Key result
t-PA and PAI-1 levels exhibit significant diurnal oscillations in acute MI, peaking midmorning.
Why the study?
Information was limited regarding diurnal changes in fibrinolysis parameters after acute myocardial infarction and their relationship with on-treatment platelet reactivity.
Cohort (n=30)
No
Fibrinolytic parameters exhibit diurnal variations in AMI patients on DAPT, with elevated evening PAI-1 in clopidogrel-resistant patients potentially increasing thrombosis risk.
Diurnal fibrinolytic oscillations may inform timed sampling post-AMI; leaves open whether they guide chronotherapy or alter outcomes in trials.
There is limited information about diurnal changes in fibrinolysis parameters after acute myocardial infarction (AMI) and their relationship with on-treatment platelet reactivity. The aim of this study was to assess tissue plasminogen activator (t-PA), plasminogen activator inhibitor type-1 (PAI-1), α2-antiplasmin (α2-AP) activity, and plasmin-antiplasmin (PAP) complexes in 30 AMI patients taking dual antiplatelet therapy (DAPT), i.e., acetylsalicylic acid and clopidogrel. Fibrinolytic parameters were assessed at four time points (6 a.m., 10 a.m., 2 p.m., and 7 p.m.) on the third day after AMI using immunoenzymatic methods. Moreover, platelet reactivity was measured using multiple-electrode aggregometry, to assess potential differences in fibrinolytic parameters in low/high on-aspirin platelet reactivity and low/high on-clopidogrel platelet reactivity subgroups of patients. We detected significant diurnal oscillations in t-PA and PAI-1 levels in the whole study group. However, PAP complexes and α2-AP activity were similar at the analyzed time points. Our study reveals a potential impact of DAPT on the time course of fibrinolytic parameters, especially regarding clopidogrel. We suggest the presence of diurnal variations in t-PA and PAI-1 concentrations in AMI patients, with the highest levels midmorning, regardless of platelet reactivity. Significantly elevated levels of PAI-1 during the evening hours in clopidogrel-resistant patients may increase the risk of thrombosis.
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Boińska et al. (2022) conducted a cohort in Acute Myocardial Infarction (n=30). Time of day (diurnal oscillations) vs. Evening (7 p.m.) was evaluated on Tissue plasminogen activator (t-PA) concentrations at 6 a.m. vs 7 p.m.. In patients with acute myocardial infarction, t-PA and PAI-1 concentrations exhibited significant diurnal oscillations with the highest levels occurring in the midmorning (6 a.m. and 10 a.m.).
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