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Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation

BACKGROUND: The risk of mortality and graft loss is higher in kidney transplant recipients with reduced estimated glomerular filtration rate (eGFR) and albuminuria. It is unclear whether these markers are also associated with cardiovascular events. METHODS: We examined linked healthcare databases in...

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Autores principales: Lam, Ngan N., Klarenbach, Scott, Quinn, Robert R., Hemmelgarn, Brenda, Tonelli, Marcello, Ye, Feng, Ravani, Pietro, Bello, Aminu K., Brennan, Daniel C., Lentine, Krista L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233669/
https://www.ncbi.nlm.nih.gov/pubmed/30498766
http://dx.doi.org/10.1097/TXD.0000000000000828
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author Lam, Ngan N.
Klarenbach, Scott
Quinn, Robert R.
Hemmelgarn, Brenda
Tonelli, Marcello
Ye, Feng
Ravani, Pietro
Bello, Aminu K.
Brennan, Daniel C.
Lentine, Krista L.
author_facet Lam, Ngan N.
Klarenbach, Scott
Quinn, Robert R.
Hemmelgarn, Brenda
Tonelli, Marcello
Ye, Feng
Ravani, Pietro
Bello, Aminu K.
Brennan, Daniel C.
Lentine, Krista L.
author_sort Lam, Ngan N.
collection PubMed
description BACKGROUND: The risk of mortality and graft loss is higher in kidney transplant recipients with reduced estimated glomerular filtration rate (eGFR) and albuminuria. It is unclear whether these markers are also associated with cardiovascular events. METHODS: We examined linked healthcare databases in Alberta, Canada to identify kidney transplant recipients between 2002 and 2013 who had at least 1 outpatient serum creatinine and albuminuria measurement at 1-year posttransplant. We determined the relationship between categories of eGFR and albuminuria and the risk of subsequent cardiovascular events. RESULTS: Among 1069 eligible kidney transplant recipients, the median age was 52 years, 37% were female, and 52% had eGFR ≥60 mL/min per 1.73 m(2). Over a median follow-up of 6 years, the adjusted rate of all-cause mortality and cardiovascular events was 2.7-fold higher for recipients with eGFR 15-29 mL/min per 1.73 m(2) and heavy albuminuria compared to recipients with eGFR ≥60 mL/min per 1.73 m(2) and normal albuminuria (rate ratio, 2.7; 95% confidence interval, 1.3-5.7). Similarly, recipients with heavy albuminuria had a threefold increased risk of all-cause mortality and heart failure compared with recipients with eGFR ≥60 mL/min per 1.73 m(2) and normal albuminuria. CONCLUSIONS: These findings suggest that eGFR and albuminuria should be used together to determine the risk of cardiovascular outcomes in transplant recipients.
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spelling pubmed-62336692018-11-29 Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation Lam, Ngan N. Klarenbach, Scott Quinn, Robert R. Hemmelgarn, Brenda Tonelli, Marcello Ye, Feng Ravani, Pietro Bello, Aminu K. Brennan, Daniel C. Lentine, Krista L. Transplant Direct Kidney Transplantation BACKGROUND: The risk of mortality and graft loss is higher in kidney transplant recipients with reduced estimated glomerular filtration rate (eGFR) and albuminuria. It is unclear whether these markers are also associated with cardiovascular events. METHODS: We examined linked healthcare databases in Alberta, Canada to identify kidney transplant recipients between 2002 and 2013 who had at least 1 outpatient serum creatinine and albuminuria measurement at 1-year posttransplant. We determined the relationship between categories of eGFR and albuminuria and the risk of subsequent cardiovascular events. RESULTS: Among 1069 eligible kidney transplant recipients, the median age was 52 years, 37% were female, and 52% had eGFR ≥60 mL/min per 1.73 m(2). Over a median follow-up of 6 years, the adjusted rate of all-cause mortality and cardiovascular events was 2.7-fold higher for recipients with eGFR 15-29 mL/min per 1.73 m(2) and heavy albuminuria compared to recipients with eGFR ≥60 mL/min per 1.73 m(2) and normal albuminuria (rate ratio, 2.7; 95% confidence interval, 1.3-5.7). Similarly, recipients with heavy albuminuria had a threefold increased risk of all-cause mortality and heart failure compared with recipients with eGFR ≥60 mL/min per 1.73 m(2) and normal albuminuria. CONCLUSIONS: These findings suggest that eGFR and albuminuria should be used together to determine the risk of cardiovascular outcomes in transplant recipients. Lippincott Williams & Wilkins 2018-09-06 /pmc/articles/PMC6233669/ /pubmed/30498766 http://dx.doi.org/10.1097/TXD.0000000000000828 Text en Copyright © 2018 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Kidney Transplantation
Lam, Ngan N.
Klarenbach, Scott
Quinn, Robert R.
Hemmelgarn, Brenda
Tonelli, Marcello
Ye, Feng
Ravani, Pietro
Bello, Aminu K.
Brennan, Daniel C.
Lentine, Krista L.
Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation
title Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation
title_full Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation
title_fullStr Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation
title_full_unstemmed Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation
title_short Renal Function, Albuminuria, and the Risk of Cardiovascular Events After Kidney Transplantation
title_sort renal function, albuminuria, and the risk of cardiovascular events after kidney transplantation
topic Kidney Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233669/
https://www.ncbi.nlm.nih.gov/pubmed/30498766
http://dx.doi.org/10.1097/TXD.0000000000000828
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