Extent of arterial calcification by conventional vitamin K antagonist treatment

PLoS One. 2020 Oct 29;15(10):e0241450. doi: 10.1371/journal.pone.0241450. eCollection 2020.

Abstract

Background and aims: Vitamin K antagonists (VKA) remain the most frequently prescribed oral anticoagulants worldwide despite the introduction of non-vitamin K antagonist oral anticoagulants (NOAC). VKA interfere with the regeneration of Vitamin K1 and K2, essential to the activation of coagulation factors and activation of matrix-Gla protein, a strong inhibitor of arterial calcifications. This study aimed to clarify whether VKA treatment was associated with the extent of coronary artery calcification (CAC) in a population with no prior cardiovascular disease (CVD).

Methods: We collected data on cardiovascular risk factors and CAC scores from cardiac CT scans performed as part of clinical examinations (n = 9,672) or research studies (n = 14,166) in the period 2007-2017. Data on use of anticoagulation were obtained from the Danish National Health Service Prescription Database. The association between duration of anticoagulation and categorized CAC score (0, 1-99, 100-399, ≥400) was investigated by ordered logistic regression adjusting for covariates.

Results: The final study population consisted of 17,254 participants with no prior CVD, of whom 1,748 and 1,144 had been treated with VKA or NOAC, respectively. A longer duration of VKA treatment was associated with higher CAC categories. For each year of VKA treatment, the odds of being in a higher CAC category increased (odds ratio (OR) = 1.032, 95%CI 1.009-1.057). In contrast, NOAC treatment duration was not associated with CAC category (OR = 1.002, 95%CI 0.935-1.074). There was no significant interaction between VKA treatment duration and age on CAC category.

Conclusions: Adjusted for cardiovascular risk factors, VKA treatment-contrary to NOAC-was associated to higher CAC category.

Publication types

  • Multicenter Study
  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anticoagulants / therapeutic use*
  • Calcinosis / drug therapy*
  • Coronary Artery Disease / drug therapy*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Risk Factors
  • Vitamin K / antagonists & inhibitors*

Substances

  • Anticoagulants
  • Vitamin K

Grants and funding

This work was supported by Novo Nordisk Foundation (NNF17OC0029268) (https://novonordiskfonden.dk/en/) and Independent Research Fund Denmark (7090-00014B) (https://dff.dk/en/front-page?set_language=en). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.