Abstract
Exercise training reduces cardiovascular mortality and improves quality of life in CAD patients. We investigated the feasibility and impact of 12 weeks of low-volume high-intensity interval training (HIIT) in CAD-patients. Patients with stable CAD were randomized 1:1 to supervised HIIT or standard care. HIIT sessions were completed three times weekly for 12 weeks on a rowing ergometer. Before and after the 12-week intervention, patients completed a physiological evaluation of cardiorespiratory performance and quality of life questionnaires. Mixed model analysis was used to evaluate differences between and within groups. A total of 142 patients (67 ± 9 years, nHIIT = 64, nStandard care = 78) completed the trial. Training adherence was 97% (range 86–100%). Six patients dropped out because of non-fatal adverse events. Weekly training duration was 54 min with an average power output of 138 W. HIIT increased peak oxygen uptake by 2.5 mL/kg/min (95% CI 2.1–3.0), whereas no change was observed in standard care (0.2 mL/kg/min, 95% CI − 0.2–0.6, P < 0.001). In addition, HIIT improved markers of quality of life, including physical functioning, limitations due to physical illness, general health and vitality (P < 0.05). Twelve weeks of low-volume whole-body HIIT increased cardiorespiratory capacity and improved quality of life in patients with stable CAD compared to standard care. In addition, our study demonstrates that the applied vigorous training regime is feasible for this patient group.
Clinical trial registration: www.clinicaltrials.gov. Identification number: NCT04268992.
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Introduction
Ischemic heart disease is a leading cause of mortality worldwide, with 8.9 million annual deaths1. Atherosclerosis is the most common cause of myocardial ischemia, and the prevalence of patients with symptomatic coronary artery disease (CAD) is accelerating globally2. Thus, feasible and efficient rehabilitation programs, including evidence-based exercise training protocols, are warranted for patients suffering from CAD.
Exercise training is a central component in the treatment of CAD, which is supported at meta-analysis level3 and by a large-scale systematic Cochrane review4. Current guidelines recommend 30–60 min of moderate-intensity exercise at least five times weekly5,6, which may be challenging for frail groups such as CAD patients.
The application of high-intensity interval training (HIIT) has accelerated during the last decade and has been tested in e.g. CAD patients, healthy young individuals and elite athletes7,8,9,10. Collectively, HIIT protocols in different groups of participants have been demonstrated to upregulate several physiological variables such as maximal oxygen uptake, cardiac function and blood volume as well as skeletal muscle mitochondrial function and angiogenesis8,11,12. In recent years, strong clinical interest has arisen in HIIT as an alternative to moderate-intensity continuous exercise13,14. Meta-analysis data confirm that HIIT appears to be superior to moderate-intensity continuous training at increasing peak oxygen uptake in patients with CAD, though the effect on quality of life seems to be similar15,16,17. One of the challenges in comparing HIIT protocols from different studies is the relatively large range in total training volume, interval intensities and duration as well as exercise modalities in the various studies being analysed. Furthermore, there is variation in the characteristics of the different CAD populations studied and limited information on the impact and feasibility of HIIT in elderly individuals18,19. Thus, further research in the application of HIIT exercise protocols in CAD patients is warranted to specify exercise recommendations that optimise health benefits and reduce risk20,21.
The primary objective of the present study was therefore to investigate the effect of low-volume whole-body HIIT on cardiorespiratory performance, physical performance and quality of life in patients with CAD. A secondary aim was to evaluate the feasibility of HIIT for this patient group. We hypothesised firstly that high-intensity rowing has beneficial effects on cardio-respiratory performance, physical performance and quality of life in patients with CAD, and secondly that high-intensity rowing is a feasible exercise protocol for this patient group.
Methods
Study design
The study, designed as a randomised controlled trial with two intervention arms, was conducted at the Department of Medicine, National Hospital of the Faroe Islands, Tórshavn, Faroe Islands. Patients were randomly allocated 1:1 to either supervised HIIT or standard care. Patients in the standard care group were asked to continue their lives as usual and did not participate in more than leisure activity. Specifically, they did not change dietary or exercise habits. We obtained written informed consent from all patients, and the Declaration of Helsinki was followed in all respects. The study was approved by the Faroese Ethics Committee and The Faroese Data Inspectorate, and registered at http://www.clinicaltrials.gov (NCT04268992, first registration 13/02/2020). The data that support the results of this study are available upon request from the corresponding author.
Participants
Patients with CAD were identified from discharge summaries from admissions where invasive coronary angiography was performed, and eligible CAD patients received a letter inviting them to participate in the study. The trial flowchart is illustrated in Fig. 1. At baseline, patients were interviewed about their medical history and the following measurements where performed: blood pressure, 12-lead electrocardiogram, blood samples (renal function, lipid profile, haemoglobin A1c), exercise stress test, transthoracic echocardiography (if more than two years since the last scan), body weight and body composition. Furthermore, all patients completed two questionnaires as detailed below. Following the baseline examination, patients were randomised to one of two groups; supervised HIIT or standard care. Each patient visited the hospital at two additional occasions for blood sampling, an exercise stress test and questionnaires (Fig. 2). The same equipment was used before and after the intervention for the exercise stress test and determination of body weight and body composition. The inclusion and the 12-week randomisation period were performed in two rounds: from July to November 2020, and from January to June 2021.
Inclusion criteria
Patients were included in the study if they were older than 18 years, had angiographically verified CAD treated with percutaneous coronary intervention or coronary artery bypass graft surgery, had previous ST-elevation myocardial infarction/non-ST-elevation myocardial infarction with no need for revascularisation, and at least 12 months since revascularisation or myocardial infarction diagnosis.
Exclusion criteria
Patients were not invited to participate in the study if they were treated with oral anticoagulants, had severe heart failure (ejection fraction < 30% or New York Heart Association > 2), had been given an implantable cardioverter-defibrillator or undergone cardiac resynchronisation therapy, had severe valvular heart disease, had been hospitalised with serious arrhythmia within the preceding 6 months, or had chronic obstructive pulmonary disease GOLD IV. Moreover, patients were excluded if they were unable to perform strenuous exercise and if they participated in ≤ 80% of the exercise sessions during the intervention period.
Randomisation
The allocation sequence and randomisation were based on a predetermined block size of 2, 4, 6, and 8 generated by a computerised random number generator in Microsoft Excel (2016). A note with “Exercise” or “Control” was wrapped in aluminium paper and placed in envelopes. An unaffiliated person performed the randomisation and numbered the envelopes from 1 to 169 in a randomised order. Following the completion of all baseline measurements at the initial visit, the patients were given a sealed envelope containing the patient’s study number.
Exercise test
Patients fasted for ≥ 1.5 h and were instructed to refrain from vigorous exercise for 24 h prior to the experimental testing, and to avoid alcohol, tobacco and caffeine on the day of testing.
Peak oxygen uptake (VO2peak) and maximal power output (Wmax) were determined using a modified protocol from a previous study in our research group22. The patients completed an incremental cycling test to exhaustion on an electronically braked cycle ergometer (Excalibur Sport, Lode, Groningen, Netherlands) with continuous measurement of VO2 using an online gas collection system (model Cosmed, Quark b2, Milano, Italy). Heart rate was monitored (HRM-Dual, Garmin, Olathe, Kansas, USA) throughout the test. Gas analysers and the flow sensor of the applied spirometer were frequently calibrated.
The exercise protocol was initiated with a 6-min warm-up period; 3 min at 30 or 50 W followed by 3 min at 50 or 70 W for women and men, respectively, after which the workload was increased by 15 or 20 W/min for women and men until exhaustion. Patients were verbally encouraged and motivated throughout the test, and they were blinded to pulmonary measurements, power output and time elapsed. Breath-by-breath VO2 values and ventilation were averaged over 30 s; the maximal pulmonary ventilation and VO2peak were defined as the highest 30-s value. Submaximal VO2 (VO2submax) was determined as the average oxygen uptake during the final 30 s of the warm-up interval. Maximal power output was calculated as Wcompl + 15 (t/60) for women and Wcompl + 20 (t/60) for men, where Wcompl is the last fully completed workload and t is the time sustained at the final workload. Maximal heart rate (HRmax) was defined as the highest measured heart rate, and submaximal heart rate (HRsubmax) was determined as average HR during the final 30 s of the warm-up bout.
Body composition
Body composition was assessed using bioelectrical impedance analysis under standardised conditions during the laboratory visits (InBody 270, Biospace, California, USA23).
Questionnaires
All patients completed questionnaires about physical activity level (International Physical Activity Questionnaire-Short Form (IPAQ-SF)24) and quality of life (Short Form 36 Health Survey Questionnaire (SF-36v2)25) at baseline and study end. IPAQ-SF reports physical activity during the last 7 days. Patients in the HIIT group were informed not to include the physical activity related to the intervention in the IPAQ-SF questionnaire. Results in SF-36v2 are presented as T-scores, which are calculated with means and standard deviations from the U.S. general population in 2009 using software from Quality Metric25. Dietary habits were not monitored, but patients were instructed to avoid marked changes during the intervention.
Exercise training
The patients completed ~ 30-min rowing sessions three times weekly for 12 weeks on a wind-braked rowing ergometer with slides (Concept 2 model D w. PM5, Vermont, United States). Ergometer rowing was chosen because it taxes the cardiorespiratory system markedly due to the large active muscle mass26. All training sessions were supervised by experienced rowing specialists.
The training program was designed according to the well-documented efficiency of HIIT for improving both cardiovascular and muscular oxidative capacity8,27. Training sessions consisted of short-duration (≤ 2 min) exhaustive high-intensity interval bouts utilising a 1:1 work-to-rest ratio. To reduce the risk of injury, the initial 6 sessions of the training intervention were predominantly focused on familiarisation with the rowing ergometer, rowing technique and training modality. Subsequently, an individual target intensity defined as 100% of the average maximum workload (W) from session 7 was provided for each training session. The target intensity was adjusted based on the average maximum workload on session 16 (week 6) and session 25 (week 9) to account for training-induced improvements (see Table S3 in the Supplementary for a detailed overview of the training program).
Power output during the exercise intervals was registered in weeks 3, 6 and 9. The average intensity during the intervals was quantified and normalised to the average power that patients were able to sustain during a 5-min all-out rowing performance test completed in week five. The patients were encouraged to perform as much work as possible during the 5 min and explicitly instructed to pace themselves for a high average power output instead of going all out from the beginning.
Adverse events
Adverse events were registered continuously and at each hospital visit. Severe adverse events were defined as all-cause mortality, hospitalisation for CAD or atrial and ventricular arrhythmia. An adverse event was considered moderate if it was an exercise injury that caused the patient to withdraw from the study because of musculoskeletal injuries (e.g. back pain, joint pain). Mild adverse events were considered self-limited if it was possible to start and/or restart training (nausea, muscle soreness, fatigue, mild vertigo).
Statistical analysis
Demographical data are presented as means with standard deviation or medians with 25th and 75th percentiles, and compared using an unpaired t-test or Mann–Whitney test. Proportions are presented in percent and compared using Pearson’s chi squared test or Fisher’s exact test if assumptions were not met for the chi-square test. Changes from baseline to after the intervention are presented as means with 95% confidence intervals [95% CI lower limit; upper limit] unless otherwise stated. Possible between-group differences in continuous endpoints were evaluated for all completed cases by a mixed-model repeated measures approach by means of the SPSS MIXED method28. Group (HIIT vs standard care), time (pre vs post intervention) and group × time interaction were specified as fixed factors. The between-group differences in response to the intervention were assessed by the group × time interaction effect. A significant group × time interaction was further evaluated by a Sidak-adjusted pairwise comparison. Random variation and repeated effects were defined from individual patients. Independence of the obtained data was assumed in the model. Visual inspection of homogeneity of residual variance and normality of the residual was performed for all data. If a clear violation of the model assumptions occurred, data were logarithmically transformed to conform to the model assumptions and presented as medians with 95% CI. Finally, possible correlations between changes in VO2peak and markers of quality of life were assessed by the Pearson’s correlation test and an intention to treat analyses was performed on absolute VO2peak, VO2peak adjusted for body weight and Wmax. The level of statistical significance was set at P < 0.05. The primary outcomes in the present study were VO2peak and the summary component related to physical health; a marker of quality of life. With an alpha level of 0.05 and a sample size of 64 patients in HIIT and 78 patients in standard care, the trial is provided with 99% and 86% power to detect expected differences in VO2peak and physical component summary, respectively29. Sample size was calculated based on markers of fibrinolysis (see clinicaltrials.gov: NCT04268992), and these data will be reported elsewhere. MM has full access to all the data in the study and takes responsibility for its integrity and the data analysis. Statistical analyses were performed using IBM SPSS statistics v.27.0.0.
Results
Baseline characteristics
Figure 1 illustrates the recruitment of CAD patients. We sent invitation letters to 478 eligible CAD patients, and 169 agreed to participate in the study. The most common reasons for declining are listed in Fig. 1. In total, 142 patients completed the study; 64 in the exercise group and 78 in the standard care group. Baseline characteristics for the study patients are presented in Table 1. The mean age for all patients was 67 years (33 patients > 75 years), and the majority of the patients (80%) were men. In the standard care group, all patients were treated with acetylsalicylic acid. In the HIIT group, 60 out of 64 patients were treated with acetylsalicylic acid, three patients were treated with clopidogrel and one patient did not take any antithrombotic medication. Treatment with angiotensin-converting enzyme-inhibitors was significantly more common in the HIIT group compared with the standard care group. Moreover, all patients had stable coronary artery disease with a Canadian cardiovascular society-score ≤ 1.
Exercise training
Each training session started with a 6 min warm-up on the rowing ergometer followed by an average of 12 min of active interval training time. Thus, the total active training time was ~ 18 min/session. The average power output during the warm-up and intervals was 86 ± 34 W and 138 ± 46 W, respectively, corresponding to 72 ± 19% and 117 ± 11% of the average power that the patients could sustain during a 5-min all-out effort. Adherence to the exercise sessions was 97% (86–100%).
Cardiovascular adaptions
The applied exercise training regime increased absolute VO2peak and VO2peak adjusted for body weight by 197 mL/min [160; 233] and 2.5 mL/kg/min [2.1; 3.0] (n = 60), respectively, whereas no changes were observed after standard care (8 mL/min [− 24; 46] and 0.2 mL/kg/min [− 0.2; 0.6], group × time interaction P < 0.001; Fig. 3A,B). In contrast, Wmax improved in both groups, but the improvement was significantly higher in HIIT compared to standard care (23 W [19; 27] (n = 60) vs 3.7 W [0.1; 7.2] (n = 76) group × time interaction P < 0.001; Fig. 3C). The intention to treat analyses on absolute VO2peak, VO2peak adjusted for body weight and Wmax showed similar results compared with the per-protocol analysis. VEmax remained constant in standard care (− 0.9 [− 3.1; 1.2] L/min) but increased by 13 L/min [11; 16] in HIIT (group × time interaction P < 0.001; Table 2). In addition, submaximal heart rate decreased by − 5 BPM [− 7; − 3] in HIIT, while it was unaffected in standard care (− 1.4 BPM [− 3.4; 0.6], group × time interaction P < 0.001; Table 2).
In addition, we performed an exploratory sub-group analysis on patients > 75 years of age. Absolute VO2peak and VO2peak adjusted for body weight increased by 129 mL/min [77; 182] and 1.7 mL/kg/min [1.1; 2.4] in HIIT while it remained unaffected in standard care (− 3 mL/kg/min [− 48; 41] and 0.1 mL/kg/min [− 0.5; 0.6], P < 0.001 for group × time interaction in both analyses).
Body composition
Exercise training reduced (P < 0.001) body fat mass and body fat percentage by − 1.5 kg [− 2.2; − 0.8] and − 1.5% [− 2.0; − 1.0], respectively, whereas no changes were observed in the standard care group (group × time interaction P < 0.05; Table 2). Due to methodological problems, body composition measures were only obtained in half of the patients.
Quality of life
In general, exercise training increased markers of quality of life associated with physical health which is illustrated by a pronounced improvement (P < 0.001) in physical component summary. Specifically, a group × time interaction (all P-values < 0.05) existed for three out of four components related to physical health; physical functioning, role limitations due to physical illness and general health (Table 3). In addition, a group × time interaction (P < 0.01) existed for one of four components related to mental health; vitality.
Associations between VO2peak and quality of life
The changes in absolute VO2peak were significantly and positively correlated with changes in physical functioning (Pearson’s r = 0.21 [0.04; 0.37], P < 0.05), general health (Pearson’s r = 0.31 [0.15; 0.45], P < 0.001), vitality (Pearson’s r = 0.37 [0.21; 0.51], P < 0.001) and social functioning [Pearson’s r = 0.19 [0.02; 0.34], P < 0.05). Accordingly, a significant correlation existed between changes in VO2peak and changes in both physical component summary (Pearson’s r = 0.24 [0.07; 0.40], P < 0.01) and mental component summary [Pearson’s r = 0.21 [0.04; 0.37], P < 0.05).
Physical activity
During the 12-week intervention, there was no between-group difference in total physical activity, vigorous activity, moderate activity or walking, nor sitting hours. The results are presented in Supplementary, Table S1. Despite no group × time interaction, it can be noted that patients in the HIIT group demonstrated a significant reduction in walking hours from pre- to post intervention (P < 0.05). Data were log transformed (excluding sitting hours) because they were not normally distributed.
Lipid profile and haemoglobin A1c
Haemoglobin A1c and lipid parameters did not change over time either between or within groups (Supplementary Table S2).
Safety and feasibility
One non-fatal severe adverse event was reported due to worsening of angina. Two patients withdrew their consent to participate because of training-related moderate adverse events (lower back pain and knee pain). Mild self-limiting adverse events were reported in three cases (ankle pain, mild vertigo/hypotension, palpitations). In general, the patients gave positive feedback on the exercise training and adherence was high. As expected, the dropout was higher in the HIIT group compared to standard care, 23% vs 9% (P = 0.02), Fig. 1. However, if dropouts before the intervention start are taken into account, the rates were 13% vs 9%, P = 0.33 (adverse event, training-related injuries and adherence ≤ 80%).
Discussion
In the present study, we randomised CAD patients to either whole-body HIIT or standard care, and demonstrated for the first time that low-volume HIIT training performed on a rowing ergometer, which involves both upper and lower body, was feasible and resulted in significant improvements in VO2peak, body fat mass and quality of life. Adherence to the prescribed exercise training sessions was high and the applied HIIT protocol was well tolerated and positively perceived by this patient group with few adverse events and training injuries. There were no fatal adverse events.
Exercise training and cardiovascular endpoints
We utilized a 12-week interval-based training program consisting predominantly of short-duration (≤ 2 min) high-intensity intervals. The high intensity of the exercise training intervention is confirmed by the average power output of ~ 140 W during the intervals, corresponding to 117% of the average power the patients could sustain during a 5-min all-out rowing test. The efficient training time, including warm-up, totalled only ~ 18 min/session, corresponding to a weekly training volume of ~ 54 min. This is considerably less than the 150 min/week of moderate-intensity aerobic physical activity recommended for patients with CAD by the European Council of Cardiology6,30. Despite the low training volume, we observed significantly different changes in VO2peak of 2.2 mL/kg/min between those assigned HIIT compared to standard care. The efficiency of the applied training intervention for upregulating cardiorespiratory fitness is additionally confirmed by the substantial improvements in submaximal heart rate and peak pulmonary ventilation after HIIT only. However, the training-induced changes in VO2peak in the present study are lower compared to a recent meta-analysis of 16 randomised controlled trials31, which reported an average VO2peak improvement of 4.52 mL/kg/min in response to 4–12 weeks of exercise training in patients with coronary artery disease. In addition, it was reported that studies with medium-to-long HIIT intervals and studies utilising a work-to-rest ratio > 1 demonstrated the most significant improvements in VO2peak16. Thus, the application of repetitive exposure to short-duration (≤ 2 min) intervals with a 1:1 work-to-rest ratio, as applied in the present study, may not be optimal for improving cardiorespiratory fitness and may therefore be one of the explanatory factors for the discrepancies between the VO2peak improvements in the present study compared to Du et al.16. In contrast, the observed changes in VO2peak in the present study are considerably higher than those reported by a recent meta-analysis31 (based on 8 randomised controlled trials) of 436 patients with heart failure with preserved ejection fraction, demonstrating an average VO2peak improvement of 1.7 mL/kg/min in response to 12–24 weeks of exercise-training compared with habitually active controls. In addition, a recent randomised clinical trial amongst 120 patients with heart failure with preserved ejection fraction assigned (1:1:1) to either HIIT (3 × 38 min/week), moderate continuous training (5 × 40 min/week) or guideline control (1 × advice on physical activity) reported numeric changes in VO2peak of 1.1, 1.6 and − 0.6 mL/kg/min, respectively, after 3 months, with no significant difference between HIIT and moderate continuous training32. Thus, comparing the training-induced increases in VO2peak after HIIT in Mueller et al.32 with the present findings, we observed more than a twofold higher training-induced increase in VO2peak (2.5 vs. 1.1 mL/kg/min) despite a ~ twofold lower weekly training volume (54 vs. 114 min/week), which may indicate a higher susceptibility to exercise training for improving cardiorespiratory fitness in CAD patients compared to heart failure patients.
No a priori-defined minimal clinically difference in VO2peak change was set in the present study. However, previous studies have set it at 2.5 mL/kg/min32, which is the exact magnitude of training-induced increase in VO2peak observed after HIIT in the present study, although the between-group difference was marginally lower (2.2 mL/kg/min). Importantly, the level of cardiorespiratory performance is strongly associated with cardiovascular endpoints in healthy individuals as well as patients with cardiovascular disease33. Specifically, epidemiological evidence shows that a 1-MET improvement in aerobic capacity is associated with a 13% reduction in all-cause mortality and a 15% reduction in cardiovascular disease events in healthy individuals34.
Although Mueller et al.32 reported no statistical difference between VO2peak changes in response to HIIT vs. moderate-intensity continuous training in patients with heart failure, accumulating meta-analysis-level evidence shows that HIIT appears to have superior cardiorespiratory benefits compared to moderate-intensity continuous training in patients with CAD15,16,17,18,35,36. Continuous training is characterised by a constant submaximal workload and steady-state oxygen uptake, whereas HIIT is characterised by short periods of extremely high workload alternated with periods of recovery. The higher efficacy of HIIT is likely caused by the repetitive cardiorespiratory and metabolic strain triggered by the repeated exposure to an intense stimulus, and this is most likely a driver of e.g. cardiovascular remodelling and a resultant increase in aerobic capacity37. It is well documented that exercise training plays a central role in the treatment of CAD patients, and current guidelines recommend a comprehensive cardiac rehabilitation program2,5. There is evidence supporting beneficial effects of exercise training in patients with CAD in relation to survival rates and a direct mechanistic impact on the pathogenesis is assumed38,39,40. A recent Cochrane meta-analysis review supports this recommendation by demonstrating that long-term exercise training significantly reduces cardiovascular death and hospital admissions in patients with CAD41. Accordingly, prior research has shown that CAD patients who continue to be physically active have the lowest mortality risk42, however, initiating physical exercise in sedentary and high-risk CAD patients was associated with the greatest reduction in cardiovascular death43. However, adhering to time-consuming and high-frequency exercise training program may be challenging for people, such as CAD patients, with a lower general health status and fitness than the general population.
Collectively, the present findings provide compelling evidence of the health-beneficial effects of low-volume HIIT for stable CAD patients compared to standard care, as well as the high feasibility of the applied training modality for this specific patient group.
HIIT and quality of life
The present study also shows that quality of life improved after the 12 week HIIT intervention compared to standard care. Moreover, there was a significant positive correlation between changes in VO2peak and markers for quality of life, which emphasizes the importance of cardiorespiratory fitness for improving quality of life. However, it is well established that exercise training improves quality of life in CAD patients41,44, and recently it was also investigated whether HIIT or moderate-intensity continuous training affected quality of life differently. Indeed, two new meta-analyses demonstrate that both moderate-intensity continuous training and HIIT are equally efficient with regard to upregulated quality of life, even if HIIT has a superior effect on peak VO2 gain in patients with CAD15,16. In addition to the beneficial effects of the training intervention on quality of life, HIIT also improved variables such as self-rated general health and vitality, which is also supported by other exercise training studies with patient groups29,45. These measures are essential for exercise motivation, continuation and adherence to a training program, which indicates that the applied training modality may be sustainable for this type of patient. Future studies should aim to further investigate the psychological effects of HIIT for CAD patients.
HIIT improves cardiovascular fitness in CAD patients older than 75 years
Patients who participated in our study were older than the patients in the majority of studies examining HIIT in CAD patients18 (see Table 1). Previous studies have reported that regular exercise training reduces the risk of cardiovascular disease and mortality in healthy, elderly individuals46. Also, a large retrospective study showed that cardiac rehabilitation is associated with decreased mortality in elderly CAD patients (> 65 years of age)47, although the underlying mechanisms remain largely unknown. However, a training-induced enhancement in the responsiveness of the β adrenergic receptor, a receptor that deteriorates with aging, may partially explain the improvements in cardiovascular health reported in elderly engaging in regular physical activity48.
Several previous reviews call for more evidence on the effect of HIIT compared to moderate-intensity continuous training in elderly with CAD. In particular, the literature calls for data on patients older than 75 years18,19. The present study showed that HIIT is safe and improves cardiorespiratory fitness in older CAD patients. Indeed, for this sub-group of CAD patients ≥ 75 years, the HIIT intervention also significantly increased absolute VO2peak and VO2peak adjusted for body weight compared to standard care. Our findings are supported by others using high-intensity interval training in elderly populations49,50.
Effect of HIIT on body composition and low-density lipoprotein cholesterol
Based on body composition assessments, patients in our study were moderately overweight. A training-induced fat loss of 1.5 kg was observed in the HIIT group without loss in total body weight. These findings are supported by previous studies reporting reduced fat mass and increased skeletal muscle mass as well-established consequences of high-intensity training8,9, also in the absence of weight loss51. Total cholesterol and low-density lipoprotein cholesterol (LDL-C) were not affected by exercise training in this study. In contrast to our findings, Pedersen et al.52 reported a reduced LDL-C in response to 12 weeks of aerobic interval training in sedentary overweight patients with CAD. However, these discrepancies may be explained by the observed weight-loss in the exercise group in Pedersen et al.52. The body composition data should be interpreted with caution due to the use of bioelectrical impedance technology and not dual-energy X-ray absorptiometry scans being the gold standard.
Safety
Despite the high intensity of the training, and the whole-body training approach, we only registered two training-related injuries and one adverse event. In conjunction with a training adherence of ~ 97% these findings clearly demonstrate the feasibility of the applied training modality for this elderly and frail patient population.
Strength and limitations
The strengths of the present study include the systematic and supervised nature of the HIIT intervention, the high compliance, the large sample size and the relatively high average age of the patient population. Moreover, the validity of the cardiorespiratory adaptations should be optimal because the cardiorespiratory test was performed on a cycle ergometer, whilst the exercise intervention was performed on rowing ergometers and thereby minimising the learning effect. Thus, the risk of habituation to the cardiorespiratory test is considered to be minimal. However, some limitations should be considered. The gender ratio was skewed (83% of the patients were males and 17% females) because CAD is more common in men than in than their women counterparts53. We cannot exclude that daily medication or comorbidities of the patients may have affected the training response. A total of 65% of the patients received treatment with a beta blocker. Beta blockers lower the heart rate, and may therefore have affected maximal heart rate and other heart rate measures in our study. However, they should not have affected exercise training and cardiorespiratory fitness54.
Conclusion
In conclusion, we demonstrated that 12 weeks of whole-body HIIT improves VO2peak and quality of life in elderly patients with stable CAD. Consequently, a combination of HIIT and standard medical treatment can be advised as a safe, feasible and efficient treatment strategy aimed at improving cardiovascular health and quality of life in patients with stable CAD.
Data availability
The dataset generated and analysed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- CAD:
-
Coronary artery disease
- HIIT:
-
High-intensity interval training
- VO2peak :
-
Peak oxygen uptake
- Wmax :
-
Maximal power output
- VO2submax :
-
Submaximal oxygen uptake
- HRmax :
-
Maximal heart rate
- HRsubmax :
-
Submaximal heart rate
- IPAQ-SF:
-
International Physical Activity Questionnaire-Short Form
- SF-36v2:
-
Short Form 36 Health Survey Questionnaire
References
World Health Organization. The Top 10 Causes of Death. https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death (Accessed 25 January 2022) (2020).
Piepoli, M. F. et al. 2016 European Guidelines on cardiovascular disease prevention in clinical practice: The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts) Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR). Eur. Heart J. 37, 2315–2381. https://doi.org/10.1093/eurheartj/ehw106 (2016).
Taylor, R. S. et al. Exercise-based rehabilitation for patients with coronary heart disease: Systematic review and meta-analysis of randomized controlled trials. Am. J. Med. 116, 682–692. https://doi.org/10.1016/j.amjmed.2004.01.009 (2004).
Dibben, G. et al. Exercise-based cardiac rehabilitation for coronary heart disease. Cochrane Database Syst. Rev. 11, CD001800. https://doi.org/10.1002/14651858.CD001800.pub4 (2021).
Smith, S. C. et al. AHA/ACCF secondary prevention and risk reduction therapy for patients with coronary and other atherosclerotic vascular disease: 2011 update: A guideline from the American Heart Association and American College of Cardiology Foundation endorsed by the World Heart Federation and the Preventive Cardiovascular Nurses Association. J. Am. Coll. Cardiol. 58, 2432–2446. https://doi.org/10.1016/j.jacc.2011.10.824 (2011).
Pelliccia, A. et al. 2020 ESC Guidelines on sports cardiology and exercise in patients with cardiovascular disease. Eur. Heart J. 42, 17–96. https://doi.org/10.1093/eurheartj/ehaa605 (2021).
Keteyian, S. J. et al. Greater improvement in cardiorespiratory fitness using higher-intensity interval training in the standard cardiac rehabilitation setting. J. Cardiopulm. Rehabil. Prev. 34, 98–105. https://doi.org/10.1097/HCR.0000000000000049 (2014).
Gibala, M. J., Little, J. P., Macdonald, M. J. & Hawley, J. A. Physiological adaptations to low-volume, high-intensity interval training in health and disease. J. Physiol. 590, 1077–1084. https://doi.org/10.1113/jphysiol.2011.224725 (2012).
Mohr, M. et al. High-intensity intermittent swimming improves cardiovascular health status for women with mild hypertension. Biomed. Res. Int. 2014, 728289. https://doi.org/10.1155/2014/728289 (2014).
Fransson, D. et al. Skeletal muscle and performance adaptations to high-intensity training in elite male soccer players: Speed endurance runs versus small-sided game training. Eur. J. Appl. Physiol. 118, 111–121. https://doi.org/10.1007/s00421-017-3751-5 (2018).
Wisloff, U. et al. Superior cardiovascular effect of aerobic interval training versus moderate continuous training in heart failure patients: A randomized study. Circulation 115, 3086–3094. https://doi.org/10.1161/CIRCULATIONAHA.106.675041 (2007).
Moholdt, T. T. et al. Aerobic interval training versus continuous moderate exercise after coronary artery bypass surgery: A randomized study of cardiovascular effects and quality of life. Am. Heart J. 158, 1031–1037. https://doi.org/10.1016/j.ahj.2009.10.003 (2009).
Gayda, M., Ribeiro, P. A., Juneau, M. & Nigam, A. Comparison of different forms of exercise training in patients with cardiac disease: Where does high-intensity interval training fit? Can. J. Cardiol. 32, 485–494. https://doi.org/10.1016/j.cjca.2016.01.017 (2016).
Winzer, E. B., Woitek, F. & Linke, A. Physical activity in the prevention and treatment of coronary artery disease. J. Am. Heart Assoc. 7, 7725. https://doi.org/10.1161/JAHA.117.007725 (2018).
Gomes-Neto, M. et al. High-intensity interval training versus moderate-intensity continuous training on exercise capacity and quality of life in patients with coronary artery disease: A systematic review and meta-analysis. Eur. J. Prev. Cardiol. 24, 1696–1707. https://doi.org/10.1177/2047487317728370 (2017).
Du, L. et al. Effect of high-intensity interval training on physical health in coronary artery disease patients: A meta-analysis of randomized controlled trials. J. Cardiovasc. Dev. Dis. https://doi.org/10.3390/jcdd8110158 (2021).
Pattyn, N., Beulque, R. & Cornelissen, V. Aerobic interval vs continuous training in patients with coronary artery disease or heart failure: An updated systematic review and meta-analysis with a focus on secondary outcomes. Sports Med. 48, 1189–1205. https://doi.org/10.1007/s40279-018-0885-5 (2018).
Hannan, A. L. et al. High-intensity interval training versus moderate-intensity continuous training within cardiac rehabilitation: A systematic review and meta-analysis. Open Access J. Sports Med. 9, 1. https://doi.org/10.2147/OAJSM.S150596 (2018).
Goncalves, C., Raimundo, A., Abreu, A. & Bravo, J. Exercise intensity in patients with cardiovascular diseases: Systematic review with meta-analysis. Int. J. Environ. Res. Public Health. https://doi.org/10.3390/ijerph18073574 (2021).
Tucker, W. J. et al. Exercise for primary and secondary prevention of cardiovascular disease: JACC focus seminar 1/4. J. Am. Coll. Cardiol. 80, 1091–1106. https://doi.org/10.1016/j.jacc.2022.07.004 (2022).
Quindry, J. C., Franklin, B. A., Chapman, M., Humphrey, R. & Mathis, S. Benefits and risks of high-intensity interval training in patients with coronary artery disease. Am. J. Cardiol. 123, 1370–1377. https://doi.org/10.1016/j.amjcard.2019.01.008 (2019).
Sjúrðarson, T. et al. Effect of angiotensin-converting enzyme inhibition on cardiovascular adaptation to exercise training. Physiol. Rep. 10, e15382. https://doi.org/10.14814/phy2.15382 (2022).
Ward, L. C. Bioelectrical impedance analysis for body composition assessment: Reflections on accuracy, clinical utility, and standardisation. Eur. J. Clin. Nutr. 73, 194–199. https://doi.org/10.1038/s41430-018-0335-3 (2019).
The IPAQ Group. International Physical Activity Questionnaire. https://sites.google.com/site/theipaq/home (Accessed 25 January 2022) (2021).
Quality Metric. Quality Metric, SF-36v2 Health Survey is Designed to Measure Functional Health and Well-Being from the Patient’s Point of View. https://www.qualitymetric.com/health-surveys-old/the-sf-36v2-health-survey/ (Accessed 3 February 2022).
Volianitis, S., Yoshiga, C. C. & Secher, N. H. The physiology of rowing with perspective on training and health. Eur. J. Appl. Physiol. 120, 1943–1963. https://doi.org/10.1007/s00421-020-04429-y (2020).
Nordsborg, N. B. et al. Oxidative capacity and glycogen content increase more in arm than leg muscle in sedentary women after intense training. J. Appl. Physiol. 119, 116–123. https://doi.org/10.1152/japplphysiol.00101.2015 (2015).
Cnaan, A., Laird, N. M. & Slasor, P. Using the general linear mixed model to analyse unbalanced repeated measures and longitudinal data. Stat. Med. 16, 2349–2380. https://doi.org/10.1002/(sici)1097-0258(19971030)16:20%3c2349::aid-sim667%3e3.0.co;2-e (1997).
Conraads, V. M. et al. Aerobic interval training and continuous training equally improve aerobic exercise capacity in patients with coronary artery disease: The SAINTEX-CAD study. Int. J. Cardiol. 179, 203–210. https://doi.org/10.1016/j.ijcard.2014.10.155 (2015).
World Health Organization. Physical Activity. https://www.who.int/news-room/fact-sheets/detail/physical-activity (Accessed 26 November 2020).
Fukuta, H., Goto, T., Wakami, K., Kamiya, T. & Ohte, N. Effects of exercise training on cardiac function, exercise capacity, and quality of life in heart failure with preserved ejection fraction: A meta-analysis of randomized controlled trials. Heart Fail. Rev. 24, 535–547. https://doi.org/10.1007/s10741-019-09774-5 (2019).
Mueller, S. et al. Effect of high-intensity interval training, moderate continuous training, or guideline-based physical activity advice on peak oxygen consumption in patients with heart failure with preserved ejection fraction: A randomized clinical trial. Jama 325, 542–551. https://doi.org/10.1001/jama.2020.26812 (2021).
Myers, J. et al. Exercise capacity and mortality among men referred for exercise testing. N. Engl. J. Med. 346, 793–801. https://doi.org/10.1056/NEJMoa011858 (2002).
Kodama, S. et al. Cardiorespiratory fitness as a quantitative predictor of all-cause mortality and cardiovascular events in healthy men and women: A meta-analysis. JAMA 301, 2024–2035. https://doi.org/10.1001/jama.2009.681 (2009).
Elliott, A. D., Rajopadhyaya, K., Bentley, D. J., Beltrame, J. F. & Aromataris, E. C. Interval training versus continuous exercise in patients with coronary artery disease: A meta-analysis. Heart Lung Circ. 24, 149–157. https://doi.org/10.1016/j.hlc.2014.09.001 (2015).
Liou, K., Ho, S., Fildes, J. & Ooi, S. Y. High intensity interval versus moderate intensity continuous training in patients with coronary artery disease: A meta-analysis of physiological and clinical parameters. Heart Lung Circ. 25, 166–174. https://doi.org/10.1016/j.hlc.2015.06.828 (2016).
Gibala, M. J. Physiological basis of interval training for performance enhancement. Exp. Physiol. 106, 2324–2327. https://doi.org/10.1113/EP088190 (2021).
Pedersen, B. K. & Saltin, B. Exercise as medicine—Evidence for prescribing exercise as therapy in 26 different chronic diseases. Scand. J. Med. Sci. Sports 25(Suppl 3), 1–72. https://doi.org/10.1111/sms.12581 (2015).
Akyuz, A. Exercise and coronary heart disease. Adv. Exp. Med. Biol. 1228, 169–179. https://doi.org/10.1007/978-981-15-1792-1_11 (2020).
Gambardella, J., Morelli, M. B., Wang, X. J. & Santulli, G. Pathophysiological mechanisms underlying the beneficial effects of physical activity in hypertension. J. Clin. Hypertens. (Greenwich) 22, 291–295. https://doi.org/10.1111/jch.13804 (2020).
Anderson, L. et al. Exercise-based cardiac rehabilitation for coronary heart disease: Cochrane systematic review and meta-analysis. J. Am. Coll. Cardiol. 67, 1–12. https://doi.org/10.1016/j.jacc.2015.10.044 (2016).
Gonzalez-Jaramillo, N. et al. Systematic review of physical activity trajectories and mortality in patients with coronary artery disease. J. Am. Coll. Cardiol. 79, 1690–1700. https://doi.org/10.1016/j.jacc.2022.02.036 (2022).
Stewart, R. A. H. et al. Physical activity and mortality in patients with stable coronary heart disease. J. Am. Coll. Cardiol. 70, 1689–1700. https://doi.org/10.1016/j.jacc.2017.08.017 (2017).
Jaureguizar, K. V. et al. Effect of high-intensity interval versus continuous exercise training on functional capacity and quality of life in patients with coronary artery disease: A randomized clinical trial. J. Cardiopulm. Rehabil. Prev. 36, 96–105. https://doi.org/10.1097/HCR.0000000000000156 (2016).
Reed, J. L. et al. The effects of high-intensity interval training, Nordic walking and moderate-to-vigorous intensity continuous training on functional capacity, depression and quality of life in patients with coronary artery disease enrolled in cardiac rehabilitation: A randomized controlled trial (CRX study). Prog. Cardiovasc. Dis. https://doi.org/10.1016/j.pcad.2021.07.002 (2021).
Barbiellini Amidei, C. et al. Association of physical activity trajectories with major cardiovascular diseases in elderly people. Heart 108, 360–366. https://doi.org/10.1136/heartjnl-2021-320013 (2022).
Suaya, J. A., Stason, W. B., Ades, P. A., Normand, S. L. & Shepard, D. S. Cardiac rehabilitation and survival in older coronary patients. J. Am. Coll. Cardiol. 54, 25–33. https://doi.org/10.1016/j.jacc.2009.01.078 (2009).
Santulli, G., Ciccarelli, M., Trimarco, B. & Iaccarino, G. Physical activity ameliorates cardiovascular health in elderly subjects: The functional role of the β adrenergic system. Front. Physiol. 4, 209. https://doi.org/10.3389/fphys.2013.00209 (2013).
Storen, O. et al. The effect of age on the VO2max response to high-intensity interval training. Med. Sci. Sports Exerc. 49, 78–85. https://doi.org/10.1249/MSS.0000000000001070 (2017).
de Guia, R. M. et al. Aerobic and resistance exercise training reverses age-dependent decline in NAD(+) salvage capacity in human skeletal muscle. Physiol. Rep. 7, e14139. https://doi.org/10.14814/phy2.14139 (2019).
Ross, R. et al. Reduction in obesity and related comorbid conditions after diet-induced weight loss or exercise-induced weight loss in men. A randomized, controlled trial. Ann. Intern. Med. 133, 92–103. https://doi.org/10.7326/0003-4819-133-2-200007180-00008 (2000).
Pedersen, L. R. et al. Weight loss is superior to exercise in improving the atherogenic lipid profile in a sedentary, overweight population with stable coronary artery disease: A randomized trial. Atherosclerosis 246, 221–228. https://doi.org/10.1016/j.atherosclerosis.2016.01.001 (2016).
Mosca, L., Barrett-Connor, E. & Wenger, N. K. Sex/gender differences in cardiovascular disease prevention: What a difference a decade makes. Circulation 124, 2145–2154. https://doi.org/10.1161/CIRCULATIONAHA.110.968792 (2011).
Gordon, N. F. & Duncan, J. J. Effect of beta-blockers on exercise physiology: Implications for exercise training. Med. Sci. Sports Exerc. 23, 668–676 (1991).
Acknowledgements
The authors would like to thank all the participants for their keen commitment and enthusiastic participation. We would also like to acknowledge the technical assistance of Toni Dam, Magnus Norðberg, Jón Bjarnason, laboratory technicians Nina Djurhuus and Gunnrið Jóanesarson, laboratory assistants Halla Weihe Reinert, Katrin Mortensen, Billa Mouritsardóttir Foldbo, and Súsanna Jacobsen and Jacob Bjørne for his help with scoring the SF-36v2 questionnaire. We also acknowledge PhD students and colleagues Sanna á Borg and Marnar Fríðheim Kristiansen for their support and help with blood sampling.
Funding
The study was funded by Aarhus University, Research Council Faroe Islands (Project Number 3029), the Betri Foundation, Central Jutland Region, the Fabrikant Karl G. Andersen Foundation, and the A.P. Moller Foundation.
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J.K., E.L.G., AM.H., S.D.K. conceived the study. J.K., E.L.G., AM.H., S.D.K., M.M., T.S. finalised the design. All authors contributed to study conduction, data analysis, result interpretation, writing and revision of the manuscript.
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Kristiansen, J., Sjúrðarson, T., Grove, E.L. et al. Feasibility and impact of whole-body high-intensity interval training in patients with stable coronary artery disease: a randomised controlled trial. Sci Rep 12, 17295 (2022). https://doi.org/10.1038/s41598-022-21655-w
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DOI: https://doi.org/10.1038/s41598-022-21655-w
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