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Published on: July 20, 2022
Digoxin and Platelet Activation in Patients With Atrial Fibrillation: In Vivo and In Vitro Study
Daniele Pastori1, Roberto Carnevale2, Cristina Nocella3
11 I Clinica Medica Department of Internal Medicine and Medical Specialties Sapienza University of Rome Italy.
Insights
Digoxin use in atrial fibrillation (AF) patients correlates with increased platelet activation, a marker of cardiovascular risk. This study suggests digoxin may promote platelet aggregation, particularly at higher concentrations, impacting cardiovascular events.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Background:
- Digoxin use is linked to increased cardiovascular events in atrial fibrillation (AF).
- The mechanism may involve digoxin's effect on platelet activation.
- Platelet activation is a key factor in cardiovascular risk.
Purpose of the Study:
- To investigate the association between serum digoxin concentration (SDC) and platelet activation in AF patients.
- To explore the in vitro effects of digoxin on platelet function.
Main Methods:
- Post hoc analysis of anticoagulated AF patients (n=520) comparing digoxin users and non-users.
- Measurement of urinary 11-dehydro-thromboxane B2 (TxB2) as a marker of platelet activation.
- In vitro experiments assessing platelet activation markers and aggregation in response to digoxin in healthy subjects and AF patients.
Main Results:
- A significant positive correlation was found between SDC and urinary 11-dehydro-TxB2 (rs=0.350, P<0.001).
- AF patients with higher SDC exhibited increased platelet activation.
- In vitro, digoxin induced platelet activation and aggregation in AF patients, but not in healthy subjects, especially after collagen pre-stimulation.
Conclusions:
- Serum digoxin concentration is significantly correlated with in vivo platelet activation.
- Supratherapeutic SDC can enhance platelet aggregation via calcium-related pathways.
- These findings suggest a potential mechanism linking digoxin use to cardiovascular risk in AF patients.
Abstract:
Background Digoxin use was shown to be associated with an increased risk of cardiovascular events in atrial fibrillation ( AF ). We hypothesized that digoxin may affect cardiovascular risk by increasing platelet activation. Methods and Results Post hoc analysis of a prospective study of anticoagulated patients with AF . Patients were divided into 2 groups balanced for age, sex, and cardiovascular risk factors: digoxin users (n=132) and nonusers (n=388). Urinary excretion of 11-dehydro-thromboxane B2 (TxB2), a marker of platelet activation, and serum digoxin concentration ( SDC ) were measured. In vitro experiments were performed on platelets from healthy subjects and AF patients, which were incubated with scalar doses of digoxin (0.6-2.4 ng/mL) with or without prestimulation with a sub-threshold of collagen. Median 11-dehydro-TxB2 was 105.0 ( interquartile range, 60.0-190.0) ng/mg creatinine, and median SDC was 0.65 ( interquartile range, 0.40-1.00) ng/mL. Urinary 11-dehydro-TxB2 and SDC were correlated ( rs=0.350, P<0.001). Patients in the upper tertile of SDC showed higher 11-dehydro-TxB2 compared with non-digoxin users ( P=0.019). In vitro study showed an increased basal platelet activation in patients with AF compared with healthy subjects . Digoxin (2.4 ng/mL) induced calcium mobilization, PAC -1 (procaspase-activating compound 1) and platelet aggregation in AF patients but not in healthy subjects . After pretreatment with a sub-threshold of collagen, digoxin dose-dependent induced calcium mobilization, arachidonic acid release, TxB2 biosynthesis, PAC -1 and soluble platelet selectin expression, and platelet aggregation, which were inhibited by antibody against digoxin. Conclusions We found a significant in vivo correlation between SDC and platelet activation. Supratherapeutic SDC increased in vitro platelet aggregation via calcium-related phospholipase A2 phosphorylation. Our findings may have clinical implications for AF patients treated with digoxin.
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