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Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation

Living kidney donation represents the optimal renal replacement therapy, but recent data suggest an increased long-term renal risk for the donor. Here, we evaluated the risk for reduced estimated glomerular filtration rate (eGFR), death, and major cardiovascular events such as nonfatal myocardial in...

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Autores principales: Kerschbaum, Julia, Bitter, Stefanie, Weitlaner, Maria, Kienzl-Wagner, Katrin, Neuwirt, Hannes, Bösmüller, Claudia, Mayer, Gert, Schneeberger, Stefan, Rudnicki, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073681/
https://www.ncbi.nlm.nih.gov/pubmed/31991745
http://dx.doi.org/10.3390/jcm9020338
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author Kerschbaum, Julia
Bitter, Stefanie
Weitlaner, Maria
Kienzl-Wagner, Katrin
Neuwirt, Hannes
Bösmüller, Claudia
Mayer, Gert
Schneeberger, Stefan
Rudnicki, Michael
author_facet Kerschbaum, Julia
Bitter, Stefanie
Weitlaner, Maria
Kienzl-Wagner, Katrin
Neuwirt, Hannes
Bösmüller, Claudia
Mayer, Gert
Schneeberger, Stefan
Rudnicki, Michael
author_sort Kerschbaum, Julia
collection PubMed
description Living kidney donation represents the optimal renal replacement therapy, but recent data suggest an increased long-term renal risk for the donor. Here, we evaluated the risk for reduced estimated glomerular filtration rate (eGFR), death, and major cardiovascular events such as nonfatal myocardial infarction or cerebrovascular event including TIA (transient ischemic attack) and stroke in 225 donors, who underwent pre-donation examinations and live donor nephrectomy between 1985 and 2014 at our center. The median follow-up time was 8.7 years (1.0–29.1). In multivariate analysis, age and arterial hypertension at baseline were significantly associated with a higher risk of adverse renal outcomes, such as (1) eGFR <60 mL/min/1.73 m(2) (age per year: HR (hazard ratio) 1.05, 95% confidence interval (CI) 1.03–1.08, hypertension: HR 2.25, 95% CI 1.22–3.98), (2) eGFR <60 mL/min/1.73 m(2) and a decrease of ≥40% from baseline (age: HR 1.08, 95% CI 1.03–1.13, hypertension: HR 4.22, 95% CI 1.72–10.36), and (3) eGFR <45 mL/min/1.73 m(2) (age: HR 1.12, 95% CI 1.05–1.20, hypertension: HR 5.06, 95% CI 1.49–17.22). In addition, eGFR at time of donation (per mL/min/1.73 m(2)) was associated with a lower risk of (1) eGFR <60 mL/min/1.73 m(2) (HR 0.98, 95% CI 0.97–1.00) and (2) eGFR <45 mL/min/1.73 m(2) (HR 0.95, 95% CI 0.90–1.00). Age was the only significant predictor for death or major cardiovascular event (HR 1.08, 95% CI 1.01–1.16). In conclusion, arterial hypertension, lower eGFR, and age at the time of donation are strong predictors for adverse renal outcomes in living kidney donors.
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spelling pubmed-70736812020-03-19 Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation Kerschbaum, Julia Bitter, Stefanie Weitlaner, Maria Kienzl-Wagner, Katrin Neuwirt, Hannes Bösmüller, Claudia Mayer, Gert Schneeberger, Stefan Rudnicki, Michael J Clin Med Article Living kidney donation represents the optimal renal replacement therapy, but recent data suggest an increased long-term renal risk for the donor. Here, we evaluated the risk for reduced estimated glomerular filtration rate (eGFR), death, and major cardiovascular events such as nonfatal myocardial infarction or cerebrovascular event including TIA (transient ischemic attack) and stroke in 225 donors, who underwent pre-donation examinations and live donor nephrectomy between 1985 and 2014 at our center. The median follow-up time was 8.7 years (1.0–29.1). In multivariate analysis, age and arterial hypertension at baseline were significantly associated with a higher risk of adverse renal outcomes, such as (1) eGFR <60 mL/min/1.73 m(2) (age per year: HR (hazard ratio) 1.05, 95% confidence interval (CI) 1.03–1.08, hypertension: HR 2.25, 95% CI 1.22–3.98), (2) eGFR <60 mL/min/1.73 m(2) and a decrease of ≥40% from baseline (age: HR 1.08, 95% CI 1.03–1.13, hypertension: HR 4.22, 95% CI 1.72–10.36), and (3) eGFR <45 mL/min/1.73 m(2) (age: HR 1.12, 95% CI 1.05–1.20, hypertension: HR 5.06, 95% CI 1.49–17.22). In addition, eGFR at time of donation (per mL/min/1.73 m(2)) was associated with a lower risk of (1) eGFR <60 mL/min/1.73 m(2) (HR 0.98, 95% CI 0.97–1.00) and (2) eGFR <45 mL/min/1.73 m(2) (HR 0.95, 95% CI 0.90–1.00). Age was the only significant predictor for death or major cardiovascular event (HR 1.08, 95% CI 1.01–1.16). In conclusion, arterial hypertension, lower eGFR, and age at the time of donation are strong predictors for adverse renal outcomes in living kidney donors. MDPI 2020-01-25 /pmc/articles/PMC7073681/ /pubmed/31991745 http://dx.doi.org/10.3390/jcm9020338 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kerschbaum, Julia
Bitter, Stefanie
Weitlaner, Maria
Kienzl-Wagner, Katrin
Neuwirt, Hannes
Bösmüller, Claudia
Mayer, Gert
Schneeberger, Stefan
Rudnicki, Michael
Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation
title Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation
title_full Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation
title_fullStr Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation
title_full_unstemmed Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation
title_short Arterial Hypertension as a Risk Factor for Reduced Glomerular Filtration Rate after Living Kidney Donation
title_sort arterial hypertension as a risk factor for reduced glomerular filtration rate after living kidney donation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073681/
https://www.ncbi.nlm.nih.gov/pubmed/31991745
http://dx.doi.org/10.3390/jcm9020338
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