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.

Related Concept Videos

Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
11.9K
Amyloid Fibrils03:03

Amyloid Fibrils

6.4K
Fibril-associated Collagen01:11

Fibril-associated Collagen

Fibril-associated collagens are a type of collagens present in the extracellular matrix with interrupted triple helices or FACIT (Fibril-associated collagens interrupted triple-helices). FACIT help connect and attach the collagen fibrils with each other as well as with other proteins of the extracellular matrix.
For example, the type II collagen fibrils in cartilage have covalently bound type IX fibril-associated collagens at regular intervals. Other types of fibril-associated collagens are...
3.4K
Equivalence: In Vitro and In Vivo Bioequivalence01:17

Equivalence: In Vitro and In Vivo Bioequivalence

Body:Bioequivalence studies are crucial in evaluating whether new drugs can match an approved one regarding pharmacological effects and clinical performance. These studies test if drugs, despite different dosage forms, share identical plasma concentration-time profiles. Three types of equivalence are central to these studies: chemical, pharmaceutical, and therapeutic. Chemical equivalence indicates that two or more drug products contain identical active ingredients in equal amounts.
224
Bioavailability Study Design: Healthy Subjects Versus Patients01:15

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...
156
Structure and Function of Platelets01:18

Structure and Function of Platelets

The cell fragments known as platelets are disc-shaped, with an average diameter of about 3 μm and a thickness of roughly 1 μm. They play a crucial role in the body's vascular clotting system, which also involves plasma proteins, blood cells, and blood vessel tissues.
Platelets are continually replenished, circulating in the bloodstream for 9-12 days before being removed by phagocytes, primarily in the spleen. A microliter of circulating blood contains between 150,000 and 450,000...
3.5K