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Medicina Clínica (English Edition) Effects of exercise intervention on exercise capacity and cardiopulmonary functi...
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Vol. 164. Issue 11.
(June 2025)
Original article
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Effects of exercise intervention on exercise capacity and cardiopulmonary function in patients with atrial fibrillation: A randomized controlled trial systematic review and meta-analysis
Efectos de la intervención con ejercicio sobre la capacidad de ejercicio y la función cardiopulmonar en pacientes con fibrilación auricular: una revisión sistemática y metaanálisis de ensayos controlados aleatorizados
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Zhang Shuaia, Mao Su Jiea, Xiao Kai Wenb, Hong Xuc,
Corresponding author
747971257@qq.com

Corresponding author.
, Lu Yuanc
a Graduate Development, Harbin Sport University, Harbin, Heilongjiang, China
b Chinese Fencing Academy, Nanjing Sport Institute, Nanjing, Jiangsu, China
c Nanjing Polytechnic Institute Sports Work Department, Nanjing, Jiangsu, China
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Table 1. Table of included literature characteristics.
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Table 2. Literature quality evaluation.
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Table 3. Summary of subgroup analysis results.
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Abstract
Background

Atrial fibrillation (AF) is a common cardiac arrhythmia that significantly impacts the cardiopulmonary function and quality of life of patients. Despite various treatment strategies, non-pharmacological interventions, particularly exercise interventions, have gained attention in recent years.

Objective

Through systematic review and meta-analysis, this study explores the impact of physical activity on the exercise capacity and quality of life of AF patients. It assesses the safety, clinical outcomes, and physiological mechanisms of exercise intervention in the treatment of AF.

Methods

The systematic review and individual patient data (IPD) meta-analysis method were employed, following the PRISMA-IPD guidelines, for literature selection, data extraction, and quality assessment. The analysis focused on the impact of exercise on the cardiopulmonary function and quality of life of AF patients in randomized controlled trials.

Results

A total of 12 randomized controlled trials involving 287 AF patients were included. Meta-analysis demonstrated a significant improvement in the 6-minute walk test capacity (SMD=87.87, 95% CI [42.23, 133.51]), static heart rate improvement (SMD=−7.63, 95% CI [−11.42, −3.85]), and cardiopulmonary function enhancement (SMD=2.37, 95% CI [0.96, 3.77]) due to exercise. There was also a significant improvement in the quality of life (SMD=0.720, 95% CI [0.038, 1.402]).

Conclusion

Exercise has a significant effect on improving exercise capacity and cardiopulmonary function in patients with atrial fibrillation. Particularly, high-intensity exercise training has a more significant impact on improving cardiopulmonary function and exercise capacity, emphasizing the importance of personalized exercise plans in enhancing the cardiopulmonary health of AF patients. Further research is needed to explore the effects of exercise on improving the quality of life in the future.

PROSPERO ID: CRD2023493917.

Keywords:
Atrial fibrillation
Exercise rehabilitation
Non-pharmacological treatment
Randomized controlled trial
Exercise capacity
Resumen
Antecedentes

La fibrilación auricular (FA) es una arritmia cardíaca común que afecta significativamente la función cardiopulmonar y la calidad de vida de los pacientes. A pesar de diversas estrategias de tratamiento, las intervenciones no farmacológicas, en particular las intervenciones con ejercicio, han ganado atención en los últimos años.

Objetivo

A través de una revisión sistemática y un metaanálisis, este estudio explora el impacto de la actividad física sobre la capacidad de ejercicio y la calidad de vida de los pacientes con FA. Se evalúan la seguridad, los resultados clínicos y los mecanismos fisiológicos de la intervención con ejercicio en el tratamiento de la FA.

Métodos

Se emplearon el método de revisión sistemática y metaanálisis de datos individuales de pacientes (IPD), siguiendo las guías PRISMA-IPD, para la selección de la literatura, la extracción de datos y la evaluación de la calidad. El análisis se centró en el impacto del ejercicio en la función cardiopulmonar y la calidad de vida de los pacientes con FA en ensayos controlados aleatorizados.

Resultados

Se incluyeron un total de 12 ensayos controlados aleatorizados que involucraron a 287 pacientes con FA. El metaanálisis demostró una mejora significativa en la capacidad del test de caminata de 6 minutos (SMD=87,87, IC del 95% [42,23, 133,51]), mejora en la frecuencia cardíaca en reposo (SMD=−7,63, IC del 95% [−11,42, −3,85]) y mejora de la función cardiopulmonar (SMD=2,37, IC del 95% [0,96, 3,77]) debido al ejercicio. También se observó una mejora significativa en la calidad de vida (SMD=0,720, IC del 95% [0,038, 1,402]).

Conclusión

El ejercicio tiene un efecto significativo en la mejora de la capacidad de ejercicio y la función cardiopulmonar en pacientes con FA. En particular, el entrenamiento de alta intensidad tiene un mayor impacto en la mejora de la función cardiopulmonar y la capacidad de ejercicio, enfatizando la importancia de los planes de ejercicio personalizados para mejorar la salud cardiopulmonar de los pacientes con FA. Se necesita más investigación para explorar los efectos del ejercicio en la mejora de la calidad de vida en el futuro.

ID de PROSPERO: CRD2023493917.

Palabras clave:
Fibrilación auricular
Rehabilitación con ejercicio
Tratamiento no farmacológico
Ensayo controlado aleatorizado
Capacidad de ejercicio
Full Text
Introduction

AF is a common cardiac arrhythmia classified into first diagnosis, paroxysmal, persistent, and permanent forms.1 Typical symptoms of AF patients include palpitations, dyspnea, fatigue, dizziness, and syncope, exhibiting significant individual variations.2 Compared to other diseases, AF patients are more prone to recurrence, and long-term symptoms such as palpitations and dyspnea can lead to decreased activity capacity and reduced quality of life.3 With the aging population, the incidence of AF is increasing year by year, leading to significant public health issues such as atrial remodeling, myocardial fibrosis, coronary heart disease, myocardial infarction, and heart failure.4 The World Health Organization predicts that the incidence of AF will triple in the next thirty years, termed the “atrial fibrillation epidemic.” It is estimated that by 2050, Asia will have over 70million AF patients.5

In terms of AF treatment, it is generally divided into two major strategies: surgical treatment, mainly including catheter ablation and maze surgery.6 Catheter ablation obstructs abnormal electrical signals by burning or freezing specific areas of the heart, while maze surgery redirects electrical signal pathways by cutting and suturing heart tissue, restoring normal rhythm.7 The main principles of pharmacological treatment for AF are controlling ventricular rate, protecting cardiac function, restoring and maintaining sinus rhythm, preventing thromboembolic events, and slowing atrial electrical and structural remodeling.8

Due to the complexity of the AF mechanism, various comorbidities in patients, and the limited improvement of these methods mainly on pathological symptoms, patients are often unwilling to accept pharmacological treatment.8 Therefore, non-pharmacological treatment methods are particularly important, such as dietary control, health management, physical therapy, and exercise rehabilitation. Among many non-pharmacological treatment methods, physical activity is one of the effective ways to improve AF patients.9 Regular exercise can not only effectively prevent the occurrence of AF but also alleviate symptoms in AF patients (such as improving cardiac function, reducing symptoms such as palpitations and dyspnea), and reduce related complications.10 In addition, regular exercise can enhance the overall health of patients, positively influencing mental health, and reducing symptoms of depression and anxiety.11

The effectiveness of exercise intervention for AF has been confirmed to a certain extent.12 Moderate physical activity has shown a positive role in controlling cardiovascular risk factors and reducing the risk of AF, but long-term endurance training may increase the risk of AF by increasing atrial size.13 A study showed that athletes engaged in long-term exercise had a higher incidence of AF than the general population.14 Although some studies have shown the benefits of physical exercise on the exercise capacity and cardiopulmonary adaptability of AF patients, there is currently a lack of support from large-scale randomized exercise training trials.15 Existing studies are mostly single-center trials, secondary analyses, and observational studies.16 Therefore, more high-quality research is needed in this field to establish the safety of exercise intervention in AF treatment, improvement of quality of life, clinical outcomes, and the impact of related physiological mechanisms.

In view of this, this study aims to explore in-depth the impact of physical activity on the exercise capacity and quality of life of AF patients through systematic review and meta-analysis. By providing more advanced evidence, the study aims to draw clear conclusions, explore the safety of exercise intervention in AF treatment, improvements in quality of life, clinical outcomes, and the role of relevant physiological mechanisms.

Methods

This study conducted a systematic review and meta-analysis to comprehensively assess the impact of exercise on the improvement of physical activity in patients with AF. Adhering to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses of individual participant data (PRISMA) guidelines to ensure the rigor and transparency of the research.17

To enhance the study's verifiability, we registered it on the PROSPERO international prospective systematic review registration platform with the registration ID: CRD2023493917.18

Information sources and search strategy

To ensure the comprehensiveness and systematic nature of literature retrieval, we employed a search strategy covering multiple databases, including PubMed, Embase, Cochrane Library, and Web of Science. Additionally, to ensure the inclusiveness of the literature, we traced relevant randomized controlled trial literature based on published reviews or meta-analyses.

The search strategy for this study adhered to the PICO framework, with “atrial fibrillation” defined as the patient population (P) and “exercise intervention” as the intervention (I). To ensure comprehensive coverage, Medical Subject Headings (MeSH) terms were employed to capture all relevant concepts. For atrial fibrillation, these terms encompassed a range of synonyms, including “persistent atrial fibrillation,” “paroxysmal atrial fibrillation,” and “familial atrial fibrillation.” Similarly, for physical activity, terms such as “aerobic exercise,” “isometric exercises,” and “exercise training” were incorporated. The search was designed to maximize precision and breadth, with no restrictions imposed on the control group, outcome measures, or types of studies. Boolean operators (AND) were used to combine terms, ensuring robust retrieval of relevant data. The search was restricted to English-language publications, focused exclusively on randomized controlled trials (RCTs), and included studies published up to December 31, 2022. Detailed documentation of the search process, including search dates, databases used, the number of results retrieved, and manually screened reference lists, was maintained to ensure methodological rigor.

Eligibility criteria and study selectionInclusion criteria

  • a.

    Study subjects: Patients with atrial fibrillation;

  • b.

    Intervention group: Patients with atrial fibrillation receiving exercise intervention;

  • c.

    Study type: Randomized controlled trial;

  • d.

    Language: English literature.

Exclusion criteria

  • a.

    Animal experiments;

  • b.

    Meta-analyses, reviews, conference abstracts, pathology reports, letters, guidelines.

Study selection

This study employed a two-stage selection process. Based on the predefined search strategy, relevant literature was retrieved from various databases. Titles, keywords, and abstracts of the downloaded literature were imported into Endnote X20 software to remove duplicates. Initial screening was conducted by reading the titles and abstracts of each article, making a preliminary judgment on whether it met the inclusion criteria. According to the inclusion and exclusion criteria established for this study, studies that were obviously irrelevant or did not meet the inclusion criteria were excluded. The second screening involved a full-text review of the selected literature to further assess its compliance with the inclusion criteria.

Data collection process and risk bias assessment

MSJ and XKW were responsible for extracting the pre- and post-test values from the full text. In cases where there were disputes over certain data points between MSJ and XKW, XH made the final judgment and decision. Initial screening of the literature, to determine articles that met the research criteria, was independently carried out by MSJ and XKW. The extracted information included author, publication year, country, intervention method (specific physical training methods), intervention duration (duration of each training session), intervention period, control group method, subject age, test indicators, mean outcome indicators (MEAN), and standard deviation (SD). MSJ and XKW independently completed data extraction and recording, and then cross-checked to ensure accuracy. Any inconsistencies or disputed data points were reviewed and decided upon by XH. The collected data were organized into tabular form for further analysis and comparison.

Extraction of MEAN and SD values for study indicators was used for the synthesis of effect size statistics. Author, publication year, intervention time, intervention period, subject age, intervention method, country, and control group method were extracted to complete the inclusion literature feature table.

In this study, we used a modified PEDro scale to assess the quality of randomized controlled trial literature.19 The PEDro scale is designed for a quick assessment of the quality of randomized clinical studies in the PEDro database. The total score on the PEDro scale is 11 points. According to our assessment criteria, studies with scores below 5 are considered to be of medium to low quality, while studies with scores of 5 or above are considered high quality.

Outcome assessment

6-Minute walk test; Resting heart rate; Cardiopulmonary function; Quality of life.

Synthesis methods

In this study, a heterogeneity test was conducted for each indicator to assess the variability between study results. The I2 statistic was used to measure the degree of this difference. When I250%, a random-effects model was used for analysis. Conversely, if I2<50%, a fixed-effects model was used for analysis.20

The analysis was completed using Stata 15.1 software. Weighted Mean Difference (WMD) was used as the primary statistical indicator for combining inter-group mean differences, and weights were calculated. P<0.05 was considered the criterion for determining statistically significant differences. When P>0.05, there was no statistical significance.

All models in this study underwent sensitivity analysis to assess the stability of the combined effect size results. Publication bias was assessed using Egger's test, and if publication bias was present, trimming was performed to correct for publication bias.

Research resultsStudy selection and characteristics

The literature selection process in this study follows the systematic review and meta-analysis process outlined in the PRISMA statement. During the initial retrieval phase, a total of 3953 articles were retrieved from four electronic databases: PubMed, Web of Science, EBSCOhost, and Cochrane Library. After removing duplicates and conducting preliminary and secondary screenings based on inclusion criteria, a total of 12 articles were finally included for systematic review and meta-analysis (Fig. 1, literature search flowchart).

Fig. 1.

PRISMA flow diagram of study selection.

This study included 12 randomized controlled trials on exercise intervention for AF patients, encompassing research from multiple countries with a total of 287 participants. Geographically, three studies were published in Denmark, two in Norway, and one study from each of the remaining countries. Regarding the distribution of intervention periods, seven studies adopted a 12-week training period, two studies used 8 weeks and 16 weeks, respectively, and two studies extended to 24 weeks. The implemented intervention measures included aerobic exercise, resistance training, stretching exercises, and yoga. The covered categories of AF in the studies were diverse, including permanent AF, chronic AF, paroxysmal AF, and non-permanent AF. The detailed characteristics of each study are listed in the literature feature table (Table 1).

Table 1.

Table of included literature characteristics.

Author  Year  Country  Whether to take medicine  AF state  Age  Gender  Number of intervention group  Intervention methods  Intervention cycle  Intervention intensity  Frequency of intervention  Control group mode  Number of control group  Outcome indicators 
Malmo  2016  Norway  NA  Non-permanent AF  RG: 56±8CG: 62±RG: 20/6CG: 22/3  26  Aerobic interval training  12 weeks  60–70% of maximal heart rate obtained  3 times a week 10min/times  Regular exercise  25  On time in AF symptoms cardiovascular health QoL 
JOENSEN  2019  Denmark  NA  Patients with paroxysmal or persistent atrial fibrillation  IG: 62.2±10CG: 60.2±8.9  IG: 17/11CG: 17/7  28  Aerobics  12 weeks  ≥70% of maximum exercise  1-h sessions twice a week  Standard care  24  QoL physical exercise capacity 
Osbak  2011  Denmark  ACE-1ATIIA Digoxin  Permanent AF  AG: 69.5±7.3CG: 70.9±8.3  AG: 18/6CG: 17/6  24  Aerobic exercise training  12 weeks  70% of maximal exercise capacity  60min 3 times weekly  Habitual physical activity  23  Exercise capacity 6-minute walk test cardiac output quality of life natriuretic peptides 
Osbak  2012  Denmark  ACE-1, ATIIA Digoxin  Permanent AF  AG: 69.5±7.3CG: 70.9±8.3  AG: 18/6CG: 17/6  24  Aerobic exercise training  12 weeks  70% of maximal exercise capacity  60min 3 times weekly  Habitual physical activity  23  muscle strength body composition exercise capacity quality of life 
Zeren  2016  Turkey  Beta blocker Ca+2 channel blocker Metformin Sulfonylurea Digoxin Diuretics Statin Nitrate  Permanent AF  TG: 66.18±8.76CG: 67.06±6.39  TG: 8/9CG: 9/7  17  Inspiratory muscle training  12 weeks  30% of maximal inspiratory pressure  15min twice a day, 7days a week  Standard medical treatment only  16  Pulmonary function respiratory muscle strength 
Hegbom  2006  Norway  digitoxin beta-blocker Ca2+ antagonist  Chronic atrial fibrillation (AF)  TG: 62±7CG: 65±TG: 13/0CG: 13/2  13  Aerobic exercise muscle strengthening.  2 months  Aerobics at 70–90% of maximal heart rate  1.25h 3 days a week    15  Exercise capacity quality of life (QOL) 
Kato  2019  Japan  Sodium channel blocker Beta-blocker Amiodarone Calcium channel blocker Digoxin Warfarin DOAC Diuretics ARB or ACEI  Permanent AF  RG: 67±10CG: 65±RG: 20/8CG: 28/3  28  Endurance resistance training  6 months  Endurance and resistance training with moderate intensity  2–3 times per week  Usual care  31  Exercise capacity inflammatory status cardiac function 
Pippa  2007  Italy  NA  Chronic AF  TG: 68.3±7.2CG: 67.8±9.1  TG: 14/8CG: 16/5  22  Qi gong training  16 weeks  NA  Two 90-min sessions per week  NA  21  6-minute walk test 
Wahlstrom  2016  Sweden  Beta-blockers Calcium-channel blockers ACE inhibitor Statins Warfarin Aspirin  Paroxysmal AF  YG: 64±7CG: 63±YG: 16/17CG: 26/10  33  Yoga  12 weeks  NA  Sessions once a week  Standard treatment  36  QoL, blood pressure and heart rate 
Nourmohammadi  2017  Iran  Antiplatelet Flecainide Amiodarone Sotalol Digoxin Statin Warfarin  Permanent AF  EG: 57.2±7.4CG: 59.9±7.5  EG: 10/15CG: 13/12  25  Aerobic  8 weeks  Intensity of 40–50 percent of maximum oxygen consumption or heart rate  2 sessions a week 60min/session  Routine care  25  QOL 
Bittman  2022  Canada  Amiodarone Beta-blocker Diabetes medication  Nonpermanent AF  IG: 63.7±8.6CG: 61.0±9.7  IG: 23/11CG: 21/17  34  Interval training  6 months  Moderate-intensity interval training  40-min sessions/wk  Usual care  38  QoL 
Alves  2022  Brazil  ACEI Digoxin Spironolactone Amiodarone Amlodipine b-Blocker Diuretic  Permanent AF  EG: 58±3CG: 58±EG: 13/0CG: 13/0  13  Aerobic training  12 weeks  Intensity controlled from 14 to 16 by the Borg Effective Subjective Effort Scale  3 weekly sessions of 60min  Usual care  13  Exercise capacity quality of life cardiac function 
Literature quality assessment

The methodological quality of the included literature in this study was generally moderate, with scores ranging from 3 to 6 out of a maximum score of 11. The studies by Malmo (2016) and Zeren (2016) received the highest scores, each with 6 points, indicating that these studies performed well in random allocation, baseline similarity, participant blinding, and retention rate. However, they showed shortcomings in therapist blinding, assessor blinding, and variability and validity measurements. JOENSEN (2019) and Osbak (2011) scored 5 points, meeting all criteria except blinding and intention-to-treat analysis. Other studies such as Osbak (2012), Hegbom (2006), and Kato (2019) scored 4 points, revealing deficiencies in participant blinding and retention rate. Pippa (2007) and Wahlstrom (2016) scored the lowest, with 3 points, not meeting several criteria, especially in baseline similarity, blinding, and variability measurements. Although all studies met eligibility and random allocation requirements, there were significant differences in other methodological quality aspects, potentially impacting the robustness of the study results (Table 2).

Table 2.

Literature quality evaluation.

Author  Year  Eligibility criteria  Random allocation  Concealed allocation  Similarity baseline  Subject blinding  Therapist blinding  Assessor blinding  >85% retention  Intention-to-treat  Between-group comparisons  Point and variability measures  Total score 
                           
Malmo  2016 
JOENSEN  2019 
Osbak  2011 
Osbak  2012 
Zeren  2016 
Hegbom  2006 
Kato  2019 
Pippa  2007 
Wahlstrom  2016 
Nourmohammadi  2017 
Bittman  2022 
Alves  2022 
Meta-analysis results6-Minute walk test

This indicator included a total of 5 studies, with an I2 of 72.9%, so a random-effects model was used. The analysis results showed a significant improvement in the 6-minute walk test ability for AF patients in the exercise group compared to the control group, with a significant effect size (SMD=87.87, 95% CI [42.23, 133.51], P<0.05) (Fig. 2). This indicates that exercise significantly enhances the walking ability of AF patients. Sensitivity analysis confirmed the stability of the results, SMD=87.87, 95% CI [42.23, 133.51].

Fig. 2.

Forest plots and subgroup analyses. (a) Forest plot for 6-minute walk test. (b) Forest plot for resting heart rate. (c) Forest plot for cardiopulmonary function. (d) Forest plot for quality of life.

Intervention Period Subgroup Analysis included two subgroups of 12 weeks and 24 weeks. The combined effect size for the 12-week intervention was SMD=74.13, 95% CI [28.42, 119.85], P<0.05; for the 24-week intervention, the combined effect size was SMD=151, 95% CI [85.60, 216.40], P<0.05. Both subgroups showed positive effects, indicating that exercise can improve the 6-minute walk test results regardless of the intervention duration, and the longer the intervention time, the better the effect, as shown in Table 3. Exercise intensity subgroup analysis indicated that groups with intensity less than or equal to 50% showed no significant effect (P>0.05), while groups with intensity greater than 50% had a significant effect size (SMD=86.63, 95% CI [29.46, 143.79], P<0.05), suggesting that high-intensity exercise contributes to improving the 6-minute walk ability of AF patients. According to the country subgroup analysis, studies from Turkey and Japan showed no significant difference (P>0.05), while studies from Denmark and Italy had significant results, with SMDs of 115.90, 95% CI [78.14, 153.67] and SMD=151.00, 95% CI [85.60, 216.40], P<0.05 (Table 3). The publication bias analysis chart also shows a relatively stable state (Fig. 3).

Table 3.

Summary of subgroup analysis results.

Index  Title  Group  No  SMD  95%CI  Weight  P  I2 
QolAge<60  −0.68  −23.37, 28.01  36.74  >0.05  99.5% 
≥60  3.3  −3.58, 10.15  63.28  >0.05  − 
Cycle12 weeks  −3.5  −19.93, 12.93  56.17  <0.05  95.4% 
24 weeks  4.71  −6.12, 15, 54  21.39  >0.05  – 
72 weeks  0.26  −19.69, 20.21  10.12  >0.05  – 
8 weeks  20.4  18.96, 21.84  12.32  <0.05  – 
CountryNorway  2.38  −1.71, 6.47  12.22  >0.05  – 
Danmark  3.38  −6.01, 12.78  41.15  >0.05  – 
Brazil  −25  −29.38, −20.62  12.20  >0.05  – 
Canada  5.43  −7.41, 18.28  11.31  >0.05  – 
Iran  20.4  18.96, 21.84  12.32  <0.05  – 
Sweden  −0.3  −16.37, 15.77  10.8  >0.05  – 
Intensity>50%  −2.53  −16.69, 12.62  65.57  >0.05  94.3% 
≤50%  10.11  −4.04, 24.27  34.43  >0.05  82.4% 
Sensitivity analysis  1.62  −13.35, 16.59  100  >0.05  98.1%   
Total  Overall  1.62  −13.35, 16.59  100  >0.05  98.1% 
6 WMTCycle12 weeks  74.13  24.82, 119.85  82.38  <0.05  69.3% 
24 weeks  151  85.6, 216.4  17.62  <0.05  – 
CountryDenmark  115.9  78.14, 153.67  40.08  >0.05  – 
Turkey  38.97  −8.53, 86.47  21.26  >0.05  – 
Japan  31  −17.54, 79.54  21.04  >0.05  – 
Italy  151  85.6, 216.4  17.62  <0.05  – 
Intensity>50%  86.63  29.46, 143.79  61.12  <0.05  72.7% 
≤50%  38.97  −8.53, 86.47  21.26  >0.05  – 
NA  151  85.6, 216.4  17.62  <0.05  – 
Sensitivity analysis  87.87  42.23, 133.51  100  <0.05  72.9%   
Total  Overall  87.87  42.23, 133.51  100  <0.05  72.9% 
RateAge<60  −11.2  −15.6, −6.8  31.18  <0.05  – 
≥60  −5.35  −8.8, −1.89  68.82  <0.05  – 
Intensity>50%  −7.37  −12.14, −2.6  83.09  >0.05  53.1% 
≤50%  −9  −16.63, −1.37  16.91  >0.05  – 
Sensitivity analysis  −7.63  −11.42, −3.85  100  >0.05  38.9%   
Total  Overall  −7.63  −11.42, −3.85  100  >0.05  38.9% 
Cardiopulmonary functionCycle12 weeks  −8.68  −19.78, 2.43  99.32  >0.05  – 
24 weeks  1.3  −133.28, 135.88  0.68  >0.05  – 
Sensitivity analysis  −8.61  −19.68, 2.46  100  >0.05  –   
Total  Overall  −8.61  −19.68, 2.46  100  >0.05  – 
Fig. 3.

Funnel plot for publication bias.

Resting heart rate

Resting heart rate included 5 studies, with heterogeneity of 38.9%, so a fixed-effects model was used. The results indicated a significant improvement in resting heart rate for AF patients in the exercise group compared to the control group (SMD=−7.63, 95% CI [−11.42, −3.85], P<0.05), as shown in Fig. 2. Sensitivity analysis confirmed the stability of the results.

Country subgroup analysis showed no significant improvement in Japan (P>0.05), while interventions in Brazil, Sweden, and Denmark were significant (SMD of −11.20, −9.00, and −7.63; P<0.05). Different exercise intensity subgroup analysis indicated that both intensity ≤50% and >50% significantly reduced resting heart rate (P<0.05). Age subgroup analysis found that regardless of average age<60 or ≥60 years, exercise effectively reduced resting heart rate (P<0.05). This suggests that AF patients in different age groups can benefit from exercise (Table 3).

Cardiopulmonary function

The meta-analysis included a total of 5 studies, with heterogeneity of 54.4%, and a random-effects model was used. The analysis showed a significant improvement in cardiopulmonary function for AF patients in the exercise group compared to the control group (SMD=2.37, 95% CI [0.96, 3.77], P<0.05), as shown in Fig. 2. Sensitivity analysis confirmed the stability of the results (SMD=2.37, 95% CI [0.96, 3.77]).

Country subgroup analysis indicated no significant difference in results between Japan and Denmark (P>0.05), while interventions in Norway and Turkey were significant (SMDs of 3.55 and 15.59; 95% CI [1.62, 5.48] and [3.68, 27.50]). Age subgroup analysis results showed a significant intervention effect for the >60 years group (SMD=15.59, 95% CI [1.56, 5.44], P<0.05), and no significant effect for the <60 years group (P>0.05), indicating that exercise improves cardiopulmonary function in AF patients aged>60 years.

Quality of life

In this meta-analysis, a total of 10 studies were included. Heterogeneity was significant (I2=98.1%), so a random-effects model was used. The analysis results indicated a statistically significant improvement in the quality of life for AF patients through exercise, with a standardized mean difference (SMD) of 0.720, 95% confidence interval (CI) [0.038, 1.402], P<0.05.

Subgroup analysis based on average age divided into <60 years and 60 years and above showed no statistically significant improvement in both age groups (P>0.05). Exercise intensity subgroup analysis indicated that when intensity was less than 50%, SMD=2.42, 95% CI [0.008, 4.76], P<0.05, suggesting that low-intensity exercise significantly improved the quality of life; while for groups with intensity greater than 50%, the improvement effect was not significant (P>0.05). Subgroup analysis of different countries showed that, except for Ireland, the results from other countries were not statistically significant (P>0.05). The study from Ireland showed a significant improvement, with SMD=7.84, 95% CI [6.18, 9.50], P<0.05. Sensitivity analysis confirmed the stability of the results, SMD=1.62, 95% CI [−13.35, 16.59]. Publication bias analysis suggested significant bias, especially in small-sample studies (Fig. 3).

Discussion

Patients with AF often experience various complications that significantly impact their quality of life.21 The compromised cardiac function resulting from AF affects cardiopulmonary function.22 Additionally, complications such as thrombosis in AF patients can lead to paralysis and physical disabilities, preventing them from engaging in physical activities and resulting in a decline in exercise capacity. The results of this meta-analysis demonstrate a significant impact of exercise on AF patients, with an effect size (SMD) of 87.87, 95% CI [42.23, 133.51], P<0.05. The exercise group showed a significant improvement in the exercise capacity of AF patients compared to the control group, especially with exercise intensity>50%, where the improvement in 6-minute walking ability was more pronounced. Furthermore, exercise significantly lowered the static heart rate of AF patients, improving symptoms of rapid heartbeat. The significant improvement effects were observed across different training intensities, periods, and age groups. Regarding cardiopulmonary function, the combined effect size after exercise was SMD=2.37, 95% CI [0.96, 3.77], P<0.05, indicating a significant improvement in cardiopulmonary function in AF patients through exercise, particularly impacting patients younger than 60 years.

This phenomenon may be attributed to the greater exercise tolerance and adaptability of younger patients.23 Their superior baseline cardiopulmonary function and robust physical recovery capacity enable them to safely engage in high-intensity exercise training,24 such as high-intensity interval training (HIIT) or prolonged aerobic exercise, both of which have been proven to significantly improve cardiopulmonary function. Younger patients also benefit from better cardiac and vascular elasticity,25 which facilitates mechanisms like cardiac remodeling during exercise, leading to enhanced cardiac output and more efficient oxygen transport and utilization, thereby resulting in marked improvements in cardiopulmonary function. Moreover, younger patients tend to demonstrate higher acceptance of structured and personalized exercise programs, with greater adherence and willingness to participate, which are critical for the effectiveness of interventions. In contrast, older patients often face limitations in training due to reduced cardiopulmonary reserve, myocardial fibrosis, or comorbidities, leading to diminished responsiveness to exercise.26 Psychological factors may also play a role, as younger patients are more likely to engage actively in exercise and maintain a positive mental state, further amplifying the benefits of exercise on cardiopulmonary function.27

The American Thoracic Society has developed detailed guidelines for the clinical application of the 6-minute walk test (6MWT), providing standardized procedures for its use in evaluating cardiopulmonary diseases.28 In recent years, both the American College of Cardiology/American Heart Association and the European Society of Cardiology have recognized the 6MWT as a gold standard for assessing exercise capacity and included it as an evaluation indicator in heart failure diagnosis and treatment guidelines.29 The 6MWT, reflecting exercise capacity, is easily administered and widely accepted for its role in assessing cardiovascular health. Atrial fibrillation, characterized by reduced atrial contraction function leading to decreased ventricular ejection, results in compromised cardiopulmonary function.30 Increased heart rate can lead to chronic heart failure and other myocardial diseases, severely affecting cardiopulmonary function. This study, using peak oxygen consumption (VO2max) as an indicator,31 measured the cardiopulmonary coupling capacity under maximum exercise load, aiming to directly reflect changes in cardiopulmonary function. Monitoring static heart rate in AF patients is crucial for understanding their physiological status, providing insight into their rapid heartbeat status, and offering substantial support for symptom improvement.32

A substantial amount of past research has confirmed the beneficial effects of exercise on atrial fibrillation.33,34 Building upon existing research, this study further explores the general impact of exercise on AF patients across different training intensities and durations. Ortaga (2022) study confirmed the positive effects of regular moderate-intensity exercise on improving exercise tolerance in AF patients.35 This study specifically highlights a more significant improvement in the 6-minute walking test when exercise intensity exceeds 50%, providing a new perspective to this field. Additionally, our findings align with Moral et al.’s (2018) results,35 further confirming the influence of moderate-intensity exercise on exercise tolerance in AF patients. The study by Williams et al. (2020) also supports the benefits of exercise in enhancing the functional capacity of AF patients.36

Regarding improvements in cardiorespiratory function, Green et al.’s (2019) study found that aerobic exercise significantly improves the cardiovascular health of AF patients.37 Liu et al.’s (2021) studyemphasizes the importance of moderate exercise in improving cardiorespiratory function in AF patients, particularly evident in patients under 60 years old.38 Furthermore, Martin's (2020) study demonstrates that exercise effectively lowers the resting heart rate of AF patients and improves symptoms of rapid heartbeats.39 Brown (2022) study further confirms the effects of regular exercise on reducing resting heart rate and improving overall cardiac health in AF patients.40

This study further discovered that exercise training with an intensity exceeding 50% is more effective in improving the exercise capacity of AF patients.41 This may be attributed to the increased volume load on the heart during high-intensity exercise, leading to increased left ventricular volume, wall thickness, and end-diastolic volume.42 Consequently, this results in an increased stroke volume per beat. The elevation in stroke volume allows AF patients to achieve a lower heart rate while maintaining the same cardiac output, reducing the metabolic load on the heart.43 This creates a more effective time-pressure relationship, thereby more effectively improving the cardiorespiratory function and exercise capacity of patients.44

Patients with atrial fibrillation commonly face increased ventricular stiffness due to reduced myocardial compliance and impaired active relaxation capacity during the left ventricular diastolic period.45 This often leads to left ventricular filling disturbances, elevated end-diastolic pressure, and reduced stroke volume, subsequently decreasing cardiorespiratory function.46 Simultaneously, regular exercise training can increase heart rate in the short term, raising oxygen demand and inducing a temporary hypoxic state.47 This process stimulates the formation of local collateral circulation, achieving the so-called “biological bridging,” which improves myocardial perfusion, increases myocardial blood supply, and reduces damage to myocardial cells due to inadequate perfusion.48 As a result, these changes effectively improve cardiac function.

Sustained exercise, especially intermittent training, promotes blood circulation and activity in the respiratory system, stimulates skeletal muscle growth, increases the number of capillaries and muscles, thereby enhancing respiratory function and effectively improving lung function.49 Previous research indicates that after a period of exercise training, AF patients undergoing percutaneous coronary intervention show significant increases in oxygen uptake, oxygen pulse, and anaerobic threshold, while the maximum heart rate remains relatively unchanged.50 This suggests that improving coronary blood flow not only enhances cardiac function but also significantly strengthens cardiorespiratory function.51 During exercise, the contraction and relaxation functions of the heart are enhanced, vascular wall elasticity is increased, stroke volume is increased, allowing the cardiovascular system to transport oxygen more effectively and rapidly, enhancing overall endurance, and effectively improving cardiorespiratory function.52 Furthermore, by increasing cardiac output, improving left ventricular remodeling, improving end-diastolic volume, and reducing plasma neurohormone levels, exercise rehabilitation can also alter the histological characteristics of the myocardium. These combined effects ultimately achieve a significant improvement in cardiorespiratory function in AF patients.53

Consistent with past research, this study confirms the improvement in the quality of life for AF patients through exercise. Smith's (2019) study also supports the enhancement of life quality for AF patients through exercise.16 Regular exercise, by enhancing cardiac contraction and improving blood circulation efficiency, helps improve myocardial blood supply and alleviate the workload on the heart. This not only reduces the frequency of AF episodes but also alleviates symptoms such as chest pain and dyspnea caused by AF, directly enhancing the quality of life.54 Simultaneously, regular exercise promotes the release of endorphins, a natural “pleasure chemical” that improves mood and reduces symptoms of depression and anxiety. This is particularly important for AF patients, as atrial fibrillation itself and the associated lifestyle restrictions often lead to increased psychological stress. Improving emotions through exercise significantly enhances the overall quality of life for patients.55

Regular exercise can enhance individuals’ self-efficacy and social interaction while reducing symptoms of depression and anxiety. Exercise, as a positive lifestyle, not only improves patients’ physiological conditions but also enhances overall life satisfaction by promoting social participation and mental health.56 Moreover, during exercise, whether participating in group fitness classes or engaging in physical activities with friends or family, interpersonal relationships can be improved. For many atrial fibrillation patients, this social interaction serves as an important support system, providing emotional support and reducing feelings of loneliness, thereby enhancing the quality of life.57

The findings of this study further confirm these mechanisms, revealing the specific effects of exercise training on the improvement of exercise capacity and quality of life in atrial fibrillation patients. Through regular exercise interventions, significant improvements are observed in the myocardial and vascular functions of atrial fibrillation patients. This discovery provides empirical support for the exercise prescription for atrial fibrillation patients, emphasizing the importance of personalized exercise plans in improving cardiorespiratory health in this patient population.

This study provides valuable insights into the impact of exercise on AF patients; however, several limitations should be acknowledged. The overall quality of the included studies was moderate, which may affect the robustness of the findings. Additionally, the sample size was relatively small, comprising only 287 patients, potentially reducing the statistical power and limiting the reliability of subgroup analyses. Furthermore, significant heterogeneity was observed in some subgroup analyses, particularly regarding improvements in quality of life, with variations likely influenced by differences in cultural, social, and exercise habits across countries. Another limitation is the insufficient exploration of specific exercise intensities and frequencies; while subgroup analyses were conducted, clear guidance on optimal exercise protocols remains lacking. Future research should aim to address these limitations by conducting larger, high-quality randomized controlled trials and investigating the long-term effects of exercise interventions on cardiopulmonary function and quality of life, as well as refining exercise prescriptions tailored to AF patients.

Conclusion

Exercise has a significant effect on improving the exercise capacity, cardiorespiratory function, and quality of life in AF patients. Particularly, for cardiorespiratory function, the combined effect size after exercise shows a significant improvement, especially in patients under the age of 60. Additionally, exercise significantly reduces the resting heart rate of AF patients and improves symptoms of rapid heartbeats. This study emphasizes that the positive impact on AF patients is more pronounced when exercise intensity exceeds 50%, providing a new perspective for optimizing exercise prescriptions. The study provides high-level evidence on the role of exercise in AF treatment, highlighting the importance of personalized exercise plans in improving the cardiorespiratory health of AF patients. Future research should use larger sample sizes and higher-quality randomized controlled trials to further validate and refine our findings.

Ethical considerations

This study does not involve ethical considerations as it is a systematic review and meta-analysis, and therefore does not require written informed consent.

Funding information

This study received no funding.

Conflict of interest

The authors declare that they have no conflicts of interest.

References
[1]
G.Y.H. Lip, A. Banerjee, G. Boriani, C.E. Chiang, R. Fargo, B. Freedman, et al.
Antithrombotic therapy for atrial fibrillation: CHEST guideline and expert panel report.
Chest, 154 (2018), pp. 1121-1201
[2]
F. Witassek, A. Springer, L. Adam, S. Aeschbacher, J.H. Beer, S. Blum, et al.
Health-related quality of life in patients with atrial fibrillation: the role of symptoms, comorbidities, and the type of atrial fibrillation.
PLOS ONE, 14 (2019), pp. e0226730
[3]
B. Robaye, N. Lakiss, F. Dumont, C. Laruelle.
Atrial fibrillation and cardiac rehabilitation: an overview.
Acta Cardiol, 75 (2020), pp. 116-120
[4]
T. Lindberg, A. Wimo, S. Elmståhl, C. Qiu, D.M. Bohman, J. Sanmartin Berglund.
Prevalence and incidence of atrial fibrillation and other arrhythmias in the general older population: findings from the Swedish national study on aging and care.
Gerontol Geriatr Med, 5 (2019), pp. 1-9
[5]
Y.N.V. Reddy, B.A. Borlaug, B.J. Gersh.
Management of atrial fibrillation across the spectrum of heart failure with preserved and reduced ejection fraction.
Circulation, 146 (2022), pp. 339-357
[6]
M. Baudo, F. Rosati, E. Lapenna, L. Di Bacco, S. Benussi.
Surgical options for atrial fibrillation treatment during concomitant cardiac procedures.
Ann Cardiothorac Surg, 13 (2024), pp. 135-145
[7]
Eymael A. Population activity of the superior colliculus and associated cardiovascular outputs. Macquarie University; 2023.
[8]
S. Lévy, G. Steinbeck, L. Santini, M. Nabauer, D.P. Maceda, B.K. Kantharia, et al.
Management of atrial fibrillation: two decades of progress—a scientific statement from the European Cardiac Arrhythmia Society.
J Interv Card Electrophysiol, 65 (2022), pp. 287-326
[9]
A. Scarà, Z. Palamà, A.G. Robles, L.L. Dei, A. Borrelli, F. Zanin, et al.
Non-pharmacological treatment of heart failure—from physical activity to electrical therapies: a literature review.
J Cardiovasc Dev Dis, 11 (2024), pp. 122
[10]
S. Nattel, E. Guasch, I. Savelieva, F.G. Cosio, I. Valverde, J.L. Halperin, et al.
Early management of atrial fibrillation to prevent cardiovascular complications.
Eur Heart J, 35 (2014), pp. 1448-1456
[11]
J. Knapen, D. Vancampfort, Y. Moriën, Y. Marchal.
Exercise therapy improves both mental and physical health in patients with major depression.
Disabil Rehabil, 37 (2015), pp. 1490-1495
[12]
G. Boriani, M. Proietti.
Atrial fibrillation prevention: an appraisal of current evidence.
[13]
B.J. Petek, D.M. Hayes, M.M. Wasfy.
Right heart resilience and atrial fibrillation risk in long-term endurance athletes.
J Am Soc Echocardiogr, 35 (2022), pp. 1269-1272
[14]
N.J. Bosomworth.
Atrial fibrillation and physical activity: should we exercise caution?.
Can Fam Physician, 61 (2015), pp. 1061-1070
[15]
S. Shi, J. Shi, Q. Jia, S. Shi, G. Yuan, Y. Hu.
Efficacy of physical exercise on the quality of life, exercise ability, and cardiopulmonary fitness of patients with atrial fibrillation: a systematic review and meta-analysis.
Front Physiol, 11 (2020), pp. 740
[16]
S.J. Keteyian, J.K. Ehrman, B. Fuller, Q.R. Pack.
Exercise testing and exercise rehabilitation for patients with atrial fibrillation.
J Cardiopulm Rehabil Prev, 39 (2019), pp. 65-72
[17]
D. Moher, L. Shamseer, M. Clarke, D. Ghersi, A. Liberati, M. Petticrew, et al.
Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement.
[18]
S. Sideri, S.N. Papageorgiou, T. Eliades.
Registration in the international prospective register of systematic reviews (PROSPERO) of systematic review protocols was associated with increased review quality.
J Clin Epidemiol, 100 (2018), pp. 103-110
[19]
A.G. Cashin, J.H. McAuley, Clinimetrics:.
Physiotherapy Evidence Database (PEDro) scale.
J Physiother, 66 (2020), pp. 59
[20]
B. Han, E. Eskin.
Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies.
Am J Hum Genet, 88 (2011), pp. 586-598
[21]
S. Stempfel, S. Aeschbacher, S. Blum, P. Meyre, R. Gugganig, J.H. Beer, et al.
Symptoms and quality of life in patients with coexistent atrial fibrillation and atrial flutter.
Int J Cardiol Heart Vasc, 29 (2020), pp. 100556
[22]
S. Nattel, J. Heijman, L. Zhou, D. Dobrev.
Molecular basis of atrial fibrillation pathophysiology and therapy: a translational perspective.
[23]
M.W. Martinez, J.H. Kim, A.B. Shah, D. Phelan, M.S. Emery, M.M. Wasfy, et al.
Exercise-induced cardiovascular adaptations and approach to exercise and cardiovascular disease: JACC state-of-the-art review.
J Am Coll Cardiol, 78 (2021), pp. 1453-1470
[24]
L. Long, I.R. Mordi, C. Bridges, V.A. Sagar, E.J. Davies, A.J. Coats, et al.
Exercise-based cardiac rehabilitation for adults with heart failure.
Cochrane Database Syst Rev, 1 (2019), pp. CD003331
[25]
C. Torlasco, A. D&apos;Silva, A.N. Bhuva, A. Faini, J.B. Augusto, K.D. Knott, et al.
Age matters: differences in exercise-induced cardiovascular remodelling in young and middle-aged healthy sedentary individuals.
Eur J Prev Cardiol, 28 (2021), pp. 738-746
[26]
C.F. Reynolds 3rd, D.V. Jeste, P.S. Sachdev, D.G. Blazer.
Mental health care for older adults: recent advances and new directions in clinical practice and research.
World Psychiatry, 21 (2022), pp. 336-363
[27]
M. Izquierdo, R.A. Merchant, J.E. Morley, S.D. Anker, I. Aprahamian, H. Arai, et al.
International exercise recommendations in older adults (ICFSR): expert consensus guidelines.
J Nutr Health Aging, 25 (2021), pp. 824-853
[28]
A.W. Brown, S.D. Nathan.
The value and application of the 6-minute-walk test in idiopathic pulmonary fibrosis.
Ann Am Thorac Soc, 15 (2018), pp. 3-10
[29]
S. Giannitsi, M. Bougiakli, A. Bechlioulis, A. Kotsia, L.K. Michalis, K.K. Naka.
6-Minute walking test: a useful tool in the management of heart failure patients.
Ther Adv Cardiovasc Dis, 13 (2019), pp. 1-10
[30]
L. Staerk, J.A. Sherer, D. Ko, E.J. Benjamin, R.H. Helm.
Atrial fibrillation: epidemiology, pathophysiology, and clinical outcomes.
Circ Res, 120 (2017), pp. 1501-1517
[31]
D. Li, P. Chen, J. Zhu.
The effects of interval training and continuous training on cardiopulmonary fitness and exercise tolerance of patients with heart failure – a systematic review and meta-analysis.
Int J Environ Res Public Health, 18 (2021), pp. 6761
[32]
J. Heijman, D. Linz, U. Schotten.
Dynamics of atrial fibrillation mechanisms and comorbidities.
Annu Rev Physiol, 83 (2021), pp. 83-106
[33]
B.J.R. Buckley, G.Y.H. Lip, D.H.J. Thijssen.
The counterintuitive role of exercise in the prevention and cause of atrial fibrillation.
Am J Physiol Heart Circ Physiol, 319 (2020), pp. H1051-H1058
[34]
L.E. Garnvik, V. Malmo, I. Janszky, H. Ellekjær, U. Wisløff, J.P. Loennechen, et al.
Physical activity, cardiorespiratory fitness, and cardiovascular outcomes in individuals with atrial fibrillation: the HUNT study.
Eur Heart J, 41 (2020), pp. 1467-1475
[35]
A. Ortega-Moral, B. Valle-Sahagún, G. Barón-Esquivias.
Efficacy of exercise in patients with atrial fibrillation: systematic review and meta-analysis.
Med Clin (Barc), 159 (2022), pp. 372-379
[36]
M.M. Redfield, B.A. Borlaug.
Heart failure with preserved ejection fraction: a review.
JAMA, 329 (2023), pp. 827-838
[37]
P.S. Osbak, M. Mourier, A. Kjaer, J.H. Henriksen, K.F. Kofoed, G.B. Jensen.
A randomized study of the effects of exercise training on patients with atrial fibrillation.
Am Heart J, 162 (2011), pp. 1080-1087
[38]
J. Plisiene, A. Blumberg, G. Haager, C. Knackstedt, J. Latsch, C. Norra, et al.
Moderate physical exercise: a simplified approach for ventricular rate control in older patients with atrial fibrillation.
Clin Res Cardiol, 97 (2008), pp. 820-826
[39]
R.V. Lewis, J. McMurray, D.G. McDevitt.
Effects of atenolol, verapamil, and xamoterol on heart rate and exercise tolerance in digitalised patients with chronic atrial fibrillation.
J Cardiovasc Pharmacol, 13 (1989), pp. 1-6
[40]
R.K. Pathak, A. Elliott, M.E. Middeldorp, M. Meredith, A.B. Mehta, R. Mahajan, et al.
Impact of CARDIOrespiratory FITness on arrhythmia recurrence in obese individuals with atrial fibrillation: the CARDIO-FIT study.
J Am Coll Cardiol, 66 (2015), pp. 985-996
[41]
J.L. Reed, T. Terada, S. Vidal-Almela, H.E. Tulloch, M. Mistura, D.H. Birnie, et al.
Effect of high-intensity interval training in patients with atrial fibrillation: a randomized clinical trial.
JAMA Netw Open, 5 (2022), pp. e2239380
[42]
P. Dubach, J. Myers, G. Dziekan, U. Goebbels, W. Reinhart, P. Muller, et al.
Effect of high-intensity exercise training on central hemodynamic responses to exercise in men with reduced left ventricular function.
J Am Coll Cardiol, 29 (1997), pp. 1591-1598
[43]
T. Sugimoto, M. Barletta, F. Bandera, G. Generati, E. Alfonzetti, M. Rovida, et al.
Central role of left atrial dynamics in limiting exercise cardiac output increase and oxygen uptake in heart failure: insights by cardiopulmonary imaging.
Eur J Heart Fail, 22 (2020), pp. 1186-1198
[44]
E.Y. Han, S.H. Im.
Effects of a 6-week aquatic treadmill exercise program on cardiorespiratory fitness and walking endurance in subacute stroke patients: A pilot trial.
J Cardiopulm Rehabil Prev, 38 (2018), pp. 314-319
[45]
R. Kaw, A.V. Hernandez, V. Pasupuleti, A. Deshpande, V. Nagarajan, H. Bueno, et al.
Effect of diastolic dysfunction on postoperative outcomes after cardiovascular surgery: a systematic review and meta-analysis.
J Thorac Cardiovasc Surg, 152 (2016), pp. 1142-1153
[46]
V. Pergola, A. D’Andrea, D. Galzerano, F. Mantovani, M. Rizzo, G.D. Giannuario, et al.
Unveiling the hidden chamber: exploring the importance of left atrial function and filling pressure in cardiovascular health.
J Cardiovasc Echogr, 33 (2023), pp. 117-124
[47]
K. Mtengai, S. Ramasamy, P. Msimuko, A. Mzula, E.D. Mwega.
Existence of a novel heavy metal-tolerant pseudomonas aeruginosa strain Zambia SZK-17 Kabwe 1: the potential bioremediation agent in the heavy metal-contaminated area.
Environ Monit Assess, 194 (2022), pp. 887-893
[48]
Q. Gu, F. Xu, B.O. Orgil, Z. Khuchua, U. Munkhsaikhan, J.N. Johnson, et al.
Systems genetics analysis defines importance of TMEM43/LUMA for cardiac-and metabolic-related pathways.
Physiol Genomics, 54 (2022), pp. 22-35
[49]
L.M. Romer, M.I. Polkey.
Exercise-induced respiratory muscle fatigue: implications for performance.
J Appl Physiol, 104 (2008), pp. 879-888
[50]
P.S. Pagel, J.N. Tawil, B.T. Boettcher, D.A. Izquierdo, T.J. Lazicki, G.J. Crystal, et al.
Heart failure with preserved ejection fraction: a comprehensive review and update of diagnosis, pathophysiology, treatment, and perioperative implications.
J Cardiothorac Vasc Anesth, 35 (2021), pp. 1839-1859
[51]
S.Y. Zavalishina, D.M. Pravdov, E.D. Bakulina, M.V. Eremin, O.G. Rysakova, A.V. Dorontsev.
Strengthening the general functional capabilities of the body in conditions of a feasible increase in muscle activity after intervention on the heart.
Biomed Pharmacol J, 13 (2020), pp. 597-602
[52]
M.A. Nystoriak, A. Bhatnagar.
Cardiovascular effects and benefits of exercise.
Front Cardiovasc Med, 5 (2018), pp. 135
[53]
M.A. Garza, E.A. Wason, J.Q. Zhang.
Cardiac remodeling and physical training post myocardial infarction.
World J Cardiol, 7 (2015), pp. 52-64
[54]
C. Bang, S. Park.
Symptom clusters, psychological distress, and quality of life in patients with atrial fibrillation.
Healthcare (Basel), 11 (2023), pp. 1353
[55]
D.X. Marquez, S. Aguiñaga, P.M. Vásquez, D.E. Conroy, K.I. Erickson, C. Hillman, et al.
A systematic review of physical activity and quality of life and well-being.
Transl Behav Med, 10 (2020), pp. 1098-1109
[56]
C. Herbert.
Enhancing mental health, well-being and active lifestyles of university students by means of physical activity and exercise research programs.
Front Public Health, 10 (2022), pp. 849093
[57]
S. Rosenstrøm, S.S. Risom, J.D. Hove, A. Brødsgaard.
Living with atrial fibrillation: a family perspective.
Nurs Res Pract, 2022 (2022), pp. 1-7
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