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Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes

AIM: Three urinary biomarkers, kidney injury molecule-1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL), and cystatin C, have been suggested as clinically relevant highly specific biomarkers of acute kidney tubular damage. Yet, the utility of these biomarkers in the prognostication of dia...

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Autores principales: Tonkonogi, Aleksandra, Carlsson, Axel C., Helmersson-Karlqvist, Johanna, Larsson, Anders, Ärnlöv, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967263/
https://www.ncbi.nlm.nih.gov/pubmed/27321055
http://dx.doi.org/10.1080/03009734.2016.1192704
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author Tonkonogi, Aleksandra
Carlsson, Axel C.
Helmersson-Karlqvist, Johanna
Larsson, Anders
Ärnlöv, Johan
author_facet Tonkonogi, Aleksandra
Carlsson, Axel C.
Helmersson-Karlqvist, Johanna
Larsson, Anders
Ärnlöv, Johan
author_sort Tonkonogi, Aleksandra
collection PubMed
description AIM: Three urinary biomarkers, kidney injury molecule-1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL), and cystatin C, have been suggested as clinically relevant highly specific biomarkers of acute kidney tubular damage. Yet, the utility of these biomarkers in the prognostication of diabetic nephropathy has been less studied. Therefore, we aimed to investigate the longitudinal association between these urinary biomarkers and cardiovascular mortality in patients with diabetes. METHODS: The study sample consisted of participants with diabetes in the community-based Uppsala Longitudinal Study of Adult Men (n = 91; mean age 77.8 years). During follow-up (median 8.3 years, interval 0.7–13.4 years), 33 participants died of cardiovascular causes. RESULTS: In a multivariable Cox regression model adjusting for age, glomerular filtration rate, and urinary albumin/creatinine ratio, higher urinary KIM-1/creatinine was associated with an increased risk for cardiovascular mortality (HR per SD increase 1.51, 95% confidence intervals 1.03–2.24, P = 0.03). Neither urinary NGAL/creatinine nor urinary cystatin C/creatinine were independently associated with an increased cardiovascular mortality risk. CONCLUSION: In elderly men with diabetes, higher urinary KIM-1/creatinine was associated with an increased long-term risk of cardiovascular mortality independently of established markers of diabetic nephropathy. Our data provide support for kidney tubular damage as an important aspect of diabetic nephropathy that merits further investigation.
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spelling pubmed-49672632016-08-25 Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes Tonkonogi, Aleksandra Carlsson, Axel C. Helmersson-Karlqvist, Johanna Larsson, Anders Ärnlöv, Johan Ups J Med Sci Original Articles AIM: Three urinary biomarkers, kidney injury molecule-1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL), and cystatin C, have been suggested as clinically relevant highly specific biomarkers of acute kidney tubular damage. Yet, the utility of these biomarkers in the prognostication of diabetic nephropathy has been less studied. Therefore, we aimed to investigate the longitudinal association between these urinary biomarkers and cardiovascular mortality in patients with diabetes. METHODS: The study sample consisted of participants with diabetes in the community-based Uppsala Longitudinal Study of Adult Men (n = 91; mean age 77.8 years). During follow-up (median 8.3 years, interval 0.7–13.4 years), 33 participants died of cardiovascular causes. RESULTS: In a multivariable Cox regression model adjusting for age, glomerular filtration rate, and urinary albumin/creatinine ratio, higher urinary KIM-1/creatinine was associated with an increased risk for cardiovascular mortality (HR per SD increase 1.51, 95% confidence intervals 1.03–2.24, P = 0.03). Neither urinary NGAL/creatinine nor urinary cystatin C/creatinine were independently associated with an increased cardiovascular mortality risk. CONCLUSION: In elderly men with diabetes, higher urinary KIM-1/creatinine was associated with an increased long-term risk of cardiovascular mortality independently of established markers of diabetic nephropathy. Our data provide support for kidney tubular damage as an important aspect of diabetic nephropathy that merits further investigation. Taylor & Francis 2016-08 2016-06-17 /pmc/articles/PMC4967263/ /pubmed/27321055 http://dx.doi.org/10.1080/03009734.2016.1192704 Text en © 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Tonkonogi, Aleksandra
Carlsson, Axel C.
Helmersson-Karlqvist, Johanna
Larsson, Anders
Ärnlöv, Johan
Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes
title Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes
title_full Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes
title_fullStr Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes
title_full_unstemmed Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes
title_short Associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes
title_sort associations between urinary kidney injury biomarkers and cardiovascular mortality risk in elderly men with diabetes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967263/
https://www.ncbi.nlm.nih.gov/pubmed/27321055
http://dx.doi.org/10.1080/03009734.2016.1192704
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