- Open Access
The role of cardiac rehabilitation using exercise to decrease natriuretic peptide levels in non-surgical patients: a systematic review
Perioperative Medicine volume 8, Article number: 14 (2019)
Exercise is recommended in patients with cardiac failure. In the perioperative patient, exercise is also gaining popularity as a form of prehabilitation. In this meta-analysis, we examine if exercise is able to reduce natriuretic peptide levels. Natriuretic peptide (NP) has strong prognostic ability in identifying patients who will develop adverse postoperative cardiovascular outcomes. The protocol was registered with PROSPERO (CRD42017051468). The database search included MEDLINE (PubMed), CINAHL (EBSCO host), EMBASE (EBSCO host), ProQuest, Web of Science, and Cochrane database. The primary outcomes were to determine whether exercise therapy was effective in reducing NP levels as compared to control group, the shortest time period required to reduce NP levels after exercise therapy, and whether reducing NP levels decreased morbidity and mortality. Full texts of 16 trials were retrieved for this review. Exercise therapy showed a significant reduction in natriuretic peptide levels between the intervention and control groups (SMD − 0.45, 95% CI − 0.88 to − 0.03) with significant heterogeneity between the included trials. This was also shown in the within a 12-week period.
Historically, exercise was commonly avoided in patients with heart failure. This has changed dramatically over the past 30 years with recommendations from international organisations such as the European Society of Cardiology and American College of Cardiology Foundation/American Heart Association for the use of exercise training to improve exercise tolerance and reduce morbidity and mortality (Cattadori et al. 2018).
Exercise is now considered part of preoperative rehabilitation, also known as prehabilitation, for patients presenting for surgery. This is based on the philosophy that improving functional capacity may improve the patient’s ability to withstand the surgical stress response and thereby improve postoperative outcomes. Outcomes such as hospital length of stay, postoperative pulmonary complications, and quality of life have been improved with this approach (Drudi et al. 2019).
There is currently no consensus on the type and duration of exercise needed to improve outcome in surgical patients (Vermillion et al. 2018) and non-surgical patients (Smart and Steele 2010). Furthermore, B-type natriuretic peptide (BNP) testing has been recommended to identify patients at high risk of perioperative cardiovascular events (Duceppe et al. 2017), yet there remains limited data on the efficacy of exercise to decrease B-type natriuretic peptides (Smart and Steele 2010) and decrease subsequent cardiovascular events.
The objective of this systematic review of clinical trials was to determine whether in adult, medical patients with cardiac failure, exercise therapy was able to decrease natriuretic peptide (NP) levels and whether this was associated with improved cardiovascular outcomes.
Protocol and registration
The protocol was registered with PROSPERO (CRD42017051468). The Preferred Reporting Items for Systematic reviews and Meta-Analysis (PRISMA) guidelines were adhered to (Moher et al. 2009). This protocol included a meta-analysis included on the effect of medical therapy on NP levels, which is presented in the accompanying paper (Alphonsus et al. 2019).
The inclusion criteria for this systematic review have been described in the systematic review on natriuretic peptide-directed medical therapy which included exercise therapy trials.
In this systematic review, we report prospective randomised clinical trials of adult medical patients who were randomised to exercise as part of cardiac rehabilitation, where the subsequent changes in natriuretic peptide levels are reported. We excluded (i) trials that monitored natriuretic peptides for prognostic or diagnostic purposes, without a strategy to lower natriuretic peptide levels; (ii) reviews of natriuretic peptide or biomarker physiology; and (iii) trials reporting natriuretic peptides in patients with acute myocardial infarction, pulmonary hypertension, cardiac resynchronisation therapy, and left ventricular assist devices.
Information sources, search, and study selection
Three searches were conducted using search terms ‘brain natriuretic peptide’ AND ‘treatment’, ‘brain natriuretic peptide’ AND ‘heart failure’, and ‘brain natriuretic peptide’ AND ‘exercise’. The following databases were accessed: MEDLINE (PubMed), CINAHL (EBSCO host), EMBASE (EBSCO host), ProQuest, Web of Science, and Cochrane database. There were no filters used for year of publication or language. Non-English titles were not excluded. An example of the search is shown in Additional file 1. The initial search was conducted on 22 December 2016 and updated on 4 March 2018.
Data collection process
Titles were screened for potential inclusion by CA and PG. Abstracts of potential papers identified through the title search were then screened using inclusion and exclusion criteria by CA and PG. The full texts of potential trials were then extracted for full text review and analysis. Reference lists were searched for additional papers that could be included in this review. Data extraction was done by one author (CA) and then checked by a co-author (BB). When required data was not presented in the publication, the authors were contacted for these data.
We extracted data on the NP reduction at the end of the exercise trials. Data on the patient characteristics, the type of exercise intervention, the physical activity in the control group, and the mortality and morbidity in the trials was also extracted.
The primary outcomes for this review were to determine (i) whether exercise therapy was effective in reducing NP levels as compared to control group, (ii) the shortest time period required to reduce NP levels after exercise therapy, and (iii) whether reducing NP levels decreased morbidity and mortality. The secondary outcome was to determine which specific exercise regimens were more effective in reducing NP levels.
Risk of bias in individual studies
Assessment of bias in the studies was conducted by CA and verified by BB following discussion. The Cochrane Collaboration risk of bias tool was used and assessed selection bias, concealment bias, performance bias, detection bias, attrition bias, and other biases. Studies were assessed as having low, unclear, or high risk of bias.
Summary measures and synthesis of results
Statistical analyses were conducted using Review Manager Version 5.3 (Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014). For NP reduction, we tabulated the absolute NP change. NP levels which were reported as median and interquartile range (IQR) were converted to mean and SD (Wan et al. 2014). As the included trials used either BNP or NT-proBNP to monitor therapeutic response, we made use of standardised mean difference (SMD) for our meta-analysis. SMD addresses the difference in the effect size for an intervention when the units of measurement differ between trials, e.g. use of BNP or NT-proBNP. The SMD is the difference between groups in mean end point divided by the SD of the control group (or pooled SD of the treatment and control groups) (Guyatt et al. 2015). These data are presented as a forest plot. Random effects models were used where the I2 statistic > 25% (representing significant heterogeneity); otherwise, a fixed effects model was used.
Risk of bias across studies
Risk of publication bias across studies was assessed with funnel plots for NP reduction.
After the initial search, 64 articles were reviewed for potential inclusion. Twenty-six trials (27 publications) were selected and 8 trials added from references, of which 18 were trials of medical therapy interventions and 16 trials were of an exercise intervention (Fig. 1).
We evaluated 2 previous systematic reviews using the AMSTAR format (Additional file 2).
Study characteristics of included studies
Cardiac rehabilitation exercise trials were conducted in adult patients 18 years and older, in an outpatient setting (Table 1). The included cardiac rehabilitation exercise trials all included some form of aerobic exercise, either walking, bicycle, or treadmill. Trials that involved interval training were considered as a separate subgroup for analysis (Aksoy et al. 2015; Nilsson et al. 2010; Stevens et al. 2015). Three trials included resistance training in addition to aerobic training in the intervention group (Gary et al. 2011; Jonsdottir et al. 2006; Malfatto et al. 2009; Norman et al. 2012). Most trials ran for up to 12 weeks, one trial for 20 weeks (Jonsdottir et al. 2006), and another for 24 weeks (Norman et al. 2012). Most trials were small, with a maximum of 40 patients in each arm, with the exception of 1 large trial (HF-ACTION) which included 477 patients (Ahmad et al. 2014). Most trials included patients with an ejection fraction (EF) < 40%, two trials had patients with EF 40–49% (Guazzi et al. 2012; Parrinello et al. 2010), and three trials had patients with mixed categories of heart failure (Aksoy et al. 2015; Jonsdottir et al. 2006; Nilsson et al. 2010). The exercise intervention protocols were not individualised to the NP levels, but the NP response to the exercise intervention was reported in all the trials.
The exercise intervention group received supervised exercise training in all the trials, except two where the exercises were home-based after participants were given instructions (Eleuteri et al. 2013; Parrinello et al. 2010). The control group were given exercise information (except Brubaker (Brubaker et al. 2009)) but did not receive supervised exercise training.
Risk of bias within studies and across studies
The risk of bias of the included trials is shown in the Additional file 3: Figure S1 and Additional file 4: Figure S2. The random sequence generation was acceptable in three trials (Ahmad et al. 2014; Guazzi et al. 2012; Maria Sarullo et al. 2006). By virtue of the intervention (supervised exercise versus exercise recommendation), blinding of patients was impossible, and investigator blinding was poor. Outcome assessors were only blinded in two trials (Ahmad et al. 2014; Brubaker et al. 2009). The funnel plots for SMD (Fig. 2) did not suggest publication bias.
Results of individual studies and synthesis of results
All trials presented data on NP levels at the end of the intervention period.
Is exercise therapy as effective in reducing NP levels as compared to control group?
The meta-analysis of the SMD in NP levels between the intervention and control group is shown in Fig. 3. The overall point estimate showed a significant reduction in NP levels between the intervention and control groups (SMD − 0.45, 95% CI − 0.88 to − 0.03) with significant heterogeneity between the included trials. Neither the continuous aerobic, nor the interval training subgroup showed a significant reduction in NP.
What is the shortest time period required to reduce NP levels after exercise therapy?
An analysis of the trials with a 12-week intervention period (the shortest exercise intervention period in the eligible trials) showed a significant NP reduction (SMD − 0.75, 95% CI − 1.17 to − 0.33) (Fig. 4).
Does reducing NP levels decreased morbidity and mortality?
Only four trials reported on mortality (Ahmad et al. 2014; Brubaker et al. 2009; Jonsdottir et al. 2006; Nilsson et al. 2010). HF-ACTION trial (Ahmad et al. 2014) reported 189 (16%) deaths in the intervention group and 198 (17%) deaths in the control group, HR 0.96 (0.79–1.17), p = 0.70, and a cardiovascular mortality at a median follow-up of 30 months of 131 (11%) deaths in the intervention group and 143 (12%) deaths in the control group, 0.92 (0.74–1.15), p = 0.47. Three other trials, Nilsson et al. (2010), Jónsdóttir et al. (2006), and Brubaker et al. (2009), reported mortality. Nilsson et al. reported one death in the control group, Jónsdóttir et al. two each in intervention and control groups, and Brubaker et al. one in each group. None of other trials reported mortality.
Secondary outcome: where specific exercise regimens were more effective in reducing NP levels?
Neither supervised continuous aerobic exercise or interval training was independently associated with a significant reduction in NP levels. A preferable exercise regimen therefore cannot be determined.
This meta-analysis examines exercise rehabilitation in adult patients with chronic heart failure in an outpatient setting. The principal finding was that exercise training can significantly decrease NP levels within 12 weeks in adult medical patients eligible for cardiac rehabilitation. The patients most likely to benefit from this intervention had stable chronic heart failure, with an EF which was predominantly < 45% (Table 1). However, significant heterogeneity exists between trials. Currently, there is insufficient data to determine whether this NP reduction is also associated with a survival benefit.
The characteristics of the exercise programmes were the following (Table 2). Almost all trials included exercise programmes that were conducted under direct supervision. All the programmes had an aerobic component and varied in exercise intensity, duration, and frequency. Few trials had interval training and resistance training. The exercise regimens were predominantly determined by patient-specific physiological parameters, e.g. AT, VT, and VO2 peak, and were thus individualised. The duration of the exercise programme was 12 weeks in most trials. These findings are applicable to patients with cardiac failure of varying severity but considered stable on medication. It is important to note that NP levels were not a criterion for inclusion in these trials, and hence, we do not know the baseline NP level necessary to determine eligibility for a supervised exercise programme.
The strength of this meta-analysis is that it shows exercise training to be associated with a reduction in NP levels within 12 weeks from randomisation. There were no reports of morbidity associated with the supervised exercise programmes.
This review has some limitations. Firstly, the protocols differed between trials making it difficult to recommend a specific exercise programme. This may partly explain the significant heterogeneity in the included studies. However, despite the significant heterogeneity, the random effects meta-analysis suggests that the reduction in NP levels associated with exercise training is possible within 12 weeks. There remains limited mortality data in the trials of cardiac rehabilitation programmes which document NP level changes over time. It is thus impossible to determine whether a reduction in NP levels secondary to exercise therapy is associated with increased survival. It is possible that an exercise intervention may improve other patient reported outcomes, although these were not uniformly reported in the included trials. Finally, as all of the trials were not blinded to the patient or investigator, it is possible that there may be co-intervention bias associated with the exercise arm of these trials.
Our review differs from the two previous systematic reviews which have examined NP levels in non-surgical patients after exercise therapy (Pearson et al. 2018; Smart and Steele 2010). These reviews also found that NP levels were reduced after exercise therapy, with a high heterogeneity in the response. The strength of our review is that it updates the previous reviews (Smart and Steele 2010) with more trials and only includes RCTs with aerobic exercise programmes (Pearson et al. 2018). We did not consider trials examining yoga, stretching, Tai chi, functional electrical stimulation, or inspiratory muscle training (Pearson et al. 2018).
Elevated preoperative NP levels have been independently associated with major adverse cardiac events and mortality following surgery (Rodseth et al. 2008, 2011, 2014). Further investigation into the role of supervised preoperative exercise programme in the surgical population may provide insight into the relationship between exercise and NP levels in this cohort of patients.
This meta-analysis shows that NP levels can be lowered with supervised exercise training and can be achieved within a 12-week programme. An exercise prehabilitation programme of 12 weeks duration may lower NP levels, and possibly perioperative risk. It is unclear whether this will improve postoperative cardiovascular outcomes.
Availability of data and materials
All articles available online and datasets are available from the corresponding author.
B-type natriuretic peptide
N-terminal pro-B-type natriuretic peptide
Standardised mean difference
- VO2 :
Maximum oxygen consumption
Ahmad T, Fiuzat M, Mark DB, Neely B, Neely M, Kraus WE, Kitzman DW, Whellan DJ, Donahue M, Zannad F, et al. The effects of exercise on cardiovascular biomarkers in patients with chronic heart failure. Am Heart J. 2014;167(2):193–202.e191.
Aksoy S, Findikoglu G, Ardic F, Rota S, Dursunoglu D. Effect of 10-week supervised moderate-intensity intermittent vs. continuous aerobic exercise programs on vascular adhesion molecules in patients with heart failure. Am J Phys Med Rehabil. 2015;94(10 Suppl 1):898–911.
Alphonsus CS, Govender P, Rodseth RN, Biccard BM. Natriuretic peptide directed medical therapy: A systematic review. Perioper Med. 2019. In press.
Brubaker PH, Moore JB, Stewart KP, Wesley DJ, Kitzman DW. Endurance exercise training in older patients with heart failure: results from a randomized, controlled, single-blind trial. J Am Geriatr Soc. 2009;57(11):1982–9.
Cattadori G, Segurini C, Picozzi A, Padeletti L, Anza C. Exercise and heart failure: an update. ESC Heart Fail. 2018;5(2):222–32.
Drudi LM, Tat J, Ades M, Mata J, Landry T, MacKenzie KS, Steinmetz OK, Gill HL. Preoperative exercise rehabilitation in cardiac and vascular interventions. J Surg Res. 2019;237:3–11.
Duceppe E, Parlow J, MacDonald P, Lyons K, McMullen M, Srinathan S, Graham M, Tandon V, Styles K, Bessissow A, et al. Canadian cardiovascular society guidelines on perioperative cardiac risk assessment and management for patients who undergo noncardiac surgery. Can J Cardiol. 2017;33(1):17–32.
Eleuteri E, Mezzani A, Di Stefano A, Vallese D, Gnemmi I, Delle Donne L, Taddeo A, Della Bella S, Giannuzzi P. Aerobic training and angiogenesis activation in patients with stable chronic heart failure: a preliminary report. Biomarkers. 2013;18(5):418–24.
Gary RA, Cress ME, Higgins MK, Smith AL, Dunbar SB. Combined aerobic and resistance exercise program improves task performance in patients with heart failure. Arch Phys Med Rehabil. 2011;92(9):1371–81.
Guazzi M, Vitelli A, Arena R. The effect of exercise training on plasma NT-pro-BNP levels and its correlation with improved exercise ventilatory efficiency in patients with heart failure. Int J Cardiol. 2012;158(2):290–1.
Guyatt G, Rennie D, Meade M, Cook D. Users’ guides to the medical literature. Essentials of evidence-based clinical practice. New York: McGraw-Hill Education Medical; 2015.
Jonsdottir S, Andersen KK, Sigurosson AF, Sigurosson SB. The effect of physical training in chronic heart failure. Eur J Heart Fail. 2006;8(1):97–101.
Kobayashi N, Tsuruya Y, Iwasawa T, Ikeda N, Hashimoto S, Yasu T, Ueba H, Kubo N, Fujii M, Kawakami M, et al. Exercise training in patients with chronic heart failure improves endothelial function predominantly in the trained extremities. Circ J. 2003;67(6):505–10.
Malfatto G, Branzi G, Osculati G, Valli P, Cuoccio P, Ciambellotti F, Parati G, Facchini M. Improvement in left ventricular diastolic stiffness induced by physical training in patients with dilated cardiomyopathy. J Card Fail. 2009;15(4):327–33.
Maria Sarullo F, Gristina T, Brusca I, Milia S, Raimondi R, Sajeva M, Maria La Chiusa S, Serio G, Paterna S, Di Pasquale P, et al. Effect of physical training on exercise capacity, gas exchange and N-terminal pro-brain natriuretic peptide levels in patients with chronic heart failure. Eur J Cardiovasc Prev Rehabil. 2006;13(5):812–7.
Meyer T, Schwaab B, Gorge G, Scharhag J, Herrmann M, Kindermann W. Can serum NT-proBNP detect changes of functional capacity in patients with chronic heart failure? Z Kardiol. 2004;93(7):540–5.
Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009;339:b2535.
Nilsson BB, Westheim A, Risberg MA, Arnesen H, Seljeflot I. No effect of group-based aerobic interval training on N-terminal pro- B-type natriuretic peptide levels in patients with chronic heart failure. Scand Cardiovasc J. 2010;44(4):223–9.
Norman JF, Pozehl BJ, Duncan KA, Hertzog MA, Krueger SK. Effects of exercise training versus attention on plasma B-type natriuretic peptide, 6-minute walk test and quality of life in individuals with heart failure. Cardiopulm Phys Ther J. 2012;23(4):19–25.
Parrinello G, Torres D, Paterna S, Di Pasquale P, Trapanese C, Licata G. Short-term walking physical training and changes in body hydration status, B-type natriuretic peptide and C-reactive protein levels in compensated congestive heart failure. Int J Cardiol. 2010;144(1):97–100.
Pearson MJ, King N, Smart NA. Effect of exercise therapy on established and emerging circulating biomarkers in patients with heart failure: a systematic review and meta-analysis. Open Heart. 2018;5(2):e000819.
Rodseth RN, Biccard BM, Le Manach Y, Sessler DI, Lurati Buse GA, Thabane L, Schutt RC, Bolliger D, Cagini L, Cardinale D, et al. The prognostic value of pre-operative and post-operative B-type natriuretic peptides in patients undergoing noncardiac surgery: B-type natriuretic peptide and N-terminal fragment of pro-B-type natriuretic peptide: a systematic review and individual patient data meta-analysis. J Am Coll Cardiol. 2014;63(2):170–80.
Rodseth RN, Lurati Buse GA, Bolliger D, Burkhart CS, Cuthbertson BH, Gibson SC, Mahla E, Leibowitz DW, Biccard BM. The predictive ability of pre-operative B-type natriuretic peptide in vascular patients for major adverse cardiac events: an individual patient data meta-analysis. J Am Coll Cardiol. 2011;58(5):522–9.
Rodseth RN, Padayachee L, Biccard BM. A meta-analysis of the utility of pre-operative brain natriuretic peptide in predicting early and intermediate-term mortality and major adverse cardiac events in vascular surgical patients. Anaesthesia. 2008;63(11):1226–33.
Sandri M, Kozarez I, Adams V, Mangner N, Hollriegel R, Erbs S, Linke A, Mobius-Winkler S, Thiery J, Kratzsch J, et al. Age-related effects of exercise training on diastolic function in heart failure with reduced ejection fraction: the Leipzig Exercise Intervention in Chronic Heart Failure and Aging (LEICA) Diastolic Dysfunction Study. Eur Heart J. 2012;33(14):1758–68.
Smart NA, Steele M. Systematic review of the effect of aerobic and resistance exercise training on systemic brain natriuretic peptide (BNP) and N-terminal BNP expression in heart failure patients. Int J Cardiol. 2010;140(3):260–5.
Stevens AL, Hansen D, Herbots L, Wens I, Creemers A, Dendale P, Eijnde BO. Exercise training improves insulin release during glucose tolerance testing in stable chronic heart failure patients. J Cardiopulm Rehabil Prev. 2015;35(1):37–46.
Vermillion SA, James A, Dorrell RD, Brubaker P, Mihalko SL, Hill AR, Clark CJ. Preoperative exercise therapy for gastrointestinal cancer patients: a systematic review. Syst Rev. 2018;7(1):103.
Wan X, Wang W, Liu J, Tong T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol. 2014;14:135.
CA has received research funding from the South African Society of Anaesthesiologists and the University of Cape Town.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Alphonsus, C.S., Govender, P., Rodseth, R.N. et al. The role of cardiac rehabilitation using exercise to decrease natriuretic peptide levels in non-surgical patients: a systematic review. Perioper Med 8, 14 (2019). https://doi.org/10.1186/s13741-019-0124-0
- Cardiac morbidity
- Preoperative factors
- Myocardial ischaemia