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Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension

BACKGROUND: This study aimed to investigate the association between a novel kidney disease index (KDI), which combines information from both estimated glomerular filtration rate (eGFR) and urinary albumin‐to‐creatinine ratio (uACR), and all‐cause and cardiovascular disease (CVD) mortality among indi...

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Autores principales: Fang, Suxia, Chen, Yuwen, Gao, Qiyue, Wei, Qucheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642315/
https://www.ncbi.nlm.nih.gov/pubmed/37605511
http://dx.doi.org/10.1002/clc.24131
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author Fang, Suxia
Chen, Yuwen
Gao, Qiyue
Wei, Qucheng
author_facet Fang, Suxia
Chen, Yuwen
Gao, Qiyue
Wei, Qucheng
author_sort Fang, Suxia
collection PubMed
description BACKGROUND: This study aimed to investigate the association between a novel kidney disease index (KDI), which combines information from both estimated glomerular filtration rate (eGFR) and urinary albumin‐to‐creatinine ratio (uACR), and all‐cause and cardiovascular disease (CVD) mortality among individuals with hypertension. METHODS: We analyzed data from 19 988 adults with hypertension who participated in the National Health and Nutrition Examination Survey from 1999 to 2018. Mortality outcomes were determined by linking to National Death Index records through December 31, 2019. Cox proportional hazards models were used to estimate hazard ratios and 95% confidence intervals for all‐cause and CVD mortality. RESULTS: Baseline KDI levels were positively associated with glucose, insulin resistance, hemoglobin A1c, triglycerides, and C‐reactive protein (p value for trend <.05). During a follow‐up period of 179 859 person‐years, a total of 5069 deaths were documented, including 1741 from cardiovascular causes. After multivariable adjustment, each standard deviation increment in KDI level was associated with a 27% increased risk of all‐cause mortality and a 31% increased risk of cardiovascular deaths (both p < .05). Further analysis showed a J‐shaped association between KDI and mortality, with the risk increasing dramatically when KDI exceeded 0.27. CONCLUSION: Elevated KDI levels were significantly associated with increased mortality from all causes and CVD among individuals with hypertension. We recommend routine testing of eGFR and uACR in hypertensive patients, and using KDI as a tool to identify individuals who are most likely to benefit from preventive therapies.
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spelling pubmed-106423152023-11-15 Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension Fang, Suxia Chen, Yuwen Gao, Qiyue Wei, Qucheng Clin Cardiol Clinical Trial Result BACKGROUND: This study aimed to investigate the association between a novel kidney disease index (KDI), which combines information from both estimated glomerular filtration rate (eGFR) and urinary albumin‐to‐creatinine ratio (uACR), and all‐cause and cardiovascular disease (CVD) mortality among individuals with hypertension. METHODS: We analyzed data from 19 988 adults with hypertension who participated in the National Health and Nutrition Examination Survey from 1999 to 2018. Mortality outcomes were determined by linking to National Death Index records through December 31, 2019. Cox proportional hazards models were used to estimate hazard ratios and 95% confidence intervals for all‐cause and CVD mortality. RESULTS: Baseline KDI levels were positively associated with glucose, insulin resistance, hemoglobin A1c, triglycerides, and C‐reactive protein (p value for trend <.05). During a follow‐up period of 179 859 person‐years, a total of 5069 deaths were documented, including 1741 from cardiovascular causes. After multivariable adjustment, each standard deviation increment in KDI level was associated with a 27% increased risk of all‐cause mortality and a 31% increased risk of cardiovascular deaths (both p < .05). Further analysis showed a J‐shaped association between KDI and mortality, with the risk increasing dramatically when KDI exceeded 0.27. CONCLUSION: Elevated KDI levels were significantly associated with increased mortality from all causes and CVD among individuals with hypertension. We recommend routine testing of eGFR and uACR in hypertensive patients, and using KDI as a tool to identify individuals who are most likely to benefit from preventive therapies. John Wiley and Sons Inc. 2023-08-21 /pmc/articles/PMC10642315/ /pubmed/37605511 http://dx.doi.org/10.1002/clc.24131 Text en © 2023 The Authors. Clinical Cardiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Trial Result
Fang, Suxia
Chen, Yuwen
Gao, Qiyue
Wei, Qucheng
Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension
title Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension
title_full Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension
title_fullStr Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension
title_full_unstemmed Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension
title_short Association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension
title_sort association of kidney disease index with all‐cause and cardiovascular mortality among individuals with hypertension
topic Clinical Trial Result
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642315/
https://www.ncbi.nlm.nih.gov/pubmed/37605511
http://dx.doi.org/10.1002/clc.24131
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