Introduction
Hypertrophic cardiomyopathy (HCM) is a cardiac disease characterized by inappropriate myocardial hypertrophy and a non-dilated left ventricle with frequent myocardial fibrosis. It is associated with variable clinical expressions and outcomes [1, 2].
Reduced exercise capacity is common in patients with HCM, affecting these patients over a broad spectrum of clinical severity [3]. Exercise stress testing has been shown to be useful for the assessment of functional capacity and risk stratification, evaluation of symptoms, and monitoring the response to therapy in patients with HCM [4]. Peak oxygen consumption (peak VO2) during cardiopulmonary exercise testing (CPET) is known to be a useful marker for the functional capacity of patients with HCM [5, 6].
Meanwhile, myocardial fibrosis in HCM has been reported to be responsible for poor clinical outcomes [7–9]. It is most commonly detected and quantified with cardiac magnetic resonance imaging (CMR) using late gadolinium enhancement (LGE) [10]. Previous reports have shown that the presence of LGE has an independent value as a prognostic factor in HCM. It has also been proposed as a factor to be considered when an implantable cardioverter-defibrillator is considered for primary prevention of sudden cardiac death [10–12].
Moreover, CPET and CMR have been described as being able to further aid in risk stratification for future clinical events [13–17]. Apart from conventional factors, additional risk stratification could be beneficial and useful for better prediction of clinical outcomes.
We sought to assess whether the extent of myocardial fibrosis depicted on CMR and exercise capacity estimated by CPET could help in determining the outcomes, assessed as independent risk factors or as additive parameters to conventional clinical parameters, in patients with HCM.
Methods
Study population and clinical characteristics
The study was performed using data obtained from the prospective observational HCM registry of the Samsung Heart Vascular Stroke Institute, Seoul, Korea. A total of 591 prospectively enrolled patients, who were diagnosed with HCM and underwent CMR between 2008 and 2015, were included. The echocardiographic criteria for inclusion in the HCM registry included the following definition of guidelines: HCM is defined by the presence of increased left ventricular (LV) wall thickness that is not solely explained by abnormal loading conditions [18, 19]. Patients with uncontrolled hypertension, uncontrolled ventricular arrhythmias, severe valvular diseases, other concomitant systemic diseases–including malignancy–and poor echocardiographic windows for analysis were excluded [3, 20–22].
The study population comprised 373 patients who were able to perform a cardiopulmonary exercise test (CPET) using a treadmill and presented with normal LV systolic function (ejection fraction ≥ 50%). CPET and CMR were performed according to a standard protocol at baseline.
All clinical characteristics were obtained by reviewing medical records. The presenting symptoms, such as dyspnea (New York Heart Association [NYHA] functional classification) or chest pain, were recorded, and a medical history of syncope or sudden cardiac death was obtained. History of other medical conditions, such as the presence of hypertension, diabetes mellitus, or atrial fibrillation, was also acquired. Information on family history (defined as history in first-degree relatives) of sudden cardiac death or HCM was also obtained. A 24-h electrocardiogram (ECG) Holter monitoring was also performed in the study population for risk stratification.
This study was approved by the Institutional Review Board of Samsung Medical Center, and the requirement for informed consent was waived.
Echocardiographic study and CPET
Conventional two-dimensional echocardiography was performed and echocardiographic parameters were obtained according to the guidelines. LV end-diastolic and end-systolic volumes were measured from apical two- and four-chamber views. The ejection fraction was calculated using Simpson’s rule. LV mass was calculated using the formula proposed by Devereux et al. and was corrected by body surface area to derive the LV mass index (LVMI) [23]. The left ventricular outflow tract (LVOT) was scanned using continuous Doppler to measure the maximal velocity and estimated pressure gradient in apical three- or five-chamber views. Left ventricular outflow tract obstruction (LVOTO) was defined as a pressure gradient of ≥ 30 mmHg at rest [19, 22, 24–26].
Left atrial volume was measured using the biplane-modified Simpson’s method and adjusted to the body surface area (left atrium volume index, LAVI). Early diastolic mitral annular velocity at the septal side (e’) and peak early diastolic transmitral flow velocity (E) were measured. E/e’ was calculated from the aforementioned values [27].
CPET was performed with symptom-limited treadmill exercise along with respiratory gas exchange analysis in all patients using the Bruce protocol [28–30]. Twelve-lead electrocardiography was performed with the use of conventional chest lead positioning before exercise, at each stage, and after stress test. Blood pressure was recorded every 2 min. Oxygen consumption (peak VO2) was measured using a Medical Graphics metabolic cart (St. Paul, MN, USA). The highest peak VO2 over a period of exercise time was expressed as absolute peak VO2 or normalized peak VO2 (percentage of age, sex, and weight predicted). Exercise was terminated if there was marked dyspnea, fatigue, chest discomfort, > 2-mm ST depression, or after 15 min of the protocol (15.6 metabolic equivalents, MET). In addition, abnormal hemodynamic response to exercise was defined as follows: (1) blunted blood pressure (BP) response, < 20 mmHg increase in systolic BP, or (2) hypotensive response, > 20 mmHg decrease in systolic BP from baseline BP, or an initial rise in systolic BP, followed by a decrease of > 20 mmHg in systolic BP [31, 32].
CMR imaging acquisition and analysis
CMR was performed using a 1.5 T system (Magnetom Avanto, Syngo MR B15 version; Siemens Medical Solutions, Erlangen, Germany) with a 32-channel phased-array receiver coil with repeated breath-holding. The CMR protocol consisted of cine, T2-weighted (T2W), first-pass perfusion, and LGE imaging. Cine imaging was performed with balanced steady-state free precession sequences along the long and short axes from the apex to the base of the LV. After localization, steady-state free precession cine images were acquired with contiguous short-axis slices (slice thickness, 6 mm; gap, 4 mm) to quantify LV function and volume.
Standard LGE images were acquired after intravenous administration of gadobutrol (0.15 mmol/kg Gadovist; Bayer Healthcare, Berlin, Germany), followed by a flush of 20 mL saline at the same rate. The LGE images from long -, short -, and apical 4-chamber views were acquired using a multi-shot turbo field echo breath-hold sequence with a phase-sensitive inversion recovery method. The inversion time was usually 280–360 ms. The LGE images were evaluated 10 min after gadolinium administration using a multi-shot turbo field echo breath-hold sequence. The field of view and image matrix were 35 × 35 cm and 256 × 256 cm [33]. LGE was considered present when the signal intensity of the index myocardial segment was 6 SD greater than the remote normal myocardial signal. LGE volume was calculated by summing the areas of LGE in all short-axis slices and was expressed as the volumetric proportion of the total LV myocardium (%LV). The CMR scans were visually interpreted by two experienced readers who were blinded to the clinical and laboratory data. The cutoff value of extensive LGE was defined as 15%LV, in accordance with previous studies that showed that this proportion of LGE by quantitative contrast enhanced CMR could help in assessing event risk [34].
Clinical outcomes
Clinical outcomes were evaluated through medical record reviews and regular telephone interviews. The primary outcome was a clinical composite of all-cause death, cardiac transplantation, stroke, heart failure requiring hospitalization (including new-onset atrial fibrillation), and implantable cardiac defibrillator implantation [24, 26]. In addition, secondary outcome analyses were performed against each component of the composite clinical outcome.
Statistical analysis
Continuous variables were compared using Student’s t-test or the Wilcoxon rank-sum test, where applicable, and are presented as mean ± standard deviation or median with interquartile range (IQR). Categorical data were tested using Fisher’s exact test or chi-square test, as appropriate. Cox proportional analysis was used to calculate the hazard ratio (HR) and 95% confidence interval (CI) to compare the risk of composite clinical outcomes. A multivariable Cox proportional hazards regression model, adjusted for age and sex, was used to identify independent predictors of composite clinical outcomes. Covariates that were either statistically significant during univariate analysis or clinically relevant were included in the multivariable models. We compared several receiver operating characteristic (ROC) curves using the area under the curve (AUC) comparison analysis method.
The variables selected for the multivariable model analyses were variables that were found to be either significant in univariable analyses (p < 0.2) or represented to be clinically meaningful parameters [35]. In addition to clinical risk factors, the incremental prognostic value of additive parameters was assessed using the net reclassification improvement (NRI) and integrated discrimination improvement (IDI) index. MODEL 1 was established for combined conventional parameters, including age, sex, history of syncope, and non-sustained ventricular tachycardia (VT) on Holter monitoring [36].
All tests were two-tailed, and statistical significance was set at p < 0.05. All analyses were performed using SPSS software (version 23.0; SPSS Inc., Chicago, IL, USA) and R statistical software version 3.6.1 (R Foundation for Statistical Computing, Vienna, Austria).
Results
Baseline characteristics and composite clinical outcomes
Baseline clinical characteristics of the patients are shown in Table 1. A total of 373 patients were referred for exercise stress testing and CMR. Patients were divided into two groups according to the presence or absence of composite clinical outcomes, comprising 84 and 289 patients, respectively. The patients in the group with composite clinical outcomes were older (56.08 ± 10.23 years vs. 52.16 ± 11.22 years, p = 0.003). The sex ratio (male) of the patients was not significantly different between the two groups (81.0% vs. 84.4% males, p = 0.51).
[Figure omitted. See PDF.]
The median follow-up period was 74.7 months (interquartile range, 50.0–103.3 months). Nine patients died regardless of cause (10.7%), and only three patients experienced cardiac-related events. Cardiac transplantation, stroke, heart failure requiring hospitalization, and implantable cardiac defibrillator implantation occurred in 1 (1.2%), 24 (28.6%), 55 (65.5%), and 14 (16.7%) patients, respectively. Among the composite clinical outcomes, heart failure that required hospitalization had the highest occurrence rate in this registry.
Association of clinical parameters and events
The composite of clinical events was associated with dyspnea on exertion (NYHA functional class II, 42.9% vs. 14.5%, p < 0.001). Patients with clinical events presented with a higher proportion of history of syncope (15.5% vs. 6.6%, p = 0.015). A history of atrial fibrillation (AF) (13.1% vs. 2.8%, p = 0.008) and non-sustained VT on 24-hour ECG monitoring (28.6% vs. 7.6%, p < 0.001) were also more frequently detected in patients with clinical events.
Echocardiographic, CMR, and CPET parameters
The parameters obtained through echocardiography, CMR, and CPET are listed in Table 2. On echocardiography, maximal LV wall thickness (18.67 ± 4.60 mm vs. 17.31 ± 4.07 mm, p = 0.009) and LV end-diastolic dimension (LVEDD) (47.37 ± 5.28 mm vs. 48.70 ± 4.88 mm, p = 0.031) were significantly higher in patients with clinical events. The incidence of LVOTO was higher in the event group (28.6% vs. 14.9%, p = 0.006). The composite outcome was also associated with larger LAVI (52.18 ± 19.22 mL/m2 vs. 40.73 ± 15.62 mL/m2, p < 0.001) and higher E/e’ (14.07 ± 5.70 vs. 11.39 ± 4.29, p < 0.001).
[Figure omitted. See PDF.]
CMR imaging revealed that the extent of LGE was larger in the event group (15.39 ± 10.53%LV vs. 11.97± 9.53%LV, p = 0.005). An ROC curve analysis was performed to obtain the cutoff value of the amount of LGE associated with prognosis. The cutoff value was 15.29% on the ROC curve, which was consistent with the findings of previous studies that defined a significant amount of LGE that could predict worse prognosis [34]. The proportion of patients with extensive LGE (≥ 15%LV) according to our cutoff value criteria was also significantly higher in the event group (50.0% vs. 28.4%, p < 0.001).
On exercise stress testing, the group with composite clinical outcomes showed lower peak VO2 (18.51 ± 13.25 mL/kg/min vs. 24.59 ± 13.28 mL/kg/min, p < 0.001) and shorter exercise duration (p < 0.001). Furthermore, an abnormal hemodynamic response to exercise (41.7% vs. 20.8%, p < 0.001) was more common in the event group. An ROC curve analysis was performed to obtain the cutoff value of the amount of peak VO2 associated with prognosis, as the cutoff value was confirmed to be 27.4 (mL/Kg/min).
Multivariate analysis of variables associated with composite clinical outcomes
The Cox regression analysis of the variables evaluated to predict composite clinical outcomes is shown in Table 3. Multivariate Cox proportional analysis, adjusted for age and sex, revealed that non-sustained VT on Holter (HR [95% CI]: 2.460 [1.444–4.190], p = 0.001), E/e’ ratio (1.051 [1.006–1.098], p = 0.027), abnormal hemodynamic response to exercise (1.661 [4.025–2.692], p = 0.04), and lower exercise capacity (≤ 27.4 mL/kg/min) (1.724 [1.004–2.962], p = 0.048) were significantly correlated with composite outcome (Table 3).
[Figure omitted. See PDF.]
Additive predictive values of various prognostic models
To establish models for the prediction of composite clinical outcomes, variables that were either indicated to be significant by multivariable analysis (p < 0.20) or deemed clinically meaningful were selected and analyzed. MODEL 1 was composed of conventional factors, such as clinical variables and non-sustained VT on Holter monitoring. Selective parameters were added in a stepwise manner to MODEL 1 and the respective models were established. MODEL 2 included echocardiographic parameters (LVEDD, LAVI, and E/e`) on top of MODEL 1. A separate model (MODEL 2–1) where CMR parameters (the presence of LGE [> 15%LV] and LV ejection fraction on CMR) were added to MODEL 1 was set up and evaluated. MODEL 3 included the CMR parameters in addition to MODEL 2. MODEL 4 included CPET parameters (abnormal hemodynamic response to exercise and lower exercise capacity) added to MODEL 3.
The incremental prognostic value of non-sustained VT on Holter, echocardiographic parameters, CMT parameters, and CPET parameters over conventional clinical variables ranged from 0.700 to 0.790 on the basis of the value of the AUC obtained by the ROC curve analysis (Table 4 and Fig 1). All models showed statistical significance for the prediction of composite clinical outcomes as the NRI value (all p-values < 0.05) (Table 4) by risk reclassification analysis. Particularly, in Model 4, where CPET variables were added to clinical, echocardiographic, and CMR parameters, definite incremental values for composite outcome prediction were significantly identified (p-values < 0.005 on NRI and IDI values).
[Figure omitted. See PDF.]
The reference model (MODEL 1) included age, sex, history of syncope as combined clinical parameters, and non-sustained ventricular tachycardia on Holter. Echocardiographic parameters were added to the left ventricular end diastolic dimension, left atrium volume index, and E/e’ ratio. Cardiac magnetic resonance parameters were included in addition to the presence of LGE (> 15%LV) and left ventricular ejection fraction. Cardiopulmonary exercise test parameters were included in addition to abnormal hemodynamic response to exercise and lower exercise capacity (peak VO2 ≤27.4 mL/Kg/min). Incremental prognostic value by ROC curve analysis was compared among 4 models. LGE: late gadolinium enhancement; LV: left ventricular; ROC: receiver operating characteristic curve.
[Figure omitted. See PDF.]
Discussion
We investigated the relationship between conventional clinical variables and additional parameters obtained from multiple modalities and composite clinical outcomes during a mid-range follow-up period. Our data showed that in addition to the clinical and echocardiographic parameters, the extent of myocardial fibrosis and information on exercise capacity obtained from CPET could be useful additional significant predictors of composite clinical outcomes in patients with HCM.
In previous studies, several factors, such as LGE on CMR, LVOT obstruction, biomarkers, and diastolic dysfunction, may have contributed to the adverse clinical outcomes with reduced exercise capacity in patients with HCM [13–15, 24]. The reduced exercise capacity could be explained by the physiology of myocardial fibrosis and hemodynamic changes in myocardial stiffness.
Among them, LGE on CMR has been found to be associated with overall mortality [11, 13, 17, 37, 38] and malignant arrhythmias in patients with HCM [12]. Our findings confirmed that the presence and amount of myocardial fibrosis could be a determinant of composite clinical outcomes in patients with HCM, and could also add value to conventional factors. The uniqueness of our study was that we demonstrated that CPET may also be an important tool for risk stratification in HCM on top of CMR findings. Moreover, we showed that functional capacity demonstrated by peak VO2 was an independent predictor of outcomes in patients with HCM, with incremental value as a risk factor when added to the alleged parameters.
Patients with HCM frequently exhibit limited exercise capacity [39–41]. The reduced exercise capacity may be attributed to the inability to increase stroke volume. This inability is due to impaired diastolic filling and LV contractile reserve for overcoming afterload [25, 42]. Exercise stress testing has previously been used to assess clinical risk [31, 43]. Here the most well-accepted prognostic factor for HCM in exercise physiology is exercise-induced abnormal BP response. This abnormal hemodynamic response can be attributed to marked LV systolic dysfunction, decreased cardiac output, and hypotension [44]. However, most studies on exercise physiology in HCM have focused on hemodynamic responses and simple exercise duration. We described the role of advanced modalities in obtaining additional risk stratification for future clinical events using all elements combined.
Patients with HCM have a high risk of sudden cardiac death; therefore, the guidelines suggest major clinical features associated with an increased risk of sudden cardiac death in adults [18]. However, in our results, there were not many events of cardiac death or sudden cardiac death because of registry data. Among the composite outcomes, heart failure events accounted for the highest rate. Therefore, our results suggest that for predicting and managing life quality and morbidity, the predictive value of functional changes, such as exercise capacity, was more statistically significant than that of pathologic changes such as fibrosis, which has been found to be associated with cardiac death. According to the results of previous studies, many methods have been suggested to increase the survival rate of patients with HCM. However, as for patients who are older or ageing, heart failure-related events such as repeated admission may be as important as sudden death, as elderly HCM patients such as subjects in our group are not prone to exhibit high rates of sudden cardiac death as their younger counterparts according to previous reports [45, 46]. As this is the case, our results may be especially important in managing older HCM patients who are increasing in number as the longevity of the general population is increasing.
Patients with HCM can present with a wide and varied spectrum of symptoms, including exertional shortness of breath, chest pain, syncope, or pre-syncope. In many situations, symptoms are equivocal. Cardiopulmonary exercise stress testing provides not only customized objective information on exercise capacity, but also information related to exertional symptoms that appear during daily activities. This is notable, as exercise-related subjective symptoms, which can be vague or equivocal, are key factors of concern during treatment planning. Objective estimation of exercise capacity and symptoms will provide a clearer picture of the patient’s clinical status. Exercise stress testing in patients with HCM is safe and rarely leads to serious adverse events [47, 48]. Therefore, we emphasize that cardiopulmonary exercise stress testing would be highly useful for patients with HCM. As our study showed, exercise capacity and hemodynamic response on CPET have additive values for predicting clinical outcomes. Performing CPET in patients with HCM would be helpful in determining both clinical outcomes and treatment plans.
Limitations
The first limitation of this study is that it was a single-center observational study. However, being conducted at a tertiary hospital, follow-up was performed on the entire study population meticulously so that we could detail the outcomes and associate them closely with baseline characteristics. Second, we included only patients who were able to perform exercise testing, which may have been the reason for the relatively small number of cases of cardiac death (n = 3) and all-cause death (n = 9). However, as patients with HCM are generally mildly symptomatic, and risk stratification for HCM was performed in relatively active patients in general, we considered our results to be acceptable for generalization in the real world. Third, we did not include additional data on post-exercise hemodynamic parameters, such as chronotropic incompetence or exercise-induced arrhythmia in our study [49]. Instead, we focused on the most widely used simple parameters for estimating exercise capacity objectively and tried not to overcomplicate the already complicated method of risk stratification in HCM.
Conclusions
This study demonstrated that CPET-derived peak oxygen consumption level, especially when combined with LGE on CMR, added value to conventional clinical risk factors as prognostic factors in patients with HCM, especially in terms of heart failure-related admissions. Dynamic objective assessment of patients with CPET may aid in elucidating various symptoms, improving treatment planning, and assessing risk stratification in patients with HCM.
Citation: Hwang J-w, Lee S-C, Kim D, Kim J, Kim EK, Chang S-A, et al. (2023) Role of cardiovascular magnetic resonance imaging and cardiopulmonary exercise test in predicting composite clinical outcomes in patients with hypertrophic cardiomyopathy. PLoS ONE 18(5): e0285887. https://doi.org/10.1371/journal.pone.0285887
About the Authors:
Ji-won Hwang
Roles: Conceptualization, Formal analysis, Investigation, Writing – original draft
Affiliation: Division of Cardiology, Department of Medicine, Ilsan Paik Hospital, Inje University School of Medicine, Goyang, Korea
Sang-Chol Lee
Roles: Conceptualization, Formal analysis, Investigation, Methodology, Project administration, Resources, Supervision, Writing – original draft, Writing – review & editing
E-mail: [email protected]
Affiliations: Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
ORICD: https://orcid.org/0000-0003-2176-0482
Darae Kim
Roles: Conceptualization, Data curation, Methodology, Project administration, Resources
Affiliations: Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
Jihoon Kim
Roles: Conceptualization, Data curation, Investigation, Methodology, Project administration
Affiliations: Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
Eun Kyoung Kim
Roles: Conceptualization, Data curation, Investigation, Methodology, Project administration, Writing – review & editing
Affiliations: Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
Sung-A. Chang
Roles: Conceptualization, Data curation, Formal analysis, Methodology, Project administration
Affiliations: Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
Sung-Ji Park
Roles: Data curation, Formal analysis, Investigation, Methodology, Project administration
Affiliations: Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
Sung Mok Kim
Roles: Data curation, Formal analysis, Investigation, Methodology, Project administration
Affiliations: Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
ORICD: https://orcid.org/0000-0001-5190-2328
Yeon Hyeon Choe
Roles: Data curation, Investigation, Methodology, Project administration
Affiliations: Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
Seung Woo Park
Roles: Data curation, Formal analysis, Methodology, Project administration, Resources, Supervision
Affiliations: Division of Cardiology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Cardiovascular Imaging Center, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
1. Todiere G, Aquaro GD, Piaggi P, Formisano F, Barison A, Masci PG, et al. Progression of myocardial fibrosis assessed with cardiac magnetic resonance in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2012; 60:922–9. https://doi.org/10.1016/j.jacc.2012.03.076 pmid:22935464
2. Hughes SE. The pathology of hypertrophic cardiomyopathy. Histopathology. 2004; 44:412–27. https://doi.org/10.1111/j.1365-2559.2004.01835.x pmid:15139989
3. Maron BJ. Hypertrophic cardiomyopathy: a systematic review. Jama. 2002; 287:1308–20. pmid:11886323
4. Argulian E, Chaudhry FA. Stress testing in patients with hypertrophic cardiomyopathy. Prog Cardiovasc Dis. 2012; 54:477–82. https://doi.org/10.1016/j.pcad.2012.04.001 pmid:22687588
5. Sharma S, Elliott P, Whyte G, Jones S, Mahon N, Whipp B, et al. Utility of cardiopulmonary exercise in the assessment of clinical determinants of functional capacity in hypertrophic cardiomyopathy. Am J Cardiol. 2000; 86:162–8. pmid:10913477
6. Arena R, Sietsema KE. Cardiopulmonary exercise testing in the clinical evaluation of patients with heart and lung disease. Circulation. 2011; 123:668–80. https://doi.org/10.1161/circulationaha.109.914788 pmid:21321183
7. Maron MS, Appelbaum E, Harrigan CJ, Buros J, Gibson CM, Hanna C, et al. Clinical profile and significance of delayed enhancement in hypertrophic cardiomyopathy. Circ Heart Fail. 2008; 1:184–91. https://doi.org/10.1161/circheartfailure.108.768119 pmid:19808288
8. Choi DS, Ha JW, Choi B, Yang WI, Choi EY, Rim SJ, et al. Extent of late gadolinium enhancement in cardiovascular magnetic resonance and its relation with left ventricular diastolic function in patients with hypertrophic cardiomyopathy. Circ J. 2008; 72:1449–53. pmid:18724020
9. Maron BJ, Spirito P. Implications of left ventricular remodeling in hypertrophic cardiomyopathy. Am J Cardiol. 1998; 81:1339–44. pmid:9631972
10. Moon JC, Reed E, Sheppard MN, Elkington AG, Ho SY, Burke M, et al. The histologic basis of late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2004; 43:2260–4. https://doi.org/10.1016/j.jacc.2004.03.035 pmid:15193690
11. Bruder O, Wagner A, Jensen CJ, Schneider S, Ong P, Kispert EM, et al. Myocardial scar visualized by cardiovascular magnetic resonance imaging predicts major adverse events in patients with hypertrophic cardiomyopathy. J Am Coll Cardiol. 2010; 56:875–87. https://doi.org/10.1016/j.jacc.2010.05.007 pmid:20667520
12. Leonardi S, Raineri C, De Ferrari GM, Ghio S, Scelsi L, Pasotti M, et al. Usefulness of cardiac magnetic resonance in assessing the risk of ventricular arrhythmias and sudden death in patients with hypertrophic cardiomyopathy. Eur Heart J. 2009; 30:2003–10. https://doi.org/10.1093/eurheartj/ehp152 pmid:19474054
13. Bouabdallaoui N, Ennezat PV, Durand E, Puymirat E, Macron L. Late gadolinium enhancement cardiac magnetic resonance imaging in prognostic assessment of hypertrophic cardiomyopathy. Eur Heart J Cardiovasc Imaging. 2013; 14:1024. https://doi.org/10.1093/ehjci/jet067 pmid:23644935
14. Desai MY, Bhonsale A, Patel P, Naji P, Smedira NG, Thamilarasan M, et al. Exercise echocardiography in asymptomatic HCM: exercise capacity, and not LV outflow tract gradient predicts long-term outcomes. JACC Cardiovasc Imaging. 2014; 7:26–36. https://doi.org/10.1016/j.jcmg.2013.08.010 pmid:24290569
15. Finocchiaro G, Haddad F, Knowles JW, Caleshu C, Pavlovic A, Homburger J, et al. Cardiopulmonary responses and prognosis in hypertrophic cardiomyopathy: a potential role for comprehensive noninvasive hemodynamic assessment. JACC Heart Fail. 2015; 3:408–18. https://doi.org/10.1016/j.jchf.2014.11.011 pmid:25863972
16. Sorajja P, Allison T, Hayes C, Nishimura RA, Lam CS, Ommen SR. Prognostic utility of metabolic exercise testing in minimally symptomatic patients with obstructive hypertrophic cardiomyopathy. Am J Cardiol. 2012; 109:1494–8. https://doi.org/10.1016/j.amjcard.2012.01.363 pmid:22356797
17. O’Hanlon R, Grasso A, Roughton M, Moon JC, Clark S, Wage R, et al. Prognostic significance of myocardial fibrosis in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2010; 56:867–74. https://doi.org/10.1016/j.jacc.2010.05.010 pmid:20688032
18. Elliott PM, Anastasakis A, Borger MA, Borggrefe M, Cecchi F, Charron P, et al. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J. 2014; 35:2733–79. https://doi.org/10.1093/eurheartj/ehu284 pmid:25173338
19. Gersh BJ, Maron BJ, Bonow RO, Dearani JA, Fifer MA, Link MS, et al. 2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Developed in collaboration with the American Association for Thoracic Surgery, American Society of Echocardiography, American Society of Nuclear Cardiology, Heart Failure Society of America, Heart Rhythm Society, Society for Cardiovascular Angiography and Interventions, and Society of Thoracic Surgeons. J Am Coll Cardiol. 2011; 58:e212–60. https://doi.org/10.1016/j.jacc.2011.06.011 pmid:22075469
20. Elliott P. Hypertrophic Cardiomyopathy. Circulation. 2018; 138:1399–401. https://doi.org/10.1161/circulationaha.118.035932 pmid:30354358
21. Elliott P, McKenna WJ. Hypertrophic cardiomyopathy. Lancet. 2004; 363:1881–91. https://doi.org/10.1016/s0140-6736(04)16358-7 pmid:15183628
22. Maron BJ, McKenna WJ, Danielson GK, Kappenberger LJ, Kuhn HJ, Seidman CE, et al. American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines. J Am Coll Cardiol. 2003; 42:1687–713. pmid:14607462
23. Devereux RB, Alonso DR, Lutas EM, Gottlieb GJ, Campo E, Sachs I, et al. Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol. 1986; 57:450–8. https://doi.org/10.1016/0002-9149(86)90771-x pmid:2936235
24. Maron MS, Olivotto I, Betocchi S, Casey SA, Lesser JR, Losi MA, et al. Effect of left ventricular outflow tract obstruction on clinical outcome in hypertrophic cardiomyopathy. N Engl J Med. 2003; 348:295–303. https://doi.org/10.1056/NEJMoa021332 pmid:12540642
25. Maron MS, Olivotto I, Zenovich AG, Link MS, Pandian NG, Kuvin JT, et al. Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction. Circulation. 2006; 114:2232–9. https://doi.org/10.1161/circulationaha.106.644682 pmid:17088454
26. Peteiro J, Bouzas-Mosquera A, Fernandez X, Monserrat L, Pazos P, Estevez-Loureiro R, et al. Prognostic value of exercise echocardiography in patients with hypertrophic cardiomyopathy. J Am Soc Echocardiogr. 2012; 25:182–9. https://doi.org/10.1016/j.echo.2011.11.005 pmid:22137254
27. Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015; 28:1–39.e14. https://doi.org/10.1016/j.echo.2014.10.003 pmid:25559473
28. Myers J, Buchanan N, Walsh D, Kraemer M, McAuley P, Hamilton-Wessler M, et al. Comparison of the ramp versus standard exercise protocols. J Am Coll Cardiol. 1991; 17:1334–42. pmid:2016451
29. Stewart RA, Kittelson J, Kay IP. Statistical methods to improve the precision of the treadmill exercise test. J Am Coll Cardiol. 2000; 36:1274–9. pmid:11028483
30. Gibbons RJ, Balady GJ, Beasley JW, Bricker JT, Duvernoy WF, Froelicher VF, et al. ACC/AHA Guidelines for Exercise Testing. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on Exercise Testing). J Am Coll Cardiol. 1997; 30:260–311. pmid:9207652
31. Olivotto I, Maron BJ, Montereggi A, Mazzuoli F, Dolara A, Cecchi F. Prognostic value of systemic blood pressure response during exercise in a community-based patient population with hypertrophic cardiomyopathy. J Am Coll Cardiol. 1999; 33:2044–51. pmid:10362212
32. Sadoul N, Prasad K, Elliott PM, Bannerjee S, Frenneaux MP, McKenna WJ. Prospective prognostic assessment of blood pressure response during exercise in patients with hypertrophic cardiomyopathy. Circulation. 1997; 96:2987–91. pmid:9386166
33. Kim EK, Lee SC, Hwang JW, Chang SA, Park SJ, On YK, et al. Differences in apical and non-apical types of hypertrophic cardiomyopathy: a prospective analysis of clinical, echocardiographic, and cardiac magnetic resonance findings and outcome from 350 patients. Eur Heart J Cardiovasc Imaging. 2016; 17:678–86. https://doi.org/10.1093/ehjci/jev192 pmid:26245912
34. Chan RH, Maron BJ, Olivotto I, Pencina MJ, Assenza GE, Haas T, et al. Prognostic value of quantitative contrast-enhanced cardiovascular magnetic resonance for the evaluation of sudden death risk in patients with hypertrophic cardiomyopathy. Circulation. 2014; 130:484–95. https://doi.org/10.1161/circulationaha.113.007094 pmid:25092278
35. Peduzzi P, Concato J, Feinstein AR, Holford TR. Importance of events per independent variable in proportional hazards regression analysis. II. Accuracy and precision of regression estimates. J Clin Epidemiol. 1995; 48:1503–10. pmid:8543964
36. Pencina MJ, D’Agostino RB Sr, D’Agostino RB Jr, Vasan RS. Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond. Stat Med. 2008; 27:157–72; discussion 207–12. https://doi.org/10.1002/sim.2929 pmid:17569110
37. Kwon DH, Smedira NG, Rodriguez ER, Tan C, Setser R, Thamilarasan M, et al. Cardiac magnetic resonance detection of myocardial scarring in hypertrophic cardiomyopathy: correlation with histopathology and prevalence of ventricular tachycardia. J Am Coll Cardiol. 2009; 54:242–9. https://doi.org/10.1016/j.jacc.2009.04.026 pmid:19589437
38. Rubinshtein R, Glockner JF, Ommen SR, Araoz PA, Ackerman MJ, Sorajja P, et al. Characteristics and clinical significance of late gadolinium enhancement by contrast-enhanced magnetic resonance imaging in patients with hypertrophic cardiomyopathy. Circ Heart Fail. 2010; 3:51–8. https://doi.org/10.1161/circheartfailure.109.854026 pmid:19850699
39. Tower-Rader A, Betancor J, Lever HM, Desai MY. A Comprehensive Review of Stress Testing in Hypertrophic Cardiomyopathy: Assessment of Functional Capacity, Identification of Prognostic Indicators, and Detection of Coronary Artery Disease. J Am Soc Echocardiogr. 2017; 30:829–44. https://doi.org/10.1016/j.echo.2017.05.017 pmid:28688858
40. Reant P, Reynaud A, Pillois X, Dijos M, Arsac F, Touche C, et al. Comparison of resting and exercise echocardiographic parameters as indicators of outcomes in hypertrophic cardiomyopathy. J Am Soc Echocardiogr. 2015; 28:194–203. https://doi.org/10.1016/j.echo.2014.10.001 pmid:25459499
41. Ohara T, Iwano H, Thohan V, Kitzman DW, Upadhya B, Pu M, et al. Role of Diastolic Function in Preserved Exercise Capacity in Patients with Reduced Ejection Fractions. J Am Soc Echocardiogr. 2015; 28:1184–93. https://doi.org/10.1016/j.echo.2015.06.004 pmid:26232892
42. Schaff HV, Dearani JA, Ommen SR, Sorajja P, Nishimura RA. Expanding the indications for septal myectomy in patients with hypertrophic cardiomyopathy: results of operation in patients with latent obstruction. J Thorac Cardiovasc Surg. 2012; 143:303–9. https://doi.org/10.1016/j.jtcvs.2011.10.059 pmid:22154797
43. Gimeno JR, Tome-Esteban M, Lofiego C, Hurtado J, Pantazis A, Mist B, et al. Exercise-induced ventricular arrhythmias and risk of sudden cardiac death in patients with hypertrophic cardiomyopathy. Eur Heart J. 2009; 30:2599–605. https://doi.org/10.1093/eurheartj/ehp327 pmid:19689975
44. Ciampi Q, Betocchi S, Lombardi R, Manganelli F, Storto G, Losi MA, et al. Hemodynamic determinants of exercise-induced abnormal blood pressure response in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2002; 40:278–84. pmid:12106932
45. Maron BJ, Rowin EJ, Casey SA, Haas TS, Chan RH, Udelson JE, et al. Risk stratification and outcome of patients with hypertrophic cardiomyopathy > = 60 years of age. Circulation. 2013; 127:585–93. https://doi.org/10.1161/circulationaha.112.136085 pmid:23275385
46. Maron BJ. Clinical Course and Management of Hypertrophic Cardiomyopathy. N Engl J Med. 2018; 379:655–68. https://doi.org/10.1056/NEJMra1710575 pmid:30110588
47. Suzuki K, Akashi YJ. Exercise stress echocardiography in hypertrophic cardiomyopathy. J Echocardiogr. 2017; 15:110–7. https://doi.org/10.1007/s12574-017-0338-4 pmid:28501918
48. Sorensen LL, Liang HY, Pinheiro A, Hilser A, Dimaano V, Olsen NT, et al. Safety profile and utility of treadmill exercise in patients with high-gradient hypertrophic cardiomyopathy. Am Heart J. 2017; 184:47–54. https://doi.org/10.1016/j.ahj.2016.10.010 pmid:27892886
49. Masri A, Pierson LM, Smedira NG, Agarwal S, Lytle BW, Naji P, et al. Predictors of long-term outcomes in patients with hypertrophic cardiomyopathy undergoing cardiopulmonary stress testing and echocardiography. Am Heart J. 2015; 169:684–92.e1. https://doi.org/10.1016/j.ahj.2015.02.006 pmid:25965716
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2023 Hwang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
We aimed to evaluate the additive value of cardiovascular magnetic resonance imaging (CMR) and cardiopulmonary exercise test (CPET) to predict clinical outcomes in patients with HCM. We enrolled 373 patients with HCM and normal left ventricular systolic function who underwent CPET and CMR. The primary outcome was a clinical composite of all-cause death, cardiac transplantation, stroke, heart failure requiring hospitalization and defibrillator implantation. During a follow-up of 70.70 ± 30.74 months, there were 84 composite clinical events. Peak oxygen consumption during CPET was significantly lower (18.51±13.25 vs. 24.59±13.28 mL/kg/min, p < 0.001) and abnormal hemodynamic response to exercise was more frequently detected (41.7 vs. 20.8%, p<0.001) in the group with composite clinical events. The extent of late gadolinium enhancement was larger in the event group (15.39±10.53 vs. 11.97±9.53%LV, p<0.001). Selective parameters were added stepwise to conventional clinical parameters; the final model, where CPET and CMR parameters were added, was verified to have the highest increment value for clinical outcome prediction (p<0.001). This study demonstrated that CPET and CMR findings may be important clinical tools for risk stratification in HCM. Exercise capacity was an independent predictor of composite outcomes in patients with HCM, with incremental value as a risk factor when added to the alleged parameters. These findings could help physicians monitor and manage patients with HCM in the real clinical field.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer