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Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up

Background: The best treatment for coronary artery disease (CAD) in patients with type 2 diabetes (DM2) and chronic kidney disease is unknown. Methods: This retrospective study included MASS registry patients with DM2 and multivessel CAD, stratified by kidney function. Primary endpoint was combined...

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Autores principales: Batista, Daniel Valente, Hueb, Whady, Lima, Eduardo Gomes, Rezende, Paulo Cury, Garzillo, Cibele Larrosa, Garcia, Rosa Maria Rahmi, Filho, Jaime Paula Pessoa Linhares, Martins, Eduardo Bello, Junior, Carlos Vicente Serrano, Ramires, Jose Antonio Franchini, Filho, Roberto Kalil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436946/
https://www.ncbi.nlm.nih.gov/pubmed/34433133
http://dx.doi.org/10.18632/aging.203476
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author Batista, Daniel Valente
Hueb, Whady
Lima, Eduardo Gomes
Rezende, Paulo Cury
Garzillo, Cibele Larrosa
Garcia, Rosa Maria Rahmi
Filho, Jaime Paula Pessoa Linhares
Martins, Eduardo Bello
Junior, Carlos Vicente Serrano
Ramires, Jose Antonio Franchini
Filho, Roberto Kalil
author_facet Batista, Daniel Valente
Hueb, Whady
Lima, Eduardo Gomes
Rezende, Paulo Cury
Garzillo, Cibele Larrosa
Garcia, Rosa Maria Rahmi
Filho, Jaime Paula Pessoa Linhares
Martins, Eduardo Bello
Junior, Carlos Vicente Serrano
Ramires, Jose Antonio Franchini
Filho, Roberto Kalil
author_sort Batista, Daniel Valente
collection PubMed
description Background: The best treatment for coronary artery disease (CAD) in patients with type 2 diabetes (DM2) and chronic kidney disease is unknown. Methods: This retrospective study included MASS registry patients with DM2 and multivessel CAD, stratified by kidney function. Primary endpoint was combined of mortality, myocardial infarction, or additional revascularization. Results: Median follow-up was 9.5 years. Primary endpoint occurrences among strata 1 and 2 were 53.4% and 40.7%, respectively (P=.020). Mortality rates were 37.4% and 24.6% in strata 1 and 2, respectively (P<.001). We observed a lower rate of major adverse cardiovascular events (MACE) (P=.027 for stratum 1 and P<.001 for stratum 2) and additional revascularization (P=.001 for stratum 1 and P<.001 for stratum 2) for those in the surgical group. In a multivariate analysis, eGFR was an independent predictor of MACE (P=.034) and mortality (P=.020). Conclusions: Among subjects with DM2 and CAD the presence of lower eGFR rate was associated with higher rates of MACE and mortality, irrespective of treatment choice. CABG was associated with lower rates of MACE in both renal function strata. eGFR was an independent predictor of MACE and mortality in a 10-year follow-up.
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spelling pubmed-84369462021-09-14 Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up Batista, Daniel Valente Hueb, Whady Lima, Eduardo Gomes Rezende, Paulo Cury Garzillo, Cibele Larrosa Garcia, Rosa Maria Rahmi Filho, Jaime Paula Pessoa Linhares Martins, Eduardo Bello Junior, Carlos Vicente Serrano Ramires, Jose Antonio Franchini Filho, Roberto Kalil Aging (Albany NY) Research Paper Background: The best treatment for coronary artery disease (CAD) in patients with type 2 diabetes (DM2) and chronic kidney disease is unknown. Methods: This retrospective study included MASS registry patients with DM2 and multivessel CAD, stratified by kidney function. Primary endpoint was combined of mortality, myocardial infarction, or additional revascularization. Results: Median follow-up was 9.5 years. Primary endpoint occurrences among strata 1 and 2 were 53.4% and 40.7%, respectively (P=.020). Mortality rates were 37.4% and 24.6% in strata 1 and 2, respectively (P<.001). We observed a lower rate of major adverse cardiovascular events (MACE) (P=.027 for stratum 1 and P<.001 for stratum 2) and additional revascularization (P=.001 for stratum 1 and P<.001 for stratum 2) for those in the surgical group. In a multivariate analysis, eGFR was an independent predictor of MACE (P=.034) and mortality (P=.020). Conclusions: Among subjects with DM2 and CAD the presence of lower eGFR rate was associated with higher rates of MACE and mortality, irrespective of treatment choice. CABG was associated with lower rates of MACE in both renal function strata. eGFR was an independent predictor of MACE and mortality in a 10-year follow-up. Impact Journals 2021-08-25 /pmc/articles/PMC8436946/ /pubmed/34433133 http://dx.doi.org/10.18632/aging.203476 Text en Copyright: © 2021 Batista et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Batista, Daniel Valente
Hueb, Whady
Lima, Eduardo Gomes
Rezende, Paulo Cury
Garzillo, Cibele Larrosa
Garcia, Rosa Maria Rahmi
Filho, Jaime Paula Pessoa Linhares
Martins, Eduardo Bello
Junior, Carlos Vicente Serrano
Ramires, Jose Antonio Franchini
Filho, Roberto Kalil
Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up
title Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up
title_full Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up
title_fullStr Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up
title_full_unstemmed Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up
title_short Effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up
title_sort effect of diabetic kidney disease on therapeutic strategies for coronary artery disease: ten year follow-up
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436946/
https://www.ncbi.nlm.nih.gov/pubmed/34433133
http://dx.doi.org/10.18632/aging.203476
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