Abstract

AimsTo determine whether fibrin clot properties are associated with clinical outcomes following acute coronary syndrome (ACS).Methods and resultsPlasma samples were collected at hospital discharge from 4354 ACS patients randomized to clopidogrel or ticagrelor in the PLATelet inhibition and patient Outcomes (PLATO) trial. A validated turbidimetric assay was employed to study plasma clot lysis time and maximum turbidity (a measure of clot density). One-year rates of cardiovascular (CV) death, spontaneous myocardial infarction (MI) and PLATO-defined major bleeding events were assessed after sample collection. Hazard ratios (HRs) were estimated using Cox proportional hazards models. After adjusting for CV risk factors, each 50% increase in lysis time was associated with CV death/spontaneous MI [HR 1.17, 95% confidence interval (CI) 1.05–1.31; P < 0.01] and CV death alone (HR 1.36, 95% CI 1.17–1.59; P < 0.001). Similarly, each 50% increase in maximum turbidity was associated with increased risk of CV death (HR 1.24, 95% CI 1.03–1.50; P = 0.024). After adjustment for other prognostic biomarkers (leukocyte count, high-sensitivity C-reactive protein, high-sensitivity troponin T, cystatin C, N-terminal pro B-type natriuretic peptide, and growth differentiation factor-15), the association with CV death remained significant for lysis time (HR 1.2, 95% CI 1.01–1.42; P = 0.042) but not for maximum turbidity. These associations were consistent regardless of randomized antiplatelet treatment (all interaction P > 0.05). Neither lysis time nor maximum turbidity was associated with major bleeding events. ConclusionFibrin clots that are resistant to lysis independently predict adverse outcome in ACS patients. Novel therapies targeting fibrin clot properties might be a new avenue for improving prognosis in patients with ACS.

Highlights

  • Adverse events, including cardiovascular (CV) death, remain common following acute coronary syndrome (ACS)

  • After adjusting for CV risk factors, each 50% increase in lysis time was associated with CV death/spontaneous myocardial infarction (MI) [Hazard ratios (HRs) 1.17, 95% confidence interval (CI) 1.05–1.31; P < 0.01] and CV death alone (HR 1.36, 95% CI 1.17–1.59; P < 0.001)

  • The prevalence of diabetes mellitus (DM), hypertension, chronic kidney disease (CKD), and female sex significantly increased with increasing lysis time quartile group

Read more

Summary

Introduction

Adverse events, including cardiovascular (CV) death, remain common following acute coronary syndrome (ACS). Intensive antithrombotic therapies, including potent P2Y12 inhibitors and the addition of low-dose anticoagulant therapy (rivaroxaban), have all resulted in improved outcomes but increased the risk of major bleeding events.[1,2,3]. There is marked overlap between risk factors for ischaemic and bleeding events.[4,5] tailoring therapy to achieve the VC The Author(s) 2018.

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call