Abstract
Background
Heart failure (HF) and atrial fibrillation (AF) are often concomitant and act in a vicious cycle. Atrial fibrillation is associated with greater functional limitations and increased morbidity and mortality in patients with HF. Moreover, AF associated with HF increases patients' physical inactivity, worsening their clinical condition, and prognosis. Exercise training is safe and has clear benefits in HF. However, these benefits have not been demonstrated when AF is associated with HF.
Case summary
We present the case of a 57-year-old man with permanent AF and HF with reduced ejection fraction, who underwent 12 weeks of exercise training that included cardiopulmonary exercise testing, neuromuscular sympathetic activity (NMSA), and muscle blood flow (MBF) before and after training.
Discussion
Exercise training was shown to have a potential benefit in reducing the activity of the sympathetic nerve and increasing muscle blood flow, as well as increasing VO2peak and decreasing the VE/VCO2 slope in a patient with AF associated with HF with reduced ejection fraction. These results may indicate favourable clinical implications in this group of patients.
Keywords: Exercise training, Heart failure, Atrial fibrillation, Muscular blood flow, Neuromuscular sympathetic activity, Case report
Learning points
Exercise training increases cardiopulmonary performance improving muscle blood flow. It should be recommended to patients with atrial fibrillation associated with heart failure.
The increased sensitivity of the arterial baroreflex re-establishing control over sympathetic activity, leading to improved muscle flow and exercise capacity.
These results may indicate favourable clinical implications in this group of patients.
Introduction
Heart failure (HF) and atrial fibrillation (AF) are often concurrent clinical conditions, and they may be the cause or consequence of each other, progressing in a vicious cycle.1 Approximately 40% of patients with HF present AF, leading to greater functional impairment and increased morbidity and mortality.2 Restoration and maintenance of sinus rhythm is challenging in these patients, with a low long-term success rate of cardioversion and ablation in patients with AF and HF.1,2
Regular physical activity is an evidence-based adjuvant therapy for HF. Exercise training attenuates the activity of the sympathetic nervous system and improves functional capacity, leading to lower rates of hospitalization and better quality of life.3–5 However, studies evaluating the effects of exercise in patients with HF and AF are lacking.
Physical inactivity may worsen the exercise intolerance in patients with AF and HF, aggravating the clinical condition, increasing the risk of hospitalization, and worsening quality of life.1,2 Physical activity can help break the vicious cycle of low functional capacity resulting from the binary AF and HF and should be recommended to these patients, as long as they are clinically stable, with optimized clinical treatment according to guidelines, with a resting heart rate ≤80 b.p.m. and ≤110% of the predicted for their maximum exercise age.6
This case report shows the changes on physical capacity, neuromuscular sympathetic activity (NMSA), and muscular blood flow (MBF) after a supervised exercise training guided by the Borg scale in a patient with AF associated with HF and reduced left ventricular ejection fraction (LVEF).
Timeline
| Time | Events |
|---|---|
| Routine medical consultation |
|
| Before to supervised exercise training (SET) |
|
| SET for a period of 12 weeks |
|
| After 12 weeks of SET |
|
| Results of SET |
|
Case presentation
A 57-year-old Caucasian man diagnosed with HF due to hypertensive dilated cardiomyopathy associated with permanent AF was referred to an exercise training program. He had non-insulin-dependent diabetes mellitus and LVEF was 35%. The functional class was III [(New York Heart Association (NYHA)] and drug therapy was according to the III Brazilian Guideline on Heart Failure and II Brazilian Guideline on Atrial Fibrillation: Losartan 100 mg, Furosemide 40 mg, Carvedilol 150 mg, Warfarin 5 mg, Simvastatin 20 mg, Metformin 1700 mg, and Omeprazole 20 mg. Because of a long history of AF, rate control strategy was implemented. The patient did not have a history of neuromuscular or pulmonary disease. He never smoke and did not drink alcohol. According to his level of physical activity, he led a sedentary life, defined as self-reported less than 1 day/week of planned, structured, and repetitive exercise. His body mass index was 36.8 kg/m2 and resting blood pressure was 115/80 mmHg. Resting electrocardiogram showed AF with an average heart rate of 75 b.p.m.
The supervised exercise training program was carried out three times a week, for a period of 12 weeks in a closed environment, with a controlled temperature between 21°C and 24°C in the afternoon (3:30 pm to 4:30 pm). The exercise training protocol consisted of 5 min of warm-up exercises, 30 min of aerobic training performed on a cycle ergometer at 60 rpm, 20 min of resistance exercises with lower and upper limbs and 5 min of relaxation exercises. The workload was adjusted during the stimulus phase of the aerobic training to keep the perceived effort intensity between 11 (relatively easy) and 13 (slightly tiring) of the Borg Scale.7 Resistance training was performed in a weight training station and consisted of 2 sets of 10 repetitions, and the following sequence of exercises: leg extension, leg curl, lat pull-down, peck deck, and press chest. The initial workload was set at 60% of 1 repetition maximum.8 He was encouraged to complete the sets of 10 prescribed repetitions, performing the appropriate movement and avoiding Valsalva manoeuvre. He was instructed to rest for 30–60 s between sets. The intensity of the exercise was increased from 5% to 10% whenever the patient adapted to the exercise workload thorough the 12 weeks of training.
After 12 weeks of supervised sessions, the patient became asymptomatic (NYHA I) and was instructed to continue exercising at home.
Table 1 displays the results of the cardiopulmonary exercise test before and after 12 weeks of exercise training, performed on a cycle ergometer, using the modified Balke protocol (25 w/min).4 Comparing the exercise test before and after 12 weeks, we observed that the rest HR reduced and the peak HR increased, and that systolic blood pressure increased, and diastolic blood pressure decreased at the peak of exercise. Peak oxygen consumption (VO2peak) increased and VE/VCO2 slope decreased after training. Figure 1 shows data on muscle sympathetic nerve activity (NMSA) before and after the intervention, obtained by a microelectrode implanted in the fibular nerve and recorded by the shots per minute and every 100 b.p.m.6 We observed that the shots decreased in both registers, indicating a reduction in NMSA. The muscle blood flow (MBF), obtained by plethysmography venous occlusion,6 increased after exercise intervention as shown in Figure 2.
Table 1.
Cardiopulmonary exercise pre- and post-12 weeks of exercise training
| Pre | Post | |
|---|---|---|
| Heart rate (b.p.m.) | ||
| Resting | 75 | 70 |
| Maximum | 111 | 116 |
| Systolic blood pressure (mmHg) | ||
| Resting | 115 | 115 |
| Maximum | 130 | 135 |
| Diastolic blood pressure (mmHg) | ||
| Resting | 80 | 75 |
| Maximum | 79 | 75 |
| VO2peak (mL/kg/min−1) | 14.7 | 16.0 |
| VE/VCO2 slope | 33 | 28 |
| Tolerance (min) | 7 | 10 |
| RER (VCO2/VO2) | 1.05 | 1.15 |
RER, respiratory exchange ratio; VO2peak, peak oxygen consumption; VE/VCO2 slope, the slope of the line between pulmonary ventilation (mL/min) and carbon dioxide production (mL/min).
Figure 1.
Muscle sympathetic nerve activity (NMSA) per minute and every 100 b.p.m. before and after the intervention.
Figure 2.
Muscle blood flow (MBS) before and after the intervention.
Figure 3.
Electrocardiogram pre- and post-12 weeks of exercise training. (A) Pre-rest; (B) pre-peak; (C) post-rest, and (D) post-peak.
Discussion
This case study highlights the known benefits of physical exercise in heart failure with reduced ejection fraction and permanent atrial fibrillation. To the best of our knowledge, this is the first report of the benefits of exercise training guided by the Borg scale on physical capacity, neuromuscular sympathetic activity, and muscle blood flow in a patient with AF and HF with reduced ejection fraction.
Muscle sympathetic nerve activity is an independent predictor of prognosis in HF.9 The reduction in the frequency of NMSA shots after exercise reinforces the idea that physical training contributes to improve prognosis in these patients. The present report shows a reduction in NMSA in AF associated with HF, but it does not elucidate its mechanisms. Nevertheless, it is reasonable to speculate that exercise training promotes increased sensitivity of the arterial baroreflex, restoring control of sympathetic nerve activity, and heart rate, which may be associated with improved sensitivity of the aortic depressor.10,11 In addition, exercise training may have reduced peripheral chemoreflex sensitivity, improving the ergoreflex control of NMSA in AF associated with HF.12
Evidence shows that exercise training increases muscle blood flow in HF,13 which was also observed in our report of a patient with AF associated with HF. This observation may have useful clinical implications because muscle blood flow is an independent predictor of mortality in HF.9 The increase in muscle blood flow after exercise training may have resulted from better endothelial function, shifting the balance between vasodilation and vasoconstriction.12
The presence of AF is related to lower exercise capacity, which is associated with reduced VO2peak and increased VE/VCO2 slope.14 The association of AF with HF has important clinical implications, with a higher risk of hospitalization and death.13 Studies have shown that exercise training increases the VO2peak and a decrease the VE/VCO2 slope in patients with HF.3,15 The findings of this case report are consistent with these studies, highlighting how the benefits of exercise training can be extended to patients with AF and HF, as long as they are clinically stable, with optimized drug therapy, using beta-blockers and with controlled heart rate at rest and exercise.
On the other hand, a sub-analysis of the HF-ACTION suggested a lack of efficacy of aerobic exercise in improving the prognosis of patients with HF and AF.16 Nevertheless, the HF-ACTION study was not designed for patients with HF and AF, and the low compliance and different aspects of exercise protocol may have contributed to an only mild increase in VO2peak. Also, the intensity of aerobic exercise using 60–70% of the heart rate reserve does not apply to patients with AF.17,18
Finally, although restoration of sinus rhythm may improve haemodynamics and prognosis in patients with HF and AF, as recent trials with catheter ablation have suggested, maintaining sinus rhythm is challenging in clinical practice and it needs to be compared with rate-control strategy in large double-blind clinical trials.19,20 Importantly, despite this patient became asymptomatic, VO2peak remained low, and his prognosis can be further improved by therapies that showed to improve survival in symptomatic patients with HFrEF, such as changing losartan to sacubitril/valsartan and adding spironolactone.21 More recently, a sodium-glucose co-transporter-2 (SGLT2) inhibitor showed to improve survival in this population.22
Exercise training is key to improve functional capacity and quality of life, with low risk of side effects and complications, being an essential and safe tool for treating patients with HF. The present case showed that exercise using the Borg scale of perceived exertion to guide intensity can improve the tolerance to exercise, increase the MBF, decrease the resting HR, and increase maximum HR, which may be related to better balance in the autonomic nervous system.23
These favourable results must be confirmed by future studies and by the replication of research that examines the impact of exercise training in patients with AF and HF with both reduced and preserved ejection fraction. They should evaluate the effects on different outcomes, such as muscle sympathetic nerve activity, muscle blood flow, and functional capacity, and include other modalities of exercise, such as interval aerobic training, water-based exercises, inspiratory muscle training, and yoga. This will help better understand the role and potential mechanisms of exercise training in patients with HF and AF, and provide specific recommendations for this population.
Conclusion
Exercise training showed potential benefits in a patient with AF associated with HF with reduced ejection fraction, reducing sympathetic nerve activity, increasing muscle blood flow and the VO2peak, and decreasing the VE/VCO2 slope and resting heart rate.
Lead author biography

Guilherme Veiga Guimarães, Phd., Researcher, School of Medicine, University of São Paulo. He is currently a cardiac rehabilitation researcher at the Heart Institute of Hospital das Clínicas, University of São Paulo, with an interest in exercise physiology.
Supplementary material
Supplementary material is available at European Heart Journal - Case Reports online.
Funding
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP # 2013/17031-6); and Conselho Nacional de Desenvolvimento Científico e Tecnologico (CNPq # 40137/2016-5). Conselho Nacional de Desenvolvimento Cientıfico e Tecnologico (CNPq # 301957/2017-7) during this project to G.V.G.
Slide sets: A fully edited slide set detailing this case and suitable for local presentation is available online as Supplementary data.
Consent: The author/s confirm that written consent for submission and publication of this case report including image(s) and associated text has been obtained from the patient in line with COPE guidelines.
Conflict of interest: none declared.
Supplementary Material
Contributor Information
Guilherme Veiga Guimarães, University of São Paulo (USP), School of Medicine, Heart Institute-Clinical Hospital (InCor/HC-FMUSP), Av Dr Enéas de Carvalho Aguiar, 44, São Paulo/SP, CEP 05403-000, Brazil.
Jean Marcelo Roque, University of São Paulo (USP), School of Medicine, Heart Institute-Clinical Hospital (InCor/HC-FMUSP), Av Dr Enéas de Carvalho Aguiar, 44, São Paulo/SP, CEP 05403-000, Brazil.
Alexander D T Machado, University of São Paulo (USP), School of Medicine, Heart Institute-Clinical Hospital (InCor/HC-FMUSP), Av Dr Enéas de Carvalho Aguiar, 44, São Paulo/SP, CEP 05403-000, Brazil.
Miguel Morita Fernandes-Silva, Federal University of Parana, Brazil.
Paul Roberto Chizzola, University of São Paulo (USP), School of Medicine, Heart Institute-Clinical Hospital (InCor/HC-FMUSP), Av Dr Enéas de Carvalho Aguiar, 44, São Paulo/SP, CEP 05403-000, Brazil.
Edimar Alcides Bocchi, University of São Paulo (USP), School of Medicine, Heart Institute-Clinical Hospital (InCor/HC-FMUSP), Av Dr Enéas de Carvalho Aguiar, 44, São Paulo/SP, CEP 05403-000, Brazil.
References
- 1. Kotecha D, Piccini JP.. Atrial fibrillation in heart failure: what should we do? Eur Heart J 2015;36:3250–3257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. Lam CS, Rienstra M, Tay WT, Liu LC, Hummel YM, van der Meer P. et al. Atrial fibrillation in heart failure with preserved ejection fraction: association with exercise capacity, left ventricular filling pressures, natriuretic peptides, and left atrial volume. JACC: Heart Failure 2017;5:92–98. [DOI] [PubMed] [Google Scholar]
- 3. Taylor RS, Sagar VA, Davies EJ, Briscoe S, Coats AJ, Dalal H. et al. Exercise-based rehabilitation for heart failure. Cochrane Database Syst Rev 2014;CD003331. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Fernandes-Silva MM, Guimarães GV, Rigaud VO, Lofrano-Alves MS, Castro RE, Cruz LGDB. et al. Inflammatory biomarkers and effect of exercise on functional capacity in patients with heart failure: Insights from a randomized clinical trial. Eur J Prev Cardiol 2017;24:808–817. [DOI] [PubMed] [Google Scholar]
- 5. Guimarães GV, Ciolac EG.. Physical activity: practice this idea. Am J Cardiovasc Dis 2014;4:1–121. [PMC free article] [PubMed] [Google Scholar]
- 6. Wyse G, Anderson JL, Antman EM, Cooper ES, Dalquist JE, Davis KB et al. Atrial fibrillation follow-up investigation of rhythm management—the AFFIRM study design. Am J Cardiol 1997;9:1198–1202. [PubMed] [Google Scholar]
- 7. Carvalho VO, Bocchi EA, Guimarães GV.. The Borg scale as an important tool of self-monitoring and self-regulation of exercise prescription in heart failure patients during hydrotherapy. A randomized blinded controlled trial. Circ J 2009;73:1871–1876. [DOI] [PubMed] [Google Scholar]
- 8. Abdul-Hameed U, Rangra P, Shareef MY, Hussain ME.. Reliability of 1-Repetition maximum estimation for upper and lower body muscular strength measurement in untrained middle aged type 2 diabetic patients. Asian J Sports Med 2012;3:267–273. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Barretto AC, Santos AC, Munhoz R, Rondon MU, Franco FG, Trombetta IC. et al. Increased muscle sympathetic nerve activity predicts mortality in heart failure patients. Int J Cardiol 2009;135:302–307. [DOI] [PubMed] [Google Scholar]
- 10. Piepoli M, Volterrani M, Ponikowski P, Giordano A, Capucci A, Coats A.. The ergoreflex activity during exercise: predictor of impaired heart rate variability in chronic heart failure. Eur J Heart Fail 2000;2:50–56. [Google Scholar]
- 11. Guimarães GV, Belli JFC, Bacal F, Bocchi EA.. Behavior of central and peripheral chemoreflex in heart failure. Arq Bras Cardiol 2011;96:161–167. [DOI] [PubMed] [Google Scholar]
- 12. Belli JFC, Bacal F, Bocchi EA, Guimarães GV.. Ergoreflex activity in heart failure. Arq Bras Cardiol 2011;97:171–178. [DOI] [PubMed] [Google Scholar]
- 13. Pearson M, Smart N.. Effect of exercise training on endothelial function in heart failure patients: a systematic review meta-analysis. Int J Cardiol 2017;231:234–243. [DOI] [PubMed] [Google Scholar]
- 14. Guimarães GV, Silva MSVD, D'avila VM, Ferreira SMA, Silva CP, Bocchi EA.. Peak VO2 and VE/VCO2 slope in the beta-blockers era in patients with heart failure: a Brazilian experience. Arq Bras Cardiol 2008;91:42–48. [DOI] [PubMed] [Google Scholar]
- 15. Downing J, Balady GJ.. The role of exercise training in heart failure. J Am Coll Cardiol 2011;58:561–569. [DOI] [PubMed] [Google Scholar]
- 16. Luo N, Merrill P, Parikh KS, Whellan DJ, Piña IL, Fiuzat M. et al. Exercise training in patients with chronic heart failure and atrial fibrillation. J Am Coll Cardiol 2017;69:1683–1691. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. O’Connor CM, Whellan DJ, Lee KL, Keteyian SJ, Cooper LS, Ellis SJ. et al. Efficacy and safety of exercise training in patients with chronic heart failure: HF-ACTION randomized controlled trial. JAMA 2009;301:1439–1450. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Cornelis J, Myers J, Heidbuchel H, Vrints C, Beckers P.. Exercise training in heart failure patients with persistent atrial fibrillation: a practical approach. Card Fail Rev 2018;4:107–111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Prabhu S, Taylor AJ, Costello BT, Kaye DM, McLellan AJA, Voskoboinik A. et al. Catheter ablation versus medical rate control in atrial fibrillation and systolic dysfunction: the CAMERA-MRI study. J Am Coll Cardiol 2017;70:1949–1961. [DOI] [PubMed] [Google Scholar]
- 20. Marrouche NF, Brachmann J, Andresen D, Siebels J, Boersma L, Jordaens L. et al. Catheter ablation for atrial fibrillation with heart failure. N Engl J Med 2018;378:417–427. [DOI] [PubMed] [Google Scholar]
- 21. Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JGF, Coats AJS, Falk V. et al. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: the Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC [published correction appears in Eur Heart J. 2016 Dec 30]. Eur Heart J 2016;37:2129–‐2200. [DOI] [PubMed] [Google Scholar]
- 22. Tamargo J. Sodium-glucose cotransporter 2 inhibitors in heart Failure: potential mechanisms of action, adverse effects and future developments. Eur Cardiol 2019;14:23–32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Malmo V, Nes BM, Amundsen BH, Tjonna AE, Stoylen A, Rossvoll O. et al. Aerobic interval training reduces the burden of atrial fibrillation in the short term: a randomized trial. Circulation 2016;133:466–473. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.



