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The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population

INTRODUCTION: One-quarter of adults worldwide meet the criteria of metabolic syndrome (MetS). MetS increases the risk of diabetes, chronic kidney disease (CKD), and cardiovascular disease. However, the association between MetS, hyperfiltration, and long-term glomerular filtration rate (GFR) decline...

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Autores principales: Bystad, Erikka W., Stefansson, Vidar T.N., Eriksen, Bjørn O., Melsom, Toralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496074/
https://www.ncbi.nlm.nih.gov/pubmed/37705899
http://dx.doi.org/10.1016/j.ekir.2023.06.022
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author Bystad, Erikka W.
Stefansson, Vidar T.N.
Eriksen, Bjørn O.
Melsom, Toralf
author_facet Bystad, Erikka W.
Stefansson, Vidar T.N.
Eriksen, Bjørn O.
Melsom, Toralf
author_sort Bystad, Erikka W.
collection PubMed
description INTRODUCTION: One-quarter of adults worldwide meet the criteria of metabolic syndrome (MetS). MetS increases the risk of diabetes, chronic kidney disease (CKD), and cardiovascular disease. However, the association between MetS, hyperfiltration, and long-term glomerular filtration rate (GFR) decline in the general population is unknown. METHODS: In the Renal Iohexol Clearance Survey (RENIS), we investigated 1551 people aged 50 to 63 years; representative of the general population without diabetes, cardiovascular disease, or kidney disease. The GFR was measured using iohexol clearance at baseline and twice during 11 years of follow-up. Hyperfiltration at baseline was defined as an absolute GFR (ml/min) above the 90th percentile adjusted for sex, age, and height, because these variables correlate with nephron number. MetS was defined as increased waist circumference and 2 risk factors among hypertension, hyperglycemia, elevated triglycerides, and low high density lipoprotein (HDL)-cholesterol levels. The GFR decline rate was calculated using linear mixed models. RESULTS: MetS was associated with hyperfiltration at baseline (odds ratio [OR] 2.4; 95% CI: 1.7–3.5, P < 0.001) and a steeper GFR decline rate during follow-up (−0.30 [−0.43 to −0.16] ml/min per 1.73 m(2)/yr). Compared to those without MetS, GFR decline was −0.83 (95% CI: −1.13 to −0.53) ml/min per 1.73 m(2)/yr in those with MetS and baseline hyperfiltration and −0.15 (−0.30 to 0.00) in those MetS without hyperfiltration, P = 0.2 for interaction. CONCLUSIONS: In the nondiabetic general population, those with MetS had an increased OR of hyperfiltration and steeper long-term GFR decline. Randomized controlled trials are needed to explore whether treatment of hyperfiltration can prevent loss of GFR in persons with MetS.
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spelling pubmed-104960742023-09-13 The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population Bystad, Erikka W. Stefansson, Vidar T.N. Eriksen, Bjørn O. Melsom, Toralf Kidney Int Rep Clinical Research INTRODUCTION: One-quarter of adults worldwide meet the criteria of metabolic syndrome (MetS). MetS increases the risk of diabetes, chronic kidney disease (CKD), and cardiovascular disease. However, the association between MetS, hyperfiltration, and long-term glomerular filtration rate (GFR) decline in the general population is unknown. METHODS: In the Renal Iohexol Clearance Survey (RENIS), we investigated 1551 people aged 50 to 63 years; representative of the general population without diabetes, cardiovascular disease, or kidney disease. The GFR was measured using iohexol clearance at baseline and twice during 11 years of follow-up. Hyperfiltration at baseline was defined as an absolute GFR (ml/min) above the 90th percentile adjusted for sex, age, and height, because these variables correlate with nephron number. MetS was defined as increased waist circumference and 2 risk factors among hypertension, hyperglycemia, elevated triglycerides, and low high density lipoprotein (HDL)-cholesterol levels. The GFR decline rate was calculated using linear mixed models. RESULTS: MetS was associated with hyperfiltration at baseline (odds ratio [OR] 2.4; 95% CI: 1.7–3.5, P < 0.001) and a steeper GFR decline rate during follow-up (−0.30 [−0.43 to −0.16] ml/min per 1.73 m(2)/yr). Compared to those without MetS, GFR decline was −0.83 (95% CI: −1.13 to −0.53) ml/min per 1.73 m(2)/yr in those with MetS and baseline hyperfiltration and −0.15 (−0.30 to 0.00) in those MetS without hyperfiltration, P = 0.2 for interaction. CONCLUSIONS: In the nondiabetic general population, those with MetS had an increased OR of hyperfiltration and steeper long-term GFR decline. Randomized controlled trials are needed to explore whether treatment of hyperfiltration can prevent loss of GFR in persons with MetS. Elsevier 2023-07-01 /pmc/articles/PMC10496074/ /pubmed/37705899 http://dx.doi.org/10.1016/j.ekir.2023.06.022 Text en © 2023 International Society of Nephrology. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Clinical Research
Bystad, Erikka W.
Stefansson, Vidar T.N.
Eriksen, Bjørn O.
Melsom, Toralf
The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population
title The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population
title_full The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population
title_fullStr The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population
title_full_unstemmed The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population
title_short The Association Between Metabolic Syndrome, Hyperfiltration, and Long-Term GFR Decline in the General Population
title_sort association between metabolic syndrome, hyperfiltration, and long-term gfr decline in the general population
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496074/
https://www.ncbi.nlm.nih.gov/pubmed/37705899
http://dx.doi.org/10.1016/j.ekir.2023.06.022
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