Association of resting heart rate with cardiovascular function: a cross-sectional study in 522 Finnish subjects
verfasst von:
Jenni K Koskela, Anna Tahvanainen, Antti Haring, Antti J Tikkakoski, Erkki Ilveskoski, Jani Viitala, Miia H Leskinen, Terho Lehtimäki, Mika AP Kähönen, Tiit Kööbi, Onni Niemelä, Jukka T Mustonen, Ilkka H Pörsti
High resting heart rate (HR) is associated with increased cardiovascular risk in general populations, possibly due to elevated blood pressure (BP) or sympathetic over-activity. We studied the association of resting HR with cardiovascular function, and examined whether the hemodynamics remained similar during passive head-up tilt.
Methods
Hemodynamics were recorded using whole-body impedance cardiography and continuous radial pulse wave analysis in 522 subjects (age 20–72 years, 261 males) without medication influencing HR or BP, or diagnosed diabetes, coronary artery, renal, peripheral arterial, or cerebrovascular disease. Correlations were calculated, and results analysed according to resting HR tertiles.
Results
Higher resting HR was associated with elevated systolic and diastolic BP, lower stroke volume but higher cardiac output and work, and lower systemic vascular resistance, both supine and upright (p < 0.05 for all). Subjects with higher HR also showed lower supine and upright aortic pulse pressure and augmentation index, and increased resting pulse wave velocity (p < 0.001). Upright stroke volume decreased less in subjects with highest resting HR (p < 0.05), and cardiac output decreased less in subjects with lowest resting HR (p < 0.009), but clear hemodynamic differences between the tertiles persisted both supine and upright.
Conclusions
Supine and upright hemodynamic profile associated with higher resting HR is characterized by higher cardiac output and lower systemic vascular resistance. Higher resting HR was associated with reduced central wave reflection, in spite of elevated BP and arterial stiffness. The increased cardiac workload, higher BP and arterial stiffness, may explain why higher HR is associated with less favourable prognosis in populations.
The online version of this article (doi:10.1186/1471-2261-13-102) contains supplementary material, which is available to authorized users.
Competing interests
The authors have no conflicts of interest to disclose.
Authors’ contributions
JK, AT, IP, JM designed and conducted the study. JK, AT, IP, AJT analysed and interpreted the data, and drafted the first version of the manuscript. JK, AT, AJT, AH, ML, IP, EI, ON and JV performed experiments. JM, AJT, EI, ON, TL, TK and MK gave critical intellectual input and contributed to drafting revised versions of the manuscript. All authors read and approved the final manuscript.
Abkürzungen
AIx
Augmentation index
BP
Blood pressure
CI
Confidence interval
CRP
C-reactive protein
HDL
High-density lipoprotein
HR
Heart rate
LDL
Low-density lipoprotein
PWV
Pulse wave velocity.
Background
Measurement of heart rate (HR) is an easily available cardiovascular phenotype in clinical practice. Increased resting HR is associated with higher cardiovascular mortality and morbidity in general populations [1‐5], even when other cardiac risk factors are taken into consideration [2, 4, 5]. Higher HR is also a risk factor for elevated blood pressure (BP) in both children and adolescents [6]. Moreover, many studies have reported that HR is associated with atherosclerosis and elevated risk of adverse cardiovascular events [1, 7‐9]. However, the results concerning possible benefits of pharmacological HR lowering are inconsistent [7, 10‐14].
The mechanisms linking elevated HR with cardiovascular pathology and pathophysiology are not well understood. The association has been assumed to be a consequence of sympathetic over-activity [15, 16]. In addition, elevated HR and reduced HR variability have been shown to accelerate atherosclerotic process in coronary arteries through local hemodynamic changes [17, 18]. Higher resting HR has also been associated with increased pulse wave velocity (PWV), i.e. increased arterial stiffness [19‐22]. High PWV is a marker of cardiovascular aging and an acknowledged independent risk factor for cardiovascular morbidity [23].
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On the other hand, there is a significant negative association between HR and central BP and central wave reflection [24]. Augmentation index (AIx) is commonly measured to evaluate central wave reflection, and higher AIx can result from increased arterial stiffness, older age, short stature, and lower HR [24]. Increased AIx and higher central wave reflection have also been associated with increased cardiovascular risk [25, 26]. Although β-blocking agents seem to increase AIx, this class of drugs appears to have a beneficial influence on prognosis in subjects with coronary artery disease, at least after myocardial infarction [14, 24, 27]. In addition to the anti-arrhythmic properties of β-blockers, this may be attributed to improved oxygen delivery due to increased time for coronary flow during prolonged diastole [24, 27].
Taken together, even though higher HR at rest is associated with lower central wave reflection which is considered to be beneficial, it is associated with less favourable prognosis in observational studies [2, 4, 5, 25, 26]. In order to understand the adverse influence of increased HR on prognosis we should identify the underlying hemodynamic differences. Previously, simultaneous analysis of central and peripheral BP, vascular resistance, cardiac function, arterial stiffness and central wave reflection during standard physical challenge has only seldom been performed. The aim of this study was to examine the association of HR with principal hemodynamic variables and their functional responses during head-up tilt in a cross-sectional study including 522 subjects without medications directly influencing HR or BP.
Methods
Study population
All study subjects participated in an on-going study, in which hemodynamics are noninvasively recorded from voluntary subjects (DYNAMIC-study; Clinical Trials registration number NCT01742702). The ethics committee of the Tampere University Hospital approved the study protocol and patients gave an informed consent, as stipulated in the Declaration of Helsinki. An announcement for the recruitment of subjects was distributed at the University of Tampere, Tampere University Hospital, several occupational health care organizations, Varala Sports Institute, and two announcements were published in a local newspaper. The subjects who responded were successively recruited in the order that they contacted the research nurse. In November 2012 a total number of 830 subjects had been recruited to the study.
In present investigation, those subjects with a history of coronary artery disease, diabetes mellitus, peripheral arterial or cerebrovascular disease, valvular regurgitation or stenosis, long QT syndrome, chronic renal insufficiency, hemochromatosis, or medication for hypertension were excluded. Also, subjects with regular medication influencing HR or BP were excluded, i.e. subjects using anti-arrhythmic agents, long-acting β2-sympathomimetics, α-adrenoceptor agonists, varenicline, or the weight-reducing agent sibutramine.
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Altogether 522 subjects (261 males, aged 20 to 72 years) with technically successful hemodynamic recordings were included in the present study. The majority of subjects were without concurrent diseases or medications (for medication details please see Additional file 1: Table S1). In total 80 of 261 women were on low-dose progesterone (intrauterine device) or combination of oestrogen and progesterone therapy (contraception or hormone replacement therapy). Subjects with the following medical conditions with established and stable drug treatment were included in the study: depression (n = 29), allergies or asthma (n = 26), dyspepsia (n = 15), hypothyroidism (n = 15), hyperlipidaemia (n = 14), musculoskeletal problems (n = 10), and epilepsy (n = 5). All subjects with thyroid problems were euthyroid clinically and on the basis of laboratory tests. Moreover, mean HR was not statistically different between any medicated versus corresponding unmedicated subgroups of subjects.
All subjects underwent a physical examination performed by a physician, who also documented medical history, lifestyle habits, and cardiovascular risk factors by interview. The amount of smoking was calculated in pack years, and the use of alcohol was evaluated as average consumption of standard drinks (corresponding to 12 grams of absolute alcohol) per week. Physical exercise frequency was interviewed, and was expressed as the number of bouts of physical activity per week that lasted for at least 30 min each time and caused sweating or shortness of breath.
Laboratory analyses
Venous blood samples were drawn after ~12 hours of fasting. Plasma sodium, potassium, glucose, creatinine, cystatin C, C-reactive protein (CRP), and total, high-density (HDL) and low-density lipoprotein (LDL) cholesterol concentrations were determined using Cobas Integra 700/800 (F. Hoffmann-LaRoche Ltd, Basel, Switzerland), or Cobas 6000, module c501 (Roche Diagnostics, Basel, Switzerland), and white blood cell count and haematocrit using ADVIA 120 or 2120 analyzers (Bayer Health Care, Tarrytown, NY, USA). Glomerular filtration rate was estimated using the Rule formula [28], since the measured creatinine values were within the normal range.
Hemodynamic measurements
Hemodynamics recordings were carried out in a quiet, temperature-controlled laboratory by a research nurse. The subjects were instructed to refrain from caffeine-containing products, smoking, and heavy meals for at least 4 h, and from alcohol for at least 24 h prior to the investigation. Before the actual measurement the subjects were resting supine for approximately 10 min, during which period electrodes for impedance cardiography were placed on the body surface, a tonometric sensor for pulse wave analysis was fixed to the left wrist on the radial pulsation, and a brachial cuff for BP calibration was placed to the right upper arm. Then hemodynamic variables were continuously captured in a beat-to-beat fashion for 5 min in supine position and for 5 min during passive head-up tilt to 60 degrees. Mean values of each measured minute of the experiment were calculated and used in statistical analyses.
Whole-body impedance cardiography
A whole-body impedance cardiography device (CircMonR, JR Medical Ltd, Tallinn, Estonia), which records the changes in body electrical impedance during cardiac cycles, was used to determine beat-to-beat HR, stroke index (stroke volume in proportion to body surface area, ml/m2), cardiac index (cardiac output/body surface area, l/min/m2), and PWV (m/s) [29‐31]. Left cardiac work index (kg*m/min/m2) was calculated by formula 0.0143*(MAP–PAOP)*cardiac index, which has been derived from the equation published by Gorlin et al. [32]. MAP is mean radial arterial pressure measured by tonometric sensor, PAOP is pulmonary artery occlusion pressure which is assumed to be normal (default 6 mmHg), and 0.0143 is the factor for the conversion of pressure from mmHg to cmH2O, volume to density of blood (kg/L), and centimetre to metre. Systemic vascular resistance index (systemic vascular resistance/body surface area, dyn*s/cm5/m2) was calculated from the signal of the tonometric BP sensor and cardiac index measured by CircMonR.
To calculate the PWV, the CircMon software measures the time difference between the onset of the decrease in impedance in the whole-body impedance signal and the popliteal artery signal. From the time difference and the distance between the electrodes, PWV can be determined. As the whole-body impedance cardiography slightly overestimates PWV when compared with Doppler ultrasound method, a validated equation was utilized to calculate values that correspond to the ultrasound method (PWV = (PWVimpedance*0.696) + 0.864) [30]. PWV was determined only in the supine position because of less accurate timing of left ventricular ejection during head-up tilt [30]. A detailed description of the method and electrode configuration has been previously reported [31]. PWV was also recorded after the head-up tilt in all subjects, and the average difference between the mean PWV before and after the head-up tilt was 0.024 ± 0.388 m/s (mean ± standard deviation), showing the good repeatability of the method (repeatability index R 98%, Bland-Altman repeatability index 0.8) [33]. The cardiac output values measured with CircMonR are in good agreement with the values measured by the thermodilution method [31], and the repeatability and reproducibility of the measurements (including PWV recordings) have been shown to be good [34, 35].
Pulse wave analysis
Radial BP and pulse wave form were continuously determined by the use of an automatic tonometric sensor (Colin BP-508 T, Colin Medical Instruments Corp., USA), which was fixed on the radial pulse with a wrist band. The extended left arm was lying on a stable bracket at the level of the heart, whether supine or upright. Radial BP signal was calibrated by brachial BP measurement at the onset of the recording. Continuous aortic BP was derived with the SphygmoCor monitoring system (SphygmoCor PWMx, AtCor Medical, Australia) using the previously validated generalized transfer function [36]. From the aortic pulse wave form AIx (augmented pressure/pulse pressure*100,%) was determined.
Stroke volume determination with cardiac ultrasound
To evaluate the accuracy of stroke volume determination with impedance cardiography during head-up tilt, echocardiography was performed by a cardiologist (author E.I.) to a subset of subjects (n = 16) during an extra visit. The 3D echocardiography (Philips ie33 ultrasound system, Bothell, USA; 1-5 MHz Matrix-array X5-1 transducer) was performed simultaneously with beat-to-beat impedance cardiography recordings during head-up tilt to 60 degrees. Mean stroke volume from 7 consecutive heart beats (6 before and 1 after echocardiography) was calculated from impedance cardiography recordings to cover approximately one respiratory cycle (~6 seconds).
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Statistical analyses
For the statistical analyses, the study population was divided into tertiles according to mean resting HR, determined as an average HR of the last 3 min during the 5-min measurement period in supine position. Analysis of variances for repeated measures was applied to study the differences in the hemodynamic variables BP, stroke index, cardiac index, left cardiac work index, systemic vascular resistance index, AIx, and PWV between the HR tertile groups during rest and head-up tilt. For post hoc testing Tukey HSD test was performed for homogenous, and Tamhane’s T2 test for nonhomogeneous variables. In adjusted analysis of variances for repeated measures, the variables sex, age, body mass index, smoking in pack years, haematocrit, leukocyte count, CRP, creatinine, cystatin C, total cholesterol, triglycerides, HDL cholesterol, fasting plasma glucose, and mean radial arterial pressure at rest were used as covariates.
Pearson’s correlation coefficients were calculated, as appropriate, and possible differences in stroke volume determined using impedance cardiography and 3D echocardiography were tested using Student’s T-test. Distributions of categorical variables among resting HR tertiles were tested using χ2 test, and differences of numerical variables among HR tertiles were studied using analysis of variances. Variable values are given as means and 95% confidence intervals (CI). Natural logarithms of CRP and triglyceride concentrations were used in analyses to normalize their distributions. P-values <0.05 were considered statistically significant. The analyses were performed using SPSS Statistics 17.0 for Windows software (SPSS Inc., Chicago, Ill., USA).
Results
Study population
The characteristics of the study population according to the HR tertiles at rest, with average values of 54, 62 and 75 beats/min in the 1st, 2nd and 3rd tertile, respectively, are shown in Table 1. Mean resting HR among men was 62 (CI: 61 to 64), and among women 64 (CI: 63 to 65) beats/min (p = 0.028). The proportion of men was higher in tertile 1 (with lowest HR) when compared with tertiles 2 and 3 (p = 0.019). Age, use of alcohol, amount of smoking, hematocrit, and plasma concentrations of sodium, potassium, HDL cholesterol, LDL cholesterol, and glucose did not differ between the HR tertiles (p > 0.05 for all). Body mass index, white blood cell count, C-reactive protein, plasma total cholesterol and triglycerides were highest within tertile 3 (p < 0.05 for all). Although plasma creatinine was lowest in tertile 3 (p < 0.005), there were no significant differences in cystatin-C concentrations or estimated glomerular filtration rate between the groups. The self-reported amount of physical exercise bouts per week was 3.4 in tertile 1 (CI: 3.1 to 3.7), 3.0 in tertile 2 (CI: 2.7 to 3.3), and 3.1 in tertile 3(CI: 2.7 to 3.5), and the differences between the tertiles were not statistically significant (p = 0.143).
Table 1
Characteristics of the study population
Resting heart rate tertiles
1
2
3
n = 172
n = 176
n = 174
Resting heart rate (1/min)
54 (53–54)
62 (62–63)*
75 (73–75)*†
Age (years)
46 (44–48)
46 (44–47)
46 (44–47)
Sex (M/F)
101/71‡
79/97
81/93
Body mass index (kg/m2)
26.2 (25.7–26.7)
26.5 (25.8–27.1)
27.3 (26.6–28.1)*
Waist circumference (cm)
92 (90–93)
92 (90–94)
94 (92–96)
Smoking (pack years)
2.3 (1.2–3.4)
1.8 (0.9–2.6)
3.5 (2.0–5.0)
Alcohol (drinks/week)
4 (3–5)
4 (3–5)
5 (4–6)
Leukocyte count (1*109/l)
5.4 (5.2–5.6)
5.9 (5.6–6.1)*
6.1 (5.8–6.4)*
Haematocrit (%)
42 (42–43)
41 (41–42)
42 (41–43)
C-reactive protein (mg/l)
1.2 (1.0–1.4)
1.6 (1.2–2.0)
2.2 (1.6–2.9)*
Creatinine (μmol/l)
77 (75–79)
72 (70–74)*
71 (70–73)*
Estimated GFR (ml/min/1.73 m2)
112 (109–114)
111 (110–113)
112 (110–114)
Cystatin C (mg/l)
0.83 (0.81–0.85)
0.82 (0.80–0.84)
0.86 (0.83–0.88)
Sodium (mmol/l)
140 (140–141)
140 (140–141)
140 (140–140)
Potassium (mmol/l)
3.8 (3.8–3.9)
3.8 (3.8–3.9)
3.8 (3.7–3.8)
Fasting plasma
Total cholesterol (mmol/l)
5.2 (5.0–5.4)
5.0 (4.8–5.1)*
5.2 (5.1–5.4)†
Triglycerides (mmol/l)
1.1 (1.0–1.2)
1.2 (1.1–1.3)
1.3 (1.2–1.5)*†
HDL cholesterol (mmol/l)
1.7 (1.6–1.7)
1.6 (1.5–1.6)
1.5 (1.5–1.6)
LDL cholesterol (mmol/l)
3.0 (2.9–3.2)
2.9 (2.7–3.0)
3.1 (3.0–3.3)
Glucose (mmol/l)
5.4 (5.3–5.5)
5.4 (5.3–5.4)
5.5 (5.4–5.6)
Values are means and 95% confidence intervals; *p < 0.05 vs. tertile 1, †p < 0.05 vs. tertile 2, analysis of variance with Tukey HSD post hoc test; ‡p < 0.05 for distributions between the tertiles, χ2 test; GFR = glomerular filtration rate using the Rule formula [28].
BP in the HR tertiles
In the entire study population HR at rest showed a moderate association with resting radial systolic BP (r = 0.14, p < 0.001) and diastolic BP (r = 0.19, p < 0.001). In tertile 3 radial systolic and diastolic BPs were higher than in other tertiles, in both supine position and during head-up tilt (Figure 1). The differences in radial BPs between HR tertile 3 versus other tertiles in supine and upright positions remained significant in adjusted analyses including the covariates given in the Statistical analyses section of Methods.
Figure 1
Radial blood pressures during rest and passive head-up tilt according to resting heart rate tertiles. (A) Systolic blood pressure, (B) diastolic blood pressure; mean (95% confidence intervals), p values denote significant differences between the tertiles depicted with different symbols.
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Aortic systolic BP did not differ between the tertiles in supine (p = 0.139) or upright positions (p = 0.452). However, supine aortic diastolic BP was higher in tertile 3 than tertiles 1 and 2 (p ≤ 0.033, unadjusted and adjusted comparisons). Upright aortic diastolic BP was higher in tertile 3 than tertile 1 (p < 0.001).
Stroke volume, cardiac work, and systemic vascular resistance among HR tertiles
All HR tertiles showed a corresponding upright chronotropic effect (11.5-13.1 beats/min, p > 0.05), and the clear differences in HR between the tertiles persisted during the head-up tilt (Figure 2A). The mean supine to upright increase in HR in the whole population was 12.4 (CI: 11.8 to 12.9) beats/min.
Figure 2
Principal hemodynamic variables during rest and passive head-up tilt according to resting heart rate tertiles. (A) Heart rate, (B) stroke index, (C) cardiac index, (D) left cardiac work index, (E) systemic vascular resistance index; mean (95% confidence intervals).
×
Supine stroke index showed a significant negative correlation with HR (r = -0.31, p < 0.001), and in tertile 3 supine stroke index was lower than in other tertiles (Figure 2B, p < 0.001 also after adjustments). In response to head-up tilt, the decrease in stroke index was smaller in the 3rd tertile (10.4 ml/m2, CI: 9.7 to 11.2) , than in the 1st (13.3 ml/m2, CI: 12.4 to 14.2), and 2nd tertiles (12.9 ml/m2, CI: 12.0 to 13.7) (unadjusted and adjusted p < 0.001). Upright stroke index was lower in tertiles 2 and 3 than in tertile 1 (p = 0.002).
In spite of the above negative correlation between stroke index and HR, supine cardiac index and also left cardiac work index were highest in tertile 3, and were also higher in tertile 2 than tertile 1 (Figures 2C and 2D, p < 0.001 also in adjusted analyses). The upright decrease in cardiac index was slightly higher in the 2nd (-0.38 ml/min/m2, CI: -0.31 to -0.44), and 3rd tertiles (-0.38 ml/min/m2, CI: -0.32 to -0.44), than in the 1st tertile (-0.28 ml/min/m2, CI: -0.22 to -0.33) (p < 0.034), but in adjusted analyses the difference remained significant only between the 1st and 3rd tertiles (p < 0.009). Importantly, the clear differences in cardiac index and left cardiac work index between the HR tertiles persisted in the upright position (p < 0.001 in unadjusted and adjusted analyses).
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Systemic vascular resistance index was lowest in tertile 3, and also lower in tertile 2 than tertile 1, and the differences remained significant in the upright position (Figure 2E, p < 0.001 also after adjustments).
HR, central wave reflection, and arterial stiffness
In the whole population, an expected negative association was found between resting HR and AIx (r = -0.19, p < 0.001), so that AIx was mathematically reduced by 2.5%-units for every 10 beats/min increase in HR. Supine aortic pulse pressure was highest in the 1st HR tertile (Figure 3A), while supine AIx was lowest in the 3rd HR tertile (Figure 3B), and corresponding differences were also observed during the head-up tilt. The differences in aortic pulse pressure and AIx remained significant in adjusted analyses (p ≤ 0.001 for all, supine and upright). As the subject’s height may influence AIx, we performed an additional analysis so that body mass index was replaced by height and weight in the adjustments, but the outcome of the analysis did not change.
Figure 3
Central pulse pressure and wave reflection during rest and passive head-up tilt according to resting heart rate tertiles. (A) Aortic pulse pressure, (B) augmentation index; mean (95% confidence intervals).
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Arterial stiffness was evaluated by measuring resting PWV, the mean value of which in the whole study population was 8.5 m/s (CI: 8.3 to 8.7). HR was notably correlated with PWV (r = 0.23, p < 0.001). PWV was significantly higher in tertiles 2 and 3 than in tertile 1 (Figure 4; p < 0.001 also in adjusted analysis).
Figure 4
Pulse wave velocity according to resting heart rate tertiles; mean(95% confidence intervals), *p < 0.001 vs. tertile 1.
×
Determination of stroke volume using impedance cardiography and echocardiography
Stroke volume during the head-up tilt was determined by means of impedance cardiography and cardiac 3D ultrasound in 16 subjects. Mean stroke volume by impedance cardiography was 72 ml (CI: 61 to 82) and by echocardiography 67 ml (CI: 59 to 75) (p > 0.05, Figure 5A). The correlation between the impedance cardiography and echocardiography recordings was good (Figure 5B).
Figure 5
Evaluation of stroke volume in 16 subjects during passive head-up tilt using echocardiography(Echo)and impedance cardiography(ICG). (A) Comparison of stroke volume measurements mean (95% confidence intervals). (B) Scatterplot depicting the measurements in each individual.
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Discussion
To our knowledge, the association of resting HR with cardiovascular response to head-up tilt has not been studied previously. Here we demonstrated that higher resting HR was associated with reduced central wave reflection and lower vascular resistance, but in spite of these beneficial characteristics, cardiac output and work were increased in tertiles with higher resting HR, both supine and upright. Moreover, BP was moderately increased in the 3rd HR tertile, while arterial stiffness was increased in both 2nd and 3rd HR tertiles when compared with the lowest HR tertile. Altogether, the present findings support the view that lower resting HR represents a more beneficial hemodynamic profile.
Since the change in posture induces significant hemodynamic changes in blood volume distribution, vascular resistance, and autonomic nervous function, head-up tilt can be regarded as a test addressing cardiovascular reactivity [37, 38]. The head-up tilt -induced decrease in stroke volume was slightly lesser in subjects with highest resting HR, while the decrease in cardiac output was somewhat lower in the subjects with lowest resting HR, despite the changes in HR between the tertiles did not differ. However, the clear differences in cardiac output and vascular resistance between the HR tertiles persisted in the upright position, and the observed differences between the hemodynamic profiles in the HR tertiles were surprisingly similar both supine and upright. This suggests that resting HR provides significant information about upright hemodynamics, so that higher resting HR indicates a more hyperdynamic upright hemodynamic profile.
The increased cardiovascular risk related to higher resting HR has been attributed to genetic factors, impaired myocardial oxygen delivery, increased BP, arrhythmias, sympathetic over-activity, and increased arterial stiffness [1‐5, 7, 15, 16], but the mechanisms are not completely understood. Elevated BP is considered one of the most potential mechanisms associating higher HR with cardiovascular risk [6, 39]. In the present study, despite lower stroke volume and vascular resistance, radial BP was highest in the 3rd tertile with the highest resting HR, in line with previous results [39]. However, as the difference in central and peripheral BP between the HR tertiles was rather small, other factors in addition to elevated BP may play a more important pathophysiological role in the cardiovascular risk associated with elevated HR. Moreover, increased HR may merely be a marker, but not a cause, for higher risk of cardiovascular end-points.
A change in heart rate is a major factor by which the cardiovascular system adjusts cardiac output [40], and in the absence of a heart disease, higher HR is commonly assumed to indicate higher cardiac output. Although cardiac output cannot be reliably predicted from HR alone [40], the present results suggest that higher HR is associated with increased cardiac output. The known determinants of cardiac output are the interaction of i) cardiac function, which is determined by heart rate, contractility, afterload and preload; and ii) return function, which is determined by vascular volume, venous compliance, blood draining from the venous compliant regions, and right atrial pressure (for a review, see [40]).
We found that higher HR was related with increased left cardiac work, and thus higher cardiac oxygen demand. In patients with coronary artery disease, reducing HR is an acknowledged treatment modality, which reduces myocardial oxygen consumption and improves subendocardial blood flow [14, 24, 27]. In an experimental study in dogs, increasing HR was found to increase cardiac oxygen demand even when the external work performed by the heart was kept constant, and this effect was attributed to the greater oxygen requirement for excitation-contraction coupling during higher HR [41]. Moreover, although the benefits of HR lowering in the treatment of hypertension have recently been questioned [10‐13], pharmacological reduction of HR and the subsequent decrease in cardiac workload by the use of drugs like β-adrenoceptor blockers might still benefit distinct subgroups of patients [15, 16].
Higher resting HR is thought to reflect enhanced sympathetic tone, and this may predispose to cardiac arrhythmias and hypertension [6, 42, 43]. In the heart increased sympathetic tone has both chronotropic and inotropic effects, while in the resistance arteries higher sympathetic tone induces vasoconstriction and thus elevates BP [44]. Counteracting these effects, parasympathetic tone plays an important role in the regulation of HR and cardiac output, and it also influences vascular resistance via secondary mechanisms [45]. In this study, we observed an inverse relation between higher HR and systemic vascular resistance and stroke index, and these findings seem to contradict with the concept of sympathetic over-activity as the cause of higher HR. On the other hand, higher HR was associated with higher BP, which suggests that vascular resistance was not sufficiently reduced to compensate for the increased cardiac output resulting from higher HR. Therefore, lower resistance in peripheral arteries cannot exclude the possibility of increased sympathetic tone in subjects with higher HR. A thorough analysis of autonomic tone would require the recording of HR variability, baroreceptor sensitivity, or direct muscle sympathetic nerve activity, and such analyses make an interesting topic for further investigations.
We found an inverse relation with HR and AIx and central pulse pressure, in line with previous reports [13, 24, 46]. Increased AIx, which is an indicator of central wave reflection, has been related to elevated cardiovascular risk [25, 26]. When higher HR leads to shorter duration of systole, this shifts the reflected wave towards diastole, and the reduction in AIx during higher HR can thus be regarded as a beneficial hemodynamic change [24]. The present results suggest that the relationship between HR and AIx could also arise from the inverse association of HR with systemic vascular resistance: the reflection point of the forward arterial pressure wave is shifted more peripherally during lower systemic vascular resistance index, and this prolongs the time to wave reflection shifting it towards diastole [24].
Our results showed a small but significant relationship between higher HR and increased PWV, a marker of arterial stiffness [23], in agreement with previous studies [19, 22, 47, 48]. However, HR itself may be an important confounder during PWV assessment. Higher HR exerted a significant increasing influence on PWV in 22 elderly subjects during cardiac pacing, in the absence of changes in BP [19]. In a study with 102 young, healthy males, left ventricular ejection time was an important determinant of PWV both under resting conditions and during adrenergic stimulation: shorter ventricular ejection time was associated with higher PWV [49]. Therefore, the associations between HR and PWV must be interpreted with caution. Although higher arterial stiffness increases pulse pressure [50], we found that aortic pulse pressure was lower in the highest HR tertile when compared with the lowest HR tertile, in spite of higher PWV in the former group. This can be explained by the lower augmentation index during higher heart rate, i.e. lower summation of the reflected pressure wave to the systolic volume wave. In addition, pulse pressure is significantly determined by stroke volume [50], and stroke index was inversely correlated (r = -0.31) with heart rate. Thus, lower aortic pulse pressure in the highest versus lowest heart rate tertile was probably a consequence of reduced augmentation index and lower stroke volume in the former group.
The majority of the present subjects were devoid of medications or prevalent diseases, while those with a diagnosed disorder were in a stable condition and on a constant medication without direct cardiovascular influences. HR was slightly higher in women versus men (64 vs. 62 beats/min), while there was no relation between HR and age. Previously, resting HR has been reported to be 2–7 beats/min higher in female than male subjects, while the effect of age on resting HR has been minor [1, 39, 51]. Importantly, age and sex were included as confounding variables in the statistical analyses. On the basis of a recent epidemiological FINRISKI survey, the present study population with a mean body mass index of 26.7, total cholesterol level of 5.1 mmol/l, and 18% proportion of smokers, represented well the prevalent Finnish population [52]. The applied methods were non-invasive, safe, and easy to perform, and the accuracy of pulse wave analysis and impedance cardiography has been tested against invasive methods [30, 31, 53]. To strengthen the results, we performed a small validation study that showed a good correlation between impedance cardiography and echocardiography -derived stroke volume.
When measuring the human hemodynamics noninvasively, many of the variables are calculations or derivatives, and most of the calculations include HR in the procedure. The formulas used here have been found to be reliable [30‐32, 54], but HR is actually a major determinant in most of the calculated cardiac and vascular hemodynamic variables. Furthermore, some of the background characteristics were strongly correlated with each other, like the associations of body mass index with age, sex, and fasting glucose. These points cause a multicollinearity problem, which cannot be completely controlled for by statistical methods, but has to be taken into consideration when evaluating the results of this study.
Conclusions
We found that the hemodynamic profile associated with higher resting HR was characterized by higher cardiac output, higher cardiac workload, and lower systemic vascular resistance. The hemodynamic features of the distinct HR tertile groups persisted during the head-up tilt. Higher resting HR was also associated with lower augmentation index and aortic pulse pressure, in spite of elevated BP and arterial stiffness. Thus, possible factors associating higher resting HR with less favourable prognosis in the population studies are higher cardiac workload, elevated BP, and increased arterial stiffness.
Acknowledgements
The authors thank Reeta Kulmala, RN, Paula Erkkilä, RN, Marika Päällysaho, RN, Pirjo Järventausta, RN, and Mirja Ikonen, RN, for invaluable technical assistance. The study was supported by Competitive State Research Financing of the Expert Responsibility Area of Tampere University Hospital, Finnish Cultural Foundation, Finnish Foundation for Cardiovascular Research, Sigrid Jusélius Foundation, Tampere Tuberculosis Foundation, Paavo Nurmi Foundation, Aarne Koskelo Foundation, Finnish Medical Foundation, and Orion-Farmos Research Foundation.
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Competing interests
The authors have no conflicts of interest to disclose.
Authors’ contributions
JK, AT, IP, JM designed and conducted the study. JK, AT, IP, AJT analysed and interpreted the data, and drafted the first version of the manuscript. JK, AT, AJT, AH, ML, IP, EI, ON and JV performed experiments. JM, AJT, EI, ON, TL, TK and MK gave critical intellectual input and contributed to drafting revised versions of the manuscript. All authors read and approved the final manuscript.
Association of resting heart rate with cardiovascular function: a cross-sectional study in 522 Finnish subjects
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