Cargando…

Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation

Aging is strictly associated with an increased incidence of cardiovascular events (CVEs) in the general population. Mechanisms underlying the risk of CVEs are still unclear. Platelet activation contributes to the onset of cardiovascular complications. The incidence of atrial fibrillation (AF) increa...

Descripción completa

Detalles Bibliográficos
Autores principales: Pastori, Daniele, Pignatelli, Pasquale, Farcomeni, Alessio, Nocella, Cristina, Bartimoccia, Simona, Carnevale, Roberto, Violi, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129920/
https://www.ncbi.nlm.nih.gov/pubmed/27270651
http://dx.doi.org/10.18632/oncotarget.9826
_version_ 1782470644609318912
author Pastori, Daniele
Pignatelli, Pasquale
Farcomeni, Alessio
Nocella, Cristina
Bartimoccia, Simona
Carnevale, Roberto
Violi, Francesco
author_facet Pastori, Daniele
Pignatelli, Pasquale
Farcomeni, Alessio
Nocella, Cristina
Bartimoccia, Simona
Carnevale, Roberto
Violi, Francesco
author_sort Pastori, Daniele
collection PubMed
description Aging is strictly associated with an increased incidence of cardiovascular events (CVEs) in the general population. Mechanisms underlying the risk of CVEs are still unclear. Platelet activation contributes to the onset of cardiovascular complications. The incidence of atrial fibrillation (AF) increases with age, and the natural history of AF is often complicated by CVEs. We prospectively investigated the relationship between age, urinary thromboxane (Tx) B(2), which reflects platelet activation, and CVEs in 833 AF patients. Median TxB(2) level was 120 [66-200] ng/mg of urinary creatinine. At multivariable linear regression analysis, age (B: 0.097, p=0.005) and previous MI/CHD (B: 0.069, p=0.047) were associated with log-TxB(2) levels. When we divided our population into age classes (i.e. < 60, 60-69, 70-79, ≥ 80 years), we found a significant difference in TxB(2) levels across classes (p=0.005), with a significant elevation at 74.6 years. During a mean follow-up of 40.9 months, 128 CVEs occurred; the rate of CVEs significantly increased with age classes (Log-rank test, p < 0.001). TxB(2) levels were higher in patients with, compared to those without, CVEs in patients aged 70-79 (p < 0.001) and ≥ 80 (p = 0.020) years. In conclusion, TxB(2) levels enhance by increasing age, suggesting that platelet activation contributes to CVEs in elderly patients with AF.
format Online
Article
Text
id pubmed-5129920
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-51299202016-12-11 Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation Pastori, Daniele Pignatelli, Pasquale Farcomeni, Alessio Nocella, Cristina Bartimoccia, Simona Carnevale, Roberto Violi, Francesco Oncotarget Research Paper: Gerotarget (Focus on Aging) Aging is strictly associated with an increased incidence of cardiovascular events (CVEs) in the general population. Mechanisms underlying the risk of CVEs are still unclear. Platelet activation contributes to the onset of cardiovascular complications. The incidence of atrial fibrillation (AF) increases with age, and the natural history of AF is often complicated by CVEs. We prospectively investigated the relationship between age, urinary thromboxane (Tx) B(2), which reflects platelet activation, and CVEs in 833 AF patients. Median TxB(2) level was 120 [66-200] ng/mg of urinary creatinine. At multivariable linear regression analysis, age (B: 0.097, p=0.005) and previous MI/CHD (B: 0.069, p=0.047) were associated with log-TxB(2) levels. When we divided our population into age classes (i.e. < 60, 60-69, 70-79, ≥ 80 years), we found a significant difference in TxB(2) levels across classes (p=0.005), with a significant elevation at 74.6 years. During a mean follow-up of 40.9 months, 128 CVEs occurred; the rate of CVEs significantly increased with age classes (Log-rank test, p < 0.001). TxB(2) levels were higher in patients with, compared to those without, CVEs in patients aged 70-79 (p < 0.001) and ≥ 80 (p = 0.020) years. In conclusion, TxB(2) levels enhance by increasing age, suggesting that platelet activation contributes to CVEs in elderly patients with AF. Impact Journals LLC 2016-06-05 /pmc/articles/PMC5129920/ /pubmed/27270651 http://dx.doi.org/10.18632/oncotarget.9826 Text en Copyright: © 2016 Pastori et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper: Gerotarget (Focus on Aging)
Pastori, Daniele
Pignatelli, Pasquale
Farcomeni, Alessio
Nocella, Cristina
Bartimoccia, Simona
Carnevale, Roberto
Violi, Francesco
Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation
title Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation
title_full Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation
title_fullStr Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation
title_full_unstemmed Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation
title_short Age-related increase of thromboxane B(2) and risk of cardiovascular disease in atrial fibrillation
title_sort age-related increase of thromboxane b(2) and risk of cardiovascular disease in atrial fibrillation
topic Research Paper: Gerotarget (Focus on Aging)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129920/
https://www.ncbi.nlm.nih.gov/pubmed/27270651
http://dx.doi.org/10.18632/oncotarget.9826
work_keys_str_mv AT pastoridaniele agerelatedincreaseofthromboxaneb2andriskofcardiovasculardiseaseinatrialfibrillation
AT pignatellipasquale agerelatedincreaseofthromboxaneb2andriskofcardiovasculardiseaseinatrialfibrillation
AT farcomenialessio agerelatedincreaseofthromboxaneb2andriskofcardiovasculardiseaseinatrialfibrillation
AT nocellacristina agerelatedincreaseofthromboxaneb2andriskofcardiovasculardiseaseinatrialfibrillation
AT bartimocciasimona agerelatedincreaseofthromboxaneb2andriskofcardiovasculardiseaseinatrialfibrillation
AT carnevaleroberto agerelatedincreaseofthromboxaneb2andriskofcardiovasculardiseaseinatrialfibrillation
AT violifrancesco agerelatedincreaseofthromboxaneb2andriskofcardiovasculardiseaseinatrialfibrillation