SYSTEMATIC REVIEW article
Sec.Movement Science and Sport Psychology
Can Exercise Reduce the Autonomic Dysfunction of Patients With Cancer and Its Survivors? A Systematic Review and Meta-Analysis
- 1PhD International School, Program of Epidemiology and Public Health (Interuniversity), Rey Juan Carlos University, Móstoles, Spain
- 2Centre for Sport Studies, Rey Juan Carlos University, Fuenlabrada, Spain
- 3GO fitLAB, Ingesport, Madrid, Spain
- 4College of Health Sciences, University of Rhode Island, Kingston, NY, United States
- 5Advanced Wellbeing Research Centre, College of Health, Wellbeing and Life Sciences, Sheffield Hallam University, Sheffield, United Kingdom
Background: Cancer therapies have increased patient survival rates, but side effects such as cardiotoxicity and neurotoxicity can lead to autonomic nervous and cardiovascular system dysfunction. This would result in a decrease in parasympathetic activity and the enhancement of sympathetic activity. Heart rate variability (HRV), which reflects autonomic modulation, is a valuable physiological tool since it correlates with cancer-related fatigue, stress, depression, and mortality in patients with cancer.
Objective: This study aimed to analyze the effects of exercise programs on the autonomic modulation, measured by the HRV of patients with cancer and its survivors.
Methods: The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were followed, and the quality of the articles was assessed with the Physiotherapy Evidence Database (PEDro) scale. The meta-analysis statistic procedure was performed by using RevMan software version 5.3.
Results: From the 252 articles found, six studies were included in the review involving 272 participants aged 30–75 years. Exercise programs had a mean length of 10.4 ± 4.6 weeks, a frequency of 3 ± 1.4 days/week, and a mean duration of 78 ± 23.9 min. In time-domain HRV measures, exercise may increase in the SD of normal-to-normal intervals [p < 0.00001, with a mean difference (MD) of 12.79 ms from 9.03 to 16.55] and a decreased root mean square of successive R–R interval differences (p = 0.002, with an MD of 13.08 ms from 4.90 to 21.27) in comparison with control groups (CG). The frequency-domain data reveal that the exercise group (EG) improve significantly more than the CGs in low frequency [absolute power: p < 0.0001, with a standardized mean difference (SMD) of 0.97 from 0.61 to 1.34; relative power: p = 0.04, with an MD = −7.70 from −15.4 to −0.36], high-frequency [absolute power: p = 0.001, with a SMD of 1.49 from 0.32 to 2.66; relative power: p = 0.04, with an MD of 8.00 normalized units (n.u.) from 0.20 to 15.80], and low-to-high frequency ratio (p = 0.007 with an MD of −0.32 from −0.55 to −0.09).
Conclusion: Exercise programs could lead to positive effects on the autonomic modulation of patients with cancer and its survivors. More beneficial changes may occur with resistance and endurance workouts. However, due to the low number of interventions performed, further research is needed to substantiate the findings and to provide additional insights regarding the exercise intensity required to increase the autonomic modulation of the patient.
Modern advances in cancer therapy have resulted in increased survival rates. However, patients are frequently affected by various negative side effects (Miller et al., 2019). In particular, both the autonomic control impairment and the increased risk of cardiovascular disease (Lakoski et al., 2015) are suffered by ~80% (Coumbe and Groarke, 2018) and 42% (Chen et al., 2012) of the patients, respectively. The autonomic nervous system (ANS) is the main homeostatic regulatory system of the body, involved in the etiology and the clinical course of cancer therapies (Simó et al., 2018). Chemotherapy and radiotherapy cause cardiotoxicity (Scott et al., 2014) and neurotoxicity (Park et al., 2013), thereby affecting ANS and cardiovascular function. The cardiovascular ANS needs to be controlled during the cancer phases to regulate levels of autonomic dysfunction of patients (Walsh and Nelson, 2002).
Heart rate variability (HRV) is a noninvasive tool to evaluate the autonomic modulation of the sinus node in healthy, cardiac, and noncardiac disease populations (Lombardi and Stein, 2011). In patients with cancer, HRV is a useful, effective, and more practical method to assess autonomic dysfunction than other validated methods, which are more complex to apply (Guo et al., 2013). HRV measures provide a multidimensional register of autonomic modulation, including the sympathetic and parasympathetic modulation of cardiac function (Arab et al., 2016), which is notably modified in patients with cancer compared with the healthy population. Studies including wide sample sizes have found significantly lower values in the root mean square of successive R–R interval measures (RMSSD), representing the parasympathetic activity, and the SD of the interbeat interval of normal sinus beats (SDNN) (i.e., overall HRV measure) of patients with cancer compared with the healthy population (De Couck and Gidron, 2013; Bijoor et al., 2016). Cancer-treating drug therapies induce cardiac abnormalities, such as heart failure, myocardial ischemia, myocarditis, hypertension, or arrhythmias, among others (Chang et al., 2017), detected with HRV even with normal systolic left ventricular function (Tjeerdsma et al., 1999) with an overactivation of the sympathetic nervous system (SNS) and a decrease in the parasympathetic nervous system (PNS) activity (Coumbe and Groarke, 2018). Consequently, this imbalance, produced by cancer drugs, may stimulate the hypothalamic-pituitary-adrenal axis and the endocannabinoid and renin-angiotensin-aldosterone systems producing an increase in oxidative stress, chronic inflammation, and atherosclerosis with a reduction in vasodilation, which affects the health of patients (Lakoski et al., 2015). Several types of research have focused on the relationship between the global HRV modifications and the health of patients with cancer obtaining an inverse correlation with cancer-related fatigue (Fagundes et al., 2011) and depression (Giese-Davis et al., 2006). Findings also show the role of HRV to predict survivorship being higher when the vagal nerve activation is stimulated (Zhou et al., 2016).
Palma et al. (2020) and Dias Reis et al. (2017) published a systematic review of supportive therapy modalities that have been developed to reduce the HRV results. They found interventions based on music therapy, traditional Chinese medicine-related treatments, exercise, relaxation, and myofascial release techniques and concluded that HRV seemed to be a safe and easily applicable method to assess cancer-related autonomic dysfunction (Palma et al., 2020). However, not only the consequences of cancer therapy need to be considered to improve HRV but also the lifestyles of patients can influence it negatively (Scott et al., 2014). Thus, a multifactorial intervention that could modify the physiological changes mentioned earlier and other health and psychological parameters is crucial to globally benefit the patients with cancer.
Exercise programs appear to promote physiological changes leading to reduce the decline of the autonomic modulation and improving its levels during (Mostarda et al., 2017) and after cancer treatments (Shin et al., 2016). Scott et al. (2014) approximated the benefits of aerobic exercise training to the autonomic modulation of patients with cancer stating that it may decrease sympathetic tone and increase vagal tone by the influence of exercise in attenuate cardiovascular abnormalities as heart failure or coronary artery disease. Aerobic exercise modifies the renin-angiotensin-aldosterone system (Scott et al., 2014) and stimulates the hypothalamic-pituitary-adrenal axis suppressing angiotensin II expression, which promotes the sympathetic activity of the ANS (Routledge et al., 2010). Consequently, the stimulation of the hypothalamic-pituitary-adrenal axis and the endocannabinoid and renin-angiotensin-aldosterone systems is produced (Arab et al., 2016). Exercise also upregulates nitric oxide promoting vasodilation (Kingwell, 2000; Scott et al., 2014) reduces reactive oxygen species induced by chemotherapy toxicity (Scott et al., 2014). Moreover, regarding the remaining physiological changes mentioned earlier, exercise can also decrease chronic inflammation (Gleeson et al., 2011), improving the immune system and the stimulation of natural killer cells (Khosravi et al., 2019). Exercise can also reduce body mass index (BMI) (Thomas et al., 2017), which may be correlated to an HRV increase (Arab et al., 2016). Although exercise may have the potential role to increase HRV, the results presented by the different interventions developed are controversial considering all the variables inside HRV. In this way, this systematic review and meta-analysis aimed to evaluate the effects of exercise interventions on the autonomic function of patients with cancer and its survivors analyzing the measures involved.
The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines have been followed to develop the systematic review (Liberati et al., 2009). Before the data extraction was performed, the study was registered in the International Prospective Register of Systematic Reviews (PROSPERO) by the following identification number: CRD42020191041.
The databases employed for searching the articles were Web of Science (including studies indexed in the KCI-Korean Journal Database, MEDLINE, Russian Science Citation Index, SciELO Citation Index, and PubMed (MEDLINE). The terms used for the search were as follows: cancer and neoplasms, separated by OR; and HRV, autonomous nervous function, autonomous nervous system, separated by OR; and exercise, training, physical activity, also separated by OR. The only filter employed was the requirement of being articles written in English or Spanish. The search was carried out from April 2020 to June 2020.
The articles found were included if they fulfilled the following criteria: (1) the target population was patients with cancer or survivors, (2) the program involves any physical exercise, (3) the investigation assesses and reports any HRV variable, (4) the study includes at least one control group (CG) whose results are compared with an exercise group (EG). Moreover, the following exclusion criteria were set: (1) the article was a review, letter to the editor, conference abstract, case report, or study protocol, (2) the study did not evaluate the HRV variables directly after the intervention, and (3) the studies were completely written in a language different from English or Spanish.
Risk of Bias Assessment
The analysis of the risk of bias was performed using the Physiotherapy Evidence Database (PEDro) scale, known as a valid and reliable instrument to assess eligibility, allocation to groups, blinding of allocation, and comparison between groups at baseline and its outcomes (Maher et al., 2003). The leading reasons for its selection were due to it being the most used in the scientific area of the Sport Sciences for Health and it is a specific tool focused on physical therapies (Moseley et al., 2020).
Participants, Interventions, Comparisons, and Study Designs Information
The main information of the articles is reported in the tables and figures in the article and the supplementary data. Regarding participants, CG and EG baseline parameters were extracted, such as sample size, mean age, BMI, physical activity level, cancer type, stage, type of treatment, and timing. The intervention characteristics included the length of the program, duration of each session, weekly frequency, exercise description, intensity, progression, and adherence. The intervention of the comparison group was also extracted.
HRV Outcome Measurements
Interventions included an HRV assessment before and after the intervention. For consistency in measures, participants were laid in a supine position (Niederer et al., 2013; Dias Reis et al., 2017; Zhou et al., 2018) or seated in chairs (Shin et al., 2016; Lee et al., 2018). HRV was recorded for 5 min of adequate stationary sign (Niederer et al., 2013; Lee et al., 2018; Zhou et al., 2018) with Polar S810 (Niederer et al., 2013), CANS 3000 (Laxtha, Daejeon, Korea) (Shin et al., 2016), or CheckMyHeart Handheld HRV (Lee et al., 2018) by using ECG (Zhou et al., 2018). The spectral analysis from the artifact-free data was performed by the fast Fourier transformation with the Kubios HRV Analysis software (Niederer et al., 2013; Dias Reis et al., 2017; Mostarda et al., 2017; Zhou et al., 2018) or AcqKnowledge (Zhou et al., 2018). The results of this review include two HRV variables in the time domain, namely, SDNN and RMSSD. In the frequency domain, the low-frequency (LF) band, the high-frequency (HF) band, the ratio of LF-to-HF (LF/HF), and the total power (TP), calculated as the sum of the energy in very-low-frequency (VLF), LF, and HF bands, were extracted (Shaffer and Ginsberg, 2017). The frequency-domain data were reported in absolute units by using milliseconds squared (ms2) or normalized units (n.u.) obtained by diving the result between the TP and multiplied to 100 [i.e., LF or HF/(TP–VLF) × 100] (Task Force of the European Society of Cardiology the North American Society of Pacing Electrophysiology, 1996). SDNN and RMSSD were measured in 1/1,000 s (milliseconds) (Shin et al., 2016), and HF was recorded from 0.15 to 0.4 Hz and LF from 0.04 to 0.15 Hz (Table 3) (Niederer et al., 2013; Shin et al., 2016; Dias Reis et al., 2017; Mostarda et al., 2017; Zhou et al., 2018).
The analysis was performed with the post-intervention means and SDs of the EG and the CG collected from the articles. The meta-analysis statistical tool used was the Review Manager Software (RevMan software version 5.3) (RevMan, 2014). The selected method was the inverse variance with random effects and a 95% CI (Schmidt et al., 2009). Additionally, the I2 model was used to calculate the heterogeneity of the results. The results were presented with a standardized mean difference (SMD) when the same variable was measured in different units (i.e., ms2 and log ms2) as occurred with the absolute power variables of HF and LF. In contrast, the mean difference (MD) was used when all studies assessed the variable using the same units (n.u. or ms). According to the Cochrane Handbook for Systematic Reviews of Intervention, the SMD effects were interpreted as small with results <0.4, moderate from 0.4 to 0.7, and large >0.7 (Higgins and Green, 2011).
About 252 articles were identified in Web of Science (n = 166) and PubMed (n = 86) scientific databases. Figure 1 shows the flow diagram where 209 articles were analyzed after removing the duplicates. Two hundred and three articles were excluded after reading the title or the abstract (n = 164) or after the full-text evaluation (n = 39). Therefore, both the systematic review and the meta-analysis were developed with six studies published between 2012 and 2018.
Figure 1. Study flow diagram following the preferred reporting items for systematic reviews and meta-analyses guidelines.
Risk of Bias
In the PEDro scale, as Table 1 shows the mean score obtained was 5, and the external validity was 5, ranging from 4–7 (10 being the highest possible mark). The five articles assessed positively reached the external validity (item 1) and the statistic items (items 10 and 11). However, the internal validity punctuation was more heterogeneous. None of the evaluated studies met items 5, 6, and 7 related to the blinding process, difficult to fulfill in sport sciences.
The baseline information of the participants is reported in Table 2. The total sample size of the systematic review was 272, out of which 126 were included in the CG and 146 in the EG, and the sample was mainly composed of women. The ages ranged from 30 to 75 years, although most of the participants were older than 45 years of age. Different types of cancer were included in this study as follows: three interventions contained only patients with breast cancer (Shin et al., 2016; Dias Reis et al., 2017; Mostarda et al., 2017) and two incorporated various types of cancer such as colorectal, lung, breast, genital, gastrointestinal, and hematological (Niederer et al., 2013; Lee et al., 2018). One study contained only nasopharyngeal cancer (Zhou et al., 2018). The patients participated in the exercise program during the treatment of cancer drugs (i.e., chemotherapy, radiotherapy, and hormonotherapy) (Niederer et al., 2013; Shin et al., 2016; Zhou et al., 2018) or after finishing the treatments (Niederer et al., 2013; Dias Reis et al., 2017; Mostarda et al., 2017; Lee et al., 2018).
The exercise interventions included in this review are detailed in Table 3. The length of the exercise program varied from 4 weeks (Mostarda et al., 2017) to 16 weeks (Niederer et al., 2013), with one intervention conducted during the entire chemotherapy cycle of 19 months (Zhou et al., 2018). Participants attended exercise sessions once per week (Lee et al., 2018), three times per week (Shin et al., 2016; Dias Reis et al., 2017; Mostarda et al., 2017), and five times per week (Zhou et al., 2018), whereas Niederer et al. (2013) suggested patients exercise 3–5 times per week. Together with the study of Zhou et al. (2018), their interventions were the only programs that included an unsupervised exercise element. Sessions lasted from 60 to 120 min (Niederer et al., 2013; Lee et al., 2018; Zhou et al., 2018), with a median of a 70-min exercise (Shin et al., 2016; Dias Reis et al., 2017; Mostarda et al., 2017).
Two exercise programs were based on oriental exercise techniques, such as Tai Chi (Zhou et al., 2018) and Qigong (Lee et al., 2018), including a meditation component. The remaining interventions involved cardiovascular and resistance training (Niederer et al., 2013; Shin et al., 2016; Dias Reis et al., 2017; Mostarda et al., 2017), including the program conducted by Niederer et al. (2013), where patients were counseled to exercise following the recommendations of the ACSM Roundtable on Exercise Guidelines for Cancer Survivors (Schmitz et al., 2010) and could participate in guided Nordic Walking sessions once per week. Dias Reis et al. (2017) and Mostarda et al. (2017) incorporated the cardiovascular cycling of 30 min and different free weight exercises, such as squats, shoulder press, hip flexion, or French press, among others (Dias Reis et al., 2017; Mostarda et al., 2017). In contrast, Shin et al. (2016) used circuit training to develop the sessions combining strength and cardiovascular exercises and using the rate of perceived exertion (RPE) to monitor and progress the intensity (Shin et al., 2016).
Most of the studies reported the outcome results after treatment. However, one study (Lee et al., 2018) only reported the change from baseline. Therefore, it was excluded from this meta-analysis. Other than the study of Niederer et al. (2013), the outcomes of the EG after cancer treatment were extracted (Niederer et al., 2013). The results were then divided into time and frequency domains to present how exercise influences patients with cancer and survivors in these domains.
Regarding the HRV time-domain measure analysis, in SDNN EG, there were significant increases compared with the CG with a p < 0.00001 (MD of 12.79 and a 95% CI from 9.03 to 16.55) (Figure 2). Also, Lee et al. (2018) found significant differences between groups analyzing the change from baseline (p = 0.001) (Lee et al., 2018). Participants in the EG also reached higher increases on RMSSD compared to those in the CG (p = 0.002 with an MD of 13.08 ms and 95% CI from 4.90 to −21.27) (Figure 3).
Figure 2. Effects of exercise in SDNN (standard deviation of the interbeat interval of normal sinus beats) heart rate variability measure.
Figure 3. Effects of exercise in RMSSD (root mean square of successive differences between normal heartbeats) heart rate variability measure.
As for the frequency-domain outcomes, the LF and HF results were obtained in SMD from the analysis of the absolute power (ms2 or log ms2), and that in MD, the relative power (n.u.). Figure 4 shows that LF was significantly increased in the EG compared to the CG in both analyses. In absolute power, results had a p-value of <0.0001 and an SMD of 0.97 with a 95% CI from 0.61 to 1.34, while in n.u., the p-value was 0.04 with an MD of −7.70 n.u. and a 95% CI from −15.04 to −0.36. The HF results, which are presented in Figure 5, of the EG in absolute power measures, were significantly higher than the CG outcomes (p = 0.001, and an SMD of 1.49 with a 95% CI from 0.32 to 2.66) and their effects on the relative power units (p = 0.04, and an MD of 8.00 n.u. with a 95% CI from 0.20 to 15.80). Moreover, Lee et al. (2018) stated that significant differences in the change from baseline reveal but not between groups (Lee et al., 2018). The ratio LF/HF showed significant differences between EG and CG with a p-value of 0.007 and an MD of −0.32 (95% CI from −0.55 to −0.09), as represented in Figure 6. Finally, the TP data was not analyzed by meta-analysis only two studies include the measure (Niederer et al., 2013; Lee et al., 2018). Niederer et al. (2013) stated the significant differences in the interaction between groups (i.e., exercise during treatment group, exercise after treatment group, and CG) and time (before and after intervention) with a p-value of 0.025. However, their post-hoc analysis showed high differences between after treatment group and the CG (p = 0.012). As for the results of Lee et al. (2018), the Qigong EG significantly increases TP with a p-value of 0.002 from baseline to after intervention.
Figure 4. Effects of exercise in HF (High Frequency) heart rate variability measure expressed in absolute (ms2) and relative (n.u) power.
Figure 5. Effects of exercise in LF (Low Frequency) heart rate variability measure expressed in absolute (ms2) and relative (n.u) power.
Figure 6. Effects of exercise in Ratio HF/LF (ratio of Low Frequency to High Frequency) heart rate variability measure.
This systematic review and meta-analysis aimed to evaluate the effects of exercise interventions in the HRV of cancer patients and survivors. The data obtained showed significant differences between the EG and the CG in all the variables analyzed as follows: SDNN, RMSSD, LF (ms2 and n.u.), HF (ms2 and n.u.), LF/HF ratio, and TP. Thus, exercise interventions may improve the autonomic control in patients with cancer and reduce the risk of autonomic dysfunction of participants. However, some specifications need to be considered due to the heterogeneity of the programs and the physiological implications of the variables analyzed.
Although we have included all the variables measured in the HRV, the physiological interpretation of some of these variables of ANS recording is controversial. Only RMSSD and HF have been proven to reflect the PNS activity to date (Shaffer and Ginsberg, 2017), whereas the reflection of SNS or PNS in SDNN, LF, and LF/HF is not clear. SDNN seems to measure the overall HRV with the contribution of sympathetic and parasympathetic modulation, but in the short-term resting recordings, the main source of the variation could be provided from the SNP (Shaffer and Ginsberg, 2017). The LF physiological interpretation is still not universally agreed since some researchers assume it as an index of cardiac sympathetic control (Reyes Del Paso et al., 2013), whereas more current literature state that it may principally reflect the baroreflex activity (Goldstein et al., 2011) or even being mainly determined by the PSN (Reyes Del Paso et al., 2013). However, it seems to depend on the band recording frequency having a possible SNS implication if it reaches 0.1 Hz (Shaffer and Ginsberg, 2017). Consequently, the physiological interpretation of the LF/HF ratio is also uncertain due to LF not being a pure SNS index (Goldstein et al., 2011; Shaffer and Ginsberg, 2017). With this in mind, the following discussion will be focused on the HF and RMSSD physiological values to argue the overall autonomic control effects.
In line with HRV parasympathetic activity variables of the CGs, several articles have revealed the effects of cancer treatments in RMSSD and HF and the overall measure of SDNN. Surgery, for instance, significantly reduces RMSSD and SDNN even 14 days post-op (Hansen et al., 2013), which is similar to what occurs after administration of a high dose of chemotherapy and its subsequent cardiotoxicity (Kloter et al., 2018). This ANS dysfunction reduces the release of catecholamine neurotransmitters, which could negatively influence the regulation of the tumor microenvironment (Hanns et al., 2019). Cancer decreases catecholamine production, with a concomitant rise in oxidative stress, inflammation, and cancer progression (Cole et al., 2015). Under normal conditions, the PNS could regulate the inflammatory response, but the decline of the vagal nerve activity produced by cancer may inhibit inflammatory regulation (Williams et al., 2019). In this way, in contrast to healthy controls with similar characteristics, patients with breast cancer have significantly lower RMSSD, HF, and SDNN values 1 year after treatment (Caro-Morán et al., 2016). Consequently, when comparing the HRV results with the normal values of healthy individuals, the differences are notable (Nunan et al., 2010). Thus, the role of PNS and its variance is so crucial in cancer prognosis that having a high HF power is positively correlated with survival in patients with advanced breast cancer (Giese-Davis et al., 2015).
Exercise seems to have a positive influence on the ANS of patients with cancer and its related physiological consequences, as shown in Figure 7, illustrates, in this case, the recovery to the normal values of HRV measures after the interventions. Exercise can induce the increase of catecholamines, which are commonly reduced due to cancer and lead to positive changes in tumor hypoxia, angiogenesis, metabolic stress, and cell immunity (Hojman et al., 2018) by the lactate production, according to the Warburg effect (San-Millán and Brooks, 2016). This would increase the parasympathetic responses and decrease the local oxidative stress and DNA damage, i.e., inflammatory reactions (De Couck et al., 2012). Consequently, the ability of cancer cells to form tumors in distinct tissues (Hojman et al., 2018) and the risk of developing metabolic abnormalities (Licht et al., 2010) related to poor cancer prognosis (De Couck et al., 2012) could be reduced. Moreover, exercise may also benefit patients by increasing the vagal nerve stimulation in the renin-angiotensin-aldosterone system (Miller and Arnold, 2019). When this occurs, there may be a reduction in the renin enzyme production (Cunha et al., 2016), with subsequent angiotensin II reduction, thereby affecting the cholinergic parasympathetic neurotransmission to the heart (Miller and Arnold, 2019). These mechanisms control angiogenesis, tumorigenesis, metastasis, and cellular proliferation (Munro et al., 2017). Few articles relate the effects of exercise in the renin-angiotensin-aldosterone of patients with cancer, but in other disease populations, it appears that exercise could prevent the increase of angiotensin-converting enzyme and plasma angiotensin II levels (Nunes-Silva et al., 2017) (Figure 7).
Figure 7. Explication of the changes in the heart rate variability of cancer patients and exercise training effects in comparation to healthy population data. Healthy population of HRV data from Nunan et al. (2010), cancer and treatments consequences and exercise effects data correspond to control and exercise group after intervention results of the current systematic review. References from the physiological changes in cancer patients and its exercise effects are reported in the systematic review discussion. SDNN, standard deviation of the interbeat interval of normal sinus beats; RMSSD, root mean square of successive RR interval measures; HF, high frequency; LF, low frequency; LF/HF, low-to-high frequency ratio; PNS, parasympathetic nervous system; ROS, reactive oxygen species.
The type of exercise and the intensity of exercise could be the important factors to consider for the PNS activation. First, to increase catecholamine production, moderate- or high-intensity exercise is needed (Zouhal et al., 2008). Additionally, in HF values, no significant differences between the control and the Qigong group were found (Lee et al., 2018), and the Tai Chi intervention presented the lowest MDs results (Zhou et al., 2018), which could mean that the intensity performed was too low to impact the PNS activity. Accordingly, low responses were also shown in the intervention in the study of Niederer et al. (2013), where participants engaged in unsupervised physical activity without a structured program (36). Still, studies carried out with other target populations show that low-intensity exercise modalities such as Tai Chi increased the parasympathetic stimulation (Cole et al., 2016). However, a study with elderly women, which compared the effects of the autonomic modulation of Tai Chi and walking programs, found no significant HRV differences between the groups (Audette et al., 2006). Perhaps higher intensities may be needed to increase the muscle recruitment associated with the rise in circulating catecholamines (Spiering et al., 2008), which has been shown to decrease HRV (Zouhal et al., 2008). Moreover, the comparison between the effects of endurance training and resistance training on the autonomic modulation, measured by HRV, is still controversial in patients with chronic diseases (Boudet et al., 2017). Although endurance training seemed to be more effective in modifying the HRV activity in healthy populations, in patients with metabolic syndrome, the high-intensity resistance training together with endurance seemed to have greater decreases in the heart rate and greater increases in the VLF domain compared with moderate resistance training with endurance workout (Boudet et al., 2017). These improvements could be produced by the role of strength training in declining the inflammatory process, an aspect shared with cancer physiology (Gleeson et al., 2011). Besides, resistance training may be utilized to prevent or to regain the decline of HRV considering that sarcopenia is a significant predictor of toxicity and time to tumor progression (Prado et al., 2009). More investigation is needed to identify the type of optimal exercise and to analyze the physiological process of resistance exercise in HRV physiology.
Most of the sport science investigations performed about HRV measure the effects of acute doses of exercise during the practice and in the recovery phase. In cancer, the acute effects of exercise have been analyzed with HF and RMSSD measures during and after yoga practice obtaining significant HF alterations in all the positions performed except in meditation and post-resting (Mackenzie et al., 2014). Hence, in line with the previous literature, a higher muscle activation may be required during exercise to stimulate the vagal nerve activity. An intervention carried out with Tai Chi Qigong added that a minimum of 4 min of practice is required to achieve the effects in HF and LF (Fong et al., 2015). Moreover, HRV measures could provide an opportunity to record how participants have responded to training in the 12–24 h post-exercise session (Javaloyes et al., 2020). These HRV outcomes, usually measured by RMSSD, can guide to decide the intensity and volume of the following session of training (Kiviniemi et al., 2007; Javaloyes et al., 2020). Nevertheless, no investigations have been performed at present with patients with cancer.
The current meta-analysis and systematic review are the first to explore the effects of exercise programs on the HRV of patients with cancer and its survivors. Some limitations need to be mentioned. The total sample size was moderate at best, although interventions that involved all types of exercise were included. Consequently, the studies analyzed were heterogeneous, limiting the generalization of the results, but still provide a wider review of the types of interventions investigated in the field. Finally, only studies written in English or Spanish, indexed in PubMed or Web of Science and articles with a before and after HRV measure or changes from baseline outcomes were included.
Exercise programs may lead to positive effects on the overall autonomic control, measured by HRV of patients with cancer and its survivors. This systematic review and meta-analysis show that exercise can increase SDNN (overall HRV), RMSSD, and HF (n.u. and ms2), reflecting the stimulation of PNS activity. Furthermore, significant differences between EG and CG were also found in the LF and the LF/HF ratio of HRV variables. Due to the low number of interventions performed on HRV, exercise, and cancer, no further conclusions can be made. Thus, future research is needed to contrast the findings and to provide more specific information about the type and intensity of exercise required to improve the overall autonomic control and to reduce the toxicity and future autonomic dysfunction of the patient with cancer.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
AL-P, DC-M, and XM: conceptualization, resources, validation, and writing the original draft preparation. AL-P, DC-M, and AJ: methodology, writing the review, and editing. AL-P and DC-M: software, formal analysis, and data curation. GL, LH, and AJ: investigation. GL, LH, and XM: supervision. DC-M and AJ: project administration. All authors have read and approved the published version of the manuscript.
The authors declare that this study received funding from GO fit LAB-Ingesport and the Industrial Doctorate Spanish National grant program of the Spanish Ministry of Science, Innovation and Universities. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
Conflict of Interest
AL-P and AJ were employed by GO fit LAB-Ingesport.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Arab, C., Dias, D. P. M., De Almeida Barbosa, R. T., De Carvalho, T. D., Valenti, V. E., Crocetta, T. B., et al. (2016). Heart rate variability measure in breast cancer patients and survivors: a systematic review. Psychoneuroendocrinology 68, 57–68. doi: 10.1016/j.psyneuen.2016.02.018
Bijoor, S. N., Subbalakshmi, N., and Banerjee, S. (2016). Influence of cancer and its severity on vagal nerve activity assessed by time domain measures of heart rate variability. Res. J. Pharm. Biol. Chem. Sci. 7, 1215–1220.
Boudet, G., Walther, G., Courteix, D., Obert, P., Lesourd, B., Pereira, B., et al. (2017). Paradoxical dissociation between heart rate and heart rate variability following different modalities of exercise in individuals with metabolic syndrome: the RESOLVE study. Eur. J. Prev. Cardiol. 24, 281–296. doi: 10.1177/2047487316679523
Caro-Morán, E., Fernández-Lao, C., Galiano-Castillo, N., Cantarero-Villanueva, I., Arroyo-Morales, M., and Díaz-Rodríguez, L. (2016). Heart rate variability in breast cancer survivors after the first year of treatments: a case-controlled study. Biol. Res. Nurs. 18, 43–49. doi: 10.1177/1099800414568100
Chang, H.-M., Moudgil, R., Scarabelli, T., Okwuosa, T. M., and Yeh, E. T. (2017). Cardiovascular complications of cancer therapy: best practices in diagnosis, prevention, and management: part 1. J. Am. Coll. Cardiol. 70, 2536–2551. doi: 10.1016/j.jacc.2017.09.1096
Chen, J., Long, J. B., Hurria, A., Owusu, C., Steingart, R. M., and Gross, C. P. (2012). Incidence of heart failure or cardiomyopathy after adjuvant trastuzumab therapy for breast cancer. J. Am. Coll. Cardiol. 60, 2504–2512. doi: 10.1016/j.jacc.2012.07.068
Cole, A. R., Wijarnpreecha, K., Chattipakorn, S. C., and Chattipakorn, N. (2016). Effects of Tai Chi exercise on heart rate variability. Complement. Ther. Clin. Pract. 23, 59–63. doi: 10.1016/j.ctcp.2016.03.007
Cole, S. W., Nagaraja, A. S., Lutgendorf, S. K., Green, P. A., and Sood, A. K. (2015). Sympathetic nervous system regulation of the tumour microenvironment. Nat. Rev. Cancer 15, 563–572. doi: 10.1038/nrc3978
Cunha, T. S., Silva, K. A. S., Sanches, A., Silva, S. D. Jr., Oliveira, V., et al. (2016). “Exercise and renin angiotensin system,” in New Aspects of the Renin Angiotensin System Cardiovascular and Renal Diseases (Sharjah: Bentham Science Publishers), 275–321.
Dias Reis, A., Silva Garcia, J. B., Rodrigues Diniz, R., Silva-Filho, A. C., Dias, C. J., Leite, R. D., et al. (2017). Effect of exercise training and detraining in autonomic modulation and cardiorespiratory fitness in breast cancer survivors. J. Sports Med. Phys. Fitness 57, 1062–1068. doi: 10.23736/S0022-4707.17.07012-8
Fagundes, C. P., Murray, D. M., Hwang, B. S., Gouin, J. P., Thayer, J. F., Sollers, J. J. 3rd, and Shapiro, C. L. . (2011). Sympathetic and parasympathetic activity in cancer-related fatigue: more evidence for a physiological substrate in cancer survivors. Psychoneuroendocrinology 36, 1137–1147. doi: 10.1016/j.psyneuen.2011.02.005
Fong, S. S. M., Wong, J. Y. H., Chung, L. M. Y., Yam, T. T. T., Chung, J. W. Y., Lee, Y. M., et al. (2015). Changes in heart-rate variability of survivors of nasopharyngeal cancer during Tai Chi Qigong practice. J. Phys. Ther. Sci. 27, 1577–1579. doi: 10.1589/jpts.27.1577
Giese-Davis, J., Wilhelm, F. H., Conrad, A., Abercrombie, H. C., Sephton, S., Yutsis, M., et al. (2006). Depression and stress reactivity in metastatic breast cancer. Psychosom. Med. 68, 675–683. doi: 10.1097/01.psy.0000238216.88515.e5
Giese-Davis, J., Wilhelm, F. H., Tamagawa, R., Palesh, O., Neri, E., Taylor, C. B., et al. (2015). Higher vagal activity as related to survival in patients with advanced breast cancer: an analysis of autonomic dysregulation. Psychosom. Med. 77:346. doi: 10.1097/PSY.0000000000000167
Gleeson, M., Bishop, N. C., Stensel, D. J., Lindley, M. R., Mastana, S. S., and Nimmo, M. A. (2011). The anti-inflammatory effects of exercise: mechanisms and implications for the prevention and treatment of disease. Nat. Rev. Immunol. 11, 607–615. doi: 10.1038/nri3041
Goldstein, D. S., Bentho, O., Park, M.-Y., and Sharabi, Y. (2011). Low-frequency power of heart rate variability is not a measure of cardiac sympathetic tone but may be a measure of modulation of cardiac autonomic outflows by baroreflexes. Exp. Physiol. 96, 1255–1261. doi: 10.1113/expphysiol.2010.056259
Guo, Y., Palmer, J. L., Strasser, F., Yusuf, S. W., and Bruera, E. (2013). Heart rate variability as a measure of autonomic dysfunction in men with advanced cancer. Eur. J. Cancer Care 22, 612–616. doi: 10.1111/ecc.12066
Hanns, P., Paczulla, A. M., Medinger, M., Konantz, M., and Lengerke, C. (2019). Stress and catecholamines modulate the bone marrow microenvironment to promote tumorigenesis. Cell stress 3, 221–235. doi: 10.15698/cst2019.07.192
Hansen, M. V., Rosenberg, J., and Gögenur, I. (2013). Lack of circadian variation and reduction of heart rate variability in women with breast cancer undergoing lumpectomy: a descriptive study. Breast Cancer Res. Treat. 140, 317–322. doi: 10.1007/s10549-013-2631-x
Higgins, J., and Green, S. (2011). Chapter 17.8.2: Study summaries using more than one patient-reported outcome, in Cochrane Handbook for Systematic Reviews of Interventions (London, UK: The Cochrane Collaboration and John Wiley & Sons Ltd), 541–543.
Javaloyes, A., Sarabia, J. M., Lamberts, R. P., Plews, D., and Moya-Ramon, M. (2020). Training prescription guided by heart rate variability vs. block periodization in well-trained cyclists. J. Strength Cond. Res. 34, 1511–1518. doi: 10.1519/JSC.0000000000003337
Khosravi, N., Stoner, L., Farajivafa, V., and Hanson, E. D. (2019). Exercise training, circulating cytokine levels and immune function in cancer survivors: a meta-analysis. Brain Behav. Immun. 81, 92–104. doi: 10.1016/j.bbi.2019.08.187
Kingwell, B. A. (2000). Nitric oxide as a metabolic regulator during exercise: effects of training in health and disease. Clin. Exp. Pharmacol. Physiol. 27, 239–250. doi: 10.1046/j.1440-1681.2000.03232.x
Kiviniemi, A. M., Hautala, A. J., Kinnunen, H., and Tulppo, M. P. (2007). Endurance training guided individually by daily heart rate variability measurements. Eur. J. Appl. Physiol. 101, 743–751. doi: 10.1007/s00421-007-0552-2
Kloter, E., Barrueto, K., Klein, S. D., Scholkmann, F., and Wolf, U. (2018). Heart rate variability as a prognostic factor for cancer survival - a systematic review. Front. Physiol. 9:623. doi: 10.3389/fphys.2018.00623
Lakoski, S. G., Jones, L. W., Krone, R. J., Stein, P. K., and Scott, J. M. (2015). Autonomic dysfunction in early breast cancer: Incidence, clinical importance, and underlying mechanisms. Am. Heart J. 170, 231–241. doi: 10.1016/j.ahj.2015.05.014
Lee, Y. H., Lai, G. M., Lee, D. C., Tsai Lai, L. J., and Chang, Y. P. (2018). Promoting physical and psychological rehabilitation activities and evaluating potential links among cancer-related fatigue, fear of recurrence, quality of life, and physiological indicators in cancer survivors. Integr. Cancer Ther. 17, 1183–1194. doi: 10.1177/1534735418805149
Liberati, A., Altman, D. G., Tetzlaff, J., Mulrow, C., Gøtzsche, P. C., Ioannidis, J. P., et al. (2009). The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J. Clin. Epidemiol. 62, e1–e34. doi: 10.1016/j.jclinepi.2009.06.006
Licht, C. M., Vreeburg, S. A., Van Reedt Dortland, A. K., Giltay, E. J., Hoogendijk, W. J., Derijk, R. H., et al. (2010). Increased sympathetic and decreased parasympathetic activity rather than changes in hypothalamic-pituitary-adrenal axis activity is associated with metabolic abnormalities. J. Clin. Endocrinol. Metab. 95, 2458–2466. doi: 10.1210/jc.2009-2801
Lombardi, F., and Stein, P. K. (2011). Origin of heart rate variability and turbulence: an appraisal of autonomic modulation of cardiovascular function. Front. Physiol. 2:95. doi: 10.3389/fphys.2011.00095
Mackenzie, M. J., Carlson, L. E., Paskevich, D. M., Ekkekakis, P., Wurz, A. J., Wytsma, K., et al. (2014). Associations between attention, affect and cardiac activity in a single yoga session for female cancer survivors: an enactive neurophenomenology-based approach. Conscious. Cogn. 27, 129–146. doi: 10.1016/j.concog.2014.04.005
Maher, C. G., Sherrington, C., Herbert, R. D., Moseley, A. M., and Elkins, M. (2003). Reliability of the PEDro scale for rating quality of randomized controlled trials. Phys. Ther. 83, 713–721. doi: 10.1093/ptj/83.8.713
Miller, A. J., and Arnold, A. C. (2019). The renin-angiotensin system in cardiovascular autonomic control: recent developments and clinical implications. Clin. Auton. Res. 29, 231–243. doi: 10.1007/s10286-018-0572-5
Miller, K. D., Nogueira, L., Mariotto, A. B., Rowland, J. H., Yabroff, K. R., Alfano, C. M., et al. (2019). Cancer treatment and survivorship statistics, 2019. CA Cancer J. Clin. 69, 363–385. doi: 10.3322/caac.21565
Moseley, A. M., Elkins, M. R., Van der Wees, P. J., and Pinheiro, M. B. (2020). Using research to guide practice: the physiotherapy evidence database (PEDro). Braz. J. Phys. Ther. 24, 384–391. doi: 10.1016/j.bjpt.2019.11.002
Mostarda, C., Castro-Filha, J., Reis, A. D., Sevilio, M. Jr., Dias, C. J., Silva-Filho, A. C., et al. (2017). Short-term combined exercise training improves cardiorespiratory fitness and autonomic modulation in cancer patients receiving adjuvant therapy. J. Exerc. Rehabil. 13, 599–607. doi: 10.12965/jer.1735048.524
Munro, M. J., Wickremesekera, A. C., Davis, P. F., Marsh, R., Tan, S. T., and Itinteang, T. (2017). Renin-angiotensin system and cancer: a review. Integr. Cancer Sci. Ther. 4, 1–6. doi: 10.15761/ICST.1000231
Nunan, D., Sandercock, G. R., and Brodie, D. A. (2010). A quantitative systematic review of normal values for short-term heart rate variability in healthy adults. Pacing Clin. Electrophysiol. 33, 1407–1417. doi: 10.1111/j.1540-8159.2010.02841.x
Nunes-Silva, A., Rocha, G. C., Magalhaes, D. M., Vaz, L. N., Salviano De Faria, M. H., and Simoes E Silva, A. C. (2017). Physical exercise and ACE2-Angiotensin-(1-7)-Mas receptor axis of the Renin Angiotensin System. Protein Pept. Lett. 24, 809–816. doi: 10.2174/0929866524666170728151401
Palma, S., Keilani, M., Hasenoehrl, T., and Crevenna, R. (2020). Impact of supportive therapy modalities on heart rate variability in cancer patients - a systematic review. Disabil. Rehabil. 42, 36–43. doi: 10.1080/09638288.2018.1514664
Park, S. B., Goldstein, D., Krishnan, A. V., Lin, C. S. Y., Friedlander, M. L., Cassidy, J., et al. (2013). Chemotherapy-induced peripheral neurotoxicity: a critical analysis. CA Cancer J. Clin. 63, 419–437. doi: 10.3322/caac.21204
Prado, C. M. M., Baracos, V. E., Mccargar, L. J., Reiman, T., Mourtzakis, M., Tonkin, K., et al. (2009). Sarcopenia as a determinant of chemotherapy toxicity and time to tumor progression in metastatic breast cancer patients receiving capecitabine treatment. Clin. Cancer Res. 15, 2920–2926. doi: 10.1158/1078-0432.CCR-08-2242
Reyes Del Paso, G. A., Langewitz, W., Mulder, L. J., Van Roon, A., and Duschek, S. (2013). The utility of low frequency heart rate variability as an index of sympathetic cardiac tone: a review with emphasis on a reanalysis of previous studies. Psychophysiology 50, 477–487. doi: 10.1111/psyp.12027
Routledge, F. S., Campbell, T. S., Mcfetridge-Durdle, J. A., and Bacon, S. L. (2010). Improvements in heart rate variability with exercise therapy. Can. J. Cardiol. 26, 303–312. doi: 10.1016/S0828-282X(10)70395-0
San-Millán, I., and Brooks, G. A. (2016). Reexamining cancer metabolism: lactate production for carcinogenesis could be the purpose and explanation of the Warburg Effect. Carcinogenesis 38, 119–133. doi: 10.1093/carcin/bgw127
Schmidt, F. L., Oh, I. S., and Hayes, T. L. (2009). Fixed-versus random-effects models in meta-analysis: Model properties and an empirical comparison of differences in results. Br. J. Math. Stat. Psychol. 62, 97–128. doi: 10.1348/000711007X255327
Schmitz, K. H., Courneya, K. S., Matthews, C., Demark-Wahnefried, W., Galvão, D. A., Pinto, B. M., et al. (2010). American College of Sports Medicine roundtable on exercise guidelines for cancer survivors. Med. Sci. Sports Exerc. 42, 1409–1426. doi: 10.1249/MSS.0b013e3181e0c112
Scott, J. M., Jones, L. W., Hornsby, W. E., Koelwyn, G. J., Khouri, M. G., Joy, A. A., et al. (2014). Cancer therapy-induced autonomic dysfunction in early breast cancer: implications for aerobic exercise training. Int. J. Cardiol. 171:e50. doi: 10.1016/j.ijcard.2013.11.113
Shin, H. C., Yang, J. O., and Kim, S. R. (2016). Effects of circuit exercise on autonomic nerve system of survivors after surgery of breast cancer. J. Phys. Ther. Sci. 28, 2898–2903. doi: 10.1589/jpts.28.2898
Spiering, B. A., Kraemer, W. J., Anderson, J. M., Armstrong, L. E., Nindl, B. C., Volek, J. S., et al. (2008). Resistance exercise biology: manipulation of resistance exercise programme variables determines the responses of cellular and molecular signalling pathways. Sports Med. 38, 527–540. doi: 10.2165/00007256-200838070-00001
Task Force of the European Society of Cardiology the North American Society of Pacing Electrophysiology (1996). Heart rate variability: standards of measurement, physiological interpretation, and clinical use. Circulation 93, 1043–1065. doi: 10.1161/01.CIR.93.5.1043
Thomas, G. A., Cartmel, B., Harrigan, M., Fiellin, M., Capozza, S., Zhou, Y., et al. (2017). The effect of exercise on body composition and bone mineral density in breast cancer survivors taking aromatase inhibitors. Obesity. 25, 346–351. doi: 10.1002/oby.21729
Tjeerdsma, G., Meinardi, M. T., Van Der Graaf, W. T., Van Den Berg, M. P., Mulder, N. H., Crijns, H. J., et al. (1999). Early detection of anthracycline induced cardiotoxicity in asymptomatic patients with normal left ventricular systolic function: autonomic versus echocardiographic variables. Heart 81, 419–423. doi: 10.1136/hrt.81.4.419
Williams, D. P., Koenig, J., Carnevali, L., Sgoifo, A., Jarczok, M. N., Sternberg, E. M., et al. (2019). Heart rate variability and inflammation: a meta-analysis of human studies. Brain Behav. Immun. 80, 219–226. doi: 10.1016/j.bbi.2019.03.009
Zhou, W., Wan, Y. H., Chen, Q., Qiu, Y. R., and Luo, X. M. (2018). Effects of Tai Chi exercise on cancer-related fatigue in patients with nasopharyngeal carcinoma undergoing chemoradiotherapy: a randomized controlled trial. J. Pain Symptom Manage. 55, 737–744. doi: 10.1016/j.jpainsymman.2017.10.021
Zhou, X., Ma, Z., Zhang, L., Zhou, S., Wang, J., Wang, B., et al. (2016). Heart rate variability in the prediction of survival in patients with cancer: a systematic review and meta-analysis. J. Psychosom. Res. 89, 20–25. doi: 10.1016/j.jpsychores.2016.08.004
Keywords: autonomic modulation, exercise programs, cardiovascular dysfunction, oncology, heart rate variability
Citation: Lavín-Pérez AM, Collado-Mateo D, Mayo X, Liguori G, Humphreys L and Jiménez A (2021) Can Exercise Reduce the Autonomic Dysfunction of Patients With Cancer and Its Survivors? A Systematic Review and Meta-Analysis. Front. Psychol. 12:712823. doi: 10.3389/fpsyg.2021.712823
Received: 09 June 2021; Accepted: 12 July 2021;
Published: 24 August 2021.
Edited by:Rodrigo Ramirez-Campillo, University of Los Lagos, Chile
Reviewed by:David Cristóbal Andrade, University of Antofagasta, Chile
Jairo Azócar Gallardo, University of Los Lagos, Chile
Copyright © 2021 Lavín-Pérez, Collado-Mateo, Mayo, Liguori, Humphreys and Jiménez. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Daniel Collado-Mateo, email@example.com