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Original article
Variation in resting heart rate over 4 years and the risks of myocardial infarction and death among older adults
  1. James S Floyd1,2,
  2. Colleen M Sitlani1,2,
  3. Kerri L Wiggins1,2,
  4. Erin Wallace1,
  5. Astrid Suchy-Dicey1,
  6. Siddique A Abbasi4,
  7. Mercedes R Carnethon5,
  8. David S Siscovick1,2,6,7,
  9. Nona Sotoodehnia1,2,
  10. Susan R Heckbert1,6,7,
  11. Barbara McKnight1,3,
  12. Kenneth M Rice1,3,
  13. Bruce M Psaty1,2,6,7
  1. 1Cardiovascular Health Research Unit, University of Washington, Seattle, Washington, USA
  2. 2Department of Medicine, University of Washington, Seattle, Washington, USA
  3. 3Department of Biostatistics, University of Washington, Seattle, Washington, USA
  4. 4Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA
  5. 5Northwestern University, Chicago, Illinois, USA
  6. 6Department of Epidemiology, University of Washington, Seattle, Washington, USA
  7. 7Group Health Research Institute, Group Health Cooperative, Seattle, Washington, USA
  1. Correspondence to Dr James Floyd, Department of Medicine, University of Washington, 1730 Minor Ave, Suite 1360, Seattle, WA 98101, USA; jfloyd{at}uw.edu

Abstract

Objective Resting heart rate (RHR) is an established predictor of myocardial infarction (MI) and mortality, but the relationship between variation in RHR over a period of several years and health outcomes is unclear. We evaluated the relationship between long-term variation in RHR and the risks of incident MI and mortality among older adults.

Methods 1991 subjects without cardiovascular disease from the Cardiovascular Health Study were included. RHR was taken from resting ECGs at the first five annual study visits. RHR mean, trend and variation were estimated with linear regression. Subjects were followed for incident MI and death until December 2010. HRs for RHR mean, trend and variation are reported for differences of 10 bpm, 2 bpm/year and 2 bpm, respectively.

Results 262 subjects had an incident MI event (13%) and 1326 died (67%) during 12 years of median follow-up. In primary analyses adjusted for cardiovascular risk factors, RHR mean (HR 1.12; 95% CI 1.05 to 1.20) and variation (HR 1.08; 95% CI 1.03 to 1.13) were associated with the risk of death while trend was not. None of the RHR variables were significantly associated with the risk of incident MI events; however, CIs were wide and the MI associations with RHR variables were not significantly different from the mortality associations. Adjusting for additional variables did not affect estimates, and there were no significant interactions with sex.

Conclusions Variation in RHR over a period of several years represents a potential predictor of long-term mortality among older persons free of cardiovascular disease.

  • MYOCARDIAL ISCHAEMIA AND INFARCTION (IHD)
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Introduction

Resting heart rate (RHR) is an established prognostic marker for mortality and cardiovascular disease among the general population,1–4 the elderly5 ,6 and individuals with a variety of conditions, including coronary heart disease (CHD)7 ,8 and congestive heart failure (CHF).9 ,10 A recent population-based study found that an increase in RHR over a 10-year period was associated with increased mortality.11 However, the use of one or two observations to approximate the average and trend in RHR may result in measurement error.12

The potential for measurement error to bias estimates of association with health outcomes has long been recognised in the blood pressure literature.13 Furthermore, variation of a measurement over time can be quantified and may yield additional prognostic information. Using repeated blood pressure measurements from four stroke prevention clinical trials, Rothwell et al14 demonstrated that long-term variation in blood pressure over a period of several years was a more powerful predictor of stroke and CHD than the average blood pressure. This analytical framework—using repeated measurements over a period of several years to estimate the mean, trend and long-term variation for each person—has not yet been applied to evaluate the association of RHR with the long-term risks of health outcomes such as mortality and myocardial infarction (MI).

We used data from the first 5 yearly study visits of a prospective population-based cohort study of older adults to estimate these RHR elements and their associations with two outcomes, incident MI and death. We sought to replicate the finding of an association between RHR trend and CHD risk, and we hypothesised that greater long-term variation in RHR is associated with a higher risk of incident MI and death, independent of the RHR mean and trend.

Methods

Study design

The Cardiovascular Health Study (CHS) is a prospective population-based cohort study of risk factors for CHD and stroke in older adults.15 In 1989–1990, 5201 non-institutionalised participants over the age of 65 years were recruited from four field centres. In 1992–1993, 687 additional minority participants were recruited. At the baseline examination, information on risk factors and medication use was collected,16 and a variety of measurements were made: seated and supine blood pressure and heart rate, ankle-arm systolic blood pressures, height and weight, laboratory tests including creatinine and fasting cholesterol, 12-lead resting ECG, duplex carotid ultrasound and echocardiography. Until 1999, medication data, blood pressure, heart rate, ECGs and information from various questionnaires were collected at yearly clinic visits. The analyses described in this manuscript have been approved by the CHS Publications & Presentations Committee. The University of Washington Human Subjects Division does not consider theses analyses, which use de-identified data on CHS participants, to be Human Subjects research.

For these analyses, the baseline period comprised the first 5 yearly clinic visits. To avoid selection bias and confounding, participants were excluded if they died, had prevalent cardiovascular disease, used medications that directly affect heart rate (inhaled anticholinergics, β-adrenergic agonists, β-blockers and non-dihydropyridine calcium channel blockers), had an implanted pacemaker or had a missing RHR measurement during the baseline period. Prevalent cardiovascular disease included angina, previous MI, angioplasty, coronary artery bypass surgery, stroke, transient ischaemic attack, carotid endarterectomy, claudication, peripheral arterial bypass surgery, CHF, atrial fibrillation or the use of digoxin or nitrates.17 Subclinical cardiovascular disease at baseline was defined as the presence of an ankle brachial index <0.9, left ventricular hypertrophy on any ECG or carotid artery stenosis ≥25%.18

RHR variables

RHR measurements during the baseline study visits were taken from resting 12-lead ECGs.15 When ECG data were missing, RHR assessed by palpation over a 30 s interval was used. For each participant, linear regression was used to estimate mean, trend and variation in RHR (figure 1). RHR trend is the slope of the line of best fit and RHR variation is the SD of the five residuals around the line of best fit.

Figure 1

Diagram of resting heart rate (RHR) measurements from baseline study visits. RHR trend is the slope of the line of best fit and RHR variation is the square root of the variance from the five residuals (the root mean squared error).

Outcomes

The two primary outcomes for these analyses were incident MI events and deaths. Follow-up began at the last baseline study visit.19 Participants were asked every 6 months about cardiovascular events and hospitalisations through 31 December 2010. Centers for Medicare and Medicaid Services data were also used to identify hospitalisations. Discharge summaries, lab results and serial ECGs were obtained for all hospitalisations. Deaths were identified through surveillance calls, scheduling calls for annual visits and local obituaries. The identification of MI was based on an algorithm that included symptoms of chest pain, increased cardiac enzymes and ECG changes.19 Fatal events that did not meet criteria for MI were classified as fatal CHD-related deaths if participants had chest pain within 72 h of death or had a history of ischaemic heart disease in the absence a known non-atherosclerotic cause. An events committee adjudicated all events. Analyses of MI events included non-fatal MIs, fatal MIs and CHD-related deaths. Deaths were classified as fatal MIs and CHD-related deaths or non-CHD related.

Analysis

For the entire study population, repeated measures analysis of variance (ANOVA) was used to partition the total variance in all baseline RHR measurements into between-subject and within-subject components of variance. The within-subject component was divided by the total variance to estimate the proportion of RHR variation in the entire study sample explained by changes from measurement to measurement within individuals. Correlation coefficients between pairs of the three RHR exposure variables were calculated.

Cox regression was used to estimate HRs for the associations of the three RHR exposure variables with outcomes. In the first set of analyses, adjustments were made for age, sex and race. In the second (primary) set of analyses, adjustments were also made for cardiovascular risk factors: current smoking (yes/no), treated diabetes mellitus (yes/no), systolic blood pressure (continuous), high-density lipoprotein cholesterol level (continuous) and the presence of subclinical cardiovascular disease (yes/no). In the third set of analyses, additional adjustments were made for marital status (married/other), education (completed high school/no), self-reported health status (very good or excellent/other), regular moderate or high-intensity exercise (yes/no), body mass index (continuous), serum creatinine (continuous), 15-foot walk speed (continuous) and grip strength (continuous). Each regression model included all three RHR exposure variables simultaneously so that estimates for one RHR variable (eg, variation) were adjusted for the other two (eg, mean and trend). In sensitivity analyses, subjects with any RHR observation from manual palpation and the first 6 months of observation were excluded.

Potential interactions of sex and subclinical cardiovascular disease with the various RHR variables were assessed using interactions terms in the primary analysis models. Potential interactions of RHR mean with RHR variation were also assessed. In exploratory analyses, associations of RHR variables with different components of the primary outcomes were evaluated in the primary analysis models: incident MI events included incident MIs and CHD-related deaths; deaths were classified as CHD-related (including fatal MI) or non-CHD-related.

Because there were far fewer MI events than deaths, the power to detect RHR variable associations with MI events was limited compared with the power to detect mortality associations. Therefore, the presence of significant associations with mortality but absence of significant associations with MI events could be due to limited power rather than heterogeneity of the underlying associations. To assess whether associations of RHR variables with the two primary outcomes were different, we calculated ratios of HRs using coefficient estimates from models for each outcome that adjusted for cardiovascular risk factors and constructed CIs from percentiles of bootstrap distributions of the log HR ratios.20 This method was also used to assess the statistical evidence for differences in associations of RHR variables with the different components of the primary outcomes. The assumption of proportional hazards was evaluated using plots of scaled Schoenfeld residuals. Stata (V.11) and R (V.3.1.0)21 were used to perform all analyses.

Results

Study population

Out of 5888 total CHS participants, 585 died before the end of the baseline period, 2119 had prevalent cardiovascular disease, 719 were on medications that affect heart rate and four had a pacemaker. Of the remaining 2461 participants, 1991 had RHR measurements at each baseline study visit and were included in these analyses (see online supplementary figure S1). In total, 33 of the 9955 total RHR observations (0.3%) were from manual palpation.

Age at baseline ranged from 68 to 96 years. During follow-up over a median of 12.4 years, 262 (13%) experienced an incident MI event and 1326 (67%) died. Of the incident MI events, 189 were non-fatal MIs, 40 were fatal MIs and 33 were CHD-related deaths. A total of 132 (10%) of the deaths were fatal MI events or CHD-related deaths, 59 of which were recurrent CHD events.

RHR variables

The mean (and SD) of the RHR mean, trend and variation were 64.6 (8.4) bpm, 0.1 (2.0) bpm/year and 4.4 (2.5) bpm. Using repeated measures ANOVA, within-individual variation in RHR over time accounted for 29% of the total study population variation. The strongest correlation between RHR variables occurred between RHR mean and RHR variation (r=0.21, see online supplementary figure S2).

Participants in the highest tertile of mean RHR were less educated, reported worse health, exercised less, had higher blood pressure and cholesterol and had more hypertension and diabetes mellitus (table 1). In contrast, there was little difference in the characteristics of participants among the different tertiles of RHR trend and RHR variation.

Table 1

Characteristics of participants by tertiles of resting heart rate variables

Associations with outcomes

HRs for associations of RHR mean, trend and variation with outcomes were standardised to units of 10 bpm, 2 bpm/year and 2 bpm, respectively, which were the population SDs for each RHR variables. In both the minimally adjusted and the primary analyses adjusted for cardiovascular risk factors, RHR trend and variation were positively associated with incident MI, but CIs were wide and included 1.0 (table 2). On the other hand, RHR mean and RHR variation were significantly associated with death while RHR trend was not. To place these findings in context with other established cardiovascular disease risk factors, in the mortality analysis adjusted for cardiovascular risk factors, the associations for RHR mean (HR 1.12; 95% CI 1.05 to 1.20) and variation (HR 1.08; 95% CI 1.03 to 1.13) were similar in magnitude to the association for systolic blood pressure (HR 1.11; 95% CI 1.05 to 1.17) standardised to the study population SD (19 mm Hg). Adjusting for additional variables did not affect RHR association estimates for either primary outcome (table 2). Forest plots of RHR variable associations with the primary outcomes are displayed in figure 2.

Table 2

HRs for RHR variables and the risk of incident MI events and death

Figure 2

Forest plots of HRs for RHR variable associations with outcomes. (A) HRs for RHR mean. (B) HRs for RHR trend. (C) HRs for RHR variation. RHR, resting heart rate; CHD, coronary heart disease; MI, myocardial infarction.

Excluding subjects with any RHR observation from manual palpation and excluding the first 6 months of observation affected estimates only slightly (see online supplementary tables S1 and S2). No significant interactions with sex or subclinical cardiovascular disease status were identified (p>0.05 for all interaction terms). There was marginal statistical evidence of an interaction between RHR mean and variation in the mortality analysis (p=0.052): RHR variation was more strongly associated with mortality among subjects with mean RHR at or below the median value (HR 1.13; 95% CI 1.05 to 1.22) than among subjects with mean RHR above the median (HR 1.03; 95% CI 0.97 to 1.09). Associations of RHR variables with the components of the primary outcomes are shown in table 3 and figure 2. Plots of Schoenfeld residuals did not demonstrate violations of the proportional hazards assumption.

Table 3

HR ratios for associations of RHR variables with different outcomes

Comparisons of associations with different outcomes

To determine whether associations of RHR variables with incident MI events were different from associations of RHR variables with mortality, we calculated ratios of HRs for the two outcomes and estimated CIs (table 3). For all RHR variables, there was no strong statistical evidence of different associations for the two primary outcomes. The evidence was strongest for RHR trend: the ratio of HRs for death compared with MI was 0.89 (95% CI 0.77 to 1.01). For the ratios of HRs comparing different components of the primary outcomes, the statistical evidence for differences in associations was similarly weak.

Discussion

In this prospective cohort study of older adults free of cardiovascular disease, we found that the mean and long-term variation in RHR, but not the trend, were associated with the risk of death. These risk estimates were similar in magnitude to the risk estimate for systolic blood pressure, an established cardiovascular risk factor. Incident MI events were less frequent than deaths, resulting in wide CIs for HR estimates, and none of the RHR variables were significantly associated with incident MI risk. However, there was little statistical evidence that the incident MI associations were different from the mortality associations with RHR variables. These analyses adjusted for established cardiovascular risk factors such as smoking and hypertension and other predictors of mortality including education, self-reported health status, physical activity and grip strength.

Our findings are consistent with the results of large population-based epidemiological studies from the 1980s, in which increased RHR was associated with an increased risk of incident CHD and death from both CHD-related and non-CHD-related causes.1–3 At least 36 additional studies had evaluated RHR and mortality with nearly all reporting similar associations.22 In most of these studies, RHR was measured only once and the highest quantiles were compared with the lowest, which estimates associations only at the extremes of the exposure distribution, limiting generalisability.22 ,23 For example, non-CHS investigators have used a publically available CHS dataset, which has limited information on covariates and outcomes, to evaluate the association of baseline RHR with mortality over 8 years of follow-up. In that analysis, the highest quartile of RHR (mean 81 bpm) was associated with a 2.2-fold increase risk of death compared with the lower quartile (mean 53 bpm).24

Recent studies have used two RHR measurements several years apart to evaluate change in RHR as a prognostic marker among persons free of prevalent cardiovascular disease. Jouven et al25 found that an increase in RHR of >4 bpm over a 4-year period compared with an increase of −3 to 4 bpm was associated with a 19% increase in mortality (HR 95% CI 1.04 to 1.37), and Nauman et al11 found that an increase in RHR from <70 to >85 bpm over a 10-year period compared with an RHR that remained <70 bpm was associated with a 1.5-fold increase in mortality (HR 95% CI 1.2 to 1.9). The associations with CHD-related death were even stronger in both of these studies. In our study, we evaluated a continuous distribution of RHR trend derived from multiple measurements, which is likely to be a more sensitive analytical method. Nonetheless, the upper bound of the 95% CI for the mortality HR was only 1.03, a null result. We also failed to detect a significant association with the risk of incident MI events, but the CIs are wide and our results are consistent with as much as much as a 24% increased risk per 2 bpm increase in RHR per year. Our failure to replicate the previous findings may be due to differences in the study populations, limited power in our study or a lack of a true association.

In our study, there was strong evidence that greater long-term variation in RHR was associated with an increased risk of death, but no significant association with an increased risk of incident MI events was identified. In a previous study of blood pressure variation that made use of repeated measurements, Rothwell et al14 also found that RHR variation across several study visits was not associated with the risk of CHD events, and they did not evaluate mortality associations. The lack of association between long-term RHR variation and primarily non-fatal CHD events in both our study and the Rothwell study may have been due to similarly limited power rather than true differences in the underlying associations of RHR variation with CHD events and with mortality. The long-term variation in RHR evaluated in our study is not the same as beat-to-beat heart rate variability during a single episode of measurement,26 which is a marker of autonomic nervous system activity that has been evaluated previously in the CHS.27

In a meta-analysis of hypertension clinical trials, effects of hypertension therapies on blood pressure variation accounted for more of the treatment effect on stroke prevention than effects on the mean blood pressure.28 This finding, together with the strong epidemiological evidence of associations with stroke and CHD risks, suggests that long-term variation in blood pressure may be pathogenic.29 In contrast, a causal mechanism by which long-term variation in RHR might lead to cardiovascular events or death remains unclear. Since the early epidemiological reports, it has been postulated that an increased RHR reflects sympathetic overactivity and autonomic imbalance, which can precipitate adverse cardiovascular events through a variety of mechanisms, including increased myocardial work, platelet activation leading to thrombosis and arrhythmia.2 ,30 Heart rate is also marker of physical fitness and perhaps general health.31 Some have argued for a direct role of heart rate in the pathogenesis of atherosclerosis,32–34 although several lines of evidence argue against this. First, meta-analyses of hypertension clinical trials have shown that β-blockers are inferior to other therapies that do not have a heart rate-lowering effect (eg, thiazide diuretics) for the prevention of CHD.35 ,36 Second, in a clinical trial of persons with stable CHD, the drug ivabradine, which has pure heart rate-lowering activity and no effect on blood pressure or myocardial contractility, failed to reduce the risk of the primary outcome, even among those with an elevated RHR at baseline.37 Lastly, the association of RHR with health outcomes is non-specific: several epidemiological studies have demonstrated that an elevated RHR is associated with the risk of cancer mortality,38 in one case as strongly as with cardiovascular mortality.39

Our study had several strengths: RHR measurements from resting ECGs, centrally adjudicated outcomes ascertained through active surveillance, high-quality data on cardiovascular risk factors collected prospectively and adjustment for a large number of variables that may have accounted for RHR associations with mortality in previous studies. Also, our analytical method allowed us to simultaneously evaluate the associations of several measures of long-term variation in RHR with health outcomes using information from repeated measurements, reducing measurement error.

There were several limitations. In an attempt to avoid confounding, we excluded persons with prevalent cardiovascular disease and who used medications that affect the heart rate, limiting generalisability. The number of incident MI events was much lower than the number of deaths, resulting in low power to detect associations. Also, with only five RHR measurements, we are limited in our ability to distinguish different patterns of RHR variation, such as consistent variability across visits or having a single low or single high measurement. Lastly, although we adjusted for a number of predictors of mortality, including socioeconomic factors, self-reported health, walking speed and grip strength, the associations between RHR and mortality could reflect unmeasured confounding.

Although the prognostic relevance of RHR is well established, the relationship between long-term changes in RHR and health outcomes is not. In this prospective cohort study of older adults, variation in RHR over a period of 4 years was a strong predictor of mortality while the trend in RHR was not, independent of known cardiovascular risk factors and average RHR. These findings require replication, and populations that include younger adults and persons with established cardiovascular disease should also be studied.

Key messages

What is already known on this subject?

  • Previous studies have established that that a single measurement of resting heart rate is an important predictor of mortality and coronary heart disease, but the relationship between long-term variation in heart rate and health outcomes has not been well studied.

What might this study add?

  • In a population of older adults free of cardiovascular disease, we used repeated measurements to estimate for each subject the average, trend and variation in heart rate over a 4-year period and we estimated associations of these variables with the risks of myocardial infarction and death. We found that both average heart rate and the variation in heart rate were strongly associated with the risk of death, and the magnitude of these associations was similar to the association for systolic blood pressure, a well-established cardiovascular risk factor. Resting heart rate variables were not associated with the risk of myocardial infarction, but there were few myocardial infarction events and CIs were wide.

How might this impact on clinical practice?

  • Newer biomarkers, some of which are expensive to measure, have added little prognostic value to well-established risk factors for cardiovascular disease. Although our findings require replication, variation in the resting heart rate over a 4-year period may be an important prognostic marker, independent of the average heart rate and other cardiovascular risk factors.

Acknowledgments

The authors would like to thank Brian Shirts, MD, PhD (University of Washington) for his comments during the drafting of this manuscript, which were provided without compensation.

References

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Supplementary materials

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Footnotes

  • Contributors All authors participated in the concept and design of the study, interpretation of data and preparation of the manuscript. JSF and CMS conducted the analyses.

  • Funding This research was supported by contracts HHSN268201200036C, HHSN268200800007C, N01HC55222, N01HC85079, N01HC85080, N01HC85081, N01HC85082, N01HC85083, N01HC85086 and grant U01HL080295 from the National Heart, Lung, and Blood Institute (NHLBI), with additional contributions from the National Institute of Neurological Disorders and Stroke (NINDS). Additional support was provided by AG023629 from the National Institute on Aging (NIA). A full list of principal CHS investigators and institutions can be found at https://chs-nhlbi.org/CHS-NHLBI.org. JSF was supported by NHLBI grant K08HL116640.

  • Competing interests None.

  • Ethics approval University of Washington IRB.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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