Catheter ablation of atrial fibrillation reduces the risk of dementia and hospitalization during a very long-term follow-up

https://doi.org/10.1016/j.ijcard.2019.12.016Get rights and content

Highlights

  • Catheter ablation (CA) in atrial fibrillation (AF) patients reduced the long-term risk of dementia and hospitalization.

  • The risk of dementia was similar between AF patients receiving CA and those without history of AF.

  • CA in AF patients has a lower risk of dementia than AF patients without CA, particularly in older patients aged >65 years.

  • The dementia risk was higher in CA patients with AF hospitalization occurred ≤ 5 years than those without hospitalization.

Abstract

Background

Atrial fibrillation (AF) is associated with increased risks of dementia and hospitalization. Whether catheter ablation (CA) for AF might reduce such risks remains unclear. We aimed to investigate the effects of CA on dementia and hospitalization risks during a very long-term follow-up.

Methods

We studied a total of 787 AF patients receiving CA for AF treatment from 2003 to 2012 (AF CA group). The propensity score of this group was matched to another two cohorts: (a) AF patients without CA (AF no CA, n = 787) and (b) control patients without AF (n = 770). New onset of dementia of each subject was identified by ICD-9-CM codes, and information on hospitalization for AF was based on medical records. The Cox proportional hazards model was used to determine the hazard ratios (HRs) for events.

Results

During 9.0 ± 2.6 year's follow-up, a total of 139 dementia events and 732 AF-related hospitalizations have occurred. AF CA group has lower incidence of dementia than AF no CA group (adjusted HR: 0.44, p = 0.005). AF related hospitalizations were also lower in the AF CA group than that in AF no CA group (adjusted HR: 0.72, p < 0.05). In AF patients aged >65 years, CA reduced the risk of dementia compared to those without CA (adjusted HR: 0.46, p = 0.03).

Conclusions

In a 9-year follow-up, we found that CA had reduced the risk of dementia and hospitalization in AF patients, compared with those without CA. Such reduction in the risk of dementia was particularly clear in older AF patients (aged >65 years).

Introduction

Atrial fibrillation (AF) is the most common sustained arrhythmia in adults, with rising incidences in the aging population [1]. AF is associated with higher risks of dementia characterized by progressive cognitive impairments with normal consciousness, regardless of the history of stroke or other shared risk factors [2]. Dementia has a 5% prevalence rate in the old population (>65 years), and the prevalence would double for every 5 years after the age of 65 [3]. The mechanisms of cognitive dysfunction and dementia associated with AF include cerebral thromboembolism, cerebral hypo-perfusion, and cerebral micro-bleeds [4]. Therefore, controlling cardiac rhythm is used to reduce the risks of dementia in AF patients [2].

In major clinical trials, pharmacological treatments aiming at rhythm control showed no beneficial effects in terms of morbidity, mortality, and dementia [5,6]. One major limitation of pharmacological approach to control rhythm in AF patients is the ineffectiveness and adverse effects associated with anti-arrhythmic drugs (AADs) [7]. To improve symptoms, exercise capacity, and quality of life, catheter ablation (CA) is a therapy in AF patients at different ages with multiple co-morbidities, while minimizing the ADD toxicities [8,9]. Although CA treatment might reduce the risk of cerebral thromboembolism and hypo-perfusion, silent cerebral infarctions (SCIs) during the CA procedure might adversely increase dementia risk [10]. Whether CA reduces the long-term dementia risks remains unclear.

In a prospective registry-based study, Bunch et al., reported that the risks of dementia and stroke are lower in AF patients undergoing CA (4212 compared with 16,848 age- and gender- matched AF patients without CA) [11]. Interestingly, AF patients receiving CA have similar long-term rates of dementia and stroke compared with patients without AF [11]. In that study, the follow-up duration is 3.1 years. But dementia is a progressive disease involving long-term cerebral degeneration, and the study of dementia is better based on longer follow-up [12]. We hypothesized that the risk of dementia is lower AF patients after CA when studied in long-term follow-up.

Section snippets

Methods

This study was approved in accordance with the Good Clinical Practice Guidelines by the Institutional Review Board (IRB Number: 201305044W and 2017-09-013BCF) of the Taipei Veterans General Hospital (TVGH). A detailed method section is included in an online supplement.

Baseline characteristics

Table 1 shows the baseline characteristics of the three groups. The three groups have similar percentage of male patients (p = 0.99) and age (p = 0.17). The prevalence of hypertension (p = 0.98), CKD (p = 0.83), and COPD (p = 0.057) were not different among the three groups. AF with CA group patients have higher prevalence of coronary artery disease (p < 0.001) and stroke/transient ischemic attack (TIA) (p < 0.001) than that in AF without CA group. Control group patients have higher prevalence

Discussion

Three major findings emerged from this study: (1) CA in AF patients reduced the risk of dementia and AF-related hospitalization compared with those without CA; (2) The risk of dementia was similar between AF patients receiving CA and those without history of AF; and (3) CA in AF patients has a lower risk of dementia than AF patients without CA, particularly clear in older patients aged >65 years.

Conclusions

CA in AF patients reduced the risk of dementia and AF-related hospitalization compared with those without CA under very long-term follow-up, and the effects on dementia were particularly clear for older patients (aged >65 years). We conclude that CA is an effective therapeutic strategy to reduce dementia and hospitalization risk in AF patients.

Sources of funding

This work was supported by Ministry of Science and Technology of Taiwan (MOST 107-2314-B-010-061-MY2, MOST 106-2314-B-010-046-MY3); Grant of Taipei Veterans General Hospital (V108C-032, C17-095); Research Foundation of Cardiovascular Medicine (107-02-036), and Szu-Yuan Research Foundation of Internal Medicine (No. 108016).

Declaration of competing interest

None for all authors.

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