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Calcification of Vascular Smooth Muscle Cells and Imaging of Aortic Calcification and Inflammation
Published on: May 31, 2016
Vitamin K antagonists and cardiovascular calcification: A systematic review and meta-analysis
Nina D Kosciuszek1,2, Daniel Kalta2, Mohnish Singh2
1New York Institute of Technology, College of Osteopathic Medicine, Academic Medicine Scholar Program, Old Westbury, NY, United States.
Insights
Vitamin K antagonists (VKA) may cause vascular and valvular calcification. This meta-analysis found VKA use linked to increased calcification in coronary arteries and the aorta, suggesting potential side effects needing further study.
Area of Science:
- Cardiology
- Pharmacology
- Medical Research
Background:
- Patients on Vitamin K antagonists (VKA) for anticoagulation often exhibit vascular or valvular calcification.
- This meta-analysis investigates the hypothesis that VKA treatment contributes to vascular and valvular calcification as a side effect.
Approach:
- A systematic literature search identified 35 studies (45,757 patients) comparing VKA users and non-users.
- Random-effects inverse variance models analyzed associations between VKA use and calcification, with meta-regression identifying effect moderators.
Key Points:
- VKA use was associated with increased coronary artery calcification (OR 1.21, p=0.001), moderated by treatment duration.
- Extra-coronary calcification (aorta, carotid, etc.) was significantly higher in VKA users (OR 1.86, p<0.00001).
- Aortic valve calcification was significantly increased (OR 3.07, p<0.00001), though publication bias was noted.
Conclusions:
- Vascular and valvular calcification appear to be potential side effects of Vitamin K antagonist therapy.
- Further research is warranted to understand the clinical implications of these VKA-associated calcifications on cardiovascular outcomes.
Background:
Many patients treated with Vitamin K antagonists (VKA) for anticoagulation have concomitant vascular or valvular calcification. This meta-analysis aimed to evaluate a hypothesis that vascular and valvular calcification is a side-effect of VKA treatment.
Methods:
We conducted a systematic literature search to identify studies that reported vascular or valvular calcification in patients treated with VKA. The associations between VKA use and calcification were analyzed with random-effects inverse variance models and reported as odds ratios (OR) and 95% confidence intervals (95% CI). In addition, univariate meta-regression analyses were utilized to identify any effect moderators.
Results:
Thirty-five studies were included (45,757 patients; 6,251 VKA users). The median follow-up was 2.3 years [interquartile range (IQR) of 1.2-4.0]; age 66.2 ± 3.6 years (mean ± SD); the majority of participants were males [77% (IQR: 72-95%)]. VKA use was associated with an increased OR for coronary artery calcification [1.21 (1.08, 1.36), p = 0.001], moderated by the duration of treatment [meta-regression coefficient B of 0.08 (0.03, 0.13), p = 0.0005]. Extra-coronary calcification affecting the aorta, carotid artery, breast artery, and arteries of lower extremities, was also increased in VKA treated patients [1.86 (1.43, 2.42), p < 0.00001] and moderated by the author-reported statistical adjustments of the effect estimates [B: -0.63 (-1.19, -0.08), p = 0.016]. The effect of VKA on the aortic valve calcification was significant [3.07 (1.90, 4.96), p < 0.00001]; however, these studies suffered from a high risk of publication bias.
Conclusion:
Vascular and valvular calcification are potential side effects of VKA. The clinical significance of these side effects on cardiovascular outcomes deserves further investigation.
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