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Published on: February 9, 2016
Long-term prognostic value of cardiopulmonary exercise testing in patients with hypertrophic cardiomyopathy
Leopoldo Ordine1, Grazia Canciello1, Salvatore Di Napoli1
1Department of Advanced Biomedical Sciences, University of Naples 'Federico II', School of Medicine, Via S Pansini, 5, Naples I-80131, Italy.
Insights
Cardiopulmonary exercise testing (CPET) is a powerful prognostic tool for hypertrophic cardiomyopathy (HCM). A reduced peak oxygen uptake (VO2) predicts major adverse cardiac events (MACE), even in asymptomatic patients.
Area of Science:
- Cardiology
- Exercise Physiology
Background:
- Hypertrophic cardiomyopathy (HCM) is a complex myocardial disease.
- The prognostic value of cardiopulmonary exercise testing (CPET) in predicting major adverse cardiac events (MACE) in HCM requires further clarification, especially in long-term outcomes and independent of initial symptoms.
Purpose of the Study:
- To evaluate the long-term predictive capability of CPET for MACE in patients with HCM.
- To determine if CPET findings can stratify risk independently of baseline symptoms.
Main Methods:
- A longitudinal study of 154 HCM patients who underwent symptom-limited CPET.
- MACE included septal reduction therapies, end-stage HCM, sudden cardiac death, and heart failure-related death or transplantation.
- Multivariable and competing risk analyses were performed over a mean follow-up of 12 years.
Main Results:
- Reduced percentage predicted peak VO2 (PVO2%) < 60% was an independent predictor of MACE (HR 4.16).
- NYHA Class >I also predicted MACE (HR 2.27).
- In asymptomatic (NYHA Class I) patients, PVO2% < 60% remained a significant predictor of MACE (HR 5.611), with risk divergence after 15 years.
Conclusions:
- CPET is a potent prognostic tool for risk stratification in HCM patients.
- A reduced peak VO2 is a key indicator of increased risk for MACE.
- CPET can enhance risk assessment, including for asymptomatic individuals.
Introduction:
Hypertrophic cardiomyopathy (HCM) is a heterogeneous myocardial disorder characterized by left ventricular hypertrophy. The role of cardiopulmonary exercise testing (CPET) in predicting major adverse cardiac events (MACE) remains incompletely understood, particularly over long-term follow-up and independently of baseline symptoms.
Methods:
We longitudinally studied 154 HCM patients (age 43 ± 16 years; 27% female), who underwent symptom-limited CPET. At baseline, 98 patients were in New York Heart Association (NYHA) Class I, 48 in Class II, and 8 in Class III. Septal reduction therapies (SRT), progression to end-stage HCM (ES-HCM), sudden cardiac death (SCD), heart failure-related death (HF), and heart transplantation (HT) represented a composite MACE endpoint.
Results:
Over a mean follow-up of 12 ± 9 years, 38 patients experienced MACE (SRT = 9; ES-HCM = 11; SCD = 10; HF/HT = 8). In multivariable analysis, independent predictors of MACE were percentage predicted peak VO2 (PVO2%) < 60 [hazard ratio (HR) 4.16, 95% confidence interval (CI) 1.89-9.14; P < .001], and NYHA Class >I (HR 2.27, 95% CI 1.06-4.89; P = .036). By using SRT as a competing risk, the only predictor of MACE became PVO2% < 60 (HR 3.966, 95% CI 1.626-9.670; P = .002). Among asymptomatic patients (i.e. NYHA Class I), only PVO2% < 60 remained a significant predictor of MACE (HR 5.611, 95% CI 1.635-19.253; P = .006), with risk divergence evident after nearly 15 years of follow-up. The result was also confirmed in the competing risk analysis.
Conclusion:
In this long follow-up study, CPET is a powerful prognostic tool in HCM. A reduced peak VO2 identifies those at higher risk, highlighting the potential for CPET to improve risk stratification, even among patients classified as NYHA Class I.
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