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The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk

INTRODUCTION: Serum uric acid (SUA) has been depicted as a contributory causal factor in metabolic syndrome (MS), which in turn, portends unfavourable prognosis. AIM: We assessed the prognostic role of SUA in patients with and without MS. METHODS: We used data from the multicentre Uric Acid Right fo...

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Autores principales: Pugliese, Nicola Riccardo, Mengozzi, Alessandro, Virdis, Agostino, Casiglia, Edoardo, Tikhonoff, Valerie, Cicero, Arrigo F. G., Ungar, Andrea, Rivasi, Giulia, Salvetti, Massimo, Barbagallo, Carlo M., Bombelli, Michele, Dell’Oro, Raffaella, Bruno, Berardino, Lippa, Luciano, D’Elia, Lanfranco, Verdecchia, Paolo, Mallamaci, Francesca, Cirillo, Massimo, Rattazzi, Marcello, Cirillo, Pietro, Gesualdo, Loreto, Mazza, Alberto, Giannattasio, Cristina, Maloberti, Alessandro, Volpe, Massimo, Tocci, Giuliano, Georgiopoulos, Georgios, Iaccarino, Guido, Nazzaro, Pietro, Parati, Gianfranco, Palatini, Paolo, Galletti, Ferruccio, Ferri, Claudio, Desideri, Giovambattista, Viazzi, Francesca, Pontremoli, Roberto, Muiesan, Maria Lorenza, Grassi, Guido, Masi, Stefano, Borghi, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238697/
https://www.ncbi.nlm.nih.gov/pubmed/33604722
http://dx.doi.org/10.1007/s00392-021-01815-0
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author Pugliese, Nicola Riccardo
Mengozzi, Alessandro
Virdis, Agostino
Casiglia, Edoardo
Tikhonoff, Valerie
Cicero, Arrigo F. G.
Ungar, Andrea
Rivasi, Giulia
Salvetti, Massimo
Barbagallo, Carlo M.
Bombelli, Michele
Dell’Oro, Raffaella
Bruno, Berardino
Lippa, Luciano
D’Elia, Lanfranco
Verdecchia, Paolo
Mallamaci, Francesca
Cirillo, Massimo
Rattazzi, Marcello
Cirillo, Pietro
Gesualdo, Loreto
Mazza, Alberto
Giannattasio, Cristina
Maloberti, Alessandro
Volpe, Massimo
Tocci, Giuliano
Georgiopoulos, Georgios
Iaccarino, Guido
Nazzaro, Pietro
Parati, Gianfranco
Palatini, Paolo
Galletti, Ferruccio
Ferri, Claudio
Desideri, Giovambattista
Viazzi, Francesca
Pontremoli, Roberto
Muiesan, Maria Lorenza
Grassi, Guido
Masi, Stefano
Borghi, Claudio
author_facet Pugliese, Nicola Riccardo
Mengozzi, Alessandro
Virdis, Agostino
Casiglia, Edoardo
Tikhonoff, Valerie
Cicero, Arrigo F. G.
Ungar, Andrea
Rivasi, Giulia
Salvetti, Massimo
Barbagallo, Carlo M.
Bombelli, Michele
Dell’Oro, Raffaella
Bruno, Berardino
Lippa, Luciano
D’Elia, Lanfranco
Verdecchia, Paolo
Mallamaci, Francesca
Cirillo, Massimo
Rattazzi, Marcello
Cirillo, Pietro
Gesualdo, Loreto
Mazza, Alberto
Giannattasio, Cristina
Maloberti, Alessandro
Volpe, Massimo
Tocci, Giuliano
Georgiopoulos, Georgios
Iaccarino, Guido
Nazzaro, Pietro
Parati, Gianfranco
Palatini, Paolo
Galletti, Ferruccio
Ferri, Claudio
Desideri, Giovambattista
Viazzi, Francesca
Pontremoli, Roberto
Muiesan, Maria Lorenza
Grassi, Guido
Masi, Stefano
Borghi, Claudio
author_sort Pugliese, Nicola Riccardo
collection PubMed
description INTRODUCTION: Serum uric acid (SUA) has been depicted as a contributory causal factor in metabolic syndrome (MS), which in turn, portends unfavourable prognosis. AIM: We assessed the prognostic role of SUA in patients with and without MS. METHODS: We used data from the multicentre Uric Acid Right for Heart Health study and considered cardiovascular mortality (CVM) as death due to fatal myocardial infarction, stroke, sudden cardiac death, or heart failure. RESULTS: A total of 9589 subjects (median age 58.5 years, 45% males) were included in the analysis, and 5100 (53%) patients had a final diagnosis of MS. After a median follow-up of 142 months, we observed 558 events. Using a previously validated cardiovascular SUA cut-off to predict CVM (> 5.1 mg/dL in women and 5.6 mg/dL in men), elevated SUA levels were significantly associated to a worse outcome in patients with and without MS (all p < 0.0001) and provided a significant net reclassification improvement of 7.1% over the diagnosis of MS for CVM (p = 0.004). Cox regression analyses identified an independent association between SUA and CVM (Hazard Ratio: 1.79 [95% CI, 1.15–2.79]; p < 0.0001) after the adjustment for MS, its single components and renal function. Three specific combinations of the MS components were associated with higher CVM when increasing SUA levels were reported, and systemic hypertension was the only individual component ever-present (all p < 0.0001). CONCLUSION: Increasing SUA levels are associated with a higher CVM risk irrespective of the presence of MS: a cardiovascular SUA threshold may improve risk stratification. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00392-021-01815-0.
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spelling pubmed-82386972021-07-09 The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk Pugliese, Nicola Riccardo Mengozzi, Alessandro Virdis, Agostino Casiglia, Edoardo Tikhonoff, Valerie Cicero, Arrigo F. G. Ungar, Andrea Rivasi, Giulia Salvetti, Massimo Barbagallo, Carlo M. Bombelli, Michele Dell’Oro, Raffaella Bruno, Berardino Lippa, Luciano D’Elia, Lanfranco Verdecchia, Paolo Mallamaci, Francesca Cirillo, Massimo Rattazzi, Marcello Cirillo, Pietro Gesualdo, Loreto Mazza, Alberto Giannattasio, Cristina Maloberti, Alessandro Volpe, Massimo Tocci, Giuliano Georgiopoulos, Georgios Iaccarino, Guido Nazzaro, Pietro Parati, Gianfranco Palatini, Paolo Galletti, Ferruccio Ferri, Claudio Desideri, Giovambattista Viazzi, Francesca Pontremoli, Roberto Muiesan, Maria Lorenza Grassi, Guido Masi, Stefano Borghi, Claudio Clin Res Cardiol Original Paper INTRODUCTION: Serum uric acid (SUA) has been depicted as a contributory causal factor in metabolic syndrome (MS), which in turn, portends unfavourable prognosis. AIM: We assessed the prognostic role of SUA in patients with and without MS. METHODS: We used data from the multicentre Uric Acid Right for Heart Health study and considered cardiovascular mortality (CVM) as death due to fatal myocardial infarction, stroke, sudden cardiac death, or heart failure. RESULTS: A total of 9589 subjects (median age 58.5 years, 45% males) were included in the analysis, and 5100 (53%) patients had a final diagnosis of MS. After a median follow-up of 142 months, we observed 558 events. Using a previously validated cardiovascular SUA cut-off to predict CVM (> 5.1 mg/dL in women and 5.6 mg/dL in men), elevated SUA levels were significantly associated to a worse outcome in patients with and without MS (all p < 0.0001) and provided a significant net reclassification improvement of 7.1% over the diagnosis of MS for CVM (p = 0.004). Cox regression analyses identified an independent association between SUA and CVM (Hazard Ratio: 1.79 [95% CI, 1.15–2.79]; p < 0.0001) after the adjustment for MS, its single components and renal function. Three specific combinations of the MS components were associated with higher CVM when increasing SUA levels were reported, and systemic hypertension was the only individual component ever-present (all p < 0.0001). CONCLUSION: Increasing SUA levels are associated with a higher CVM risk irrespective of the presence of MS: a cardiovascular SUA threshold may improve risk stratification. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00392-021-01815-0. Springer Berlin Heidelberg 2021-02-18 2021 /pmc/articles/PMC8238697/ /pubmed/33604722 http://dx.doi.org/10.1007/s00392-021-01815-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Pugliese, Nicola Riccardo
Mengozzi, Alessandro
Virdis, Agostino
Casiglia, Edoardo
Tikhonoff, Valerie
Cicero, Arrigo F. G.
Ungar, Andrea
Rivasi, Giulia
Salvetti, Massimo
Barbagallo, Carlo M.
Bombelli, Michele
Dell’Oro, Raffaella
Bruno, Berardino
Lippa, Luciano
D’Elia, Lanfranco
Verdecchia, Paolo
Mallamaci, Francesca
Cirillo, Massimo
Rattazzi, Marcello
Cirillo, Pietro
Gesualdo, Loreto
Mazza, Alberto
Giannattasio, Cristina
Maloberti, Alessandro
Volpe, Massimo
Tocci, Giuliano
Georgiopoulos, Georgios
Iaccarino, Guido
Nazzaro, Pietro
Parati, Gianfranco
Palatini, Paolo
Galletti, Ferruccio
Ferri, Claudio
Desideri, Giovambattista
Viazzi, Francesca
Pontremoli, Roberto
Muiesan, Maria Lorenza
Grassi, Guido
Masi, Stefano
Borghi, Claudio
The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk
title The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk
title_full The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk
title_fullStr The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk
title_full_unstemmed The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk
title_short The importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk
title_sort importance of including uric acid in the definition of metabolic syndrome when assessing the mortality risk
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238697/
https://www.ncbi.nlm.nih.gov/pubmed/33604722
http://dx.doi.org/10.1007/s00392-021-01815-0
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