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Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate

It has been reported that an increase in urinary albumin excretion (UAE) within the normal range could be a risk factor for incident hypertension. However, it remains unclear how the subtle increases in UAE and renal function interact in the development of hypertension. We examined the modification...

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Autores principales: Munakata, Masanori, Hattori, Tomomi, Konno, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746590/
https://www.ncbi.nlm.nih.gov/pubmed/28933781
http://dx.doi.org/10.1038/hr.2017.77
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author Munakata, Masanori
Hattori, Tomomi
Konno, Satoshi
author_facet Munakata, Masanori
Hattori, Tomomi
Konno, Satoshi
author_sort Munakata, Masanori
collection PubMed
description It has been reported that an increase in urinary albumin excretion (UAE) within the normal range could be a risk factor for incident hypertension. However, it remains unclear how the subtle increases in UAE and renal function interact in the development of hypertension. We examined the modification of UAE as a risk factor for incident hypertension by glomerular filtration rate (GFR) in the Japanese population. We prospectively followed 1281 normotensive individuals from Watari town (34.3% men; mean age, 58.0±12.3 years old) whose UAE was <30 mg g(−1)· Cr. Hypertension was diagnosed as a systolic blood pressure (BP)⩾140 mm Hg and/or a diastolic BP⩾90 mm Hg, or antihypertensive medication use. The relationship between sex-specific quartiles of UAE and incident hypertension was examined with Cox proportional hazard analysis. During a mean follow-up of 3.7 years, 315 individuals developed hypertension. Multivariate Cox proportional hazard analysis revealed that a subtle increase in UAE was a risk factor for incident hypertension, but there was a significant interaction between UAE and estimated GFR (eGFR) (P=0.018). The risk of incident hypertension dose dependently increased in the highest eGFR quartile (⩾90 ml min(−1) per 1.73 m(2)). Decline in renal function alone increased the risk of incident hypertension but the increased risk with a subtle increase in UAE became smaller and less clear in the lower eGFR quartiles. The present data suggest that UAE as a risk factor for incident hypertension is largely dependent on eGFR levels.
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spelling pubmed-57465902018-01-13 Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate Munakata, Masanori Hattori, Tomomi Konno, Satoshi Hypertens Res Original Article It has been reported that an increase in urinary albumin excretion (UAE) within the normal range could be a risk factor for incident hypertension. However, it remains unclear how the subtle increases in UAE and renal function interact in the development of hypertension. We examined the modification of UAE as a risk factor for incident hypertension by glomerular filtration rate (GFR) in the Japanese population. We prospectively followed 1281 normotensive individuals from Watari town (34.3% men; mean age, 58.0±12.3 years old) whose UAE was <30 mg g(−1)· Cr. Hypertension was diagnosed as a systolic blood pressure (BP)⩾140 mm Hg and/or a diastolic BP⩾90 mm Hg, or antihypertensive medication use. The relationship between sex-specific quartiles of UAE and incident hypertension was examined with Cox proportional hazard analysis. During a mean follow-up of 3.7 years, 315 individuals developed hypertension. Multivariate Cox proportional hazard analysis revealed that a subtle increase in UAE was a risk factor for incident hypertension, but there was a significant interaction between UAE and estimated GFR (eGFR) (P=0.018). The risk of incident hypertension dose dependently increased in the highest eGFR quartile (⩾90 ml min(−1) per 1.73 m(2)). Decline in renal function alone increased the risk of incident hypertension but the increased risk with a subtle increase in UAE became smaller and less clear in the lower eGFR quartiles. The present data suggest that UAE as a risk factor for incident hypertension is largely dependent on eGFR levels. Nature Publishing Group 2017-12 2017-09-21 /pmc/articles/PMC5746590/ /pubmed/28933781 http://dx.doi.org/10.1038/hr.2017.77 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Munakata, Masanori
Hattori, Tomomi
Konno, Satoshi
Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate
title Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate
title_full Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate
title_fullStr Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate
title_full_unstemmed Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate
title_short Relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate
title_sort relationship between subtle urinary albumin excretion and risk of incident hypertension: modification by glomerular filtration rate
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746590/
https://www.ncbi.nlm.nih.gov/pubmed/28933781
http://dx.doi.org/10.1038/hr.2017.77
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