AI Article Synopsis

  • The study investigates the role of Fibrinopeptide A (FPA) in patients with Acute Coronary Syndrome (ACS), which is linked to high mortality rates and caused by atherosclerosis and blood clot formation.
  • The research involved comparing serum FPA levels in 107 ACS patients and 69 patients with chronic coronary syndrome, revealing that ACS patients were older, more likely to be male, and had higher rates of hypertension and smoking.
  • Findings show that elevated serum FPA levels, particularly above 3.38 ng/mL, can effectively indicate ACS and suggest the need for more aggressive antithrombotic treatment options.

Article Abstract

Objective: Acute coronary syndrome (ACS) is one of the leading causes of mortality, globally. Atherosclerosis is an underlying factor in ACS process and coagulative cascade is activated secondary to atherosclerotic plaque rupture. Fibrinopeptide A (FPA) takes an active role in thrombus formation and is an indicator of coagulative process. We aimed to evaluate serum FPA level in patients with ACS.

Methods: Patients diagnosed with ACS and chronic coronary syndrome (CCS), with non-obstructive coronary artery disease as a control group, were included in the study. Blood samples and demographic data of all patients were obtained at admission. Obtained data were compared between ACS and control groups.

Results: The study consisted of 107 patients with ACS and 69 patients with CCS. ACS group was older (p<0.001) with male preponderance (p<0.001), more likely to had hypertension (p<0.001), and had a higher smoking rate (p<0.001). Serum FPA level was highest in the ST elevated myocardial infarction group (p<0.001). FPA>3.38 ng/mL predicted ACS with 89.7% sensitivity and 78% specificity (AUC: 0.825, 95% CI 0.745-0.905; p<0.001).

Conclusion: Serum FPA may be used for the differential diagnosis of ACS. In addition, patients with increased FPA may be considered to be given more aggressive antithrombotic medication.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996658PMC
http://dx.doi.org/10.14744/nci.2021.12499DOI Listing

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