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Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction

Survivors after a myocardial infarction (MI), especially those with diabetes mellitus (DM), remain at high risk of further events. Identifying and treating factors that may influence survival may open new therapeutic strategies. We assessed the impact on prognosis of DM and hypovitaminosis D (hypovi...

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Autores principales: Aleksova, Aneta, Ferro, Federico, Gagno, Giulia, Padoan, Laura, Saro, Riccardo, Santon, Daniela, Stenner, Elisabetta, Barbati, Giulia, Cappelletto, Chiara, Rossi, Maddalena, Beltrami, Antonio Paolo, Sinagra, Gianfranco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408858/
https://www.ncbi.nlm.nih.gov/pubmed/32640692
http://dx.doi.org/10.3390/jcm9072127
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author Aleksova, Aneta
Ferro, Federico
Gagno, Giulia
Padoan, Laura
Saro, Riccardo
Santon, Daniela
Stenner, Elisabetta
Barbati, Giulia
Cappelletto, Chiara
Rossi, Maddalena
Beltrami, Antonio Paolo
Sinagra, Gianfranco
author_facet Aleksova, Aneta
Ferro, Federico
Gagno, Giulia
Padoan, Laura
Saro, Riccardo
Santon, Daniela
Stenner, Elisabetta
Barbati, Giulia
Cappelletto, Chiara
Rossi, Maddalena
Beltrami, Antonio Paolo
Sinagra, Gianfranco
author_sort Aleksova, Aneta
collection PubMed
description Survivors after a myocardial infarction (MI), especially those with diabetes mellitus (DM), remain at high risk of further events. Identifying and treating factors that may influence survival may open new therapeutic strategies. We assessed the impact on prognosis of DM and hypovitaminosis D (hypovitD), alone or combined. In this prospective, observational study, 1081 patients were enrolled surviving an MI and divided into four groups according to their diabetic and VitD status. The primary end-point was composite of all-cause mortality, angina/MI and heart failure (HF). Secondary outcomes were mortality, HF and angina/MI. During a follow-up of 26.1 months (IQR 6.6–64.5), 391 subjects experienced the primary end-point. Patients with DM or hypovitD had similar rate of the composite end-point. Patients with only hypovitD or DM did not differ regarding components of composite end-point (angina p = 0.97, HF p = 0.29, mortality p = 0.62). DM and VitD deficiency had similarly adjusted risks for primary end-point (HR 1.3, 95%CI 1.05–1.61; HR 1.3, 95% CI 1.04–1.64). The adjusted HR for primary composite end-point for patients with hypovitD and DM was 1.69 (95%CI 1.25–2.29, p = 0.001) in comparison to patients with neither hypoD nor DM. In conclusion, DM and hypovitD, individually and synergistically, are associated with a worse outcome after MI.
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spelling pubmed-74088582020-08-13 Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction Aleksova, Aneta Ferro, Federico Gagno, Giulia Padoan, Laura Saro, Riccardo Santon, Daniela Stenner, Elisabetta Barbati, Giulia Cappelletto, Chiara Rossi, Maddalena Beltrami, Antonio Paolo Sinagra, Gianfranco J Clin Med Article Survivors after a myocardial infarction (MI), especially those with diabetes mellitus (DM), remain at high risk of further events. Identifying and treating factors that may influence survival may open new therapeutic strategies. We assessed the impact on prognosis of DM and hypovitaminosis D (hypovitD), alone or combined. In this prospective, observational study, 1081 patients were enrolled surviving an MI and divided into four groups according to their diabetic and VitD status. The primary end-point was composite of all-cause mortality, angina/MI and heart failure (HF). Secondary outcomes were mortality, HF and angina/MI. During a follow-up of 26.1 months (IQR 6.6–64.5), 391 subjects experienced the primary end-point. Patients with DM or hypovitD had similar rate of the composite end-point. Patients with only hypovitD or DM did not differ regarding components of composite end-point (angina p = 0.97, HF p = 0.29, mortality p = 0.62). DM and VitD deficiency had similarly adjusted risks for primary end-point (HR 1.3, 95%CI 1.05–1.61; HR 1.3, 95% CI 1.04–1.64). The adjusted HR for primary composite end-point for patients with hypovitD and DM was 1.69 (95%CI 1.25–2.29, p = 0.001) in comparison to patients with neither hypoD nor DM. In conclusion, DM and hypovitD, individually and synergistically, are associated with a worse outcome after MI. MDPI 2020-07-06 /pmc/articles/PMC7408858/ /pubmed/32640692 http://dx.doi.org/10.3390/jcm9072127 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
Aleksova, Aneta
Ferro, Federico
Gagno, Giulia
Padoan, Laura
Saro, Riccardo
Santon, Daniela
Stenner, Elisabetta
Barbati, Giulia
Cappelletto, Chiara
Rossi, Maddalena
Beltrami, Antonio Paolo
Sinagra, Gianfranco
Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction
title Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction
title_full Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction
title_fullStr Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction
title_full_unstemmed Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction
title_short Diabetes Mellitus and Vitamin D Deficiency: Comparable Effect on Survival and a Deadly Association after a Myocardial Infarction
title_sort diabetes mellitus and vitamin d deficiency: comparable effect on survival and a deadly association after a myocardial infarction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408858/
https://www.ncbi.nlm.nih.gov/pubmed/32640692
http://dx.doi.org/10.3390/jcm9072127
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