Vascular Calcification Clinical Trial
Official title:
Aortic Calcification and Vitamin K Antagonists
The vitamin K antagonists (VKA) are necessary drugs of prevention and treatment of thrombo-embolic disease. The AVKAL study assesses the impact of VKA treatment on the aortic calcifications development. This is a biomedical research without health product, transversal and monocentric study which compares the aortic calcifications levels of two populations : one treated by VKA and the other which has never been treated by VKA.
The vitamin K antagonists exercise their anticoagulant effect by preventing the vitamin K
dependant gamma-carboxylation of coagulation II, VII, IX and X factors which forms the final
step of their activation.
They inhibit the vitamin K epoxide reductase VKORC1 enzyme, which is responsible of the
vitamin K epoxide recycling in vitamin K hydroquinone (its reduced form). The carboxylation
also can be inhibited by the Matrix Gla protein (MGP), inhibitor factor of vascular
calcifications.
Warfarin (the most used VKA at the word level) is employed on animal for produce vascular
calcifications by inhibiting the MGP activation.
Epidemiologic data indicate that warfarin could increase the calcifications of cardiac
valves and coronary arteries. However, these studies were not interested in abdominal
aorta's calcifications which are considered like an important marker of cardiovascular risk
and did not concern the fluindione which is the most used VKA in France. Even if a class
effect seems logical, the investigators can't dismiss the local effects, different to
warfarin. In these studies, the calcifications assessment were rarely quantitative and the
MGP levels were not measured. The vascular calcifications constitute a potential adverse
effect of VKA which could limit their benefit in certain populations.
In this work there is an assumption that the aortic calcifications levels are upper in
patients receiving VKA than in patients who are not receiving VKA and the aortic
calcifications increase is owed to the non-activation of MGP.
The main objective is to assess if the taking of VKA is associated with the aortic
calcifications development in patients receiving VKA.
Investigators will compare 2 populations: one group treated by VKA treatment for at least 6
months and one focus group which have never been treated by VKA treatment.
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