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- Publisher Website: 10.1016/j.hrthm.2020.01.007
- Scopus: eid_2-s2.0-85080889063
- PMID: 31931172
- WOS: WOS:000531537700006
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Article: Oral anticoagulant and reduced risk of dementia in patients with atrial fibrillation: A population-based cohort study
Title | Oral anticoagulant and reduced risk of dementia in patients with atrial fibrillation: A population-based cohort study |
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Authors | |
Keywords | Atrial fibrillation Cognitive impairment Dementia Oral anticoagulant Vascular dementia |
Issue Date | 2020 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/heartrhythmjournal |
Citation | Heart Rhythm, 2020, v. 17, p. 706-713 How to Cite? |
Abstract | Background:
Whether oral anticoagulation (OAC) can prevent dementia or cognitive impairment (CI) in patients with atrial fibrillation (AF) remains unclear.
Objective:
The purpose of this study was to investigate the risk of dementia/CI among AF patients with and without OAC treatment.
Methods:
We conducted a retrospective cohort study using United Kingdom (UK) primary care data (2000–2017). Participants with newly diagnosed AF without a history of dementia/CI were identified. Inverse probability of treatment weights based on propensity scores and Cox regression were used to compare the dementia outcomes.
Results:
Among 84,521 patients with AF, 35,245 were receiving OAC treatment and 49,276 received no OAC treatment; of these patients, 29,282 were receiving antiplatelets. Over a mean follow-up of 5.9 years, 5295 patients developed dementia/CI. OAC treatment was associated with a lower risk of dementia/CI compared to no OAC treatment (hazard ratio [HR] 0.90; 95% confidence interval 0.85–0.95; P <.001) or antiplatelets (HR 0.84; 95% confidence interval 0.79–0.90; P <.001). No significant difference in dementia risk was observed for direct oral anticoagulants (DOACs) vs warfarin (HR 0.89; 95% confidence interval 0.70–1.14; P = .373), whereas dual therapy (OAC plus an antiplatelet agent) was associated with a higher risk of dementia/CI compared with no treatment (HR 1.17; 95% confidence interval 1.05–1.31; P = .006).
Conclusion:
OAC use was associated with a lower risk of dementia/CI compared to non-OAC and antiplatelet treatment among AF patients. The evidence for DOAC on cognitive function is insufficient, and further studies including randomized clinical trials are warranted. |
Persistent Identifier | http://hdl.handle.net/10722/284984 |
ISSN | 2023 Impact Factor: 5.6 2023 SCImago Journal Rankings: 2.072 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Mongkhon, P | - |
dc.contributor.author | Fanning, L | - |
dc.contributor.author | Lau, WCY | - |
dc.contributor.author | Tse, G | - |
dc.contributor.author | Lau, KK | - |
dc.contributor.author | Wei, L | - |
dc.contributor.author | Kongkaew, C | - |
dc.contributor.author | Wong, ICK | - |
dc.date.accessioned | 2020-08-07T09:05:12Z | - |
dc.date.available | 2020-08-07T09:05:12Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Heart Rhythm, 2020, v. 17, p. 706-713 | - |
dc.identifier.issn | 1547-5271 | - |
dc.identifier.uri | http://hdl.handle.net/10722/284984 | - |
dc.description.abstract | Background: Whether oral anticoagulation (OAC) can prevent dementia or cognitive impairment (CI) in patients with atrial fibrillation (AF) remains unclear. Objective: The purpose of this study was to investigate the risk of dementia/CI among AF patients with and without OAC treatment. Methods: We conducted a retrospective cohort study using United Kingdom (UK) primary care data (2000–2017). Participants with newly diagnosed AF without a history of dementia/CI were identified. Inverse probability of treatment weights based on propensity scores and Cox regression were used to compare the dementia outcomes. Results: Among 84,521 patients with AF, 35,245 were receiving OAC treatment and 49,276 received no OAC treatment; of these patients, 29,282 were receiving antiplatelets. Over a mean follow-up of 5.9 years, 5295 patients developed dementia/CI. OAC treatment was associated with a lower risk of dementia/CI compared to no OAC treatment (hazard ratio [HR] 0.90; 95% confidence interval 0.85–0.95; P <.001) or antiplatelets (HR 0.84; 95% confidence interval 0.79–0.90; P <.001). No significant difference in dementia risk was observed for direct oral anticoagulants (DOACs) vs warfarin (HR 0.89; 95% confidence interval 0.70–1.14; P = .373), whereas dual therapy (OAC plus an antiplatelet agent) was associated with a higher risk of dementia/CI compared with no treatment (HR 1.17; 95% confidence interval 1.05–1.31; P = .006). Conclusion: OAC use was associated with a lower risk of dementia/CI compared to non-OAC and antiplatelet treatment among AF patients. The evidence for DOAC on cognitive function is insufficient, and further studies including randomized clinical trials are warranted. | - |
dc.language | eng | - |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/heartrhythmjournal | - |
dc.relation.ispartof | Heart Rhythm | - |
dc.subject | Atrial fibrillation | - |
dc.subject | Cognitive impairment | - |
dc.subject | Dementia | - |
dc.subject | Oral anticoagulant | - |
dc.subject | Vascular dementia | - |
dc.title | Oral anticoagulant and reduced risk of dementia in patients with atrial fibrillation: A population-based cohort study | - |
dc.type | Article | - |
dc.identifier.email | Lau, WCY: wallisy@hku.hk | - |
dc.identifier.email | Lau, KK: gkklau@hku.hk | - |
dc.identifier.email | Wong, ICK: wongick@hku.hk | - |
dc.identifier.authority | Lau, KK=rp01499 | - |
dc.identifier.authority | Wong, ICK=rp01480 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.hrthm.2020.01.007 | - |
dc.identifier.pmid | 31931172 | - |
dc.identifier.scopus | eid_2-s2.0-85080889063 | - |
dc.identifier.hkuros | 311786 | - |
dc.identifier.volume | 17 | - |
dc.identifier.spage | 706 | - |
dc.identifier.epage | 713 | - |
dc.identifier.isi | WOS:000531537700006 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1547-5271 | - |