male (mean age, 67 ± 11 years) and 1,101 were female (mean age, 69 ± 9 years). All participants were part of the Nomura Cohort Study in 2002 (cohort 1) and 2014 (cohort 2), as well as the follow-up period (2002 follow-up rate, 94.8%; 2014 follow-up rate, 98.0%). We obtained adjusted relative risk estimates for all-cause mortality from a basic resident register. In addition, we employed a Cox proportional hazards model and adjusted it for possible confounders to determine the hazard ratio (HR) and 95% confidence interval (CI). RESULTS: Of the total participants, 639 (31.7%) were deceased; of these, 327 (35.7%) were male and 312 (28.3%) were female. We found an independent association between a higher ratio of SUA/Cr and a higher risk of all-cause mortality in female participants only (HR, 1.10; 95% CI, 1.02–1.18). The multivariable-adjusted HRs (95% CI) for all-cause mortality across quintiles of baseline SUA/Cr were 1.28 (0.91–1.80), 1.00, 1.38 (0.95–1.98), 1.37 (0.94–2.00), and 1.57 (1.03–2.40) for male participants, and 0.92 (0.64–1.33), 1.00, 1.04 (0.72–1.50), 1.56 (1.06–2.30), and 1.59 (1.06–2.38) for female participants. When the data were further stratified on the basis of age (< 65 or ≥ 65 years), body mass index (< 22.0 or ≥ 22.0 kg/m(2)), estimated glomerular filtration rate (< 60 or ≥ 60 mL/min/1.73 m(2)), and presence of SUA-lowering medication, trends similar to those of the full population were found in all groups. CONCLUSION: Baseline SUA/Cr is independently and significantly associated with future all-cause mortality among hypertensive patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40885-023-00235-8. BioMed Central 2023-04-01 /pmc/articles/PMC10067315/ /pubmed/37004085 http://dx.doi.org/10.1186/s40885-023-00235-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kawamoto, Ryuichi Kikuchi, Asuka Ninomiya, Daisuke Tokumoto, Yoshio Kumagi, Teru Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients |
title | Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients |
title_full | Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients |
title_fullStr | Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients |
title_full_unstemmed | Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients |
title_short | Serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients |
title_sort | serum uric acid to creatinine ratio is a useful predictor of all-cause mortality among hypertensive patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067315/ https://www.ncbi.nlm.nih.gov/pubmed/37004085 http://dx.doi.org/10.1186/s40885-023-00235-8 |
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