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Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes
Soluble urokinase-type plasminogen activator receptor (suPAR) is associated with chronic kidney disease (CKD) severity and peripheral artery disease (PAD). We hypothesize an association of PAD severity and suPAR in patients without advanced CKD and further risk stratification according to the Kidney...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879231/ https://www.ncbi.nlm.nih.gov/pubmed/33448911 http://dx.doi.org/10.1177/1358863X20982077 |
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author | Höbaus, Clemens Ursli, Martin Yussef, Sarah Mohammed Wrba, Thomas Koppensteiner, Renate Schernthaner, Gerit-Holger |
author_facet | Höbaus, Clemens Ursli, Martin Yussef, Sarah Mohammed Wrba, Thomas Koppensteiner, Renate Schernthaner, Gerit-Holger |
author_sort | Höbaus, Clemens |
collection | PubMed |
description | Soluble urokinase-type plasminogen activator receptor (suPAR) is associated with chronic kidney disease (CKD) severity and peripheral artery disease (PAD). We hypothesize an association of PAD severity and suPAR in patients without advanced CKD and further risk stratification according to the Kidney Disease: Improving Global Outcomes (KDIGO) guidelines. For study purposes, suPAR was measured in 334 PAD patients (34% women, age 69 (62–78) years, eGFR 68 ± 20 mL/min/1.72 m(2)) by commercial ELISA. Patients were followed for 10 years to assess long-term all-cause survival by Cox regression. Higher suPAR levels were associated with lower ankle–brachial index (R = −0.215, p = 0.001) in patients with PAD without media-sclerosis (n = 236). suPAR levels inversely correlated with decreased glomerular filtration rate (R = −0.476, p < 0.001) and directly correlated with urinary albumin-to-creatinine ratio (R = 0.207, p < 0.001). Furthermore, higher suPAR levels associated with a higher KDIGO risk score (p < 0.001). Baseline suPAR was significantly associated with all-cause mortality (HR 1.40 (95% CI 1.16–1.68), p < 0.001) over 10 years. suPAR remained associated with mortality (HR 1.29 (1.03–1.61), p = 0.026) after multivariable adjustment for age, sex, cardiovascular risk factors, and eGFR. Future research may define a standard role for suPAR assessment in PAD’s work-up and treatment, especially in patients with CKD. |
format | Online Article Text |
id | pubmed-7879231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78792312021-02-22 Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes Höbaus, Clemens Ursli, Martin Yussef, Sarah Mohammed Wrba, Thomas Koppensteiner, Renate Schernthaner, Gerit-Holger Vasc Med Original Articles Soluble urokinase-type plasminogen activator receptor (suPAR) is associated with chronic kidney disease (CKD) severity and peripheral artery disease (PAD). We hypothesize an association of PAD severity and suPAR in patients without advanced CKD and further risk stratification according to the Kidney Disease: Improving Global Outcomes (KDIGO) guidelines. For study purposes, suPAR was measured in 334 PAD patients (34% women, age 69 (62–78) years, eGFR 68 ± 20 mL/min/1.72 m(2)) by commercial ELISA. Patients were followed for 10 years to assess long-term all-cause survival by Cox regression. Higher suPAR levels were associated with lower ankle–brachial index (R = −0.215, p = 0.001) in patients with PAD without media-sclerosis (n = 236). suPAR levels inversely correlated with decreased glomerular filtration rate (R = −0.476, p < 0.001) and directly correlated with urinary albumin-to-creatinine ratio (R = 0.207, p < 0.001). Furthermore, higher suPAR levels associated with a higher KDIGO risk score (p < 0.001). Baseline suPAR was significantly associated with all-cause mortality (HR 1.40 (95% CI 1.16–1.68), p < 0.001) over 10 years. suPAR remained associated with mortality (HR 1.29 (1.03–1.61), p = 0.026) after multivariable adjustment for age, sex, cardiovascular risk factors, and eGFR. Future research may define a standard role for suPAR assessment in PAD’s work-up and treatment, especially in patients with CKD. SAGE Publications 2021-01-15 2021-02 /pmc/articles/PMC7879231/ /pubmed/33448911 http://dx.doi.org/10.1177/1358863X20982077 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Höbaus, Clemens Ursli, Martin Yussef, Sarah Mohammed Wrba, Thomas Koppensteiner, Renate Schernthaner, Gerit-Holger Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes |
title | Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes |
title_full | Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes |
title_fullStr | Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes |
title_full_unstemmed | Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes |
title_short | Soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes |
title_sort | soluble urokinase-type plasminogen activator receptor predicts peripheral artery disease severity and outcomes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879231/ https://www.ncbi.nlm.nih.gov/pubmed/33448911 http://dx.doi.org/10.1177/1358863X20982077 |
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