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Updated: Aug 20, 2026

Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Regional left atrial coagulation and fibrinolytic activities in patients with mitral stenosis
Ayca Boyaci1, Serkan Topaloglu, Sevinc Yilmaz
1Departments of Cardiology, Turkiye Yuksek Ihtisas Hospital, Ankara, Turkey.
Abstract:
Systemic thromboembolism is a major complication of mitral stenosis (MS), especially in those patients having atrial fibrillation (AF). Recent evidence has suggested that regional left atrial coagulation activity may be increased in MS and may contribute to the pathophysiology of left atrial thrombus. However, the relation of left atrial coagulation activity to factors that predispose to left atrial thrombus formation is unknown. Also, the relations between left atrial and systemic coagulation activity, fibrinolysis, and platelet activation remain unresolved. Left atrial and peripheral venous levels of fibrinogen, antithrombin III, factor VII and factor VIII for coagulation, D-dimer, tPA and PAI-I, plasmin and antiplasmin for fibrinolysis, and platelet factor 4 and vWF for platelet activation, and endothelial dysfunction were measured in 46 patients with MS and normal clotting times who were undergoing percutaneous mitral valvuloplasty. Left atrial tPA, plasmin, PAI-I, antiplasmin, PF4, and vWF levels exceeded the corresponding peripheral venous levels (P < 0.05) in patients with MS, being more significant in the AF subgroup. There were no significant differences between left atrial and peripheral venous levels of fibrinogen, D-dimer, factor VII, and factor VIII within the patient group (P > 0.05). The results suggest that there are significant variations in the indices of coagulation, fibrinolytic system and platelet activation, and endothelial dysfunction between left atrial and peripheral venous blood samples of patients with MS that may be due to limited spillover from the left atrium to the systemic circulation.
Insights
In mitral stenosis (MS) patients, left atrial coagulation and fibrinolysis differ significantly from systemic circulation, particularly in those with atrial fibrillation (AF). These localized changes may explain thrombus formation risks.
Area of Science:
- Cardiology
- Hematology
- Thrombosis Research
Background:
- Systemic thromboembolism is a serious complication of mitral stenosis (MS), particularly in patients with atrial fibrillation (AF).
- Increased left atrial coagulation activity is suspected in MS, potentially contributing to thrombus formation.
- The relationship between left atrial coagulation, fibrinolysis, platelet activation, and systemic markers in MS remains unclear.
Purpose of the Study:
- To investigate the differences in left atrial versus systemic coagulation, fibrinolysis, and platelet activation markers in patients with MS.
- To explore the association of these markers with thrombus formation risk factors.
Main Methods:
- Measurement of coagulation (fibrinogen, factors VII, VIII), fibrinolysis (D-dimer, tPA, PAI-I, plasmin, antiplasmin), platelet activation (PF4, vWF), and endothelial dysfunction markers.
- Comparison of left atrial and peripheral venous blood levels in 46 MS patients undergoing percutaneous mitral valvuloplasty.
- Subgroup analysis for patients with atrial fibrillation (AF).
Main Results:
- Left atrial levels of tPA, plasmin, PAI-I, antiplasmin, PF4, and vWF were significantly higher than peripheral venous levels (P < 0.05).
- These differences were more pronounced in the AF subgroup.
- No significant differences were observed in fibrinogen, D-dimer, factor VII, or factor VIII levels between left atrial and peripheral venous blood.
Conclusions:
- Significant regional variations exist in coagulation, fibrinolysis, and platelet activation markers within the left atrium compared to systemic circulation in MS patients.
- These localized prothrombotic changes in the left atrium may be due to limited systemic spillover.
- Findings highlight potential mechanisms for thrombus formation in MS, especially in AF patients.
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