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Clinical research

Higher cardiorespiratory fitness predicts long-term survival in patients with heart failure and preserved ejection fraction: the Henry Ford Exercise Testing (FIT) Project

Olusola A. Orimoloye, Swetha Kambhampati, Albert J. Hicks III, Mahmoud Al Rifai, Michael G. Silverman, Seamus Whelton, Waqas Qureshi, Jonathan K. Ehrman, Steven J. Keteyian, Clinton A. Brawner, Zeina Dardari, Mouaz H. Al-Mallah, Michael J. Blaha

Arch Med Sci 2019; 15, 2: 350–358
Online publish date: 2019/03/04
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Introduction

Heart failure with preserved ejection fraction (HFpEF) accounts for nearly half of heart failure hospitalizations and more than half of the heart failure mortality in the US [1]. A combination of its prevalence, outcomes, and future projections has led to a description of HFpEF as the single largest unmet need in cardiovascular medicine [1]. Despite this high prevalence of HFpEF in the heart failure subpopulation, there are few effective therapies to improve mortality outcomes in these patients and few methods for risk stratification [2, 3].

The assessment of cardiorespiratory fitness (CRF), a health-related component of physical fitness defined as the ability of the circulatory and respiratory systems to supply oxygen to skeletal muscles during sustained physical activity [4], has been proposed as a tool for risk stratification in this heart failure subpopulation. There have also been suggestions that improving this measure may lead to better outcomes in patients with HFpEF.

Numerous studies have shown graded inverse associations of morbidity and mortality with CRF across multiple populations [5], including healthy [6], diabetic [7], overweight [8], and hypertensive individuals [9], as well as in patients with heart disease [10], and following myocardial infarction [11]. Similarly, in heart failure with reduced ejection fraction (HFrEF), low CRF has been shown to be associated with increased mortality in patients with ischemic cardiomyopathy, non-ischemic cardiomyopathy, and patients being evaluated for heart transplantation [1214].

High levels of CRF have been shown to improve or prevent many of the comorbidities commonly seen with HFpEF, including hypertension, obesity, anemia, diabetes, renal dysfunction, and impaired left ventricular compliance [1]. Although these comorbidities have been shown to be associated with HFpEF or the ventricular-vascular dysfunction seen in patients with HFpEF, they do not fully account for the poor outcomes seen in the HFpEF population [15]. When HFpEF patients were compared to matched patients enrolled in clinical trials, the HFpEF population still demonstrated significantly higher mortality [15].

Currently, there are limited data examining the association of CRF and survival in HFpEF patients [16]. Trials of exercise training in HFpEF populations have only reported short-term follow-up data, and are thus not adequately powered to evaluate mortality [1719]. This lack of large HFpEF cohorts, multiple negative treatment trials, and lack of long-term follow-up have contributed to the paucity of interventions in HFpEF and methods for HFpEF risk stratification. Understanding the association of CRF and mortality in patients with HFpEF is an important step toward developing interventions aimed at prolonging life in patients with HFpEF. Programs such as cardiac rehabilitation may be better supported and reimbursed with data suggesting that such interventions may improve survival in these patients.

Given the foregoing, we aimed to study the association between CRF and long-term mortality in patients with HFpEF isolated from the Henry Ford Exercise Testing Project (the FIT Project) cohort. We hypothesized that higher CRF would be independently associated with lower risk of death and that this association would be similar for both HFpEF and non-HFpEF individuals.

Material and methods

Study design

We examined data from the FIT Project, an investigator-initiated retrospective cohort study of 69,885 patients who underwent a physician-referred exercise stress testing at Henry Ford Health System affiliated subsidiaries in metropolitan Detroit, MI between 1991 and 2009. The FIT Project rationale and design have been previously described [20]. Briefly, the FIT Project was assembled using directly measured exercise data, and retrospectively collected medical and medication history. Verification and supplementation of missing data was performed using electronic medical records (EMR), administrative databases, and pharmacy claims files. The FIT Project determined total mortality via linkage with the Social Security Administration Death Master File, and select nonfatal outcomes through medical claims files [20].

Study cohort and identification of HFpEF

The study sample consists of individuals within the FIT project who had a prior clinical diagnosis of congestive heart failure and available treadmill data, who demonstrated ejection fraction of ≥ 50% within 1 year of the clinical treadmill test.

The clinical diagnosis of heart failure was made either during the intake report taken by the nurse at the start of the test or by an EMR-based diagnosis requiring at least three occurrences of heart failure ICD-9 code 428.XX in the patient’s chart. In all cases, the history of heart failure was confirmed by linkage with administrative claims files confirming a history of a billing diagnosis of heart failure.

Specifically, we first considered 1,596 patients who had documented heart failure within the FIT project. Of this number, 575 had a clinical treadmill test within 1 year of an echocardiogram (the median time from treadmill test to echocardiogram in our HFpEF cohort was 53 days). Of this number, a total of 165 patients had an echocardiogram with a documented ejection fraction (EF) ≥ 50%, and these comprise the study population. HFpEF was thus defined in this study as an established clinical diagnosis of heart failure with an associated ejection fraction (EF) ≥ 50% on echocardiogram.

Mortality assessment

The primary outcome was all-cause mortality with a median follow-up time of 9.7 (5.2–13.9) years. Mortality ascertainment was conducted using social security number, first name, last name, and date of birth to search the Social Security Death Index Death Master File until April 2013. A complete search was done in over 99.5% of all the patients in the FIT database [20].

Treadmill stress testing and estimation of cardiorespiratory fitness

All patients underwent routine clinical treadmill stress testing using the standard protocol [21]. Indication for stress test referral was provided by the referring physician, and subsequently categorized into common indications (chest pain, shortness of breath, “rule out” ischemia, or other). The treadmill test was symptom-limited and was terminated if the patient had exercise-limiting chest pain, shortness of breath, or other limiting symptoms as assessed by the supervising clinician. In accordance with American Heart Association and American College of Cardiology (AHA/ACC) guidelines [22], testing could be terminated early at the discretion of the clinician for significant arrhythmias, abnormal hemodynamic responses, diagnostic ST-segment changes, or if the participant was unwilling or unable to continue.

Resting heart rates and blood pressures were taken in the seated position prior to stress testing, and percent of maximal heart rate achieved was based on the age-predicted maximal heart rate formula: 220 – age. CRF was expressed in metabolic equivalents of task (METs), which was calculated by the Quinton treadmill controller based on achieved speed and elevation [23]. Full MET credit for a stage was provided once a patient completed at least 1.5 min of the 3-minute stage. The following CRF categories were used: poor (1–4 METs), intermediate (5–6 METs), and moderate-high (≥ 7 METs). The poor CRF category was defined based on previous systolic heart failure fitness data which showed worse mortality for patients who achieved 4 or less METs [13].

Measurement of covariates

Demographic information, indication for stress test, risk factor burden, past medical history, and active medication use were obtained by a nurse and/or exercise physiologist immediately prior to the stress test. A smoking history was defined as self-reported history of smoking. Other risk factors, medical history, and medication data were then augmented by a retrospective search of the EMR. A database-verified diagnosis was considered present when the appropriate International Classification of Diseases, 9th Revision (ICD-9) code was present on more than 3 separate encounters within the Henry Ford health system. Hypertension was defined as a prior diagnosis of hypertension, use of anti-hypertensive medications, or a database-verified diagnosis of hypertension. The blood pressure at the time of the test was not used to diagnose hypertension. Diabetes mellitus was defined as a prior diagnosis of diabetes, use of hypoglycemic medications including insulin, or EMR problem list-based diagnosis of diabetes. A history of coronary artery disease (CAD) was defined as prior myocardial infarction, coronary angioplasty, coronary artery bypass surgery, or prior documented obstructive CAD on a prior angiogram. Weight was measured at the time of initial stress testing. Estimated glomerular filtration rates (GFR) were calculated using the Levey Modification of Diet in Renal Disease formula, where GFR = 175 × standardized Screatinine –1.154 × age–0.203 × 1.212 (if Black) × 0.742 (if female) [24].

Statistical analysis

Baseline characteristics of the study cohort were summarized for each of the 3 CRF groups. Categorical variables were reported as percent frequencies and compared using the χ2 test, while continuous variables were presented as means ± standard deviation and compared using ANOVA.

Crude incidence rates of all-cause mortality were calculated and reported per 1000 person-years. Kaplan-Meier survival curves for each CRF group were constructed and compared via log rank testing. The proportional hazards assumption was tested and confirmed using complementary log-log plots. Multivariable Cox regression models were used to assess the association between METs and all-cause mortality using the lowest CRF category as the reference (METs ≤ 4). Model 1 was adjusted for demographics of age, sex, and race. Model 2 was further adjusted for modifiable risk factors including hypertension, diabetes mellitus, smoking status, and weight. Model 3 was additionally adjusted for medication use including β-blockers, angiotensin-converting enzyme inhibitors (ACEI), angiotensin receptor blockers, and medications for chronic lung disease (i.e. inhalers). Model 4 was further adjusted for history of CAD to account for potential ischemia-related limitations in CRF. We also modeled METs continuously and calculated the risk of all-cause mortality per 1 unit increase of METs.

Additionally, we sought to evaluate the risk of mortality associated with a HFpEF diagnosis when compared to non-HFpEF patients with similar traditional risk factors and similar CRF. To do this, we created a propensity score-matched cohort of non-HFpEF patients drawn from the larger FIT cohort, excluding patients with heart failure with reduced ejection fraction. Propensity score matching was performed using nearest-neighbor matching in a 1 : 3 fashion accounting for 5 variables (the limit of our statistical power): age, sex, race, hypertension and diabetes mellitus. In subsequent survival analyses using this matched cohort, models were adjusted for smoking status, β-blockers, ACEI, lung disease medications, known CAD, and statins, as these variables remained residually significantly different between the 2 cohorts.

Finally, to study whether there was a differential benefit of CRF in the HFpEF versus non-HFpEF cohort, we fit separate survival models for CRF and mortality in patients with and without HFpEF to formally test for effect measure modification.

All reported p-values were two-sided and a p-value < 0.05 was considered statistically significant. All analyses were performed using Stata version 13.1 (StataCorp, College Station, Texas).

Results

Baseline characteristics are summarized in Table I. The mean age of the overall HFpEF cohort was 64 ±13 years, 55% were female, 46% were Black and 52% were white. There were 90 (54%) HFpEF patients in the poor CRF group, 33 (20%) in the intermediate group, and 44 (26%) in the moderate-high group. Patients in the lower CRF categories were older, had a lower eGFR, and were more likely to be female and diabetic (p < 0.05). 92.9% of the entire HFpEF cohort had hypertension, while usage of medications such as β-blockers and ACE Inhibitors was 40.1% and 47.3% respectively.

Table I

Baseline characteristics of the study population stratified by METs categories

ParameterTotal population (N = 167)Poor CRF METs 1–4 (N = 90)Intermediate CRF METs 5–6 (N = 33)Moderate-high CRF METs ≥ 7 (N = 44)P-value
Demographic characteristics:
 Age [years]63.9 ±12.567 ±10.959.1 ±15.961.0 ±11.10.002
 Gender, n, %:    0.01
  Female91, 54.518, 54.618, 54.628, 63.6 
  Male76, 45.533, 36.715, 45.516, 36.4 
 Race, n, %:    0.57
  White86, 51.545, 50.014, 42.427, 61.4 
  Black77, 46.143, 47.818, 54.616, 36.4 
  Others4, 2.42, 2.21, 3.01, 2.3 
Clinical characteristics:
 Hypertension, n, %155, 92.886, 95.631, 93.938, 86.40.15
 Diabetes, n, %70, 41.947, 52.211, 33.312, 27.30.01
 History of CAD, n, %94, 56.351, 56.718, 54.625, 56.80.98
 Smoking history, n, %55, 32.929, 32.29, 27.317, 38.60.56
 Estimated glomerular filtration rate66.9 ±30.360.6 ±33.675.8 ±22.974.3 ±24.00.03
 Weight [lbs]179.6 ±44.3176.1 ±45.3176.2 ±40.8189.8 ±44.10.16
Medication use, n, %:
 β-Blocker use67, 40.131, 34.418, 54.618, 40.90.13
 ACEi use79, 47.345, 50.017, 51.517, 38.60.40
 ARB use3, 1.81, 1.11, 3.01, 2.270.75
 Use of lung disease medications30, 18.018, 203, 9.19, 20.450.045

[i] ACEi – angiotensin-converting enzyme inhibitors, ARB – angiotensin receptor blockers, CAD – coronary artery disease. Data represent proportions or means ± standard deviations.

There were 103 (62%) deaths in the entire HFpEF cohort during the follow-up period. After 5 years, 36% of patients in the poor CRF category, 18% of those in the intermediate CRF group, and 4.6% in the moderate to high CRF group were deceased (Table II). Throughout the follow-up, patients in higher fitness groups maintained a survival advantage over those in lower fitness groups (Figure 1).

Table II

Mortality rates of the study population with HFpEF stratified by METs categories

DeathTotal, n, %1–4 METs, n, %5–6 METs, n, %≥ 7 METs, n, %P-value
At 1 year10, 6.07, 7.83, 9.10, 00.14
At 2 years17, 10.213, 14.44, 12.10, 00.03
At 3 years26, 15.620, 22.225, 15.21, 2.30.01
At 4 years31, 18.625, 27.85, 15.21, 2.30.001
At 5 years40, 24.032, 35.66, 18.22, 4.6< 0.001
At 7 years59, 35.341, 45.613, 39.45, 11.4< 0.001
At 10 years78, 46.750, 55.616, 48.512, 27.30.008
Figure 1

Kaplan-Meier curves of all-cause mortality by METs group for the HFpEF study population

/f/fulltexts/AOMS/35958/AMS-15-35958-g001_min.jpg

The crude incidence rate of death decreased from 84 to 37 deaths per 1000 person-years going from poor to moderate-high CRF. In unadjusted models, compared to the poor CRF group, moderate-high CRF was associated with 64% lower risk of mortality (HR = 0.36, 95% CI: 0.19–0.67) (Figure 2). The survival advantage in the moderate-high CRF group persisted in the fully adjusted model (HR = 0.37, 95% CI: 0.18–0.73). No significant risk reduction in mortality was seen when the intermediate CRF group was compared to the poor CRF group. There was a 13% reduction in mortality per 1 unit higher METs (HR = 0.87, 95% CI: 0.78–0.96), which remained significant and unchanged after full adjustment (HR = 0.86, 95% CI: 0.77–0.97).

Figure 2

Multivariable-adjusted hazard ratios (95% confidence interval) for the association of CRF and all-cause mortality in the HFpEF population

/f/fulltexts/AOMS/35958/AMS-15-35958-g002_min.jpg

Risk factor and CRF-adjusted effect of HFpEF on mortality risk

Baseline characteristics of propensity-matched study population are as described in Table III. After multivariable adjustments, the long-term mortality risk of the HFpEF cohort was significantly higher than the propensity-matched non-HFpEF cohort (HR = 2.3, 95% CI: 1.7–3.2). After further adjustment for CRF (modeled as continuous METs), the mortality risk associated with HFpEF diminished but was still significant (HR = 1.8, 95% CI: 1.3–2.5), suggesting that CRF partly accounted for the association between HFpEF and mortality. Similar results were obtained when we adjusted for METs as a categorical variable (Table IV).

Table III

Baseline characteristics of propensity-matched study population

ParameterCase (N = 167)Control (N = 501)P-value
Mean METs4.7 ±2.56.3 ±2.8< 0.001
METs categories, n, %:
 1–490, 53.9131, 26.2< 0.001
 5–633, 19.8111, 22.2 
 ≥ 744, 26.4259, 51.7 
Matched on:
 Age [years]63.9 ±12.563.9 ±11.30.99
 Gender, n, %:  0.89
  Females91, 54.5270, 53.9 
  Males76, 45.5231, 46.11 
 Race, n, %:  0.96
  White86, 51.5264, 52.7 
  Black77, 46.1226, 45.1 
  Other4, 2.411, 2.2 
 Diabetes, n, %70, 41.9224, 44.70.53
 Hypertension, n, %155, 92.9457, 91.220.52
Not matched on:
 Smoking, n, %55, 32.9197, 39.30.14
 β-Blockers, n, %67, 40.1242, 48.30.07
 ACEI, n, %79, 47.3147, 29.3< 0.001
 ARB, n, %3, 1.807, 1.400.71
 Use of lung disease medications, n, %30, 18.040, 8.0< 0.001
 Known CAD, n, %94, 56.3223, 44.5 
 GFR66.9 ±30.377.1 ±24.7< 0.001
 Weight179.6 ±44.3181.6 ±39.40.60
 Statin, n, %42, 25.2157, 31.30.13
Death percentage, n, %78, 46.7104, 20.8< 0.001

[i] ACEI – angiotensin-converting enzyme inhibitors, ARB – angiotensin receptor blockers, CAD – coronary artery disease, GFR – glomerular filtration. Data represent proportions or means ± standard deviations.

Table IV

Association between HFpEF and incident all-cause mortality with and without adjustment for cardiorespiratory fitness

HFpEFUnadjusted HR (95% CI)Adjusted* HR (95% CI)
Without METs2.6 (2.0–3.5)2.3 (1.7–3.2)
With METs (continuous)1.9 (1.4–2.6)1.8 (1.3–2.5)
With METs (categorical)2.0 (1.5–2.7)1.9 (1.4–2.6)

* Models adjusted for smoking status, use of β-blockers, use of ACE inhibitors, use of lung disease medications, known CAD and statin use, as these variables remained residually statistically significant following propensity matching.

Assessment of modification of CRF effect by HFpEF status

The analysis shown in Figure 3 A presents hazard ratios of mortality with increasing METs for both the HFpEF and non-HFpEF cohorts, with the METs 1–4 category as the reference in each respective group. Higher CRF from poor to moderate-high was significantly associated with lower mortality risk in both the HFpEF and non-HFpEF cohorts, without evidence of interaction (p = 0.32), suggesting that the association between CRF and mortality appears similar regardless of HFpEF status.

Figure 3

A – Multivariable-adjusted hazard ratios (95% confidence interval) for the association between CRF and incident all-cause mortality by HFpEF status. B – Interaction analysis: multivariable-adjusted hazard ratios (95% confidence interval) for the association between CRF and all-cause mortality

/f/fulltexts/AOMS/35958/AMS-15-35958-g003_min.jpg

Figure 3 B presents hazard ratios of mortality comparing HFpEF and non-HFpEF using the non-HFpEF cohort with poor CRF (METs 1–4) as the reference category. This analysis demonstrated that while moderate-high CRF had a statistically lower mortality risk compared to poor CRF in non-HFpEF patients, HFpEF patients regardless of CRF had similar mortality to the poor CRF non-HFpEF group.

Discussion

The results of our study demonstrate that in HFpEF patients, higher CRF levels were inversely associated with all-cause mortality compared to poor CRF. We confirm, through a propensity matched analysis, that the diagnosis of HFpEF is independently associated with mortality, and extend existing literature by showing that this risk is partially explained by diminished CRF levels. Furthermore, we found no significant interaction between CRF and HFpEF, suggesting that the improved survival associated with higher CRF appears to be similar for both HFpEF and non-HFpEF cohorts matched for age, gender, and cardiovascular risk factors.

The results of this study are of marked clinical importance as they indicate that data from the straightforward and widely available treadmill exercise stress test can provide important prognostic information in patients with HFpEF, and suggest that improving CRF may potentially yield a mortality benefit in this population.

Our study has several strengths. First, the FIT dataset is the largest epidemiologic database of objectively assessed clinical exercise data to date. Our study population was racially diverse, with nearly 50% Black subjects, and was also sex-balanced, with nearly 50% women. In addition, the duration of follow-up extends to 15 years for all-cause mortality, with more than 50% of patients followed for at least 10 years.

In the present study, we showed that HFpEF patients in the FIT Project had a significantly worse mortality per CRF category compared to a propensity-matched cohort, even after multivariable adjustment for other residual differences. We showed however, that this association between HFpEF and mortality is at least partly explained by decreased CRF. This is consistent with other cardiovascular studies that have shown higher mortality rates for HFpEF compared to non-HFpEF patients and suggests that HFpEF is associated with mortality via both CRF-dependent and CRF-independent mechanisms. Studies on HFpEF hemodynamic responses to exercise have described a number of maladaptations that may contribute to the worse outcomes in this population including chronotropic incompetence [25], poor augmentation of cardiac output [26], reduced peripheral arterial blood flow [27], and impaired skeletal muscle metabolism [28]. Indeed, HFpEF patients are known to have poor exercise tolerance demonstrated by a lower peak oxygen uptake, a blunted cardiac output increase during exercise, and a robust rise in left ventricular and pulmonary filling pressures compared to healthy non-HFpEF populations [29].

Even though our data suggest improved long-term survival in HFpEF patients who achieved an estimated MET level of 7 or more (moderate-high CRF) on treadmill exercise testing, it is unknown whether targeting exercise training in HFpEF patients to achieve a CRF level of at least 7 METs will improve mortality. Our cohort did show a significant 18% lower risk for long-term mortality for every MET achieved, so it is possible that improvements in METs through exercise training might show similar long-term mortality benefit in the HFpEF population. Further studies are required to examine whether CRF-oriented exercise training in HFpEF patients will improve survival. Nevertheless, this study demonstrates that the low-cost intervention of a treadmill exercise stress test can provide significant risk stratification for HFpEF patients regardless of multiple comorbidities.

Our results extend the evidence from the findings of prior studies, which have demonstrated that exercise training and improved CRF in patients with HFpEF are associated with clinical improvement. Some studies have also shown that exercise training improves exercise capacity and quality of life, and this benefit is associated with atrial reverse remodeling and improved left ventricular diastolic function through favorable cardiac remodeling [30]. Similarly, a large meta-analysis evaluating the efficacy of exercise training in patients with HFpEF found that exercise training was associated with an improvement in CRF and quality of life [18].

Overall, in the absence of effective pharmacologic treatments available for patients with HFpEF, regular exercise training has shown strong objective evidence in improving quality of life and functional capacity for patients with HFpEF [31, 32]. This study therefore sheds light on improved mortality over long-term follow-up with CRF in patients with HFpEF, which has not been sufficiently demonstrated in the existing literature.

Our study has a number of limitations that warrant acknowledgment. First, the FIT Project reports the experience of a single health system with its unique practice patterns and modes of operation. Although the study population is diverse, it may not be representative of the general US population. Patients who completed a different protocol for stress testing were not included in the FIT Project, potentially excluding patients who are less fit, unable to exercise on a treadmill or those who were referred for pharmacological stress testing. This may have excluded the sickest heart failure patients, given that the protocol used can be challenging for heart failure patients.

Some subjects were allowed to use handrails, so our exercise data may not be fully representative of true exercise capacity. While this may attenuate our effect estimates, this is more representative of what would be obtained in a clinical setting, as it is reflective of clinical safety practices.

In conclusion, moderate-to-high CRF (≥ 7 METs) on baseline treadmill testing is associated with a survival benefit in HFpEF patients. The benefit observed in HFpEF patients is similar to the well-described benefit of CRF in non-HFpEF patients. Future studies should investigate whether targeted exercise training to achieve at least moderate-high CRF would reduce mortality in this high-risk population.

The results of our study demonstrate the importance of measuring CRF in HFpEF patients, with a moderate-high CRF (METs ≥ 7) inversely associated with all-cause mortality after multivariable adjustment. We confirm that a HFpEF diagnosis is independently associated with mortality, and extend existing literature by showing that this risk is partially explained by diminished CRF levels. Furthermore, there appears to be no evidence of interaction between CRF and HFpEF, suggesting that improved survival associated with higher CRF appears to be similar for both HFpEF and non-HFpEF populations matched for age, gender, and cardiovascular risk factors.

Our data alert clinicians to the importance of CRF in determining long-term survival in patients with HFpEF. This study also suggests that strategies to increase CRF, such as cardiac rehabilitation, may potentially be beneficial in the management of patients with HFpEF.

Acknowledgments

Olusola A. Orimoloye and Swetha Kambhampati are joint first authors.

The authors thank the staff and participants of the FIT Project for their important contributions.

Conflict of interest

The authors declare no conflict of interest.

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