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Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population
INTRODUCTION: Although lower high-density lipoprotein cholesterol (HDL-C) levels are considered a risk factor for cardiovascular disease (CVD), experimental evidence suggest that aging, inflammation, and oxidative stress may remodel HDL-C, leading to dysfunctional HDL-C. Population studies on HDL-C...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343778/ https://www.ncbi.nlm.nih.gov/pubmed/34386657 http://dx.doi.org/10.1016/j.ekir.2021.05.007 |
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author | Melsom, Toralf Norvik, Jon Viljar Enoksen, Inger Therese Stefansson, Vidar Rismo, Renathe Jenssen, Trond Solbu, Marit D. Eriksen, Bjørn O. |
author_facet | Melsom, Toralf Norvik, Jon Viljar Enoksen, Inger Therese Stefansson, Vidar Rismo, Renathe Jenssen, Trond Solbu, Marit D. Eriksen, Bjørn O. |
author_sort | Melsom, Toralf |
collection | PubMed |
description | INTRODUCTION: Although lower high-density lipoprotein cholesterol (HDL-C) levels are considered a risk factor for cardiovascular disease (CVD), experimental evidence suggest that aging, inflammation, and oxidative stress may remodel HDL-C, leading to dysfunctional HDL-C. Population studies on HDL-C and loss of the glomerular filtration rate (GFR) reported inconsistent results, but they used inaccurate estimates of the GFR and may have been confounded by comorbidity. METHODS: We investigated the association of HDL-C levels with risk of GFR loss in a general population cohort; the participants were aged 50–62 years and did not have diabetes, CVD, or chronic kidney disease (CKD) at baseline. The GFR was measured using iohexol-clearance at baseline (n=1627) and at the follow-up (n=1324) after a median of 5.6 years. We also investigated any possible effect modification by low-grade inflammation, physical activity, and sex. RESULTS: Higher HDL-C levels were associated with steeper GFR decline rates and increased risk of rapid GFR decline (>3 ml/min per 1.73 m(2) per year) in multivariable adjusted linear mixed models and logistic regression (–0.64 ml/min per 1.73 m(2) per year [95% CI –0.99, –0.29; P < 0.001] and odds ratio 2.7 [95% CI 1.4, 5.2; P < 0.001] per doubling in HDL-C). Effect modifications indicated a stronger association between high HDL-C and GFR loss in physically inactive persons, those with low-grade inflammation, and men. CONCLUSION: Higher HDL-C levels were independently associated with accelerated GFR loss in a general middle-aged nondiabetic population. |
format | Online Article Text |
id | pubmed-8343778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83437782021-08-11 Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population Melsom, Toralf Norvik, Jon Viljar Enoksen, Inger Therese Stefansson, Vidar Rismo, Renathe Jenssen, Trond Solbu, Marit D. Eriksen, Bjørn O. Kidney Int Rep Clinical Research INTRODUCTION: Although lower high-density lipoprotein cholesterol (HDL-C) levels are considered a risk factor for cardiovascular disease (CVD), experimental evidence suggest that aging, inflammation, and oxidative stress may remodel HDL-C, leading to dysfunctional HDL-C. Population studies on HDL-C and loss of the glomerular filtration rate (GFR) reported inconsistent results, but they used inaccurate estimates of the GFR and may have been confounded by comorbidity. METHODS: We investigated the association of HDL-C levels with risk of GFR loss in a general population cohort; the participants were aged 50–62 years and did not have diabetes, CVD, or chronic kidney disease (CKD) at baseline. The GFR was measured using iohexol-clearance at baseline (n=1627) and at the follow-up (n=1324) after a median of 5.6 years. We also investigated any possible effect modification by low-grade inflammation, physical activity, and sex. RESULTS: Higher HDL-C levels were associated with steeper GFR decline rates and increased risk of rapid GFR decline (>3 ml/min per 1.73 m(2) per year) in multivariable adjusted linear mixed models and logistic regression (–0.64 ml/min per 1.73 m(2) per year [95% CI –0.99, –0.29; P < 0.001] and odds ratio 2.7 [95% CI 1.4, 5.2; P < 0.001] per doubling in HDL-C). Effect modifications indicated a stronger association between high HDL-C and GFR loss in physically inactive persons, those with low-grade inflammation, and men. CONCLUSION: Higher HDL-C levels were independently associated with accelerated GFR loss in a general middle-aged nondiabetic population. Elsevier 2021-05-19 /pmc/articles/PMC8343778/ /pubmed/34386657 http://dx.doi.org/10.1016/j.ekir.2021.05.007 Text en © 2021 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 Melsom, Toralf Norvik, Jon Viljar Enoksen, Inger Therese Stefansson, Vidar Rismo, Renathe Jenssen, Trond Solbu, Marit D. Eriksen, Bjørn O. Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population |
title | Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population |
title_full | Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population |
title_fullStr | Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population |
title_full_unstemmed | Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population |
title_short | Association of High-Density Lipoprotein Cholesterol With GFR Decline in a General Nondiabetic Population |
title_sort | association of high-density lipoprotein cholesterol with gfr decline in a general nondiabetic population |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343778/ https://www.ncbi.nlm.nih.gov/pubmed/34386657 http://dx.doi.org/10.1016/j.ekir.2021.05.007 |
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