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Long-term risk for end-stage kidney disease and death in a large population-based cohort

Knowledge of metabolic risk factors for end-stage kidney disease (ESKD) in the general population is limited when considering the competing event death in risk analysis. The aim of our prospective observational study was to investigate how blood pressure and metabolic factors might influence the ris...

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Autores principales: Zitt, Emanuel, Pscheidt, Constanze, Concin, Hans, Kramar, Reinhard, Peter, Raphael S., Beyersmann, Jan, Lhotta, Karl, Nagel, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955909/
https://www.ncbi.nlm.nih.gov/pubmed/29769597
http://dx.doi.org/10.1038/s41598-018-26087-z
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author Zitt, Emanuel
Pscheidt, Constanze
Concin, Hans
Kramar, Reinhard
Peter, Raphael S.
Beyersmann, Jan
Lhotta, Karl
Nagel, Gabriele
author_facet Zitt, Emanuel
Pscheidt, Constanze
Concin, Hans
Kramar, Reinhard
Peter, Raphael S.
Beyersmann, Jan
Lhotta, Karl
Nagel, Gabriele
author_sort Zitt, Emanuel
collection PubMed
description Knowledge of metabolic risk factors for end-stage kidney disease (ESKD) in the general population is limited when considering the competing event death in risk analysis. The aim of our prospective observational study was to investigate how blood pressure and metabolic factors might influence the risks for ESKD and death before ESKD in a large Austrian population-based cohort with long-term follow-up. 177,255 participants (53.8% women; mean age 42.5 years) were recruited between 1988 and 2005 and linked to the Austrian Dialysis and Transplant Registry and the National Mortality Registry. Over a mean follow-up of 16 years 358 participants reached ESKD and 19,512 participants died. Applying fully adjusted cause-specific Cox proportional hazards models elevated fasting blood glucose, hypertension, hypertrigylceridemia and hypercholesterolemia were associated with a higher relative risk for ESKD than for death before ESKD, whereas elevated γ-glutamyltransferase was associated with an increased relative risk of death but not ESKD. Results were similar using continuous or categorical exposure variable measures in the general cohort but differed in selected high-risk populations. These findings might help improve the design of renal risk factor modification trials and kidney disease awareness and prevention programs in the general population, which may ultimately decrease the burden of ESKD.
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spelling pubmed-59559092018-05-21 Long-term risk for end-stage kidney disease and death in a large population-based cohort Zitt, Emanuel Pscheidt, Constanze Concin, Hans Kramar, Reinhard Peter, Raphael S. Beyersmann, Jan Lhotta, Karl Nagel, Gabriele Sci Rep Article Knowledge of metabolic risk factors for end-stage kidney disease (ESKD) in the general population is limited when considering the competing event death in risk analysis. The aim of our prospective observational study was to investigate how blood pressure and metabolic factors might influence the risks for ESKD and death before ESKD in a large Austrian population-based cohort with long-term follow-up. 177,255 participants (53.8% women; mean age 42.5 years) were recruited between 1988 and 2005 and linked to the Austrian Dialysis and Transplant Registry and the National Mortality Registry. Over a mean follow-up of 16 years 358 participants reached ESKD and 19,512 participants died. Applying fully adjusted cause-specific Cox proportional hazards models elevated fasting blood glucose, hypertension, hypertrigylceridemia and hypercholesterolemia were associated with a higher relative risk for ESKD than for death before ESKD, whereas elevated γ-glutamyltransferase was associated with an increased relative risk of death but not ESKD. Results were similar using continuous or categorical exposure variable measures in the general cohort but differed in selected high-risk populations. These findings might help improve the design of renal risk factor modification trials and kidney disease awareness and prevention programs in the general population, which may ultimately decrease the burden of ESKD. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955909/ /pubmed/29769597 http://dx.doi.org/10.1038/s41598-018-26087-z Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zitt, Emanuel
Pscheidt, Constanze
Concin, Hans
Kramar, Reinhard
Peter, Raphael S.
Beyersmann, Jan
Lhotta, Karl
Nagel, Gabriele
Long-term risk for end-stage kidney disease and death in a large population-based cohort
title Long-term risk for end-stage kidney disease and death in a large population-based cohort
title_full Long-term risk for end-stage kidney disease and death in a large population-based cohort
title_fullStr Long-term risk for end-stage kidney disease and death in a large population-based cohort
title_full_unstemmed Long-term risk for end-stage kidney disease and death in a large population-based cohort
title_short Long-term risk for end-stage kidney disease and death in a large population-based cohort
title_sort long-term risk for end-stage kidney disease and death in a large population-based cohort
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955909/
https://www.ncbi.nlm.nih.gov/pubmed/29769597
http://dx.doi.org/10.1038/s41598-018-26087-z
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