Abstract
Purpose of Review
Strong evidence is evolving that physical exercise prevents hypertension and reduces blood pressure in patients with pre- and manifest HTN. Yet, identifying and confirming the effectiveness of exercise are challenging. Herein, we discuss conventional and novel biomarkers such as extracellular vesicles (EVs) which may track responses to HTN before and after exercise.
Recent Findings
Evolving data shows that improved aerobic fitness and vascular function as well as lowered oxidative stress, inflammation, and gluco-lipid toxicity are leading biomarkers considered to promote HTN, but they explain only about a half of the pathophysiology. Novel biomarkers such as EVs or microRNA are providing additional input to understand the complex mechanisms involved in exercise therapy for HTN patients.
Summary
Conventional and novel biomarkers are needed to fully understand the integrative “cross-talk” between tissues to regulate vasculature physiology for blood pressure control. These biomarker studies will lead to more specific disease markers and the development of even more personalized therapy in this field. However, more systematic approaches and randomized controlled trials in larger cohorts are needed to assess exercise effectiveness across the day and with different exercise types.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Arterial hypertension (HTN) is a major modifiable risk factor for cardiovascular diseases (CVD) affecting over a billion people worldwide. Its prevalence will increase by 50% in the next 30 years assuming that current behaviors (e.g., sedentary, excess sodium and caloric intake, smoking, poor sleep) continue unabated [1]. Yet, prevention and treatment of HTN remain challenging. Only 50% of hypertensive patients have controlled HTN. Lifestyle modification consisting of regular physical activity (e.g., 30 min/day) most days of the week is considered a key factor in the prevention and management of HTN. Exercise can also improve long-term survival [2,3,4]. Despite these well-known effects, only 5–15% of US adults meet physical activity recommendations by the World Health Organization [5]. Tracking response to these interventions with biomarkers might be important to guide for hypertension treatment and even the personalization of care. As HTN is a silent disease, sensitive and early biomarkers are also needed to better describe early hypertensive target end-organ damage.
Biomarkers have already been of great interest in sports for athletes. They have been utilized to measure performance (e.g., lactate, cortisol) and progress and to identify overtraining [6]. During the last decade, growing interest has focused on biomarkers aimed at evaluating health-related factors associated with regular physical activity and sport [7]. These biomarkers of fitness, vascular function, oxidative stress, and inflammation as well as gluco-lipid toxicity have also the potential to reveal possible adverse physiological consequences of exercise. Nevertheless, the exact mechanism(s) by which exercise affects HTN favorably is not totally clear.
Many exercise studies in HTN are observational, self-reported, and, therefore, biased. Tools are still needed to understand minimal and optimal frequency, intensity, and duration of exercise. In addition, the type/modality of exercise required for prevention or treatment of HTN awaits determination. In addition, several effect modifiers must be considered. These include sex, obesity, lifestyle, and pre-existing conditions [8]. Reference standards of these confounders are lacking for different groups, including athletes and populations with known cardiovascular or metabolic diseases.
This article is aimed at briefly summarizing the effects of exercise on the physiology in HTN. In addition, current recommendations for exercise prescription for prevention and treatment of HTN will be outlined. It is important to note that most research to date has focused on aerobic exercise. Future emphasis should include more research on resistance exercise and/or the combination of aerobic and resistance exercise [9, 10]. As such, aerobic exercise will be the focus unless otherwise specified. We will then explore different types of conventional biomarkers already used, as well as provide an overview for the novel biomarkers referred to as extracellular vesicles (EVs) to provide a basic and clinical perspective in this field.
Physiology of Exercise in HTN
Regional vasodilation in active muscle groups is of prime importance to deliver sufficient oxygen to muscles during exercise. Local control of vascular vasodilation is initiated by the effect of increased cardiac output (CO) on shear stress on arterial endothelium. This signal promotes NO synthesis via endothelial nitric oxide synthetase (eNOS) leading to regional vasodilation. These regional events in the vascular beds of contracting muscles allow blood flow to match metabolic demand. Although CO increases significantly during exercise, blood pressure does not as much [11]. Nevertheless, the adaptations of blood pressure to exercise are complex and different responses to exercise exist in different individuals.
A pre-exercise response reflects adaptations of the CO before the beginning of any exercise, called the “mild mental stress” [12]. Compared with rest, heart rate increases usually by a few beats per minute just before the exercise test while the subjects are preparing themselves mentally for exercise. This is explained by a simultaneous vagal withdrawal and release of norepinephrine by the nerve endings. Increase of blood flow is the first adaptive response that helps the redistribution from the circulatory system to the active muscles (responsible for the movement).
An immediate response during exercise leads to further increase of blood pressure and redirects the flow to provide an appropriate level of increased blood flow to active muscles [13]. CO increases as does oxygen extraction. Of note, the diastolic blood pressure remains flat or even decreases but the systolic BP continuously increases. This increase, along with regional NO-facilitated vasodilation, increases blood flow to contracting muscles. Also of interest, some patients have a hypertensive response to exercise (HRE) defined as the delta between peak and baseline systolic blood pressure (SBP > 60 mmHg for men and > 50 mmHg for women) [14]. This may reflect suboptimal eNOS-induced vasodilation. Excess blood pressure elevation in response to exercise has been linked with increased CVD and mortality [15•]. In contrast, a post-exercise hypotensive response occurs in 75% of patients and can last up to 22 h after exercise. This is caused by reduced norepinephrine levels and thus by inhibition of sympathetic activity and reduction in circulating angiotensin II, adenosine, and endothelin levels and their receptors in the central nervous system. These events lead to decreased total peripheral resistance (TPR) and increased baroreflex sensitivity [16]. The post-exercise hypotensive response is dose dependent and stronger in patients with higher baseline blood pressure.
A chronic physiologic response and thus the preventive or antihypertensive effect of exercise are mediated through four major effects including improvement of endothelial function, vascular structural changes, metabolic/oxidative/inflammatory changes, and modulation of the nervous system stimulation. Different modalities such as aerobic or resistance training or combinations of modalities can be used to achieve these changes. We will refer the reader for in-depth understanding of the different effects of each exercise modality to other review articles [17]. The four major chronic physiological responses with exercise are also visualized in Fig. 1 and described in detail in the legend.
Prescription of Exercise in HTN
There is significant evidence that an inverse dose response between cardiorespiratory fitness and incidence of HTN is independent of baseline cardiorespiratory fitness [18]. This suggests that any type of exercise at any stage can potentially improve outcome. In addition, regular physical activity is highly effective in improving aerobic fitness and reaches a 30–40% reduction in the risk of heart disease in all populations [19]. It is also established that lowering systolic blood pressure with pharmacological intervention by only 5 mmHg will reduce risk, for example, for stroke by 14% and myocardial infarction by 9%. This degree of blood pressure lowering can easily be achieved with exercise in patients with HTN (8.7 mmHg for endurance, 7.2 mmHg for resistance exercise, and 13.5 mmHg for combined exercise) [20, 21].
WHO: 150 min/week of moderate aerobic or 75 min/week vigorous exercise combined with muscle strengthening 2 days/week.
AHA 2017: “BP-lowering effects have been reported with lower- and higher-intensity exercise and with continuous and interval exercise training. Meta-analyses suggest isometric exercise results in substantial lowering of BP” [22].
ACSM 2018: aerobic exercise 5–7 days/week, plus resistance exercise 2–3 days/week and flexibility exercise 2-3 days/week, ranging from moderate to vigorous (50–70% VO2max) [22].
More recently, the European Association of Preventive Cardiology (EAPC) and the ESC Council on HTN provide a consensus document to personalize prescription in the prevention and treatment of arterial HTN [23•]. Biomarkers have the potential to guide this personalization of treatment.
In summary, abundant evidence shows that prescribing moderate exercise can lower blood pressure and even prevent HTN [24]; however, many knowledge gaps exist. It is not known exactly what the minimal and optimal amount of aerobic exercise is to prevent HTN. Furthermore, how different modes of exercise impact HTN remains to be determined with regard to frequency, intensity, and duration of exercise. More recently, interest has grown in efforts to understand how even breaking up sedentary behavior can modify health independent of exercise. This approach is consistent with timing physical activity before or after meals as well as time of day to optimize CVD risk reduction.
Biomarkers Tracking Response of Exercise in HTN
-
1.
Biomarkers
Biomarkers are objective, quantifiable characteristics of biological processes, measurable accurately and reproducibly. In healthy people, measurement of biomarkers has improved the understanding of the physiology underlying exercise and its potential beneficial effects in disease states. Biomarkers can describe several adaptive processes of the body to exercise in HTN including the effects of acute exercise as well as the impact of long-term training [7]. Most studied biomarkers of exercise response include markers of fitness, vascular function, oxidative stress, and inflammation.
Biomarkers may also be guides of exercise therapy. As such, they have the potential to personalize treatment of HTN. However, it is still unclear if single or multiple biomarkers are needed. The adaptive processes of exercise in HTN are complex and a single biomarker might not be able to capture the broad physiologic dysfunctions associated with HTN. Reference ranges are also not well defined [6]. In this review, we will discuss traditional as well as novel biomarkers of exercise. We will focus on the most studied biomarkers and summarize their important findings in human cohorts. The reader will be referred to other review articles for each biomarker for further in-depth review. Only a limited number of trials exist for novel biomarkers. We will outline the potential of these novel biomarkers.
-
2.
Physical Fitness as a Biomarker
Physical fitness is a primary biomarker to trace the effects of exercise in HTN. In fact, cardiorespiratory fitness (CRF) has been studied as a biomarker to track response of exercise in HTN. CRF is the gold standard to quantify the state of fitness [8]. A recent umbrella review by Pescatello and colleagues included a review of 18 meta-analyses and systematic reviews comprising 594,129 adults [25]. The authors concluded that physical exercise prevents HTN and reduces it in patients with pre- and manifest HTN [25]. CRF was used in many of these studies to assess the fitness of the patients studied. A prospective study with 4.7-year follow-up of 6278 participants confirmed this benefit. Moderate- and high-intensity exercises were associated with 26 and 42% lower risk of HTN [18]. These studies also show that different exercise modalities (aerobic, resistant, combined) are similarly effective to lower blood pressure [20, 25]. This suggests that muscular strength might be another distinct biomarker from that of CRF in contributing to lower HTN and CVD risk. In particular, MacDonald and colleagues demonstrated in a meta-analysis that dynamic resistance training can be a single treatment modality to reduce blood pressure. Noone and colleagues performed the largest meta-analysis to analyze the impact of exercise on blood pressure in hypertensive patients but also compared the antihypertensive effect of exercise to pharmacological treatment of HTN alone [26••]. Overall, 93 randomized controlled trials were assessed. In 32 of those (404 patient with HTN), exercise together with medications lowered effectively blood pressure than controls. They also concluded that antihypertensive medications alone were slightly more effective than exercise; however, there was insufficient evidence to say that first-line antihypertensive medication reduced BP to a greater extent than exercise. In particular, in mild HTN, exercise is therefore still recommended to be the first-line therapy [26••]. For further in depth review, we will refer the reader to several reviews about this topic [8, 18]. It is of note that exercise can also lead to weight loss and thus lower blood pressure through this pathway [27].
-
3.
Biochemical Biomarkers
Biochemical biomarkers reflecting different physiological pathways such as oxidative stress, inflammation, glucose metabolism, dyslipidemia, and hemostasis have been explored. This is visualized in Fig. 2 as an overview.
Oxidative stress is involved in the pathogenesis of HTN and reflects an imbalance between free radicals (reactive oxygen species (ROS), e.g., superoxide, hydrogen peroxide, and hydroxyl radical) and antioxidants (e.g., superoxide dismutase (SOD), catalase (CAT), peroxidases, glutathione, and thioredoxin) [28]. ROS modulate several pathways in HTN leading to decreased bioavailability of NO, increased inflammation, hyperactivity of the sympathetic nervous system, and disturbance of the renin–angiotensin–aldosterone system (RAAS) [29, 30]. Available evidence shows a clear relationship between HTN, oxidative stress/levels of antioxidants, and different types of exercise, also summarized in several recent reviews [31, 32, 33•]. Markers of oxidative stress tested include those of lipid peroxidation, DNA/RNA damage, ROS, antioxidants, and urinary NO metabolites. Therefore, these markers can track responses to exercise. However, each study uses a different panel and detection techniques of biomarkers, thereby making direct comparison across studies difficult. In order to establish them as clinical markers for personalized treatment, reference standards for each biomarker and type of exercise intervention need to be developed.
The effect of different exercise modalities has been tested on markers of oxidative stress. These modalities include aerobic, isometric, and alternative exercise such as walking/Tai Chi/yoga. For example, aerobic exercise for 3, 6, or 12 months has shown to improve blood pressure and levels of NO and superoxide (O2) and increase levels of antioxidants [34, 35]. Resistance exercise (isometric or static contractions) on the other hand has been less studied in regard to these biomarkers [36, 37]. In a group of 40 HTN patients, isometric exercise training for 6 weeks decreased ROS and increased antioxidants [37]. Combined exercise training (of aerobic and resistance exercise) and its effect on oxidative stress were also investigated. In a recent single-blinded, randomized control trial of 54 older men and women, combined exercise training showed a better hypotensive and antioxidant effect, which could also be due to a greater adherence and attendance [38].
Some alternative training modes such as walking/Tai Chi/yoga offer more gentle, slow, deliberate movements. They are associated with less lowering of diastolic blood pressure. However, in 140 hypertensive patients assessed with pedometers for 5 consecutive days, those with > 10,000 steps a day had significantly less oxidative stress (higher CAT and SOD levels and low malondialdehyde levels) [39]. A recent meta-analysis of the efficacy of Tai Chi on HTN was conducted in 9 randomized controlled trials with exercise interventions of 1.5 to 6 months. The meta-analysis showed that compared to controls, exercise lowered more effectively systolic and diastolic blood pressure and contributed to higher levels of NO and lower levels of endothelin-1 [40]. However, it is not clear which marker of oxidative stress describes best response to exercise.
Of note, human studies (and also most animal studies) on oxidative stress have only been associative [32, 41,42,43]. More mechanistic studies are needed. There is also evidence that acute exercise can induce oxidative stress as a result of the inefficiency of the mitochondrial respiratory chain and the increase in fluid shear stress on the endothelium [33•, 44]. Nevertheless, human and animal studies have shown that repeated exposure to mild oxidative stress with exercise may initiate adaptive processes and reduce oxidative stress long-term-wise. Therefore, their levels are not harmful but beneficial with chronic exercise [45]. However, caution is needed for patients who perform extreme sport or have significant CVD and an exaggerated blood pressure response to HTN. This topic is beyond this review and we will refer to other manuscripts [15•].
Persistent inflammation in HTN can lead to vascular remodeling and end-organ damage of the vessels, kidneys, heart, and brain [46]. Evolving evidence demonstrates that exercise is anti-inflammatory through different actions, by (a) increasing stress hormones affecting leukocyte trafficking; (b) reducing visceral fat, which in turn decreases release of adipokines; (c) increase in anti-inflammatory myokines (IL-6,-7,-8,-10,-15, irisin, VEGF, and more); and (d) lowering toll-like receptors (TLRs) in immune cells [47]. For example, acute bouts of exercise redistribute lymphocytes to peripheral tissues [48] and activate the innate immune system (natural killer cells, macrophages, neutrophils) [47]. More recently, a study looked at subtypes of WBC s in 31 patients with “pre-HTN” (SBP 130–139) and could only identify CD11cCD16 + monocytes to be elevated, with no change in T-cell levels [49]. However, this group studied only a small study group with pre-HTN or mild HTN. Regarding cytokines, IL-6 stands out as an inflammatory marker as it has a dual function, being pro-inflammatory in sedentary people but anti-inflammatory in more active people. A likely reason for this discrepancy relates to release of IL-6 from adipose versus skeletal muscle in the former and later groups based on physical activity levels [50]. IL-6 is also one of the most studied inflammatory biomarkers in exercise and HTN. Interestingly, pro-inflammatory cytokines can decrease NO bioavailability by stimulation of ROS [51], linking oxidative stress with the immune response.
Two more recent studies randomized HTN patients into groups performing either aerobic exercise or being sedentary. In 90 patients with mild HTN, blood pressure and inflammatory markers (TNFa, IL6) decreased after 3 months of treadmill training. IL-6 levels positively correlated with systolic blood pressure [52]; this finding is also confirmed by Wagner and colleagues [53]. Other investigators studied C-reactive protein (CRP) as an inflammatory marker in 245 male patients with mild to moderate HTN. Eight [8] weeks of interval training decreased CRP and white blood count (WBC) levels. Blood pressure levels correlated also positively with changes in CRP whereas VO2max correlated negatively with WBC counts [54]. Overall studies are very heterogeneous using different modes of exercise and study size, different panels of inflammatory biomarkers, and patients with different severity of HTN. Often, these studies do not account for other lifestyle factors such as diet, smoking, and medication effects.
It is also unclear if a panel of inflammatory markers (e.g., cytokines and activated proteins such as CRP) or individual markers provide a powerful biomarker panel to assess the inflammatory response to exercise.
Myokines and adipokines belong to a group of circulating proteins/cytokines that communicate with cells in an autocrine and paracrine fashion with cross-talk to other tissues. Skeletal muscle tissue–derived proteins function as myokines (e.g., IL-15 or myonectin) and are involved in energy metabolism, angiogenesis, and myogenesis. However, some myokines are also secreted by adipocytes called adipo-myokines like IL-6 or myostatin. These myokines and in particular IL-6 can counter the harmful effects of pro-inflammatory adipokines (see above paragraph). Yet, there are also “pure” adipokines. For in-depth review of these protein messengers,we will refer the reader to other reviews [55]. These proteins secreted during exercise are also called exerkines and have been tested as biomarkers in HTN. For example, adiponectin levels were tested in 24 overweight patients with grade 1 HTN who underwent 8 weeks of moderate-intensity aerobic exercise and compared to 24 age- and sex-matched patients. Exercise led to weight loss and increase in adiponectin plasma levels. These changes preceded blood pressure changes and therefore might have a predictive function as a biomarker [56]. A more recent study of 52 patients with metabolic syndrome and high-normal blood pressure showed that yoga training with 3 1-h weekly sessions decreased pro-inflammatory adipokines and increased anti-inflammatory ones [57]. Consistent with this work, we showed that interval and continuous exercise training for 2 weeks in older adults with prediabetes who also have high-normal blood pressure lowered mean arterial pressure comparably in parallel with improved total adiponectin and lowered leptin [58]. However, larger studies are needed to confirm these findings.
Lipoproteins have been studied as a significant risk factor for CVD. A prospective analysis demonstrated that combining exercise with statin therapy leads to decreased mortality and improved fitness after 10 years of treatment [59]. In addition, a large meta-analysis of 25 randomized controlled studies comparing exercise alone (without medication) to medical therapy with statins showed that high-density lipoprotein (HDL) could be increased with exercise alone [60•]. Interestingly, HDL seems to respond better to exercise than low-density lipoprotein (LDL) and triglycerides (TG); however, most studies by our group and others show that the lipid profile can favorably be improved with exercise in people with normal to elevated blood pressure [61,62,63,64], particularly in a dose-dependent manner [65]. Taken together, though the data for LDL and TG are less consistent following exercise, HDL might be the preferred biomarker to assess the effect of exercise.
Different exercise types have been studied on the lipid profile in relation to HTN. A recent randomized controlled trial compared the impact of aerobic vs resistance vs combined aerobic resistance training matched on exercise time (i.e., 60 min/d) in 69 adults (58 + 7 years) with HTN, obesity, and sedentary lifestyle. Combined training showed a greater reduction of a composite score of CVD including lipids [66]. Another study confirmed that combined strength and endurance training can improve HDL levels (not LDL) [67]. For further in-depth review of the effect of exercise on lipids, we will refer the reader to the review by Wang and Xu [68].
Glucose metabolism disturbances are documented in people with HTN, and nearly 80% of people with type 2 diabetes have HTN [69]. This highlights a common soil in the pathophysiology. Aerobic exercise training in adults with type 2 diabetes is effective at improving glycemia with fewer daily hyperglycemic excursions and 0.5–0.7% reductions in hemoglobin A1C [70,71,72,73]. Furthermore, the US Diabetes Prevention Program (DPP) trial utilized an intensive lifestyle approach with a goal of 5–7% weight loss. Although results showed that T2D risk was reduced by 16% for each 1 kg of body weight loss [74], individuals meeting the PA goal with no weight loss had a 44% reduction in diabetes incidence. These findings support aerobic exercise as an effective tool to manage blood glucose. It should be noted that resistance training may increase lean skeletal muscle mass and reduce A1C threefold more in older adults with T2D compared to a calorie-restricted, non-exercising group that lost skeletal muscle mass [75]. This highlights that either aerobic or resistance exercise is effective at lowering glucose. While debates exist as to whether intensity of exercise induces greater gains in glycemia [76], most studies show that when calories are matched, there are no intensity differences [76]. Recent work has shown, however, that exercise timing may matter for optimal exercise-induced glycemic benefit. In fact, exercise in the post-prandial state and/or in the afternoon may promote better glycemia than pre-prandial or morning exercise [76]. However, it should be noted that pre-prandial and morning exercises still induce benefit on glucose tolerance.
Hemostatic and fibrinolytic properties change after acute strenuous exercise and can lead to an increased thrombotic tendency and increased cardiovascular risk in HTN patients [77]. Of note, inflammation is additionally contributing to activation of the coagulation system. This thrombotic tendency occurs in normotensive and hypertensive patients [78], but can be more prolonged and exaggerated in the latter group after exercise. Elevated levels of fibrinogen, increased plasma viscosity, and abnormal clotting activity have been described [77]. However, this increased pro-coagulable state can be improved with HTN treatment with angiotensin receptor blockers [79] and angiotensin-converting enzyme inhibitors [80]. As moderate exercise can lead to platelet activation and aggregation, a recovery period and a gradual progression of exercise intensity are suggested for people at risk for CVD [81, 81]. Fortunately, long-term exercise training will likely lead to sustained benefits regarding the fibrinolytic activity. Nevertheless, it is unclear which intensity and duration of exercise seem to lower the thrombogenic activity (TA) best in HTN and other CVDs. To our knowledge, a specific hemostatic or fibrinolytic marker has not been identified to assess an individual patient’s risk for cardiovascular complications due to thrombotic tendency [77]. For a very detailed analysis on effects of exercise on the coagulation system in normotensive and hypertensive patients, we will refer the reader to a recent review by Braschi [77].
Other Non-traditional Biomarkers
Hypertensive target end-organ damage should ideally be detected in its early stages. As HTN is a silent disease, early biomarkers are crucially needed, but unfortunately are lacking. Screening for left ventricular hypertrophy (cardiac damage), HTN retinopathy (eye damage), or elevated albuminuria or increased serum creatinine levels (kidney damage) is routinely performed; however, when detected, it indicates that significant end-organ damage is already present. However, a recent meta-analysis of 13 randomized controlled studies showed that exercise therapy could benefit non-dialysis CKD patients by increasing estimated glomerular filtration rate (eGFR) while reducing systolic and diastolic blood pressure and body mass index [82]. Improvements of other end-organ damage such as cardiac fibrosis and cardiac remodeling in HTN patients after exercise have also been studied [83, 84].
Endothelial function (flow-mediated dilation, FMD) and arterial stiffness (augmentation index AI and pulse wave velocity PWV) are mostly measured by experienced hands in clinical research labs, but provide pre-clinical insight towards vascular damage. A meta-analysis by Ashor and colleagues showed that exercise improves endothelial function (measured by FMD) and arterial stiffness (measured by AI, PWV) with a dose response between exercise intensity and improvement of vascular changes [85••]. Interestingly, while this was also confirmed in patients with pre-HTN and HTN [86], not all studies agree. Indeed, we have shown that interval and continuous aerobic exercise induce similar improvements in AI during the post-prandial state in older adults with obesity and prediabetes [87]. Moreover, we have observed no effect of either a single bout [61] or 2 weeks of exercise [88] by intensity in adults with prediabetes when using an oral glucose tolerance test. In contrast, a recent work we performed in middle-aged adults with obesity showcases that a single bout of exercise at 65% of VO2max can improve large conduit artery diameter and microcirculatory blood flow in response to insulin during euglycemic conditions [89]. Given that shear stress is considered a key stimulus for NO, these later results suggest that exercise may influence how endothelial cells respond to insulin prior to shear stress. Indeed, we have seen that insulin acts directly on central hemodynamic and AI in adults with metabolic syndrome who have HTN on or off medications [90]. However, these “biomarkers” of vascular dysfunction and damage are not yet routinely executed in clinical practice and most works to date have focused on fasting measures only in the literature. Also, few studies have assessed microvascular function compared with large conduit arteries. This is another important consideration as large conduit artery function may clinically relate better to atherosclerosis whereas microvascular function connects with end-organ damage [91]. Additional work characterizing the “fed” state is needed since post-prandial glucose and lipids are known to induce CVD risk to a greater extent than fasting milieus [92,93,94].
Novel Biomarkers
Extracellular vesicles are evolving as novel cell to cell and organ to organ communicators in exercise physiology [95•, 96]. They are also tested as novel biomarkers in HTN [96, 97]. These submicron vesicles can either derive from the vesicular membrane of cells through a blebbing process or are released from multivesicular bodies from within the cell into the extracellular space [98]. They are found in all types of bodily fluids, but also in the interstitial space, e.g., of skeletal muscles [99]. Exercise provides a strong stimulus for EV release; however, their phenotype and cargo depend on exercise mode and time of investigation [96]. Of note, the skeletal muscle, the largest organ in the body, is also seen as an endocrine organ, releasing myokines and exerkines. EVs are likely delivery molecules of these exerkines and might play an important role in mechanism and adaptation to exercise as messengers have local and systemic effect [100]. Skeletal muscle–derived EVs have been found to increase in particular after exercise [101, 99]. EVs, named also ExerVs, have also been found to be involved in exercise adaptations in angiogenesis, immune signaling, glycolysis, and transportation of myokines [96, 102•]. Acute and chronic effects of exercise and its effects on EVs have been studied only in a few studies in HTN. For example, we showed in individuals with mild HTN and very poor fitness (VO2peak = about 15 ml/kg/min) that EVs were higher compared with people who were considered to have similar blood pressure but poor fitness (VO2peak = about 25 ml/kg/min) [103]. These results may have clinical relevance since EVs correlated with AI (a surrogate for arterial stiffness/pulse waveforms) and 2-h glucose levels as well as low HDL. Interestingly, we followed up this work by examining the effect of exercise intensity for 2 weeks on EVs in older adults with obesity and prediabetes who had high-normal blood pressure. The results showed prior to clinically meaningful weight loss that interval exercise lowered endothelial-derived EVs (CD105) compared with continuous exercise matched on energy expenditure [87]. Our work is consistent with Kim et al. who studied adults with pre-hypertension and found that the 3 days per week of 40 min of exercise at 65% predicted heart rate for 6 months decreased endothelial-derived EV counts (CD31+/CD42a- and CD62E+) [104]. Babbitt and colleagues confirmed this finding by showing that endothelial-derived EVs and markers of inflammation also decreased after 6 months of aerobic exercise training in African Americans with increased risk for HTN [105]. These studies together though likely included only larger EVs as conventional flow cytometry was used to characterize EVs. Larger studies and more comprehensive EV characterization to include also small EVs are needed to optimize treatment towards the exact pathophysiology of HTN [97, 106].
MicroRNAs have been studied with increased interest in exercise training of HTN patients [107]. MicroRNAs (miRNAs) are a class of non-coding RNAs that play important roles in post-transcriptional regulation of gene expression. Many different miRNAs are dysregulated in HTN and are associated with pathophysiological mechanisms involved in HTN including vascular dysfunction and activation of the renin–angiotensin–aldosterone system or autonomic nervous system [107]. MiRNA profiles are dynamic and different in the acute and chronic phase of exercise. Several studies have looked at how exercise improves HTN through specific miRNAs in the heart, vascular system, and skeletal muscle, all players of HTN pathophysiology [118]. Interestingly, different miRNAs have opposite expression profiles in HTN and after exercise, indicating their possible regulatory role. For example, microRNA-29b, which regulates VEDG and collagen genes, was highly expressed in HTN, but reduced with exercise [108]. Mir-324, however, was downregulated in HTN, but increased after aerobic exercise. MiR 324 regulates mitochondrial function [109]. Studies of other small RNA and epigenetics in ET and HTN have not been reported. Many of these findings need to be validated and also different modalities of exercise studied.
Proteomics has also been utilized to study the different molecules providing tissue cross-talk during exercise. Early studies linked changes in function with changes in protein expression and post-translational modification which also showed the potential to uncover novel mechanisms underlying benefits of physical activity [110]. More recently, the interest focused to study the EV proteome in exercise [102•]. Whitham and colleagues studied the EV proteome in healthy humans following a 1-h bout of cycling exercise. They observed an increase of over 300 proteins in the circulation and identified novel candidate myokines released during exercise [102•]. To our knowledge, studies looking at the proteome of EVs after exercise in hypertensive humans have not been studied; however, it would allow deeper analysis of EV protein cargo and identification of additional biomarker candidates.
Outlook/Conclusion/Summary
Strong evidence is evolving that physical exercise prevents HTN and reduces blood pressure in patients with pre- and manifest HTN [25]. Yet, the minimal and optimal frequency, intensity, and/or duration as well as type of exercise in HTN remain to be elucidated. Further, how exercise interacts with diet, sleep, and/or medication remains understudied. Examining additional behaviors surrounding exercise is critical towards understanding how to maximize the effects of exercise to lower blood pressure. This said, identifying and confirming effectiveness of exercise are challenging. This review has discussed conventional and novel candidate biomarkers that can reflect the beneficial effect of exercise on HTN. While other evolving fields include the study of proteostasis, autophagy, and metabolomics, these studies are also in their infancies. Collectively, biomarkers reflect not only the complex mechanisms involved in exercise therapy for HTN patients but also the integrative “cross-talk” between tissues to regulate vasculature physiology for blood pressure control. More systematic approaches and randomized controlled trials in larger cohorts are needed to assess exercise effectiveness across the day. Indeed, much of the research on blood pressure exists from clinical readings (e.g., single morning read). More work is needed to understanding blood pressure across the 24-h period given that nocturnal blood pressure is an independent risk factor from that of clinical blood pressure for CVD [111]. An important consideration for the field in understanding mechanism(s) of exercise on HTN will be to consider novel biomarkers since classic biomarkers (e.g., glucose, lipids) may only predict about 20–40% of CVD risk [112,113,114,115]. As such, to implement more cost-effective strategies to combat CVD, we propose that novel biomarkers such as EVs or microRNA will lead to more specific disease markers and the development of personalized therapy in this field.
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
Dikalov SI, Ungvari Z. Role of mitochondrial oxidative stress in hypertension. Am J Physiol Heart Circ Physiol. 2013;305(10):H1417–27.
Whelton PK, He J, Appel LJ, Cutler JA, Havas S, Kotchen TA, et al. Primary prevention of hypertension: clinical and public health advisory from the National High Blood Pressure Education Program. JAMA. 2002;288(15):1882–8.
Blair SN, Kampert JB, Kohl HW 3rd, Barlow CE, Macera CA, Paffenbarger RS Jr, et al. Influences of cardiorespiratory fitness and other precursors on cardiovascular disease and all-cause mortality in men and women. JAMA. 1996;276(3):205–10.
Valenzuela PL, Carrera-Bastos P, Galvez BG, Ruiz-Hurtado G, Ordovas JM, Ruilope LM, et al. Lifestyle interventions for the prevention and treatment of hypertension. Nat Rev Cardiol. 2021;18(4):251–75.
Sabbahi A, Arena R, Elokda A, Phillips SA. Exercise and hypertension: uncovering the mechanisms of vascular control. Prog Cardiovasc Dis. 2016;59(3):226–34.
Lee EC, Fragala MS, Kavouras SA, Queen RM, Pryor JL, Casa DJ. Biomarkers in sports and exercise: tracking health, performance, and recovery in athletes. J Strength Cond Res. 2017;31(10):2920–37.
Palacios G, Pedrero-Chamizo R, Palacios N, Maroto-Sanchez B, Aznar S, Gonzalez-Gross M, et al. Biomarkers of physical activity and exercise. Nutr Hosp. 2015;31(Suppl 3):237–44.
Lin X, Zhang X, Guo J, Roberts CK, McKenzie S, Wu WC, et al. Effects of exercise training on cardiorespiratory fitness and biomarkers of cardiometabolic health: a systematic review and meta-analysis of randomized controlled trials. J Am Heart Assoc. 2015;4(7).
Pescatello LS, MacDonald HV, Ash GI, Lamberti LM, Farquhar WB, Arena R, et al. Assessing the existing professional exercise recommendations for hypertension: a review and recommendations for future research priorities. Mayo Clin Proc. 2015;90(6):801–12.
Igarashi Y. Effects of differences in exercise programs with regular resistance training on resting blood pressure in hypertensive adults: a systematic review and meta-analysis. J Strength Cond Res. 2023;37(1):253–63.
Gielen S, Schuler G, Adams V. Cardiovascular effects of exercise training: molecular mechanisms. Circulation. 2010;122(12):1221–38.
Jouven X, Schwartz PJ, Escolano S, Straczek C, Tafflet M, Desnos M, et al. Excessive heart rate increase during mild mental stress in preparation for exercise predicts sudden death in the general population. Eur Heart J. 2009;30(14):1703–10.
Ghadieh AS, Saab B. Evidence for exercise training in the management of hypertension in adults. Can Fam Physician. 2015;61(3):233–9.
Nayor M, Gajjar P, Murthy VL, Miller PE, Velagaleti RS, Larson MG, et al. Blood pressure responses during exercise: physiological correlates and clinical implications. Arterioscler Thromb Vasc Biol. 2023;43(1):163–73.
• Thanassoulis G, Lyass A, Benjamin EJ, Larson MG, Vita JA, Levy D, et al. Relations of exercise blood pressure response to cardiovascular risk factors and vascular function in the Framingham Heart Study. Circulation. 2012;125(23):2836–43. Excess blood pressure elevation in response to exercise has been linked with increased CVD and mortality as discussed in this paper.
Eicher JD, Maresh CM, Tsongalis GJ, Thompson PD, Pescatello LS. The additive blood pressure lowering effects of exercise intensity on post-exercise hypotension. Am Heart J. 2010;160(3):513–20.
Pescatello LS, Wu Y, Panza GA, Zaleski A, Guidry M. Development of a novel clinical decision support system for exercise prescription among patients with multiple cardiovascular disease risk factors. Mayo Clin Proc Innov Qual Outcomes. 2021;5(1):193–203.
Bakker EA, Sui X, Brellenthin AG, Lee DC. Physical activity and fitness for the prevention of hypertension. Curr Opin Cardiol. 2018;33(4):394–401.
Myers J. Cardiology patient pages. Exercise and cardiovascular health. Circulation. 2003;107(1):e2-5.
Naci H, Salcher-Konrad M, Dias S, Blum MR, Sahoo SA, Nunan D, et al. How does exercise treatment compare with antihypertensive medications? A network meta-analysis of 391 randomised controlled trials assessing exercise and medication effects on systolic blood pressure. Br J Sports Med. 2019;53(14):859–69.
Corso LM, Macdonald HV, Johnson BT, Farinatti P, Livingston J, Zaleski AL, et al. Is concurrent training efficacious antihypertensive therapy? A meta-analysis Med Sci Sports Exerc. 2016;48(12):2398–406.
Riebe D, Ehrman JK, Liguori G, Magal M, Medicine ACoS. ACSM’s guidelines for exercise testing and prescription: Wolters Kluwer; 2018.
• Hanssen H, Boardman H, Deiseroth A, Moholdt T, Simonenko M, Krankel N, et al. Personalized exercise prescription in the prevention and treatment of arterial hypertension: a consensus document from the European Association of Preventive Cardiology (EAPC) and the ESC Council on Hypertension. Eur J Prev Cardiol. 2022;29(1):205–15. Latest consensus document form the European Association of Preventive Cardiology (EAPC) and the ESC Council on HTN to prove a document to personalize prescription in the prevention and treatment of arterial HTN.
Sharma S, Merghani A, Mont L. Exercise and the heart: the good, the bad, and the ugly. Eur Heart J. 2015;36(23):1445–53.
Pescatello LS, Buchner DM, Jakicic JM, Powell KE, Kraus WE, Bloodgood B, et al. Physical activity to prevent and treat hypertension: a systematic review. Med Sci Sports Exerc. 2019;51(6):1314–23.
•• Noone C, Leahy J, Morrissey EC, Newell J, Newell M, Dwyer CP, et al. Comparative efficacy of exercise and anti-hypertensive pharmacological interventions in reducing blood pressure in people with hypertension: a network meta-analysis. Eur J Prev Cardiol. 2020;27(3):247–55. Largest meta-analysis to analyse the impact of exercise on blood pressure in hypertensive patients, but also comparing the anti-hypertensive effect of exercise to pharmacological treatment of HTN alone.
Swift DL, McGee JE, Earnest CP, Carlisle E, Nygard M, Johannsen NM. The effects of exercise and physical activity on weight loss and maintenance. Prog Cardiovasc Dis. 2018;61(2):206–13.
Montezano AC, Dulak-Lis M, Tsiropoulou S, Harvey A, Briones AM, Touyz RM. Oxidative stress and human hypertension: vascular mechanisms, biomarkers, and novel therapies. Can J Cardiol. 2015;31(5):631–41.
Rodrigo R, Prat H, Passalacqua W, Araya J, Guichard C, Bachler JP. Relationship between oxidative stress and essential hypertension. Hypertens Res. 2007;30(12):1159–67.
Hendre AS, Shariff AK, Patil SR, Durgawale PP, Sontakke AV, Suryakar AN. Evaluation of oxidative stress and anti-oxidant status in essential hypertension. J Indian Med Assoc. 2013;111(6):377–8, 80–1.
Weston KS, Wisloff U, Coombes JS. High-intensity interval training in patients with lifestyle-induced cardiometabolic disease: a systematic review and meta-analysis. Br J Sports Med. 2014;48(16):1227–34.
Larsen RT, Christensen J, Tang LH, Keller C, Doherty P, Zwisler AD, et al. A systematic review and meta-analysis comparing cardiopulmonary exercise test values obtained from the arm cycle and the leg cycle respectively in healthy adults. Int J Sports Phys Ther. 2016;11(7):1006–39.
• Dekleva M, Lazic JS, Arandjelovic A, Mazic S. Beneficial and harmful effects of exercise in hypertensive patients: the role of oxidative stress. Hypertens Res. 2017;40(1):15–20. This manuscript among others shows a clear relationship between HTN, oxidative stress/levels of antioxidants and different types of exercise.
Rafiq A, Aslam K, Malik R, Afroze D. C242T polymorphism of the NADPH oxidase p22PHOX gene and its association with endothelial dysfunction in asymptomatic individuals with essential systemic hypertension. Mol Med Rep. 2014;9(5):1857–62.
Touyz RM, Yao G, Schiffrin EL. c-Src induces phosphorylation and translocation of p47phox: role in superoxide generation by angiotensin II in human vascular smooth muscle cells. Arterioscler Thromb Vasc Biol. 2003;23(6):981–7.
Higashi Y, Yoshizumi M. Exercise and endothelial function: role of endothelium-derived nitric oxide and oxidative stress in healthy subjects and hypertensive patients. Pharmacol Ther. 2004;102(1):87–96.
Padilla J, Simmons GH, Bender SB, Arce-Esquivel AA, Whyte JJ, Laughlin MH. Vascular effects of exercise: endothelial adaptations beyond active muscle beds. Physiology (Bethesda). 2011;26(3):132–45.
Ruangthai R, Phoemsapthawee J. Combined exercise training improves blood pressure and antioxidant capacity in elderly individuals with hypertension. J Exerc Sci Fit. 2019;17(2):67–76.
Ten Caten ME, Dos Santos RZ, Dos Santos AB, Fiorin PBG, Sandri YP, Frizzo MN, et al. Detectable levels of eHSP72 in plasma are associated with physical activity and antioxidant enzyme activity levels in hypertensive subjects. Cell Stress Chaperones. 2018;23(6):1319–27.
Liu D, Yi L, Sheng M, Wang G, Zou Y. The efficacy of Tai Chi and Qigong exercises on blood pressure and blood levels of nitric oxide and endothelin-1 in patients with essential hypertension: a systematic review and meta-analysis of randomized controlled trials. Evid Based Complement Alternat Med. 2020;2020:3267971.
Faulx MD, Wright AT, Hoit BD. Detection of endothelial dysfunction with brachial artery ultrasound scanning. Am Heart J. 2003;145(6):943–51.
Roque FR, Briones AM, Garcia-Redondo AB, Galan M, Martinez-Revelles S, Avendano MS, et al. Aerobic exercise reduces oxidative stress and improves vascular changes of small mesenteric and coronary arteries in hypertension. Br J Pharmacol. 2013;168(3):686–703.
de Andrade LH, de Moraes WM, Matsuo Junior EH, de Orleans Carvalho de Moura E, Antunes HK, Montemor J, et al. Aerobic exercise training improves oxidative stress and ubiquitin proteasome system activity in heart of spontaneously hypertensive rats. Mol Cell Biochem. 2015;402(1–2):193–202.
Yung LM, Laher I, Yao X, Chen ZY, Huang Y, Leung FP. Exercise, vascular wall and cardiovascular diseases: an update (part 2). Sports Med. 2009;39(1):45–63.
Holloway TM, Spriet LL. CrossTalk opposing view: High intensity interval training does not have a role in risk reduction or treatment of disease. J Physiol. 2015;593(24):5219–21.
Solak Y, Afsar B, Vaziri ND, Aslan G, Yalcin CE, Covic A, et al. Hypertension as an autoimmune and inflammatory disease. Hypertens Res. 2016;39(8):567–73.
Scheffer DDL, Latini A. Exercise-induced immune system response: anti-inflammatory status on peripheral and central organs. Biochim Biophys Acta Mol Basis Dis. 2020;1866(10): 165823.
Campbell JP, Turner JE. Debunking the myth of exercise-induced immune suppression: redefining the impact of exercise on immunological health across the lifespan. Front Immunol. 2018;9:648.
Mazur M, Glodzik J, Szczepaniak P, Nosalski R, Siedlinski M, Skiba D, et al. Effects of controlled physical activity on immune cell phenotype in peripheral blood in prehypertension - studies in preclinical model and randomised crossover study. J Physiol Pharmacol. 2018;69(6).
Mathur N, Pedersen BK. Exercise as a mean to control low-grade systemic inflammation. Mediators Inflamm. 2008;2008:109502.
Peters PG, Alessio HM, Hagerman AE, Ashton T, Nagy S, Wiley RL. Short-term isometric exercise reduces systolic blood pressure in hypertensive adults: possible role of reactive oxygen species. Int J Cardiol. 2006;110(2):199–205.
Xie W, Su JH, Wang J. Changes of blood pressure, serum inflammatory factors and endothelin levels in patients with hypertension under rehabilitative aerobic exercise. J Biol Regul Homeost Agents. 2019;33(2):531–6.
Wagner EN, Hong S, Wilson KL, Calfas KJ, Rock CL, Redwine LS, et al. Effects of caloric intake and aerobic activity in individuals with prehypertension and hypertension on levels of inflammatory, adhesion and prothrombotic biomarkers-secondary analysis of a randomized controlled trial. J Clin Med. 2020;9(3).
Lamina S, Okoye GC. Effect of interval exercise training programme on C-reactive protein in the non-pharmacological management of hypertension: a randomized controlled trial. Afr J Med Med Sci. 2012;41(4):379–86.
Heiston EM, Malin SK. Impact of exercise on inflammatory mediators of metabolic and vascular insulin resistance in type 2 diabetes. Adv Exp Med Biol. 2019;1134:271–94.
Pasqualini L, Schillaci G, Innocente S, Pucci G, Coscia F, Siepi D, et al. Lifestyle intervention improves microvascular reactivity and increases serum adiponectin in overweight hypertensive patients. Nutr Metab Cardiovasc Dis. 2010;20(2):87–92.
Supriya R, Yu AP, Lee PH, Lai CW, Cheng KK, Yau SY, et al. Yoga training modulates adipokines in adults with high-normal blood pressure and metabolic syndrome. Scand J Med Sci Sports. 2018;28(3):1130–8.
Heiston EM, Eichner NZ, Gilbertson NM, Malin SK. Exercise improves adiposopathy, insulin sensitivity and metabolic syndrome severity independent of intensity. Exp Physiol. 2020;105(4):632–40.
Kokkinos PF, Narayan P, Colleran J, Fletcher RD, Lakshman R, Papademetriou V. Effects of moderate intensity exercise on serum lipids in African-American men with severe systemic hypertension. Am J Cardiol. 1998;81(6):732–5.
• Kodama S, Tanaka S, Saito K, Shu M, Sone Y, Onitake F, et al. Effect of aerobic exercise training on serum levels of high-density lipoprotein cholesterol: a meta-analysis. Arch Intern Med. 2007;167(10):999–1008. Large meta-analysis of 25 randomized controlled studies comparing exercise alone to medical therapy with statins showed that high density lipoprotein (HDL) could be increased with exercise alone.
Malin SK, Navaneethan SD, Mulya A, Huang H, Kirwan JP. Exercise-induced lowering of chemerin is associated with reduced cardiometabolic risk and glucose-stimulated insulin secretion in older adults. J Nutr Health Aging. 2014;18(6):608–15.
Malin SK, Huang H, Mulya A, Kashyap SR, Kirwan JP. Lower dipeptidyl peptidase-4 following exercise training plus weight loss is related to increased insulin sensitivity in adults with metabolic syndrome. Peptides. 2013;47:142–7.
Gilbertson NM, Eichner NZM, Khurshid M, Rexrode EA, Kranz S, Weltman A, et al. Impact of pre-operative aerobic exercise on cardiometabolic health and quality of life in patients undergoing bariatric surgery. Front Physiol. 2020;11:1018.
Bateman LA, Slentz CA, Willis LH, Shields AT, Piner LW, Bales CW, et al. Comparison of aerobic versus resistance exercise training effects on metabolic syndrome (from the Studies of a Targeted Risk Reduction Intervention Through Defined Exercise - STRRIDE-AT/RT). Am J Cardiol. 2011;108(6):838–44.
Dipietro L, Zhang Y, Mavredes M, Simmens SJ, Whiteley JA, Hayman LL, et al. Physical activity and cardiometabolic risk factor clustering in young adults with obesity. Med Sci Sports Exerc. 2020;52(5):1050–6.
Schroeder EC, Franke WD, Sharp RL, Lee DC. Comparative effectiveness of aerobic, resistance, and combined training on cardiovascular disease risk factors: a randomized controlled trial. PLoS ONE. 2019;14(1):e0210292.
Kyrolainen H, Hackney AC, Salminen R, Repola J, Hakkinen K, Haimi J. Effects of combined strength and endurance training on physical performance and biomarkers of healthy young women. J Strength Cond Res. 2018;32(6):1554–61.
Wang Y, Xu D. Effects of aerobic exercise on lipids and lipoproteins. Lipids Health Dis. 2017;16(1):132.
Ormazabal V, Nair S, Elfeky O, Aguayo C, Salomon C, Zuniga FA. Association between insulin resistance and the development of cardiovascular disease. Cardiovasc Diabetol. 2018;17(1):122.
Boule NG, Haddad E, Kenny GP, Wells GA, Sigal RJ. Effects of exercise on glycemic control and body mass in type 2 diabetes mellitus: a meta-analysis of controlled clinical trials. JAMA. 2001;286(10):1218–27.
Umpierre D, Ribeiro PA, Kramer CK, Leitao CB, Zucatti AT, Azevedo MJ, et al. Physical activity advice only or structured exercise training and association with HbA1c levels in type 2 diabetes: a systematic review and meta-analysis. JAMA. 2011;305(17):1790–9.
Chudyk A, Petrella RJ. Effects of exercise on cardiovascular risk factors in type 2 diabetes: a meta-analysis. Diabetes Care. 2011;34(5):1228–37.
Snowling NJ, Hopkins WG. Effects of different modes of exercise training on glucose control and risk factors for complications in type 2 diabetic patients: a meta-analysis. Diabetes Care. 2006;29(11):2518–27.
Hamman RF, Wing RR, Edelstein SL, Lachin JM, Bray GA, Delahanty L, et al. Effect of weight loss with lifestyle intervention on risk of diabetes. Diabetes Care. 2006;29(9):2102–7.
Dunstan DW, Daly RM, Owen N, Jolley D, De Courten M, Shaw J, et al. High-intensity resistance training improves glycemic control in older patients with type 2 diabetes. Diabetes Care. 2002;25(10):1729–36.
Remchak ME, Piersol KL, Bhatti S, Spaeth AM, Buckman JF, Malin SK. Considerations for maximizing the exercise “drug” to combat insulin resistance: role of nutrition, sleep, and alcohol. Nutrients. 2021;13(5).
Braschi A. Acute exercise-induced changes in hemostatic and fibrinolytic properties: analogies, similarities, and differences between normotensive subjects and patients with essential hypertension. Platelets. 2019;30(6):675–89.
Gleerup G, Vind J, Winther K. Platelet function and fibrinolytic activity during rest and exercise in borderline hypertensive patients. Eur J Clin Invest. 1995;25(4):266–70.
Gavriilaki E, Gkaliagkousi E, Nikolaidou B, Triantafyllou G, Chatzopoulou F, Douma S. Increased thrombotic and impaired fibrinolytic response to acute exercise in patients with essential hypertension: the effect of treatment with an angiotensin II receptor blocker. J Hum Hypertens. 2014;28(10):606–9.
Galea V, Triantafyllidi H, Theodoridis T, Koutroumbi M, Christopoulou-Cokkinou V, Kremastinos D, et al. Long-term treatment with ramipril favourably modifies the haemostatic response to acute submaximal exercise in hypertensives. J Renin Angiotensin Aldosterone Syst. 2013;14(4):322–9.
Hong S, Adler KA, Von Kanel R, Nordberg J, Ziegler MG, Mills PJ. Prolonged platelet activation in individuals with elevated blood pressure in response to a moderate exercise challenge. Psychophysiology. 2009;46(2):276–84.
Zhang L, Wang Y, Xiong L, Luo Y, Huang Z, Yi B. Exercise therapy improves eGFR, and reduces blood pressure and BMI in non-dialysis CKD patients: evidence from a meta-analysis. BMC Nephrol. 2019;20(1):398.
Lin YY, Hong Y, Zhou MC, Huang HL, Shyu WC, Chen JS, et al. Exercise training attenuates cardiac inflammation and fibrosis in hypertensive ovariectomized rats. J Appl Physiol (1985). 2020;128(4):1033–43.
Lopes S, Afreixo V, Teixeira M, Garcia C, Leitao C, Gouveia M, et al. Exercise training reduces arterial stiffness in adults with hypertension: a systematic review and meta-analysis. J Hypertens. 2021;39(2):214–22.
•• Ashor AW, Lara J, Siervo M, Celis-Morales C, Mathers JC. Effects of exercise modalities on arterial stiffness and wave reflection: a systematic review and meta-analysis of randomized controlled trials. PLoS ONE. 2014;9(10):e110034. Meta analysis showing that exercise improves endothelial function (measure by FMD) and arterial stiffness (measured by AI, PWV) with a dose response between exercise intensity and improvement of vascular changes.
Pedralli ML, Marschner RA, Kollet DP, Neto SG, Eibel B, Tanaka H, et al. Different exercise training modalities produce similar endothelial function improvements in individuals with prehypertension or hypertension: a randomized clinical trial exercise, endothelium and blood pressure. Sci Rep. 2020;10(1):7628.
Eichner NZM, Gilbertson NM, Heiston EM, Musante L, S LAS, Weltman A, et al. Interval exercise lowers circulating CD105 extracellular vesicles in prediabetes. Med Sci Sports Exerc. 2020;52(3):729–35.
Malin SK, Gilbertson NM, Eichner NZM, Heiston E, Miller S, Weltman A. Impact of short-term continuous and interval exercise training on endothelial function and glucose metabolism in prediabetes. J Diabetes Res. 2019;2019:4912174.
Heiston EM, Liu Z, Ballantyne A, Kranz S, Malin SK. A single bout of exercise improves vascular insulin sensitivity in adults with obesity. Obesity (Silver Spring). 2021;29(9):1487–96.
Dotson BL, Heiston EM, Miller SL, Malin SK. Insulin stimulation reduces aortic wave reflection in adults with metabolic syndrome. Am J Physiol Heart Circ Physiol. 2021;320(6):H2305–12.
Love KM, Barrett EJ, Malin SK, Reusch JEB, Regensteiner JG, Liu Z. Diabetes pathogenesis and management: the endothelium comes of age. J Mol Cell Biol. 2021;13(7):500–12.
de Vegt F, Dekker JM, Ruhe HG, Stehouwer CD, Nijpels G, Bouter LM, et al. Hyperglycaemia is associated with all-cause and cardiovascular mortality in the Hoorn population: the Hoorn Study. Diabetologia. 1999;42(8):926–31.
Temelkova-Kurktschiev TS, Koehler C, Henkel E, Leonhardt W, Fuecker K, Hanefeld M. Postchallenge plasma glucose and glycemic spikes are more strongly associated with atherosclerosis than fasting glucose or HbA1c level. Diabetes Care. 2000;23(12):1830–4.
Bansal S, Buring JE, Rifai N, Mora S, Sacks FM, Ridker PM. Fasting compared with nonfasting triglycerides and risk of cardiovascular events in women. JAMA. 2007;298(3):309–16.
• Trovato E, Di Felice V, Barone R. Extracellular vesicles: delivery vehicles of myokines. Front Physiol. 2019;10:522. Review article demonstrating EVs as novel cell to cell and organ to organ communicators in exercise physiology.
Brahmer A, Neuberger EWI, Simon P, Kramer-Albers EM. Considerations for the analysis of small extracellular vesicles in physical exercise. Front Physiol. 2020;11:576150.
La Salvia S, Gunasekaran PM, Byrd JB, Erdbrugger U. Extracellular vesicles in essential hypertension: hidden messengers. Curr Hypertens Rep. 2020;22(10):76.
van Niel G, D’Angelo G, Raposo G. Shedding light on the cell biology of extracellular vesicles. Nat Rev Mol Cell Biol. 2018;19(4):213–28.
Rome S, Forterre A, Mizgier ML, Bouzakri K. Skeletal muscle-released extracellular vesicles: state of the art. Front Physiol. 2019;10:929.
Vechetti IJ Jr, Valentino T, Mobley CB, McCarthy JJ. The role of extracellular vesicles in skeletal muscle and systematic adaptation to exercise. J Physiol. 2021;599(3):845–61.
Rigamonti AE, Bollati V, Pergoli L, Iodice S, De Col A, Tamini S, et al. Effects of an acute bout of exercise on circulating extracellular vesicles: tissue-, sex-, and BMI-related differences. Int J Obes (Lond). 2020;44(5):1108–18.
• Whitham M, Parker BL, Friedrichsen M, Hingst JR, Hjorth M, Hughes WE, et al. Extracellular vesicles provide a means for tissue crosstalk during exercise. Cell Metab. 2018;27(1):237–51 e4. Protein cargo of “Exercise EVs”, ExerVs, are studied by proteomic analysis, identifying them to be involved in exercise adaptations in angiogenesis, immune signaling, glycolysis and transportation of myokines.
Kucera M. Aging of the population in Czechoslovakia according to projections from 1966. Cesk Zdrav. 1966;14(7):415–8.
Kim JS, Kim B, Lee H, Thakkar S, Babbitt DM, Eguchi S, et al. Shear stress-induced mitochondrial biogenesis decreases the release of microparticles from endothelial cells. Am J Physiol Heart Circ Physiol. 2015;309(3):H425–33.
Babbitt DM, Diaz KM, Feairheller DL, Sturgeon KM, Perkins AM, Veerabhadrappa P, et al. Endothelial activation microparticles and inflammation status improve with exercise training in African Americans. Int J Hypertens. 2013;2013:538017.
Darragh IAJ, O’Driscoll L, Egan B. Exercise training and circulating small extracellular vesicles: appraisal of methodological approaches and current knowledge. Front Physiol. 2021;12:738333.
De Sousa RAL, Improta-Caria AC, Aras-Junior R, de Oliveira EM, Soci UPR, Cassilhas RC. Physical exercise effects on the brain during COVID-19 pandemic: links between mental and cardiovascular health. Neurol Sci. 2021;42(4):1325–34.
Clauss S, Wakili R, Hildebrand B, Kaab S, Hoster E, Klier I, et al. MicroRNAs as biomarkers for acute atrial remodeling in marathon runners (the miRathon study–a sub-study of the Munich Marathon Study). PLoS ONE. 2016;11(2):e0148599.
Radom-Aizik S, Zaldivar FP Jr, Haddad F, Cooper DM. Impact of brief exercise on circulating monocyte gene and microRNA expression: implications for atherosclerotic vascular disease. Brain Behav Immun. 2014;39:121–9.
Burniston JG, Hoffman EP. Proteomic responses of skeletal and cardiac muscle to exercise. Expert Rev Proteomics. 2011;8(3):361–77.
Banegas JR, Ruilope LM, de la Sierra A, Vinyoles E, Gorostidi M, de la Cruz JJ, et al. Clinic versus daytime ambulatory blood pressure difference in hypertensive patients: the impact of age and clinic blood pressure. Hypertension. 2017;69(2):211–9.
DeFronzo RA, Abdul-Ghani M. Assessment and treatment of cardiovascular risk in prediabetes: impaired glucose tolerance and impaired fasting glucose. Am J Cardiol. 2011;108(3 Suppl):3B-24B.
Hozawa A, Folsom AR, Sharrett AR, Chambless LE. Absolute and attributable risks of cardiovascular disease incidence in relation to optimal and borderline risk factors: comparison of African American with white subjects–Atherosclerosis Risk in Communities Study. Arch Intern Med. 2007;167(6):573–9.
Aronow WS. Association of obesity with hypertension. Ann Transl Med. 2017;5(17):350.
Tsimihodimos V, Gonzalez-Villalpando C, Meigs JB, Ferrannini E. Hypertension and diabetes mellitus: coprediction and time trajectories. Hypertension. 2018;71(3):422–8.
Higashi Y, Sasaki S, Kurisu S, Yoshimizu A, Sasaki N, Matsuura H, et al. Regular aerobic exercise augments endothelium-dependent vascular relaxation in normotensive as well as hypertensive subjects: role of endothelium-derived nitric oxide. Circulation. 1999;100(11):1194–202.
Korsager Larsen M, Matchkov VV. Hypertension and physical exercise: the role of oxidative stress. Medicina (Kaunas). 2016;52(1):19–27.
das Neves VJ, Fernandes T, Roque FR, Soci UPR, Melo SFS, de Oliveira EM. Exercise training in hypertension: role of microRNAs. World J Cardiol. 2014;6(8):713. https://doi.org/10.4330/wjc.v6.i8.713.
Funding
Funding for the work was supported by the National Institutes of Health RO1-HL130296 (SKM), K23-HL126101, UVA Diabetes LaunchPad Grant (SKM and UE), UVA Thelma R. Swortzel Award (SKM), and Diabetes Action Research and Education Award (SKM).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of Interest
The authors report no conflict of interest.
Human and Animal Rights and Informed Consent
Our review article cites studies which have been approved by the local ethical approval boards of the respective universities.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Trillaud, E., Klemmer, P., Malin, S.K. et al. Tracking Biomarker Responses to Exercise in Hypertension. Curr Hypertens Rep 25, 299–311 (2023). https://doi.org/10.1007/s11906-023-01252-6
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11906-023-01252-6