Abstract

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) B2, which reflects platelet activation, and CVEs in 833 AF patients. Median TxB2 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-TxB2 levels. When we divided our population into age classes (i.e. < 60, 60-69, 70-79, ≥ 80 years), we found a significant difference in TxB2 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). TxB2 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, TxB2 levels enhance by increasing age, suggesting that platelet activation contributes to CVEs in elderly patients with AF.

Highlights

  • Cardiovascular events (CVEs) represent the main cause of morbidity and mortality in the elderly population [1]

  • In this study we analyzed the relationship between platelet activation and aging by classifying Atrial fibrillation (AF) patients according to decades of age and analyzing the association between platelet activation and CVEs

  • The novel finding of the present study is that TxB2 biosynthesis is closely related with aging, with a progressive increase across the decades and a significant elevation at age > 74 years

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Summary

Introduction

Cardiovascular events (CVEs) represent the main cause of morbidity and mortality in the elderly population [1]. To explore www.impactjournals.com/oncotarget this hypothesis we measured the urinary excretion of TxB2 which is a reliable marker of in vivo platelet activation and is independently associated with CVEs in AF.

Results
Conclusion

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