Abstract
Background
We previously reported changes in the serum metabolome associated with impaired myocardial relaxation in an asymptomatic older community cohort. In this prospective parallel-group randomized control pilot trial, we subjected community adults without cardiovascular disease to exercise intervention and evaluated the effects on serum metabolomics.
Methods
Between February 2019 to November 2019, thirty (83% females) middle-aged adults (53 ± 4 years) were randomized with sex stratification to either twelve weeks of moderate-intensity exercise training (Intervention) (n = 15) or Control (n = 15). The Intervention group underwent once-weekly aerobic and strength training sessions for 60 min each in a dedicated cardiac exercise laboratory for twelve weeks (ClinicalTrials.gov: NCT03617653). Serial measurements were taken pre- and post-intervention, including serum sampling for metabolomic analyses.
Results
Twenty-nine adults completed the study (Intervention n = 14; Control n = 15). Long-chain acylcarnitine C20:2-OH/C18:2-DC was reduced in the Intervention group by a magnitude of 0.714 but increased in the Control group by a magnitude of 1.742 (mean difference −1.028 age-adjusted p = 0.004). Among Controls, alanine correlated with left ventricular mass index (r = 0.529, age-adjusted p = 0.018) while aspartate correlated with Lateral e’ (r = −764, age-adjusted p = 0.016). C20:3 correlated with E/e’ ratio fold-change in the Intervention group (r = −0.653, age-adjusted p = 0.004). Among Controls, C20:2/C18:2 (r = 0.795, age-adjusted p = 0.005) and C20:2-OH/C18:2-DC fold-change (r = 0.742, age-adjusted p = 0.030) correlated with change in E/A ratio.
Conclusions
Corresponding relationships between serum metabolites and cardiac function in response to exercise intervention provided pilot observations. Future investigations into cellular fuel oxidation or central carbon metabolism pathways that jointly impact the heart and related metabolic systems may be critical in preventive trials.
Plain language summary
Prior studies have found changes in cellular biological processes in both cardiac aging and heart failure suggesting a common underlying mechanism. I has also been shown that exercise in healthy participants can reverse the signs of early cardiac aging. In this experimental study, we examined the effects of exercise on biological markers and cardiac function among healthy community older adults. After twelve weeks of exercise, there were changes in biological components associated with cardiac function. These findings highlight the potential of exercise as a strategy to target biological alterations in early cardiac aging and potentially prevent it.
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Introduction
Age-related alterations in the cardiovascular system, such as ventricular and arterial stiffening, contribute to the risks of developing heart failure in aging1. Aging is commonly associated with changes in myocardial systolic and diastolic function, although diastolic dysfunction is a predominant feature that frequently precedes symptomatic systolic dysfunction1,2,3,4. Diastolic dysfunction also plays an important role in the pathophysiology of overt clinical heart failure with preserved ejection fraction (HFpEF), a subset of heart failure of substantial prevalence in aging cohorts5,6. While the underlying pathophysiological mechanisms behind diastolic dysfunction are complex, impairments in mitochondrial oxidation and fuel metabolism pathways have delineated diastolic failure from systolic failure7,8. These pathways were similarly observed among aging, asymptomatic older adults with impairments in myocardial relaxation and mitochondrial fuel metabolism9,10. Thus, understanding early metabolic changes in aging-related ventricular stiffness may reveal mechanistic insights before the onset of clinical diastolic failure.
The aging heart is associated with a decline in mitochondrial content and function with knock-on effects on major fuel metabolism pathways11,12. Recent evidence has linked the accumulation of amino acids such as leucine and long-chain acyl-carnitines with early impaired myocardial relaxation and arterial stiffness in an aging population9,13. Metabolomic studies in HFpEF have also revealed similar associations between disease and accumulation of long-chain acyl-carnitines14,15. Thus, in both cardiovascular aging and HFpEF, changes in markers of fuel metabolism link dysfunctional mitochondrial metabolism and central carbon pathways to the development of cardiovascular disease9,16. Given these similar functional and metabolic changes for cardiovascular aging and HFpEF, we hypothesize that interventions targeting these common pathways in the early stages may represent novel strategies applicable to aging-related diastolic dysfunction as an early upstream approach.
Aging-related changes in cardiac compliance are accelerated by physical inactivity and can be partially reversed by exercise17. Increases in long-chain acyl-carnitines have been linked to lower aerobic capacity18, while exercise upregulates mitochondrial and related fuel metabolism pathways in the heart and can reverse aging-related decline in skeletal muscle mitochondrial function19,20. Increased physical activity upregulates fatty oxidation and Krebs cycle genes, activating central carbon metabolism and mitochondrial pathways21. These findings suggest that exercise may reverse the metabolic underpinnings of cardiac aging and potentially prevent early aging-related diastolic dysfunction.
Given the importance of exercise as an essential modifiable lifestyle factor in mitigating aging-related cardiovascular risk, a better understanding of the effect of physical activity on underlying cellular metabolic processes will improve our understanding of disease pathophysiology and highlight new potential targets for disease prevention. In this paper, we examine the effects of exercise on human metabolism in the early stages of healthy aging that can be detected using metabolomic signatures. We additionally explore the associations between serum metabolomic markers in relation to cardiac function and hemodynamic parameters.
Methods
Study population
Community adults with no prior evidence of cardiovascular disease underwent transthoracic echocardiography as part of the Cardiac Aging Study, a prospective study that examines characteristics and determinants of cardiac structural and functional changes at age18. Thirty participants volunteered to participate in this exercise trial between February 2019 and November 2019 (Fig. 1). Participants were recruited if they were 40 and above, were willing and able to provide informed consent, and had at least grade 1 diastolic dysfunction on echocardiography based on the latest guidelines22. Participants with a history of cardiovascular disease, stroke, cancer, uncontrolled hypertension (i.e., systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥ 90 mmHg despite being on treatment for hypertension), low blood pressure (i.e., systolic blood pressure < 90 mmHg or diastolic blood pressure < 40 mmHg), acute pulmonary embolus or pulmonary infarction, acute myocarditis or pericarditis, suspected or known dissecting aneurysm, acute systemic infection, or uncontrolled metabolic disease (e.g., diabetes, thyrotoxicosis or myxoedema) were excluded. Patients with neuromuscular, musculoskeletal, or rheumatoid disorders that are exacerbated by exercise were also excluded. Written informed consent was obtained from participants upon enrolment. The study was conducted in accordance with the Declaration of Helsinki, and the SingHealth Centralized Institutional Review Board (CIRB/2018/2118) approved the study protocol. They were randomized with sex stratification into either twelve weeks of exercise training (Intervention, n = 15) or no exercise (Control, n = 15). Before exercise intervention, participants underwent a treadmill stress test to exclude undiagnosed obstructive coronary artery disease. One participant with an equivocal treadmill test result was excluded from the study. Treadmill test results were read by independent board-certified cardiologists blinded to participation details.
Data acquisition
Participants underwent baseline measurements before intervention and repeated measurements after 12 weeks since randomization. These measurements include anthropometry, body composition, central hemodynamics, transthoracic echocardiogram, and serum sampling for metabolomic analyses.
Skeletal muscle mass was measured by a multifrequency bioimpedance body composition analyzer (InBody 370, Biospace Company). Appendicular lean mass (ALM) was calculated as the sum of muscles for the bilateral upper and lower limbs, and ALM/height2 was calculated as follows: ALM (kg)/height (m2), respectively.
Central blood pressure and pulse wave analysis were measured with the Schiller BR-102 PLUS pulse wave analysis device (Schiller AG, Baar, Switzerland) using the oscillometric method on the brachial artery. Brachial diastolic and systolic blood pressure values were obtained from the portable automatic blood pressure function. Blood pressure was recorded multiple times during the day. Each participant was seated comfortably in a quiet room before blood pressure was recorded23. A single examiner performed all measurements. The pulse wave analysis was based on auscultatory/oscillometric blood pressure measurement and pulse contour analysis, providing information about arterial behavior and pulse wave velocity. The following parameters were obtained: (1) aortic augmentation index (%) with and without correction for a heart rate of 75 (AIx@HR75), (2) pulse wave velocity (m/s), (3) peripheral resistance (s*mmHg/ml), (4) estimated central systolic and diastolic pressure and (5) central pulse pressure calculated as the difference between estimated systolic and diastolic BP.
Two-dimensional transthoracic echocardiography was performed using ALOKA α10 with a 3.5 MHz probe. In each subject, standard echocardiography, which included 2-D, M-mode, pulse Doppler, and tissue Doppler imaging, was performed in the standard parasternal and apical (apical 4-chamber, apical 2-chamber, and apical long) views, and three cardiac cycles were recorded. Left ventricular ejection fraction and left atrial volume were measured. The trans-mitral flow E and A wave with the sample volume position at the tip of the mitral valve leaflets from the apical 4-chamber view were recorded by Doppler echocardiography. The E/A ratio was computed as a ratio of peak velocity flow in early diastole E (m/s) to peak velocity flow in late diastole by atrial contraction A (m/s). Pulsed wave tissue Doppler imaging was performed with the sample volume at the septal and lateral annulus from the apical 4-chamber view. The frame rate was between 80 and 100 frames per second. The tissue velocity patterns were recorded and expressed as E’ and A.’ Stroke volume (SV) was calculated using the Doppler volume time integral (VTI) method by multiplying left ventricular outflow tract VTI with its cross-sectional area24,25. Cardiac output was calculated by multiplying SV with pulse rate. Total arterial compliance was estimated using the SV/PP method by dividing stroke volume with pulse pressure (PP)26,27. Effective arterial elastance was calculated using the Pes/SV method by dividing the LV end-systolic pressure (Pes) by stroke volume28. Echocardiograms were performed by ultrasonographers blinded to the allocation of groups and interpreted by independent board-certified cardiologists blinded to participation details. Blood samples were collected on the day of echocardiography acquisition. Urinary microalbumin was measured using standard assays.
Metabolomics profiling
Antecubital venous blood samples (20–30 ml) were taken from consenting participants in the morning; fasting was not required before blood collection. After collection, the blood samples were immediately placed on ice for transportation and were processed within six hours to obtain serum samples. Serum metabolomic profiling analysis was performed in the Duke-NUS Metabolomics Facility. Serum samples (50 μl) were spiked with a 10 μl deuterium-labeled amino acid mixture and diluted with 400 µl methanol. After centrifugation of the mixture at 17,000 g for 5 min at 4 °C, the supernatant fraction was collected (10 μl) for amino acid analysis. A pooled quality control (QC) sample was prepared by mixing equal amounts (10 μl) of each extracted serum sample. Extraction and measurement of amino acid panels (quantified in units of μM) were performed as previously described in ref. 10. The methanol extracts were derivatized with 3 M Hydrochloric acid in butanol (Sigma Aldrich, USA) for amino acid analysis and diluted in water for analysis in LC-MS. For amino acid analysis, a C18 column (Phenomenex, 100 × 2.1 mm, 1.6 μm, Luna® Omega) on an Agilent 1290 Infinity LC system (Agilent Technologies, CA, USA) coupled with quadrupole-ion trap mass spectrometer (QTRAP 5500, AB Sciex, DC, USA) were used. Mobile phase A (Water) and Mobile phase B (Acetonitrile) containing 0.1% Formic acid were used for chromatography separation. The LC run was performed at a flow rate of 0.4 mL min−1 with an initial gradient of 2% B for 0.8 min, then increased to 15% B in 0.1 min, 20% B in 5.7 min, 50% B in 0.5 min, 70% B in 0.5 min, followed by re-equilibration of the column to the initial run condition (2% B) for 0.9 min. All compounds were ionized in positive mode using electrospray ionization. The chromatograms were integrated using MultiQuant™ 3.0.3 software (AB Sciex, DC, USA). For acyl-carnitines, serum samples (100 μl) were spiked with a 20 μl deuterium-labeled acyl-carnitine mixture and diluted with 800 µl methanol. Extraction and measurement of acyl-carnitine were performed as previously described9. Measurements were taken from distinct samples. Data acquisition and analysis were performed on an Agilent MassHunter Workstation B.06.00 Software.
Exercise Intervention
The exercise group received once-weekly exercise sessions for twelve sessions. Each weekly session consisted of aerobic exercise on treadmill machines lasting 20 –30 min (at a moderate pace of 75–85% peak heart rate), followed by strength training of major muscle groups (shoulders, chest, arms, and legs) lasting 20 min, with warm-up and cool-down using simple stretches and gentle aerobics movements lasting 10 min each.
Exercise physiologists met with participants personally throughout the intervention. Exercise sessions were conducted in person. Exercise physiologists directly supervised the exercise sessions and reviewed the participant’s progress and adherence to the intervention. No adverse effects were recorded in this trial.
Participants randomized to the Control group were advised not to participate in outside formal exercise training programs. They were allowed to do their leisure exercise.
Study endpoints
The study’s primary outcome measure was the change in metabolomic markers after 12 weeks of exercise intervention. Post-hoc analyses were carried out to examine associations between metabolomic markers, echocardiographic left ventricle indices, and vascular compliance at baseline and with respect to their change over time.
Statistics and Reproducibility
Continuous variables are expressed as mean (standard deviation), and categorical variables as n (%). Baseline and post-intervention characteristics between the groups were compared using Fisher’s exact tests for categorical variables and Mann-Whitney U test for continuous variables. Wilcoxon signed-rank test was used for matched pre- and post-intervention comparisons within the groups. Fold-change was calculated by dividing post-intervention values with pre-intervention values. Spearman’s rank-order correlation and scatter plots were used to examine the associations between the changes in metabolites, echocardiography, and vascular compliance. Subsequently, for outcomes between groups with p < 0.050, multiple regression was further applied to adjust for clinical characteristics that were different between the groups (i.e., age). For metabolites, analytes with > 10% outlier values were excluded. Outliers were defined as values below the limit of detection for the analyte. Missingness was replaced by the lowest detected value for that analyte. These metabolites are usually of low abundance and uncertain biological importance. Metabolites were standardized during laboratory analysis9,10. Log-transformation and scaling were not performed. Statistical analyses were done using IBM SPSS Statistics for Windows, Version 23 (IBM Corp, Armonk, NY, USA).
Reporting summary
Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.
Results
Participant characteristics
Thirty participants were randomized by sex stratification into Control (54.8 years ±3.55, males 13.3%) and Intervention groups (51.4 years ±4.34, males 20%). The Intervention group was younger by 3.2 years on average (p = 0.037); otherwise, both groups exhibited similar clinical characteristics, including body mass index, waist circumference, blood pressure, and maximal oxygen uptake (Table 1). In total, 29 participants completed the twelve-week study, with 14 participants in the Intervention group and 15 in the Control group. All Intervention group participants completed twelve sessions of exercise. There were no deviations from the pre-specified trial protocol.
Effect of exercise intervention: Changes in Metabolomics
We evaluated the change in metabolomic markers after 12 weeks of exercise intervention as the primary outcome measure. There were accumulations of medium-chain acylcarnitine C12:2-OH/C10:2-DC in the Intervention group by a magnitude of 1.825 (fold-change), with corresponding reductions in the Control group by a magnitude of 0.9376 (mean difference in fold-change 0.888, p = 0.033, age-adjusted p = 0.070) (Table 2). Levels of long-chain acylcarnitine C20:2-OH/C18:2-DC were reduced in the Intervention group by a magnitude of 0.7136 (fold-change) but increased in the Control group by a magnitude of 1.741 (mean difference in fold-change 1.028, p < 0.001, age-adjusted p = 0.004). Alanine (fold-change 1.1733 vs. 0.95344, mean difference 0.220, p = 0.029, age-adjusted p = 0.070) and arginine (fold-change 1.1379 vs. 0.9501, mean difference 0.188 p = 0.046, age-adjusted p = 0.133) were both increased in the Intervention group and decreased in the Control group (see Fig. 2). Adjusting for age, only the changes in C20:2-OH/C18:2-DC persisted. A heatmap of serum metabolites after the intervention is shown in Supplementary Fig. 1.
Effect of exercise intervention: cardiovascular parameters
We then performed post-hoc analyses on the associations between metabolomic markers, echocardiographic markers, and hemodynamic parameters at baseline and with respect to their change over time.
Hemodynamics and arterial stiffness
In the Control group, central diastolic blood pressure by 8.34 mmHg (p = 0.036), and central systolic blood pressure increased by 13.5 mmHg (p = 0.028); there was a trend towards increased pulse wave velocity by 0.986 m/s (p = 0.059) which did not achieve statistical significance (Table 3). Comparing both groups post-intervention, the Intervention group had a lower pulse wave velocity by 0.70 m/s (p = 0.036), which was not significant after adjusting for age (p = 0.485) (see Table 4). We did not observe significant changes in the total arterial compliance index between the groups (Table 4 and Supplementary Table 1).
Left ventricular diastolic and systolic function
In the Intervention group, Lateral e’ increased by 0.10 cm/s (p = 0.462, age-adjusted p = 0.003). In the Control group, Lateral e’ decreased by 1.3 cm/s (p = 0.033, age-adjusted p = 0.585) but was not significant after age adjustment (Table 3, Supplementary Table 2). Changes in E/e’ ratio or E/A ratio were non-significant. (Table 4 and Fig. 3a–d). We did not observe significant changes in left ventricular ejection fraction, cardiac index, or stroke volume index between the groups (Table 4 and Supplementary Table 1).
Correlations between metabolomics and echocardiographic indices
Changes in several metabolites corresponded with changes in cardiac parameters. C20:2/C18:2 and C20:2-OH/C18:2-DC were positively correlated with the E/A ratio in the Control group but not the Intervention group (Fig. 4). Correlations between other long-chain acyl-carnitines and cardiac parameters were also observed, such as negative correlations between C20:3 with Lateral e’ in the Intervention group and positive correlations between C18 species with left ventricular mass index (LVMI) in the Control group (Fig. 5). For amino acids, aspartate negatively correlated with Lateral e’ while alanine positively correlated with LVMI in the Control group but not in the Intervention group (Fig. 5).
Discussion
After twelve weeks of exercise training, we found alterations in serum metabolites corresponding to changes in cellular fuel oxidation and amino acid pathways that correlated with echocardiographic markers of diastolic function. The use of exercise to observe changes in serum metabolome in relation to cardiovascular parameters is a highlight of this work.
After twelve weeks of exercise, we observed reductions in levels of the long-chain acylcarnitine C20:20-OH/C18:2-DC in the Intervention group relative to Controls. Although no clinically relevant post-exercise changes in ventricular diastolic function were observed, non-cardiac mechanisms, such as skeletal muscle oxygen uptake and mitochondrial function suggested by circulating metabolites, may deepen mechanistic insights into exercise improvements in functional capacity29. Although C20:20-OH/C18:2-DC is a minor species of acylcarnitine, this finding suggests that alterations in fatty oxidation pathways occurred after the period of exercise. Accumulations in long-chain acylcarnitines (LCAC) are previously thought to have resulted from dysregulated fatty acid oxidation and mitochondrial insults and have been associated with impaired myocardial relaxation, preclinical heart failure, and predicted future myocardial dysfunction and major adverse cardiovascular events15,30,31,32. Previous studies have also found associations between LCACs with physical performance33,34. Positive associations between exercise and mitochondrial health also suggest biological plausibility35,36. Unlike short-chain acylcarnitines, long-chain acylcarnitines are derived exclusively from fatty acid metabolism. They are primarily metabolized in mitochondria, thus fulfilling their utility as a diagnostic tool for inborn fatty oxidation defects and a marker of mitochondrial dysfunction37,38. Other metabolomic studies have also identified evidence of skeletal mitochondrial dysfunction in patients HFpEF, reported by citrate synthase activity and porin expression, and biopsies of vastus lateralis muscles have also demonstrated decreased Type 1 oxidative fibres, which are dependent on aerobic respiration39,40. Incorporating these lines of evidence with our findings of reduced LCAC levels post-exercise, we postulate that exercise led to activations in mitochondrial pathways through metabolic switches at the proteomic or genomic levels, preventing the development of preclinical diastolic and vascular dysfunction observed in the Control group. These findings further support existing evidence that mitochondrial dysfunction in cardiac and skeletal muscles may be critical drivers of early cardiovascular aging, and exercise may reverse this41,42,43.
Corresponding relationships between serum metabolites and cardiac function in response to exercise intervention may shed some light on how exercise affects changes in the heart. Long-chain acylcarnitines (LCAC) C20:2, C20:2/C18:2, and C20:2-OH/C18:2-DC correlated with diastolic function and LV mass indices. This finding is unsurprising because LCACs are primarily metabolized in the heart and skeletal mitochondria. Thus, changes in plasma LCACs may reflect the activity of mitochondrial fatty oxidation in the heart and skeletal muscle37,44. We demonstrate this outside of a heart failure setting, suggesting a role to incorporate similar interventions that tackle upstream deteriorations in diastolic function among aging adults.
Besides acylcarnitines, there were also changes in amino acid levels, suggesting that the effect of exercise might be exerted through multiple metabolic pathways. Specifically, there was a trend towards higher arginine levels in the Intervention group. Arginine is involved in synthesizing other amino acids and compounds, including nitric oxide, which plays a crucial role in modulating vascular endothelial stiffness and left ventricular relaxation45,46. Declining levels of arginine have been associated with HFpEF8,10,14. However, arginine was not significant after adjusting for age.
While the Control group experienced decreases in Lateral e’ in and increases in markers of vascular stiffness, such as central diastolic blood pressure and pulse wave velocity, we did not find improvements in some other markers of LV diastolic function, such as the E/A ratio or E/e’ ratio. Age is an important determinant of vascular properties and diastolic function and could have contributed to observed differences between groups despite randomization. The differences in Lateral e’ and pulse wave velocity were non-significant after adjusting for age, indicating the possible influence of age. Central blood pressure was increased among Controls compared to baseline but were not different comparing post-Control with post-Exercise groups. Other randomized trials involving exercise interventions of longer durations have shown improvements in cardiovascular stiffness post-exercise, including central aortic stiffness (20 weeks) and invasive markers of LV myocardial stiffness (2 years)47,48. However, other study cohorts of shorter exercise duration have also not reported clear improvements in LV structure or function post-exercise49,50. In one such study, eight weeks of three sessions per week of supervised endurance and resistance training in patients post-myocardial infarction failed to show any significant improvement in Lateral e’ or E/e’ ratio51. A meta-analysis of eight RCTs of exercise training in HFpEF patients found that 12–24 weeks of exercise training improved functional tolerance without significant change in e’ or E/e’ ratio49. While increases in exercise frequency or duration may produce more observable changes in cardiac structure and function, our short-term exercise intervention was designed to capture changes in the metabolome within the defined period. Exercise trials in older patients have produced mixed-to-neutral effects on cardiac structure and function52,53,54. By identifying changes in the serum metabolome that were affected by exercise, our trial provides human molecular insights into the effect of exercise training, which may not be elucidated from gross cardiac functions.
There were several unexpected findings in our study. A medium-chain acylcarnitine (MCAC) (C12:2-OH/C10:2-DC) increased in the Intervention group but decreased in the Control group. Like LCAC, MCAC accumulation was thought to be associated with defects in fatty acid oxidation and mitochondrial dysfunction, such as the inadequate capacity of the tricarboxylic acid cycle (Krebs cycle) relative to acetyl-CoA generation13,55. Observational studies have linked MCACs to arterial stiffness and increased cardiovascular risk13. One possible explanation is that exercise increased fatty-acid oxidation and chain-shortening of long-chain acyl-carnitines, resulting in increased chain-shortened metabolites, including MCAC55,56,57. However, C12:2-OH/C10:2-DC was not significant after adjusting for age.
Another unexpected finding was the increase in alanine levels in the Intervention group relative to the Control group. Other observational studies have associated higher alanine levels with abnormal E/A function and HFpEF8,10,14. Alanine is an amino acid involved in several essential metabolic pathways, most notably in glucose and protein metabolism, such as nitrogen transport from peripheral tissues to the liver via the glucose-alanine cycle58,59. One possible explanation for the increase in alanine is an increase in demand for fuel metabolism post-exercise, resulting in higher amino acid catabolism to feed anaplerotic substrates and activation of hepatic glucose recovery pathways via gluconeogenesis in skeletal muscles60. However, alanine was not significant after adjusting for age.
There are several limitations to consider. Firstly, the marginal values in some of the observed changes may be underpowered due to the small study size. Despite the low power, these participants were from a low-risk community cohort for which observed relationships are likely to be underestimated rather than over-estimated. Nevertheless, this pilot study provides estimations of effect sizes for future trials in this field. Secondly, there was a female predominance in the study, which needs to be considered in future larger studies to account for sex dimorphisms in the serum metabolome. Differences in age between the Control and Exercise groups may also affect the interpretation of metabolomic, cardiac, and vascular data61,62. However, studies have shown that age and female sex are associated with greater ventricular stiffness in community adults without cardiovascular disease. Thus, our findings are relevant to real-world scenarios1,6. Thirdly, dietary, and other lifestyle factors pertinent to metabolomic perturbations were not adjusted, although randomization may correct inherent differences between groups. No restrictions on diet or exercise were prescribed during the intervention period, and the fasting state of blood tests was not specified in this real-world study of older adults9. While diet and exercise levels may affect metabolites in the blood63, fasting has not been a major source of variability in most metabolites although acylcarnitines may demonstrate some variability based on fasting status64,65. For future studies, correlations between hexoses and essential amino acids with markers of mitochondrial metabolism may provide insights into the nutritional status of participants66. Fourth, using targeted metabolomic profiling allowed for quantifying absolute metabolite concentrations but resulted in a limited breadth of analysis. However, targeted profiling allowed us to demonstrate a quantifiable extent of change post-exercise. Although these metabolites represent a small portion of the human metabolome, they report on critical pathways for cellular metabolism. Fifth, the trial involved moderately low-intensity exercise over a short duration, which might have led to null effects on skeletal muscle mass, a relevant variable of interest in aging studies67. Despite clinically indistinguishable changes in skeletal muscle mass, circulating LCAC and alanine levels may help track changes in metabolic pathways common to cardiac and skeletal muscle. Future studies that include biomarkers, such as muscle mass-derived cystatin C or nitric oxide-mediated epithelial signalling citrate/arginine ratio, may provide further mechanistic insights68,69. Sixth, while the lower prevalence of cardiovascular risk factors in this sample may limit generalizability, the results are less influenced by factors such as diabetes mellitus and hypertension, which may be differentially associated with branched-chain amino acids and other lipid pathways70,71. Finally, non-invasively obtained echocardiographic data to calculate stroke volume, cardiac output, arterial elastance, and arterial compliances are estimates and may not be accurate for interpretation compared to invasive angiographic data. However, it may be impractical to subject healthy patients to invasive angiography in clinical practice, and more helpful to rely on echocardiographic data.
Despite these limitations, our findings deepen our understanding of the mechanistic benefits of exercise in aging-associated cardiovascular disease. Further studies with larger cohorts or longer follow-ups may better depict the clinical impact of these mechanisms.
Conclusion
Our pilot data demonstrated improvements in diastolic function after an exercise intervention with corresponding changes in cellular fuel oxidation and central carbon metabolism post-exercise. Corresponding relationships between serum metabolites and cardiac function were mapped out in response to exercise intervention. These findings highlight the potential for exercise strategies to target cellular fuel oxidation or central carbon metabolism pathways to concurrently impact the heart and related metabolic systems in prevention.
Data availability
The individual participant data underlying this article are not publicly available and cannot be shared outside of the study site unless explicit approval from the SingHealth Centralized Institutional Review Board, following an approved proposal by an independent review committee and a signed data access agreement; proposals should be directed to the corresponding author. The source data for the figures are available as Supplementary Data. The study protocol will be shared on reasonable request to the corresponding author immediately following publication.
References
Redfield, M. M., Jacobsen, S. J., Borlaug, B. A., Rodeheffer, R. J. & Kass, D. A. Age- and Gender-Related Ventricular-Vascular Stiffening. Circulation 112, 2254–2262 (2005).
Strait, J. B. & Lakatta, E. G. Aging-associated cardiovascular changes and their relationship to heart failure. Heart Fail. Clin. 8, 143–164 (2012).
Lakatta, E. G. & Levy, D. Arterial and Cardiac Aging: Major Shareholders in Cardiovascular Disease Enterprises. Circulation 107, 346–354 (2003).
Obokata, M., Reddy, Y. N. V. & Borlaug, B. A. Diastolic Dysfunction and Heart Failure With Preserved Ejection Fraction: Understanding Mechanisms by Using Noninvasive Methods. JACC Cardiovasc. Imaging 13, 245–257 (2020).
Tromp, J. et al. Heart Failure With Preserved Ejection Fraction in the Young. Circulation 138, 2763–2773 (2018).
Andersson, C. & Vasan, R. S. Epidemiology of heart failure with preserved ejection fraction. Heart Fail. Clin. 10, 377–388 (2014).
Borlaug, B. A. The pathophysiology of heart failure with preserved ejection fraction. Nat. Rev. Cardiol. 11, 507–515 (2014).
Hage, C. et al. Metabolomic Profile in HFpEF vs HFrEF Patients. J. Card. Fail. 26, 1050–1059 (2020).
Gao, F. et al. Exacerbation of cardiovascular ageing by diabetes mellitus and its associations with acyl-carnitines. Aging 13, 14785–14805 (2021).
Kovalik, J. P. et al. Amino acid differences between diabetic older adults and non-diabetic older adults and their associations with cardiovascular function. J. Mol. Cell Cardiol. 158, 63–71 (2021).
Carter, H. N., Chen, C. C. & Hood, D. A. Mitochondria, muscle health, and exercise with advancing age. Physiology (Bethesda) 30, 208–223 (2015).
Hebert, S. L., Lanza, I. R. & Nair, K. S. Mitochondrial DNA alterations and reduced mitochondrial function in aging. Mech. Ageing Dev. 131, 451–462 (2010).
Koh, A. et al. Metabolomic profile of arterial stiffness in aged adults. Diabetes Vasc. Dis. Res. 15, 147916411773362 (2017).
Zordoky, B. N. et al. Metabolomic fingerprint of heart failure with preserved ejection fraction. PLoS One 10, e0124844 (2015).
Hunter, W. G. et al. Metabolomic Profiling Identifies Novel Circulating Biomarkers of Mitochondrial Dysfunction Differentially Elevated in Heart Failure With Preserved Versus Reduced Ejection Fraction: Evidence for Shared Metabolic Impairments in Clinical Heart Failure. J. Am. Heart. Assoc. 5, https://doi.org/10.1161/jaha.115.003190 (2016).
Doehner, W., Frenneaux, M. & Anker, S. D. Metabolic impairment in heart failure: the myocardial and systemic perspective. J. Am. Coll. Cardiol. 64, 1388–1400 (2014).
Fujimoto, N. et al. Effect of ageing on left ventricular compliance and distensibility in healthy sedentary humans. J. Physiol. 590, 1871–1880 (2012).
Koh, A. S. et al. Metabolomic correlates of aerobic capacity among elderly adults. Clin. Cardiol. 41, 1300–1307 (2018).
Melov, S., Tarnopolsky, M. A., Beckman, K., Felkey, K. & Hubbard, A. Resistance exercise reverses aging in human skeletal muscle. PLoS One 2, e465 (2007).
Vega, R. B., Konhilas, J. P., Kelly, D. P. & Leinwand, L. A. Molecular Mechanisms Underlying Cardiac Adaptation to Exercise. Cell. Metab. 25, 1012–1026 (2017).
Lim, R. M. H. & Koh, A. S. Cardiovascular Aging and Physical Activity: Insights From Metabolomics. Front. Cardiovasc. Med. 8, 728228 (2021).
Nagueh, S. F. et al. Recommendations for the Evaluation of Left Ventricular Diastolic Function by Echocardiography: An Update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J. Am. Soc. Echocardiogr. 29, 277–314 (2016).
Denchev, S. V., Simova, I. I. & Matveev, M. G. Evaluation of the SCHILLER BR-102 plus noninvasive ambulatory blood pressure monitor according to the International Protocol introduced by the Working Group on Blood Pressure Monitoring of the European Society of Hypertension. Blood Press Monit. 12, 329–333 (2007).
Tan, C. et al. Left ventricular outflow tract velocity time integral outperforms ejection fraction and Doppler-derived cardiac output for predicting outcomes in a select advanced heart failure cohort. Cardiovasc. Ultrasound 15, 18 (2017).
Blanco, P. Rationale for using the velocity-time integral and the minute distance for assessing the stroke volume and cardiac output in point-of-care settings. Ultrasound J. 12, 21 (2020). 21.
Chemla, D. et al. Total arterial compliance estimated by stroke volume-to-aortic pulse pressure ratio in humans. Am. J. Physiol. 274, H500–505, (1998).
de Simone, G. et al. Stroke volume/pulse pressure ratio and cardiovascular risk in arterial hypertension. Hypertension 33, 800–805 (1999).
Kelly, R. P. et al. Effective Arterial Elastance as Index of Arterial Vascular Load in Humans. Circulation 86, 51S 521 (1992).
Bowen, T. S. et al. Heart failure with preserved ejection fraction induces molecular, mitochondrial, histological, and functional alterations in rat respiratory and limb skeletal muscle. Eur. J. Heart Fail. 17, 263–272 (2015).
Carley, A. N., Taegtmeyer, H. & Lewandowski, E. D. Matrix revisited: mechanisms linking energy substrate metabolism to the function of the heart. Circ. Res. 114, 717–729 (2014).
Stanley, W. C., Recchia, F. A. & Lopaschuk, G. D. Myocardial substrate metabolism in the normal and failing heart. Physiol. Rev. 85, 1093–1129 (2005).
Cheng, M. L. et al. Metabolic disturbances identified in plasma are associated with outcomes in patients with heart failure: diagnostic and prognostic value of metabolomics. J Am. Coll. Cardiol. 65, 1509–1520 (2015).
Lum, H. et al. Plasma acylcarnitines are associated with physical performance in elderly men. J. Gerontol. A Biol. Sci. Med. Sci. 66, 548–553 (2011).
Rodríguez-Gutiérrez, R. et al. Impact of an exercise program on acylcarnitines in obesity: a prospective controlled study. J. Int. Soc. Sports Nutr. 9, 22 (2012).
Memme, J. M., Erlich, A. T., Phukan, G. & Hood, D. A. Exercise and mitochondrial health. J. Physiol. 599, 803–817 (2021).
Flockhart, M. et al. Excessive exercise training causes mitochondrial functional impairment and decreases glucose tolerance in healthy volunteers. Cell Metab. 33, 957–970.e956 (2021).
Makrecka-Kuka, M. et al. Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues. Sci. Rep. 7, 17528 (2017).
Rinaldo, P., Cowan, T. M. & Matern, D. Acylcarnitine profile analysis. Genet. Med. 10, 151–156 (2008).
Haykowsky, M. J. et al. Skeletal muscle composition and its relation to exercise intolerance in older patients with heart failure and preserved ejection fraction. Am. J. Cardiol. 113, 1211–1216 (2014).
Molina, A. J. et al. Skeletal Muscle Mitochondrial Content, Oxidative Capacity, and Mfn2 Expression Are Reduced in Older Patients With Heart Failure and Preserved Ejection Fraction and Are Related to Exercise Intolerance. JACC Heart Fail. 4, 636–645 (2016).
Tocchi, A., Quarles, E. K., Basisty, N., Gitari, L. & Rabinovitch, P. S. Mitochondrial dysfunction in cardiac aging. Biochim. Biophys. Acta. 1847, 1424–1433 (2015).
Dai, D. F., Rabinovitch, P. S. & Ungvari, Z. Mitochondria and cardiovascular aging. Circ. Res. 110, 1109–1124 (2012).
Boengler, K., Kosiol, M., Mayr, M., Schulz, R. & Rohrbach, S. Mitochondria and ageing: role in heart, skeletal muscle and adipose tissue. J. Cachexia Sarcopenia Muscle 8, 349–369 (2017).
Lopaschuk, G. D., Ussher, J. R., Folmes, C. D., Jaswal, J. S. & Stanley, W. C. Myocardial fatty acid metabolism in health and disease. Physiol. Rev. 90, 207–258 (2010).
Salmani, M. et al. Effect of l-arginine on cardiac reverse remodeling and quality of life in patients with heart failure. Clin. Nutr. 40, 3037–3044 (2021).
Tang, W. H. et al. Differential effects of arginine methylation on diastolic dysfunction and disease progression in patients with chronic systolic heart failure. Eur. Heart J. 29, 2506–2513 (2008).
Howden, E. J. et al. Reversing the Cardiac Effects of Sedentary Aging in Middle Age-A Randomized Controlled Trial: Implications For Heart Failure Prevention. Circulation 137, 1549–1560 (2018).
Brinkley, T. E. et al. Effects of Exercise and Weight Loss on Proximal Aortic Stiffness in Older Adults With Obesity. Circulation 144, 684–693 (2021).
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 (2019).
Gates, P. E., Tanaka, H., Graves, J. & Seals, D. R. Left ventricular structure and diastolic function with human ageing: Relation to habitual exercise and arterial stiffness. Eur. Heart J. 24, 2213–2220 (2003).
Fontes-Carvalho, R. et al. The Effect of Exercise Training on Diastolic and Systolic Function After Acute Myocardial Infarction: A Randomized Study. Medicine (Baltimore) 94, e1450 (2015).
Grace, F. et al. High intensity interval training (HIIT) improves resting blood pressure, metabolic (MET) capacity and heart rate reserve without compromising cardiac function in sedentary aging men. Exp. Gerontol. 109, 75–81 (2018).
Boileau, R. A. et al. Aerobic Exercise Training and Cardiorespiratory Fitness in Older Adults: A Randomized Control Trial. J. Aging Phys. Activity 7, 374–383 (1999).
Guirado, G. N. et al. Combined exercise training in asymptomatic elderly with controlled hypertension: effects on functional capacity and cardiac diastolic function. Med. Sci. Monit. 18, CR461–CR465 (2012).
Wanders, R. J., Komen, J. & Kemp, S. Fatty acid omega-oxidation as a rescue pathway for fatty acid oxidation disorders in humans. Febs J. 278, 182–194 (2011).
Karl, J. P. et al. Military training elicits marked increases in plasma metabolomic signatures of energy metabolism, lipolysis, fatty acid oxidation, and ketogenesis. Physiol. Rep. 5, https://doi.org/10.14814/phy2.13407 (2017).
Vessey, D. A., Kelley, M. & Warren, R. S. Characterization of the CoA ligases of human liver mitochondria catalyzing the activation of short- and medium-chain fatty acids and xenobiotic carboxylic acids. Biochim. Biophys. Acta. 1428, 455–462 (1999).
Kohlmeier, M. In Nutrient Metabolism (ed. Kohlmeier, M.) 308–314 (Academic Press, 2003).
Litwack, G. In Human Biochemistry (ed G. Litwack) 183–198 (Academic Press, 2018).
Wasserman, D. H., Williams, P. E., Lacy, D. B., Green, D. R. & Cherrington, A. D. Importance of intrahepatic mechanisms to gluconeogenesis from alanine during exercise and recovery. Am. J. Physiol. 254, E518–525 (1988).
Panyard, D. J., Yu, B. & Snyder, M. P. The metabolomics of human aging: Advances, challenges, and opportunities. Sci. Adv. 8, eadd6155 (2022).
Singam, N. S. V., Fine, C. & Fleg, J. L. Cardiac changes associated with vascular aging. Clin. Cardiol. 43, 92–98 (2020).
Koh, A. S. & Kovalik, J.-P. Metabolomics and cardiovascular imaging: a combined approach for cardiovascular ageing. ESC Heart Fail. 8, 1738–1750 (2021).
Townsend, M. K. et al. Impact of Pre-analytic Blood Sample Collection Factors on Metabolomics. Cancer Epidemiol. Biomarkers Prev. 25, 823–829 (2016).
Wedekind, R. et al. Determinants of blood acylcarnitine concentrations in healthy individuals of the European Prospective Investigation into Cancer and Nutrition. Clin. Nutr. 41, 1735–1745 (2022).
Sedlmeier, A. et al. The human metabolic profile reflects macro- and micronutrient intake distinctly according to fasting time. Sci. Rep. 8, 12262 (2018).
Keng, B. M. H. et al. Associations between Skeletal Muscle and Myocardium in Aging: A Syndrome of “Cardio-Sarcopenia”? J. Am. Geriatr. Soc 67, 2568–2573 (2019).
Kusunoki, H. et al. Estimation of Muscle Mass Using Creatinine/Cystatin C Ratio in Japanese Community-Dwelling Older People. J. Am. Med. Directors Assoc. 23, 902.e921–902.e931 (2022).
Wyatt, A. W., Steinert, J. R. & Mann, G. E. Modulation of the L-arginine/nitric oxide signalling pathway in vascular endothelial cells. Biochem. Soc. Symp. 71, 143–156 (2004).
Onuh, J. O. & Aliani, M. Metabolomics profiling in hypertension and blood pressure regulation: a review. Clin. Hypertens. 26, 23 (2020).
Chen, Z. Z. & Gerszten, R. E. Metabolomics and Proteomics in Type 2 Diabetes. Circ. Res. 126, 1613–1627 (2020).
Acknowledgements
We thank the staff of the laboratories involved for participating in the conduct of the study and the cardiac rehabilitation laboratory for their contributions to this study. This work was funded by the National Medical Research Council of Singapore.
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Jien Sze Ho, Louis LY Teo, Swee Yaw Tan, Ru San Tan, Jean-Paul Kovalik, and Angela S. Koh and contributed to the study conception and design and edited the manuscript. Material preparation and data collection were performed by Hai Ning Wee, Kee Voon Chua, and Jianhong Ching. Fei Gao and Jie Jun Wong provided statistical analyses. Jie Jun Wong and wrote the first draft of the manuscript and edited the subsequent versions. All authors read and approved the final manuscript.
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The study has received funding from the National Medical Research Council of Singapore (MOH-000153), Duke-NUS Medical School, Hong Leong Foundation, Estate of Tan Sri Khoo Teck Puat, and Singhealth Foundation. The funders had no role in the design and conduct of the study, collection, management, analysis, and interpretation of the data, and preparation, review, or approval of the manuscript. The authors declare no competing interests.
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Wong, J.J., Ho, J.S., Teo, L.L.Y. et al. Effects of short-term moderate intensity exercise on the serum metabolome in older adults: a pilot randomized controlled trial. Commun Med 4, 80 (2024). https://doi.org/10.1038/s43856-024-00507-w
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DOI: https://doi.org/10.1038/s43856-024-00507-w