Effect of hyperthyroidism on the hypercoagulable state and thromboembolic events in patients with atrial fibrillation

Cardiology. 2014;127(3):176-82. doi: 10.1159/000356954. Epub 2014 Jan 14.

Abstract

Objective: To clarify whether hyperthyroidism (HT) itself confers an additional effect on the hypercoagulable state and the risk of ischemic stroke among patients with hyperthyroid atrial fibrillation (AF).

Methods: We prospectively evaluated plasma D-dimer levels and thromboembolic events among three groups of patients (hyperthyroid AF, n = 62; nonthyroid AF, n = 107, and HT without AF, n = 100). Plasma D-dimer levels were used to evaluate the hypercoagulable state.

Results: The D-dimer level was significantly higher in patients with hyperthyroid AF than in nonthyroid AF (0.66 ± 0.06 vs. 0.34 ± 0.02 mg/l, p < 0.001) and HT without AF (0.66 ± 0.06 vs. 0.27 ± 0.02 mg/l, p < 0.001). During a 3-year follow-up, patients with hyperthyroid AF had a significantly higher incidence of ischemic stroke compared with patients with nonthyroid AF (hazard ratio, HR: 3.2, 95% confidence interval, CI: 1.01-5.59, p = 0.04). Cox regression analysis revealed that age (HR: 2.5, 95% CI: 1.01-1.21, p = 0.05), CHADS2-VAS score (HR: 5.5, 95% CI: 1.51-7.43, p = 0.01) and anticoagulation (HR: 0.45, 95% CI: 0.07-0.54, p = 0.01) were independent predictors of risk for the occurrence of ischemic stroke.

Conclusions: The present study suggests that HT may enhance the hypercoagulable state and the risk of ischemic stroke in patients with AF.

MeSH terms

  • Anticoagulants / therapeutic use
  • Atrial Fibrillation / blood
  • Atrial Fibrillation / complications*
  • Female
  • Fibrin Fibrinogen Degradation Products / metabolism
  • Fibrinolysis / physiology
  • Humans
  • Hyperthyroidism / blood
  • Hyperthyroidism / complications*
  • Male
  • Middle Aged
  • Prospective Studies
  • Stroke / blood
  • Stroke / etiology
  • Stroke / prevention & control
  • Thromboembolism / blood
  • Thromboembolism / etiology*
  • Thromboembolism / prevention & control
  • Thrombophilia / blood
  • Thrombophilia / etiology*
  • Thrombophilia / prevention & control

Substances

  • Anticoagulants
  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D