Advertisement
Original Article| Volume 4, ISSUE 1, P65-74, January 2022

A Population-Based Study of Unexplained/Lone Atrial Fibrillation: Temporal Trends, Management, and Outcomes

Open AccessPublished:September 13, 2021DOI:https://doi.org/10.1016/j.cjco.2021.09.006

      Abstract

      Background

      Previous studies on lone/unexplained atrial fibrillation and atrial flutter (AF) did not exclude patients with contemporary secondary AF triggers. We characterized unexplained AF using a strict definition, and compared it to secondary AF.

      Methods

      In this population-based study, unexplained AF was defined by the lack of any identifiable triggering medical/surgical diagnosis. Comparisons by AF type (unexplained vs secondary), age-of-onset (≤ / > 65 years), and sex were undertaken. Data were acquired by linking 6 population databases maintained by the Alberta Ministry of Health over a 9-year period (April 2006 to March 2015). The primary composite outcome of stroke, transient ischemic attack, thromboembolism, and/or death was assessed.

      Results

      There were 33,150 incident AF diagnoses identified, including 1145 patients (3.5%) with unexplained AF, 931 (81.2%) of whom were aged ≤ 65 years (2.8% of diagnoses, and 79% male). Patients with unexplained AF less often received rate/rhythm-control drugs (P < 0.0001), but they more often underwent electrical cardioversion (P < 0.0001) vs secondary AF patients. Men were younger at unexplained AF diagnosis (45 [interquartile range: 34-59] vs 58 [interquartile range: 40-69] years; P < 0.001). After adjusting for age at diagnosis, there were no sex-based differences in the primary outcome. Event-free survival in young unexplained AF (age ≤ 65 years) was 99.4% at 1 year and 98.3% at 3 years. At 3 years, hospitalization(s)/emergency visit(s) for noncardiovascular reasons and for AF occurred in 56.6% and 23.8% of these patients, respectively.

      Conclusions

      Using a strict contemporary definition of unexplained AF, this study shows that the condition is rare, predominantly male, and has excellent event-free survival. However, the high rate of acute hospital utilization after diagnosis is concerning.

      Résumé

      Contexte

      Les études précédentes sur le flutter auriculaire et la fibrillation auriculaire (FA) idiopathiques/inexpliqués n’excluaient pas les patients présentant des déclencheurs contemporains de FA secondaire. Nous avons caractérisé la FA inexpliquée en utilisant une définition stricte, et l’avons comparée à la FA secondaire.

      Méthodologie

      Dans cette étude basée sur une population, la FA inexpliquée a été définie par l’absence de tout diagnostic médical/chirurgical de déclencheur identifiable. Des comparaisons par type de FA (inexpliquée vs secondaire), par âge d’apparition (≤ / > 65 ans) et par sexe ont été effectuées. Les données ont été acquises en reliant six bases de données de population maintenues par le ministère de la Santé de l’Alberta sur une période de neuf ans (avril 2006 à mars 2015). Le paramètre d’évaluation principal comprenant l’accident vasculaire cérébral (AVC), l’accident ischémique transitoire, la thromboembolie et/ou le décès a été évalué.

      Résultats

      Au total, 33 150 diagnostics de FA ont été recensés, dont 1 145 patients (3,5 %) présentant une FA inexpliquée, parmi lesquels 931 (81,2 %) étaient âgés de ≤ 65 ans (2,8 % des diagnostics, et 79 % d’hommes). Les patients atteints de FA inexpliquée ont moins souvent reçu de médicaments pour contrôler la fréquence ou le rythme cardiaque (p < 0,0001), mais ils ont plus souvent subi une cardioversion électrique (p < 0,0001) par rapport aux patients atteints de FA secondaire. Les hommes étaient plus jeunes au moment du diagnostic d’une FA inexpliquée (45 [intervalle interquartile : 34 à 59] vs 58 [intervalle interquartile : 40 à 69] ans; p < 0,001). Après un ajustement pour l’âge au moment du diagnostic, il n’y avait pas de différence entre les sexes quant au paramètre d’évaluation principal. La survie sans événement chez les patients jeunes ayant présenté une FA inexpliquée (âge ≤ 65 ans) était de 99,4 % à un an, et de 98,3 % à trois ans. À trois ans, une ou plusieurs hospitalisations/consultations à l’urgence pour des raisons non cardiovasculaires et pour une FA sont survenues chez 56,6 % et 23,8 % de ces patients, respectivement.

      Conclusions

      En utilisant une définition contemporaine stricte de la FA inexpliquée, cette étude montre que cette affection est rare, majoritairement masculine, et qu’elle est associée à une excellente survie sans événement. Cependant, le taux élevé d’utilisation de soins actifs dans les hôpitaux après le diagnostic est préoccupant.
      Atrial fibrillation and atrial flutter (AF is used to designate the combined incidence—ie, either one or both, although these are not specified separately) are common arrhythmias that affect ∼2% of the population and lead to substantial morbidity and mortality, mainly due to an increased risk of stroke.
      • Zoni-Berisso M.
      • Lercari F.
      • Carazza T.
      • Domenicucci S.
      Epidemiology of atrial fibrillation: European perspective.
      Acquired, environmental, and genetic factors play a role in the pathogenesis of AF,
      • Zoni-Berisso M.
      • Lercari F.
      • Carazza T.
      • Domenicucci S.
      Epidemiology of atrial fibrillation: European perspective.
      ,
      • Fox C.S.
      • Parise H.
      • D'Agostino Sr., R.B.
      • et al.
      Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring.
      including male sex, advancing age, and family history.
      • Fox C.S.
      • Parise H.
      • D'Agostino Sr., R.B.
      • et al.
      Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring.
      ,
      • Fumagalli S.
      • Said S.A.M.
      • Laroche C.
      • et al.
      Age-related differences in presentation, treatment, and outcome of patients with atrial fibrillation in Europe: The EORP-AF General Pilot Registry (EURObservational Research Programme-Atrial Fibrillation).
      In most, AF occurs “secondary” to a comorbid condition, either cardiac in origin, such as coronary artery disease and heart failure, or extracardiac in nature, such as infectious and chronic pulmonary disease.
      • Zoni-Berisso M.
      • Lercari F.
      • Carazza T.
      • Domenicucci S.
      Epidemiology of atrial fibrillation: European perspective.
      However, in a proportion of predominantly young individuals, AF develops as a primary disorder without an identifiable trigger, often termed unexplained, idiopathic, or lone AF.
      • Brand F.N.
      • Abbott R.D.
      • Kannel W.B.
      • Wolf P.A.
      Characteristics and prognosis of lone atrial fibrillation: 30-year follow-up in the Framingham Study.
      ,
      • Jahangir A.
      • Lee V.
      • Friedman P.A.
      • et al.
      Long-term progression and outcomes with aging in patients with lone atrial fibrillation: a 30-year follow-up study.
      Although event-free survival is better in unexplained AF,
      • Fumagalli S.
      • Said S.A.M.
      • Laroche C.
      • et al.
      Age-related differences in presentation, treatment, and outcome of patients with atrial fibrillation in Europe: The EORP-AF General Pilot Registry (EURObservational Research Programme-Atrial Fibrillation).
      ,
      • Jahangir A.
      • Lee V.
      • Friedman P.A.
      • et al.
      Long-term progression and outcomes with aging in patients with lone atrial fibrillation: a 30-year follow-up study.
      its definition with respect to age of onset and comorbidity burden is inconsistent.
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      For example, the Framingham Heart Study of unexplained AF included patients with high blood pressure and advanced age,
      • Brand F.N.
      • Abbott R.D.
      • Kannel W.B.
      • Wolf P.A.
      Characteristics and prognosis of lone atrial fibrillation: 30-year follow-up in the Framingham Study.
      both now considered to be strong risk factors for secondary AF.
      • Andrade J.G.
      • Verma A.
      • Mitchell L.B.
      • et al.
      2018 Focused Update of the Canadian Cardiovascular Society Guidelines for the Management of Atrial Fibrillation.
      Understanding unexplained AF is important because diagnostic/screening approaches, therapeutic recommendations, and natural history can differ from those for acquired/secondary AF.
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      In this study, we characterized unexplained AF in a dataset from a large population, using a stringent contemporary definition, which accounted for a multitude of potentially AF-predisposing comorbidities, and compared it to secondary AF.

      Methods

      Study population

      We included all patients with an incident diagnosis of AF between April 1, 2006 and March 31, 2015 (the 2006-2014 fiscal years) evaluated in the single-payer healthcare system across the entire province of Alberta. The first diagnosis of AF was identified from inpatient and ambulatory databases using the validated
      • Cozzolino F.
      • Montedori A.
      • Abraha I.
      • et al.
      A diagnostic accuracy study validating cardiovascular ICD-9-CM codes in healthcare administrative databases. The Umbria Data-Value Project.
      ,
      • Rix T.A.
      • Riahi S.
      • Overvad K.
      • et al.
      Validity of the diagnoses atrial fibrillation and atrial flutter in a Danish patient registry.
      International Classification of Diseases, 9th edition (ICD9: code 427.3) and 10th edition (ICD10: code I48) codes from the primary diagnostic fields during the study period. Prevalent AF cases were excluded, defined as a preexisting AF diagnosis in any database (inpatient, ambulatory, and claims) from 1994 onward to current diagnosis. All patients with incident AF were categorized into 3 groups based on the location/setting of the first presentation: outpatient clinic, emergency department, and hospitalization; these groups were mutually exclusive. Given that administrative coding to distinguish between atrial fibrillation and atrial flutter is not reliable,
      • Rix T.A.
      • Riahi S.
      • Overvad K.
      • et al.
      Validity of the diagnoses atrial fibrillation and atrial flutter in a Danish patient registry.
      these conditions were combined.

      Data sources

      Data were acquired by linking 6 population databases maintained by the Alberta Ministry of Health as reported previously.
      • Roston T.M.
      • Tran D.T.
      • Sanatani S.
      • et al.
      A population-based study of syncope in the young.
      These consist of the following: (i) the Ambulatory Care database, which tracks all visits to the 101 emergency departments (EDs) in Alberta; (ii) the Discharge Abstract Database, which records all admissions to acute care facilities; (iii) the Physician Claims Database, which tracks all fee-for-service claims for insured health services; (iv) the Alberta Population Registry and Alberta Vital Statistics, which track vital statistics for Alberta inhabitants; and (v) the Pharmacy Information Network, which provides all prescriptions filled in Alberta from 2008 onward. Thus, only patients diagnosed in the 2008-2014 fiscal years were included in the prescription analysis. Medications were classified using the 2016 Guidelines for Anatomical Therapeutic Chemical Classification and Defined Daily Dose Assignment, 9th Edition.
      World Health Organization Collaborating Centre for Drug Statistics Methodology (WHO-CCDS)
      Guidelines for ATC Classification and DD Assignment.
      The Canadian Classification of Health Interventions (CCI), volume 3, was used for procedural interventions,
      Canadian Institute of Health Information (CIHI)
      which included 1.HH.59 and 1.HZ.59 (cardiac ablation) and 1.HZ.09 (electrical cardioversion; Supplemental Table S1).

      Definitions

      Unexplained AF was diagnosed when incident AF occurred in the absence of (i) chronic predisposing comorbidities 3 years before and 1 year after the index AF diagnosis and (ii) predisposing acute events present 1 month before and 1 month after the index AF diagnosis. In selecting these periods for detecting chronic comorbidities, we intended to balance the importance of identifying relevant diagnoses with the historical availability of data in the linked administrative datasets. A 1-year period following AF diagnosis was selected to allow for standard outpatient follow-up and risk-factor assessment to occur after any ED presentation with AF. These AF-predisposing comorbid and acute conditions were identified using ICD9 and ICD10 codes from inpatient, ambulatory, and physician office databases and are listed comprehensively in Supplemental Tables S2 and S3. In brief, chronic AF-predisposing comorbidities included any diagnosis of thyroid disorder, circulatory system disease (including congenital heart disease), lung disease, diabetes, malignancy, and/or obesity. Acute AF-predisposing events included infections, major trauma, poisonings/overdoses and/or major surgeries. Surgical procedures were identified using CCI, volume 3; a surgery requiring overnight hospitalization was defined as an acute AF-predisposing event. If any of these aforementioned factors were present within the pre-specified time periods, the case was classified as “secondary AF,” with all the remaining cases considered to be unexplained AF. Patients were further subdivided by age (≤ 65 years or > 65 years) at the time of diagnosis, to define younger and older AF onset, respectively. We used a cutoff of 65 years to define young onset of AF because this was similar to that used in recent studies
      • Jahangir A.
      • Lee V.
      • Friedman P.A.
      • et al.
      Long-term progression and outcomes with aging in patients with lone atrial fibrillation: a 30-year follow-up study.
      ,
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      and reflects the age at which oral anticoagulants (OACs) would be started in Canada, regardless of other stroke risk factors.
      • Andrade J.G.
      • Verma A.
      • Mitchell L.B.
      • et al.
      2018 Focused Update of the Canadian Cardiovascular Society Guidelines for the Management of Atrial Fibrillation.

      Outcomes

      The primary outcome of interest was a composite of stroke, transient ischemic attack (TIA), systemic thromboembolism, or death at 1 and 3 years of follow-up. Other endpoints examined were AF repeat healthcare encounters in the hospital or ED (as a primary diagnosis) and re-presentation/hospitalization for noncardiovascular causes at 1 and 3years. We also examined the impact of sex and age on unexplained AF diagnosis and outcomes. Death was considered to be a competing risk during follow-up for repeat AF healthcare encounters.

      Statistical analysis

      Categorical variables are presented as frequencies with percentages and are compared across groups, using χ2 tests. Annual household income and age were presented as median with interquartile range (25th, 75th percentiles) and compared across groups using the Mann-Whitney U test. We examined baseline characteristics, outcomes, and medication uptake among young AF patients, stratified by unexplained AF and secondary AF, and among unexplained AF patients, stratified by age group (young: ≤ 65 years vs old: > 65 years) and sex (male vs female). We also calculated the incidence of AF indexed to the Alberta population by fiscal year overall, stratified by type of AF (unexplained vs secondary), and by age group (young vs old). To examine the temporal trend in the incidence, we applied Poisson regression models or negative binomial models in case of over dispersion, as appropriate.
      In addition, we examined medication uptake and outcomes at 3 years from the diagnosis of AF, specifically examining the trends based on age and type of AF. For this analysis, we excluded patients who were diagnosed with incident AF after March 31, 2012, to provide the same opportunity for 3-year follow up for each patient. Cumulative incidences for primary endpoint and for recurrent AF at 3 years were plotted using Kaplan-Meier curves. Composite outcome at 3 years was compared by type of AF, age group (young vs old), and sex, using Cox’s proportional hazard regression model. We also compared use of evidence-based medication including OAC, rate-control medication, by AF type, as well as by age and sex, among young patients with unexplained AF.
      • Andrade J.G.
      • Verma A.
      • Mitchell L.B.
      • et al.
      2018 Focused Update of the Canadian Cardiovascular Society Guidelines for the Management of Atrial Fibrillation.
      For all analyses, statistical significance was defined as a 2-sided P value of < 0.05. Analyses were performed using SAS software, version 9.4 (SAS Institute, Cary, NC). No correction for multiple testing was performed, because the study was exploratory in nature.

      Results

      AF diagnosis and incidence in the entire cohort

      Of 53,059 patients with AF, 33,150 (62.5%) received a new diagnosis of AF during the study period, 1145 (3.5%) of whom had unexplained AF. We subdivided this latter group further by age > 65 years (214; 18.7% of unexplained AF) vs ≤ 65 years (931; 81.3% of unexplained AF) at diagnosis, to reflect the point in life at which AF may be related primarily to aging, and which is the indication for anticoagulation in Canada, regardless of other secondary risk factors. Supplemental Figure S1 summarizes the study population grouped by age and AF type. The incidence rate of all-cause AF (unexplained and secondary) rose steadily, on average by 1.7% per year, over the study period (rate ratio 1.017; 95% confidence interval [CI]: 1.012-1.22); P < 0.001; Fig. 1).
      Figure thumbnail gr1
      Figure 1Incidence rate of all-cause (unexplained and secondary) atrial fibrillation and atrial flutter (AF) indexed to 100,000 of the Alberta population.

      Diagnosis and outcomes of AF regardless of age

      We first compared unexplained AF to secondary AF, regardless of age at diagnosis (Table 1). Over the study period, the incidence of both unexplained AF and secondary AF increased (4.1%, P = 0.003; 1.6%; P < 0.001, respectively, Fig. 1). As anticipated, at 1 and 3 years, there was a greater risk of all adverse endpoints in secondary AF compared to unexplained AF (Fig. 2; Table 2). In unexplained AF, electrical cardioversion was attempted more frequently, compared with its use for secondary AF patients (24.4% vs 12.7% at 30 days; P < 0.001), whereas secondary AF patients were more likely to undergo catheter ablation, compared with patients with unexplained AF (1.7% vs 0.3% at 1 year; P < 0.001; Table 2).
      Table 1Characteristics of new-onset atrial fibrillation and atrial flutter (AF) patients—unexplained vs secondary
      CharacteristicsUnexplained AFSecondary AFTotalP
      n114532,00533,150
      Age at presentation, y47 (35, 61)72 (61, 80)71 (60, 80)< 0.0001
      Age group, y
      20–44512 (44.7)2097 (6.6)2609 (7.9)< 0.0001
      45–54216 (18.9)2759 (8.6)2975 (9.0)
      55–65203 (17.7)5422 (16.9)5625 (17.0)
      66–79154 (13.4)12,896 (40.3)13,050 (39.4)
      ≥ 8060 (5.2)8831 (27.6)8891 (26.8)
      Sex (male)852 (74.4)16,970 (53.0)17,822 (53.8)< 0.0001
      Chronic comorbid diagnoses
      Malignancy0 (0)11,399 (35.6)11,399 (34.4)
      Thyroid disease0 (0)6032 (18.8)6032 (18.2)
      Cardiovascular and cerebrovascular disease0 (0)30,247 (94.5)30,247 (91.2)
      Chronic lung disease0 (0)11,090 (34.7)11,091 (33.5)
      Diabetes0 (0)8258 (25.8)8258 (24.9)
      Obesity and metabolic disorders0 (0)17,255 (53.9)17,255 (52.1)
      Acute comorbid events/diagnoses
      Selected injuries and poisonings0 (0)1222 (3.8)1224 (3.7)
      Burns0 (0)26 (0.1)26 (0.1)
      Acute respiratory infection0 (0)1719 (5.4)1744 (5.3)
      Pneumonia and influenza0 (0)1889 (5.9)1892 (5.7)
      Appendicitis0 (0)20 (0.1)20 (0.1)
      Other infections0 (0)2802 (8.8)2811 (8.5)
      Locale of diagnosis
      Specialist’s outpatient clinic223 (19.5)9373 (29.3)9596 (28.9)< 0.0001
      Emergency department803 (70.1)15,352 (48.0)16,155 (48.7)
      Inpatient119 (10.4)7280 (22.7)7399 (22.3)
      Residence
      Rural207 (18.1)6060 (18.9)6267 (18.9)0.4673
      Urban938 (81.9)25,945 (81.1)26,883 (81.1)
      Median household total income in 2010, $75,143 (67,856, 94,410)73,385 (66,341, 90,652)73,385 (66,341, 90,652)0.0022
      Values are n (%) or median (interquartile range), unless otherwise indicated.
      Figure thumbnail gr2
      Figure 2Cumulative incidence composite outcomes (death/stroke/transient ischemic attack/embolism) at 3 years since the diagnosis of atrial fibrillation and atrial flutter (AF).
      Table 2Treatments and outcomes of new-onset atrial fibrillation and atrial flutter (AF)—unexplained vs secondary
      VariableUnexplained AFSecondary AFTotalP
      n114532,00533,150
      Catheter ablation
       7-d1 (0.1)94 (0.3)95 (0.3)0.1993
       30-d1 (0.1)135 (0.4)136 (0.4)0.0819
       1-y3 (0.3)533 (1.7)536 (1.6)0.0002
      Electrical cardioversion
       7-d273 (23.8)3812 (11.9)4085 (12.3)< 0.0001
       30-d282 (24.6)4069 (12.7)4351 (13.1)< 0.0001
       1-y312 (27.2)5667 (17.7)5979 (18.0)< 0.0001
      1-y outcome
       Deaths12 (1.0)2640 (8.2)2652 (8.0)< 0.0001
       Stroke2 (0.2)539 (1.7)541 (1.6)< 0.0001
       Stroke/TIA/embolism4 (0.3)806 (2.5)810 (2.4)< 0.0001
       Death/stroke/TIA/embolism16 (1.4)3262 (10.2)3278 (9.9)< 0.0001
       Bleeding3 (0.3)1525 (4.8)1528 (4.6)< 0.0001
       Hospitalization/ED visit for AF187 (16.3)6762 (21.1)6949 (21.0)< 0.0001
       Non-CV hospitalization/ED visit362 (31.6)16,81217,174 (51.8)< 0.0001
      3-y outcome
       n68920,28620,975
       Deaths20 (2.9)3415 (16.8)3435 (16.4)< 0.0001
       Stroke6 (0.9)793 (3.9)799 (3.8)< 0.0001
       Stroke/TIA/embolism/death27 (3.9)4205 (20.7)4232 (20.2)< 0.0001
       Bleeding20 (2.9)1993 (9.8)2013 (9.6)< 0.0001
       Hospitalization/ED visit for AF169 (24.5)5920 (29.2)6089 (29.0)0.0081
       Non-CV hospitalization/ED visit378 (54.9)15,013 (74.0)15,391 (73.4)< 0.0001
      Values are n (%), unless otherwise indicated.
      CV, cardiovascular; ED, emergency department; TIA, transient ischemic attack.

      Diagnosis and outcomes of AF in the young

      We then focused on younger patients with AF (aged ≤ 65 years at diagnosis; Table 3). Age of onset in unexplained AF in the young (42 years, interquartile range [IQR] 32-53) was lower, compared with that for secondary AF in the young (55 years, IQR 47-61; P < 0.001). The incidence of AF in the young rose on average by 2.1% per year over the study period (P < 0.001), including increases in both unexplained (3.8% per year) and secondary AF (2.2% per year; Fig. 3). In the young population, the location of diagnosis also differed, with secondary AF more likely to be diagnosed in outpatient and inpatient settings, and unexplained AF more likely to be diagnosed in the ED; Table 3). At 1 and 3years, a higher proportion of secondary AF patients, compared with patients with unexplained AF, experienced all adverse endpoints (Table 4; Fig. 4). Important to note is that in young-onset unexplained AF, the risk of the primary outcome was low (at 1 year, 6 patients [0.6%]; at 3 years, 10 patients [1.7%]). This finding contrasts with results for those with young-onset secondary AF, which was associated with a risk of the primary outcome of 4.0% at 1 year and 8.0% at 3 years. Trends in hospital utilization during follow-up in patients aged ≤ 65 years are shown in Table 4.
      Table 3Comparisons of characteristics among young (age ≤ 65 years) patients—unexplained vs secondary atrial fibrillation and atrial flutter (AF)
      CharacteristicsUnexplained AFSecondary AFTotalP
      n93110,27811,209
      Age at presentation42 (32, 53)55 (47, 61)55 (45, 60)< 0.0001
      Age group, y
      20–44512 (55.0)2097 (20.4)2609 (23.3)< 0.0001
      45–54216 (23.2)2759 (26.8)2975 (26.5)
      55–65203 (21.8)5422 (52.8)5625 (50.2)
      Sex (male)735 (78.9)6637 (64.6)7372 (65.8)< 0.0001
      Locale of diagnosis
      Specialist’s outpatient clinic160 (17.2)2805 (27.3)2965 (26.5)< 0.0001
      Emergency department673 (72.3)5448 (53.0)6121 (54.6)
      Inpatient98 (10.5)2025 (19.7)2123 (18.9)
      Residence
      Rural165 (17.7)1871 (18.2)2036 (18.2)0.7154
      Urban766 (82.3)8407 (81.8)9173 (81.8)
      Median household total income in 2010, $75,684 (68,090, 96,257)75,857 (68,090, 94,410)75,857 (68,090, 94,410)0.8748
      Values are n (%) or median (interquartile range), unless otherwise indicated.
      Figure thumbnail gr3
      Figure 3Incidence rate of atrial fibrillation and atrial flutter (AF) among the young (age ≤ 65 years) population.
      Table 4Cardiac intervention and outcomes among young (age ≤ 65 years) patients with unexplained vs secondary atrial fibrillation and atrial flutter (AF)
      VariableUnexplained AFSecondary AFTotalP
      n93110,27811,209
      Catheter ablation
       7-d0 (0.0)50 (0.5)50 (0.4)0.0329
       30-d0 (0.0)74 (0.7)74 (0.7)0.0094
       1-y2 (0.2)298 (2.9)300 (2.7)< 0.0001
      Electrical cardioversion
       7-d250 (26.9)1873 (18.2)2123 (18.9)< 0.0001
       30-d257 (27.6)1977 (19.2)2234 (19.9)< 0.0001
       1-y283 (30.4)2693 (26.2)2976 (26.6)0.0055
      1-y outcome
       Death5 (0.5)309 (3.0)314 (2.8)< 0.0001
       Stroke1 (0.1)79 (0.8)80 (0.7)0.0217
       Death/stroke/TIA/embolism6 (0.6)410 (4.0)416 (3.7)< 0.0001
       Bleeding2 (0.2)283 (2.8)285 (2.5)< 0.0001
       Hospitalization/ED visit for AF156 (16.8)2325 (22.6)2481 (22.1)< 0.0001
       Non-CV hospitalization/ED visit305 (32.8)4855 (47.3)5160 (46.0)< 0.001
      3-y outcome
       n56264246986
       Death8 (1.4)378 (5.9)386 (5.5)< 0.0001
       Stroke0 (0.0)119 (1.9)119 (1.7)0.0011
       Stroke/TIA/embolism/death10 (1.8)524 (8.2)534 (7.6)< 0.0001
       Bleeding16 (2.8)364 (5.7)380 (5.4)0.0047
       Hospitalization/ED visit for AF134 (23.8)2001 (31.1)2135 (30.6)0.0003
       Non-CV hospitalization/ED visit314 (55.9)4381 (68.2)4695 (67.2)< 0.0001
      Values are n (%), unless otherwise indicated.
      CV, cardiovascular; ED, emergency department; TIA, transient ischemic attack.
      Figure thumbnail gr4
      Figure 4Hazards of composite outcome (death/stroke/transient ischemic attack/embolism) at 3 years; hazards are adjusted for age and sex. AF, atrial fibrillation and atrial flutter; CI, confidence interval; HR, hazard ratio.
      Management strategies were then studied in this younger age group. Specifically, we evaluated the prescription and procedural utilization trends, but we did not undertake analyses examining the interaction between outcome and therapy, owing to the large number of confounding factors that could not be accurately adjusted for in the cohort. Tables 2 and 4 summarize catheter ablation and electrical cardioversion interventions at 1 year. In both the older and younger populations, electrical cardioversion was more commonly used for unexplained AF, whereas ablation was more commonly used for secondary AF. Specifically, 3 patients with unexplained AF (0.3%) underwent ablation within 1 year, vs 533 patients with secondary AF (1.7%; P < 0.001). Electrical cardioversion by 1 year occurred in 27.7% with unexplained AF vs 17.7% with secondary AF (P < 0.001). A rate-control strategy using atrioventricular nodal blockers was attempted in a small number of young patients with unexplained AF (Supplemental Tables S4-S6), with most beta-blocker prescriptions occurring in the first 30 days after diagnosis (166 of 223 patients; 74.4%). In young-onset secondary AF, beta-blockers were used in 37.7% at 30 days (3234 patients) and in 56.3% by 1 year (4836 patients) after diagnosis. All types of rate-control drugs were prescribed more often in secondary AF than in unexplained AF at 30 days and 1 year (P < 0.001) after diagnosis. Patients with unexplained AF were less likely to receive an anti-arrhythmic drug at all follow-up points examined (P < 0.001). Supplemental Table S4 summarizes OAC prescriptions in the young.

      Sex- and age-based trends by AF type, diagnosis, and outcomes

      We next assessed for sex- and age-based trends (Table 5; Supplemental Table S7). Women with unexplained AF were older (58 [IQR 40-69] vs 45 [IQR 34-59] years; P < 0.001), were more often diagnosed as outpatients (28% vs 17%; P < 0.001), and were more likely to experience the primary composite endpoint at 1 and 3 years, compared with men (2.7% vs 0.9%; P = 0.024 and 7.8% vs 2.6%; P = 0.002, respectively). However, after adjusting for age at diagnosis, women and men had similar outcomes (Fig. 4). There were also no significant differences based on sex for OAC prescription at 1 year (Supplemental Table S8). Women were more likely to receive calcium-channel blockers (10.8 vs 6.3%; P = 0.018) and digoxin (2.8 vs 0.7%; P = 0.009) in the first year after diagnosis. A higher proportion of men underwent electrical cardioversion, compared with women (31.2% vs 15.7% at 1year; P < 0.001). Hospitalization/ED visit for AF after index diagnosis were greater at 1 year in men vs women (17.7% vs 12.3%; P = 0.029), including among young patients with unexplained AF (18.2% vs 11.1%; P = 0.018). Age also predicted diagnosis and outcomes (Table 5; Fig. 4). When combining both AF classifications, those in the earlier-onset group (age ≤ 65 years) were more likely to be male (78.9 vs 54.7%; P < 0.001) and to be diagnosed in the emergency/inpatient setting than women. For unexplained AF, older-onset patients were more likely to suffer from the primary composite outcome than younger patients at 1 year (4.7 vs 0.6%; P < 0.001) and 3 years (13.2 vs 1.7%, P < 0.001). There were no significant differences in AF or noncardiovascular disease hospitalization/ED visit by age in follow-up (Table 5). As expected, OAC (38.0 vs 14.0%; P < 0.001), beta-blocker (37.4 vs 28.3%; P = 0.017), and calcium-channel blocker (15.1 vs 5.7%; P < 0.001) prescription occurred more in older patients with unexplained AF at 1 year than in younger AF patients (Supplemental Table S6).
      Table 5Characteristics of patients with unexplained atrial fibrillation and atrial flutter (AF) patients, stratified by age (young vs old) and by sex (women vs men)
      VariableAge ≤ 65 yAge > 65 yPWomen, all agesMen, all agesP
      n931214293852
      Age,y42 (32, 53)73 (68, 81)< 0.00158 (40, 69)45 (34, 57)< 0.001
      Sex (male)735 (78.9)117 (54.7)< 0.001
      Locale of diagnosis
       Specialist’s outpatient clinic160 (17.2)63 (29.4)< 0.00181 (27.6)142 (16.7)< 0.001
       ED673 (72.3)130 (60.7)184 (62.8)619 (72.7)
       Inpatient98 (10.5)21 (9.8)28 (9.6)91 (10.7)
      Residence
       Rural165 (17.7)42 (19.6)0.5151 (17.4)156 (18.3)0.73
       Urban766 (82.3)172 (80.4)242 (82.6)696 (81.7)
      Neighborhood household income in 2010, $75,684 (68,090, 96,257)72,369 (64,996, 90,935)0.0573,590 (65269, 94,410)75,406 (68,090, 96,257)0.16
      Electrical cardioversion
       7-d250 (26.9)23 (10.7)< 0.00142 (14.3)231 (27.1)< 0.001
       30-d257 (27.6)25 (11.7)< 0.00144 (15.0)238 (27.9)< 0.001
       1-y283 (30.4)29 (13.6)< 0.00146 (15.7)266 (31.2)< 0.001
      1-y outcome
       Death5 (0.5)7 (3.3)< 0.0015 (1.7)7 (0.8)0.20
       Stroke1 (0.1)1 (0.5)0.261 (0.3)1 (0.1)0.43
       Death/stroke/TIA/embolism6 (0.6)10 (4.7)< 0.0018 (2.7)8 (0.9)0.024
       Bleeding2 (0.2)1 (0.5)0.521 (0.3)2 (0.2)0.76
       Hospitalization/ED visit for AF156 (16.8)31 (14.5)0.4236 (12.3)151 (17.7)0.03
       Non-CV hospitalization/ED visit305 (32.8)57 (26.6)0.07995 (32.4)267 (31.3)0.73
      3-y outcome
       n572129166535
       Death8 (1.4)12 (9.3)< 0.0018 (4.8)12 (2.2)0.08
       Stroke/TIA/embolism/death10 (1.7)17 (13.2)< 0.00113 (7.8)14 (2.6)0.002
       Bleeding16 (2.8)5 (3.9)0.525 (3.0)16 (3.0)0.99
       Hospitalization/ED visit for AF136 (23.8)35 (27.1)0.4230 (18.1)141 (26.4)0.029
       Non-CV hospitalization/ED visit324 (56.6)66 (51.2)0.2692 (55.4)298 (55.7)0.95
      Values are n (%) or median (interquartile range), unless otherwise indicated.
      CV, cardiovascular; ED, emergency department; TIA, transient ischemic attack.

      Discussion

      This population study demonstrates that unexplained AF, defined using stringent contemporary criteria, has a lower than previously reported incidence and carries a small risk of serious complications during short- and medium-term follow-up. However, acute hospital encounters for AF and noncardiovascular diagnoses frequently follow the unexplained AF diagnosis. Important sex-based differences exist, highlighted by a disproportionately young age at onset in men, who carry a higher chance of AF re-presenting during follow-up. However, no sex-based differences for the primary outcome existed after adjusting for age. Collectively, these data suggest that unexplained AF is less common than previously reported, and it has unique demographic characteristics and outcomes that warrant further study.
      In keeping with established trends in all-cause AF, the impact of male sex on unexplained AF susceptibility was pronounced in our study, with a 13-year lower median age of disease onset. Although previous studies have not clearly identified biological explanations for sex differences, elevated bioavailable testosterone appeared to increase AF risk in the Multi-Ethnic Study of Atherosclerosis, and X-linked recessive factors may play a role in kindred AF.
      • O'Neal W.T.
      • Nazarian S.
      • Alonso A.
      • et al.
      Sex hormones and the risk of atrial fibrillation: The Multi-Ethnic Study of Atherosclerosis (MESA).
      ,
      • Chen L.Y.
      • Herron K.J.
      • Tai B.C.
      • Olson T.M.
      Lone atrial fibrillation: influence of familial disease on gender predilection.
      In our study, we could not rule out lifestyle as an environmental contributor, such as potential sex-based differences in alcohol intake, obesity, exercise, and smoking. Despite observing a preponderance of men with earlier-onset unexplained AF, women were at a similar risk for death, stroke, TIA, and systemic thromboembolism, after adjusting for age at diagnosis. Recent studies on nonvalvular AF have attempted to clarify the controversial role of sex on stroke risk.
      • Schnabel R.B.
      • Pecen L.
      • Ojeda F.M.
      • et al.
      Gender differences in clinical presentation and 1-year outcomes in atrial fibrillation.
      ,
      • Arnson Y.
      • Hoshen M.
      • Berliner Senderey A.
      • et al.
      Comparing management and outcomes in men and women with nonvalvular atrial fibrillation: data from a population-based cohort.
      These data show that men and women face a similar risk of stroke, with the exception of elderly women, who are at slightly higher risk.
      • Arnson Y.
      • Hoshen M.
      • Berliner Senderey A.
      • et al.
      Comparing management and outcomes in men and women with nonvalvular atrial fibrillation: data from a population-based cohort.
      Important to note is that we found no sex-based trends in OAC prescription. However, digoxin and calcium-channel blockers were more often used in women; these are traditionally viewed as second-line rate-control agents. We could not determine whether physician bias or beta-blocker intolerance/refractoriness drove this difference.
      The incidence of unexplained and secondary AF rose throughout the study period. This increase may be due to recent increasing awareness and subclinical detection of AF. Another possibility is that metabolic risk factors, such as obesity, were incompletely coded and contributed to this trend. Important to note is that when we applied a more stringent definition to unexplained AF, including young age of onset, the incidence compared to secondary AF was lower (2.8% of all new AF diagnoses) than historical estimates (up to 30% of all AF diagnoses),
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      and was in keeping with recent registry data (3%).
      • Weijs B.
      • Pisters R.
      • Nieuwlaat R.
      • et al.
      Idiopathic atrial fibrillation revisited in a large longitudinal clinical cohort.
      This variation is likely due to under-recognized secondary AF triggers and use of inconsistent definitions of unexplained AF over time.
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      Indeed, the very existence of truly unexplained, lone, or idiopathic AF is increasingly being challenged, especially with the advent of complex genetic analysis.
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      ,
      • Khera A.V.
      • Chaffin M.
      • Aragam K.G.
      • et al.
      Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
      The incidence of unexplained AF, and the growing role of genetic testing, has important clinical relevance. Emerging data show that many young patients and their families afflicted by early-onset AF have predisposing Mendelian
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      and complex genetic substrate.
      • Khera A.V.
      • Chaffin M.
      • Aragam K.G.
      • et al.
      Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
      In the past few years, truncating variants in the gene encoding Titin have emerged as strong risk factors for unexplained AF, especially in the young.
      • Ahlberg G.
      • Refsgaard L.
      • Lundegaard P.R.
      • et al.
      Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation.
      ,
      • Choi S.H.
      • Weng L.C.
      • Roselli C.
      • et al.
      Association between titin loss-of-function variants and early-onset atrial fibrillation.
      Similarly, polygenic risk models suggest that early-onset unexplained AF can be accounted for by the cumulative burden of common susceptibility variants.
      • Khera A.V.
      • Chaffin M.
      • Aragam K.G.
      • et al.
      Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
      Future opportunities to detect unexplained early-in-life AF may improve outcomes and lead to tailored therapy.
      • Piccini J.P.
      • Abraham W.T.
      • Dufton C.
      • et al.
      Bucindolol for the maintenance of sinus rhythm in a genotype-defined HF population: the GENETIC-AF trial.
      The present study provides an estimate of the number of AF cases that could benefit from further genomic analysis. We argue that the emerging relevance of genetic testing in this field necessitates that unexplained AF be defined more stringently, to illuminate who is most likely to benefit from clinically indicated genetic sequencing, family screening, and eventually precision therapy.

      Limitations

      This is a population-level study of retrospective administrative data. The amount, frequency, and symptoms of AF could not be ascertained. We could not adjust for some environmental contributors to AF such as alcohol intake, exercise, diet, and smoking, as they are either poorly coded or not coded at all. Similarly, the ICD codes for comorbidities and procedures were not universally validated; however, AF codes have strong positive and negative predictive value in validation cohorts.
      • Cozzolino F.
      • Montedori A.
      • Abraha I.
      • et al.
      A diagnostic accuracy study validating cardiovascular ICD-9-CM codes in healthcare administrative databases. The Umbria Data-Value Project.
      ,
      • Rix T.A.
      • Riahi S.
      • Overvad K.
      • et al.
      Validity of the diagnoses atrial fibrillation and atrial flutter in a Danish patient registry.
      ,
      • Yao R.J.R.
      • Andrade J.G.
      • Deyell M.W.
      • et al.
      Sensitivity, specificity, positive and negative predictive values of identifying atrial fibrillation using administrative data: a systematic review and meta-analysis.
      To increase the probability that unexplained AF was truly unexplained/idiopathic, we classified all cases with an identifiable AF-predisposing condition as being secondary AF. However, some of these conditions may not contribute to the pathogenesis of AF. Thus, patients may have been included in the secondary AF group who did not develop AF due to a comorbidity (eg, hypothyroidism or minor infection), meaning that the pathogenesis of AF was unexplained. Unfortunately, it is not possible to determine the precise cause of AF in many clinical circumstances, regardless of study design.
      The definition of the maximal age at which unexplained AF can be diagnosed remains ambiguous. Here, we used a cutoff of age 65 years to define young-onset AF, because this was similar to the age used in recent classifications,
      • Jahangir A.
      • Lee V.
      • Friedman P.A.
      • et al.
      Long-term progression and outcomes with aging in patients with lone atrial fibrillation: a 30-year follow-up study.
      ,
      • Wyse D.G.
      • Van Gelder I.C.
      • Ellinor P.T.
      • et al.
      Lone atrial fibrillation: Does it exist?.
      and it reflects the age at which OACs are indicated in Canada, regardless of other stroke risk factors.
      • Andrade J.G.
      • Verma A.
      • Mitchell L.B.
      • et al.
      2018 Focused Update of the Canadian Cardiovascular Society Guidelines for the Management of Atrial Fibrillation.
      These challenges related to disease definitions and coding consistency are inherent to all administrative population datasets, and the trends described here are hypothesis-generating. The data may be most useful to clinicians and researchers needing to understand the approximate number and proportion of AF patients who may benefit from future biological or genetic studies aimed at identifying factors involved in the pathogenesis of unexplained AF.
      When conducting event analyses, we adjusted for the 2 covariates most likely to influence outcomes (age and sex), based on existing data. Owing to the small population of patients with unexplained AF and the limited number of patients with composite outcome events at 3 years in this group (27 patients), we could not adjust for additional covariates in our modeling. Death was considered to be a competing risk for repeat AF healthcare encounters (Supplemental Fig. S2). However, for the exploratory outcome of repeat non–AF related hospital encounters, a competing risk model was not constructed because mortality was very low at 3 years in the unexplained AF group (1.7%), and death as a competing risk did not significantly influence the primary outcome or repeat AF encounter outcome. The secondary AF group may have shown a higher probability of being rehospitalized for a non-AF diagnosis, had a competing risk model been developed. However, secondary AF was not the focus of the present study.

      Conclusions

      The incidence of unexplained AF is lower than that previously reported when a stringent contemporary definition of the condition is applied. Unexplained AF is a predominantly male disorder complicated by a high rate of recurrent hospital utilization but low rates of stroke, TIA, systemic thromboembolism, and death over 3 years of follow-up. Additional studies are needed to provide an explanation for AF in these individuals, and to identify factors that lead to recurrent hospitalization.

      Funding Sources

      The Canadian Arrhythmia Network (CANet) and the University Hospital Foundation supported this study. T.M.R. is funded by the University of British Columbia Clinician Investigator Program, and is a Friedman Scholar in Health and a George Mines Traveling Fellow in Cardiac Electrophysiology. A.D.K. receives support from the Sauder Family and Heart and Stroke Foundation Chair in Cardiology (Vancouver, British Columbia), the Paul Brunes Chair in Heart Rhythm Disorders (Vancouver, British Columbia), and the Paul Albrechsten Foundation (Winnipeg, Manitoba). Z.L. received support from the Michael Smith Foundation for Health Research and the Cardiology Academic Partnership Plan, University of British Columbia.

      Disclosures

      The authors have no conflicts of interest to disclose. This study is based in part on data provided by Alberta Health. The interpretation and conclusions contained herein are those of the researchers and do not necessarily represent the views of the Government of Alberta. Neither the Government of Alberta nor Alberta Health expresses any opinion in relation to this study.

      Supplementary Material

      References

        • Zoni-Berisso M.
        • Lercari F.
        • Carazza T.
        • Domenicucci S.
        Epidemiology of atrial fibrillation: European perspective.
        Clin Epidemiol. 2014; 6: 213-220
        • Fox C.S.
        • Parise H.
        • D'Agostino Sr., R.B.
        • et al.
        Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring.
        JAMA. 2004; 291: 2851-2855
        • Fumagalli S.
        • Said S.A.M.
        • Laroche C.
        • et al.
        Age-related differences in presentation, treatment, and outcome of patients with atrial fibrillation in Europe: The EORP-AF General Pilot Registry (EURObservational Research Programme-Atrial Fibrillation).
        JACC Clin Electrophysiol. 2015; 1: 326-334
        • Brand F.N.
        • Abbott R.D.
        • Kannel W.B.
        • Wolf P.A.
        Characteristics and prognosis of lone atrial fibrillation: 30-year follow-up in the Framingham Study.
        JAMA. 1985; 254: 3449-3453
        • Jahangir A.
        • Lee V.
        • Friedman P.A.
        • et al.
        Long-term progression and outcomes with aging in patients with lone atrial fibrillation: a 30-year follow-up study.
        Circulation. 2007; 115: 3050-3056
        • Wyse D.G.
        • Van Gelder I.C.
        • Ellinor P.T.
        • et al.
        Lone atrial fibrillation: Does it exist?.
        J Am Coll Cardiol. 2014; 63: 1715-1723
        • Andrade J.G.
        • Verma A.
        • Mitchell L.B.
        • et al.
        2018 Focused Update of the Canadian Cardiovascular Society Guidelines for the Management of Atrial Fibrillation.
        Can J Cardiol. 2018; 34: 1371-1392
        • Cozzolino F.
        • Montedori A.
        • Abraha I.
        • et al.
        A diagnostic accuracy study validating cardiovascular ICD-9-CM codes in healthcare administrative databases. The Umbria Data-Value Project.
        PLoS One. 2019; 14e0218919
        • Rix T.A.
        • Riahi S.
        • Overvad K.
        • et al.
        Validity of the diagnoses atrial fibrillation and atrial flutter in a Danish patient registry.
        Scan Cardiovasc J. 2012; 46: 149-153
        • Roston T.M.
        • Tran D.T.
        • Sanatani S.
        • et al.
        A population-based study of syncope in the young.
        Can J Cardiol. 2018; 34: 195-201
        • World Health Organization Collaborating Centre for Drug Statistics Methodology (WHO-CCDS)
        Guidelines for ATC Classification and DD Assignment.
        9th ed. WHO-CCDS, Oslo2016
        • Canadian Institute of Health Information (CIHI)
        Canadian Classification of Health Interventions. Vol 3. CIHI, Ottawa2012
        • O'Neal W.T.
        • Nazarian S.
        • Alonso A.
        • et al.
        Sex hormones and the risk of atrial fibrillation: The Multi-Ethnic Study of Atherosclerosis (MESA).
        Endocrine. 2017; 58: 91-96
        • Chen L.Y.
        • Herron K.J.
        • Tai B.C.
        • Olson T.M.
        Lone atrial fibrillation: influence of familial disease on gender predilection.
        J Cardiovasc Electrophysiol. 2008; 19: 802-806
        • Schnabel R.B.
        • Pecen L.
        • Ojeda F.M.
        • et al.
        Gender differences in clinical presentation and 1-year outcomes in atrial fibrillation.
        Heart. 2017; 103: 1024-1030
        • Arnson Y.
        • Hoshen M.
        • Berliner Senderey A.
        • et al.
        Comparing management and outcomes in men and women with nonvalvular atrial fibrillation: data from a population-based cohort.
        JACC Clin Electrophysiol. 2018; 4: 604-614
        • Weijs B.
        • Pisters R.
        • Nieuwlaat R.
        • et al.
        Idiopathic atrial fibrillation revisited in a large longitudinal clinical cohort.
        Europace. 2012; 14: 184-190
        • Khera A.V.
        • Chaffin M.
        • Aragam K.G.
        • et al.
        Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
        Nat Genet. 2018; 50: 1219-1224
        • Ahlberg G.
        • Refsgaard L.
        • Lundegaard P.R.
        • et al.
        Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation.
        Nat Comm. 2018; 9: 4316
        • Choi S.H.
        • Weng L.C.
        • Roselli C.
        • et al.
        Association between titin loss-of-function variants and early-onset atrial fibrillation.
        JAMA. 2018; 320: 2354-2364
        • Piccini J.P.
        • Abraham W.T.
        • Dufton C.
        • et al.
        Bucindolol for the maintenance of sinus rhythm in a genotype-defined HF population: the GENETIC-AF trial.
        JACC Heart Fail. 2019; 7: 586-598
        • Yao R.J.R.
        • Andrade J.G.
        • Deyell M.W.
        • et al.
        Sensitivity, specificity, positive and negative predictive values of identifying atrial fibrillation using administrative data: a systematic review and meta-analysis.
        Clin Epidemiol. 2019; 11: 753-767