Association of anticoagulant therapy with risk of dementia among patients with atrial fibrillation

被引:39
作者
Kim, Daehoon [1 ]
Yang, Pil-Sung [2 ]
Jang, Eunsun [3 ,4 ]
Yu, Hee Tae [1 ]
Kim, Tae-Hoon [1 ]
Uhm, Jae-Sun [1 ]
Kim, Jong-Youn [1 ]
Sung, Jung-Hoon [2 ]
Pak, Hui-Nam [1 ]
Lee, Moon-Hyoung [1 ]
Lip, Gregory Y. H. [3 ,4 ]
Joung, Boyoung [1 ]
机构
[1] Yonsei Univ, Severance Cardiovasc Hosp, Dept Internal Med, Div Cardiol,Coll Med, 50-1 Yonseiro, Seoul 03722, South Korea
[2] CHA Univ, CHA Bundang Med Ctr, Dept Cardiol, Seongnam, South Korea
[3] Univ Liverpool, Liverpool Ctr Cardiovasc Sci, Liverpool, Merseyside, England
[4] Liverpool Heart & Chest Hosp, Liverpool, Merseyside, England
来源
EUROPACE | 2021年 / 23卷 / 02期
关键词
Atrial fibrillation; Oral anticoagulant; Non-vitamin K antagonist oral anticoagulant; Warfarin; Dementia; RIVAROXABAN; WARFARIN; OUTCOMES;
D O I
10.1093/europace/euaa192
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims To investigate the risk of dementia in atrial fibrillation (AF) patients treated with different oral anticoagulants (OACs). Methods and results This observational, population-based cohort study enrolled 53 236 dementia-free individuals with non-valvular AF who were aged >= 50 years and newly prescribed OACs from 1 January 2013 to 31 December 2016 from the Korean National Health Insurance Service database. Propensity score matching was used to compare the rates of dementia between users of non-vitamin K antagonist oral anticoagulant (NOAC) (dabigatran, rivaroxaban, and apixaban) and warfarin and to compare each individual NOAC with warfarin. Propensity score weighting analyses were also performed. In the study population (41.3% women; mean age: 70.7 years), 2194 had a diagnosis of incident dementia during a mean follow-up of 20.2 months. Relative to propensity-matched warfarin users, NOAC users tended to be at lower risk of dementia [hazard ratio (HR) 0.78, 95% confidence interval (CI) 0.69-0.90]. When comparing individual NOACs with warfarin, all the three NOACs were associated with lower dementia risk. In pairwise comparisons among NOACs, rivaroxaban was associated with decreased dementia risk, compared with dabigatran (HR 0.83, 95% CI 0.74-0.92). Supplemental propensity-weighted analyses showed consistent protective associations of NOACs with dementia relative to warfarin. The associations were consistent irrespectively of age, sex, stroke, and vascular disease and more prominent in standard dose users of NOAC. Conclusion In this propensity-matched and -weighted analysis using a real-world population-based cohort, use of NOACs was associated with lower dementia risk than use of warfarin among non-valvular AF patients initiating OAC treatment.
引用
收藏
页码:184 / 195
页数:12
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