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Can uric acid blood levels in renal transplant recipients predict allograft outcome?
BACKGROUND: Hyperuricemia is common after renal transplantation, especially in those receiving calcineurin inhibitors. Little, however, is known about the relationship between uric acid (UA) levels and allograft outcome. METHODS: We conducted a retrospective single-center analysis (N = 368) in order...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405090/ https://www.ncbi.nlm.nih.gov/pubmed/34433378 http://dx.doi.org/10.1080/0886022X.2021.1969246 |
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author | Isakov, Ofer Patibandla, Bhanu K. Shwartz, Doron Mor, Eytan Christopher, Kenneth B. Hod, Tammy |
author_facet | Isakov, Ofer Patibandla, Bhanu K. Shwartz, Doron Mor, Eytan Christopher, Kenneth B. Hod, Tammy |
author_sort | Isakov, Ofer |
collection | PubMed |
description | BACKGROUND: Hyperuricemia is common after renal transplantation, especially in those receiving calcineurin inhibitors. Little, however, is known about the relationship between uric acid (UA) levels and allograft outcome. METHODS: We conducted a retrospective single-center analysis (N = 368) in order to assess UA blood levels post-transplant association with allograft outcome. For this study, a median serum UA level of all measured UA levels from 1 month to 1 year post renal transplantation was calculated. RESULTS: Patients were divided into 2 groups based on the median UA level measured between 1 and 12 months post-transplant. Those with median UA level ≥ 7 and ≥ 6 mg/dL (N = 164) versus median UA level < 7 and < 6 mg/dL for men and women respectively (N = 204) had lower GFR values at 1, 3 and 5 years posttransplant (mean GFR ± SD of 43.4 ± 20.6 and 58 ± 19.9 at 3 years post-transplant, p < 0.001). In multivariate models, UA levels were no longer significantly associated with renal allograft function. In a multivariate cox proportional hazard model, UA level was found to be independently associated with increased risk for death-censored graft loss (HR of 1.3, 95% CI 1.0–1.7, p < 0.05 for every increase of 1 mg/dL in UA level). CONCLUSION: Hyperuricemia was found to be associated with increased death- censored graft loss but not with allograft function. Increased UA levels were not found to be an independent predictor of long-term allograft function despite the known association of hyperuricemia with the progression of cardiovascular and renal disease. |
format | Online Article Text |
id | pubmed-8405090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-84050902021-08-31 Can uric acid blood levels in renal transplant recipients predict allograft outcome? Isakov, Ofer Patibandla, Bhanu K. Shwartz, Doron Mor, Eytan Christopher, Kenneth B. Hod, Tammy Ren Fail Clinical Study BACKGROUND: Hyperuricemia is common after renal transplantation, especially in those receiving calcineurin inhibitors. Little, however, is known about the relationship between uric acid (UA) levels and allograft outcome. METHODS: We conducted a retrospective single-center analysis (N = 368) in order to assess UA blood levels post-transplant association with allograft outcome. For this study, a median serum UA level of all measured UA levels from 1 month to 1 year post renal transplantation was calculated. RESULTS: Patients were divided into 2 groups based on the median UA level measured between 1 and 12 months post-transplant. Those with median UA level ≥ 7 and ≥ 6 mg/dL (N = 164) versus median UA level < 7 and < 6 mg/dL for men and women respectively (N = 204) had lower GFR values at 1, 3 and 5 years posttransplant (mean GFR ± SD of 43.4 ± 20.6 and 58 ± 19.9 at 3 years post-transplant, p < 0.001). In multivariate models, UA levels were no longer significantly associated with renal allograft function. In a multivariate cox proportional hazard model, UA level was found to be independently associated with increased risk for death-censored graft loss (HR of 1.3, 95% CI 1.0–1.7, p < 0.05 for every increase of 1 mg/dL in UA level). CONCLUSION: Hyperuricemia was found to be associated with increased death- censored graft loss but not with allograft function. Increased UA levels were not found to be an independent predictor of long-term allograft function despite the known association of hyperuricemia with the progression of cardiovascular and renal disease. Taylor & Francis 2021-08-25 /pmc/articles/PMC8405090/ /pubmed/34433378 http://dx.doi.org/10.1080/0886022X.2021.1969246 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Isakov, Ofer Patibandla, Bhanu K. Shwartz, Doron Mor, Eytan Christopher, Kenneth B. Hod, Tammy Can uric acid blood levels in renal transplant recipients predict allograft outcome? |
title | Can uric acid blood levels in renal transplant recipients predict allograft outcome? |
title_full | Can uric acid blood levels in renal transplant recipients predict allograft outcome? |
title_fullStr | Can uric acid blood levels in renal transplant recipients predict allograft outcome? |
title_full_unstemmed | Can uric acid blood levels in renal transplant recipients predict allograft outcome? |
title_short | Can uric acid blood levels in renal transplant recipients predict allograft outcome? |
title_sort | can uric acid blood levels in renal transplant recipients predict allograft outcome? |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405090/ https://www.ncbi.nlm.nih.gov/pubmed/34433378 http://dx.doi.org/10.1080/0886022X.2021.1969246 |
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