Warfarin Accelerates Aortic Calcification by Upregulating Senescence-Associated Secretory Phenotype Maker Expression.
Ningle WeiLiuyi LuHuan-Ji ZhangMing GaoSounak GhoshZhaoyu LiuJunhua QiJing-Feng WangJie ChenHui HuangPublished in: Oxidative medicine and cellular longevity (2020)
Warfarin, a vitamin K antagonist (VKA), is known to promote arterial calcification (AC). In the present study, we conducted a case-cohort study within the Multi-Ethnic Study of Atherosclerosis (MESA); 6655 participants were included. From MESA data, we found that AC was related to both age and vitamin K; furthermore, the score of AC increased with SASP marker including interlukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) rising. Next, a total of 79 warfarin users in our center developed significantly more calcified coronary plaques as compared to non-VKA users. We investigated the role of warfarin in phosphate-induced AC in different ages by in vitro experimental study. Furthermore, dose-time-response of warfarin was positively correlated with AC score distribution and plasma levels of the SASP maker IL-6 among patients < 65 years, but not among patients ≥ 65 years. In addition, in vitro research suggested that warfarin treatment tended to deteriorate calcification in young VSMC at the early stage of calcification. Our results suggested that aging and warfarin-treatment were independently related to increased AC. Younger patients were more sensitive to warfarin-related AC than older patients, which was possibly due to accumulated warfarin-induced cellular senescence.
Keyphrases
- atrial fibrillation
- direct oral anticoagulants
- venous thromboembolism
- oral anticoagulants
- early stage
- chronic kidney disease
- end stage renal disease
- rheumatoid arthritis
- cardiovascular disease
- endothelial cells
- heart failure
- high glucose
- poor prognosis
- dna damage
- left ventricular
- peritoneal dialysis
- squamous cell carcinoma
- prognostic factors
- mass spectrometry
- stress induced
- combination therapy
- single molecule
- pulmonary artery
- atomic force microscopy