Department of Cardiology, Odense University Hospital, Odense, Denmark.
Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
PLoS One. 2020 Oct 29;15(10):e0241450. doi: 10.1371/journal.pone.0241450. eCollection 2020.
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).
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.
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.
Adjusted for cardiovascular risk factors, VKA treatment-contrary to NOAC-was associated to higher CAC category.
尽管新型非维生素 K 拮抗剂口服抗凝剂(NOAC)已问世,但维生素 K 拮抗剂(VKA)仍是全球最常开的口服抗凝药物。VKA 会干扰维生素 K1 和 K2 的再生,这对于凝血因子的激活和基质 Gla 蛋白(一种强烈抑制动脉钙化的物质)的激活是必需的。本研究旨在阐明在无既往心血管疾病(CVD)的人群中,VKA 治疗是否与冠状动脉钙化(CAC)的严重程度相关。
我们收集了 2007-2017 年期间在临床检查(n=9672)或研究中进行的心脏 CT 扫描的心血管危险因素和 CAC 评分的数据。抗凝药物使用的数据来自丹麦国家卫生服务处方数据库。通过调整协变量的有序逻辑回归,研究了抗凝时间与 CAC 评分分类(0、1-99、100-399、≥400)之间的关系。
最终研究人群包括 17254 名无既往 CVD 的参与者,其中 1748 名和 1144 名分别接受了 VKA 或 NOAC 治疗。VKA 治疗时间越长,CAC 分类越高。每接受一年的 VKA 治疗,处于更高 CAC 分类的几率增加(比值比(OR)=1.032,95%CI 1.009-1.057)。相比之下,NOAC 治疗时间与 CAC 分类无关(OR=1.002,95%CI 0.935-1.074)。VKA 治疗时间与 CAC 分类之间没有显著的交互作用。
在调整了心血管危险因素后,与 NOAC 相反,VKA 治疗与更高的 CAC 分类相关。