Abstract

The authors used cluster analysis of data from cardiovascular domains associated with exercise intolerance to help define prognostic phenotypes of patients with heart failure with preserved ejection fraction (HFpEF). Resting and postexercise echocardiography was performed in 177 patients with HFpEF and 51 asymptomatic control subjects sharing a common clinical profile. Patterns of features that determine exercise capacity were sought from automated hierarchical clustering of left ventricular (LV) diastolic and systolic function, left atrial function, right ventricular function, ventricular-arterial coupling, chronotropic reserve and myocardial fibrosis. Automated clustering separated a distinct subgroup characterized by a relatively isolated impairment of LV systolic reserve. The clinical factors identified by this process were used to define two phenotypes of patients with symptomatic HFpEF: those with reduced chronotropic and/or diastolic reserve (abnormal CR/DR; n=137) and those with preserved heart rate reserve and exertional E/e' ratio<14 (normal CR/DR; n=40). Change in global LV strain rate from rest to exercise was similar in patients with abnormal CR/DR (0.16±0.18sec-1) and those with normal CR/DR (0.21±0.17sec-1) and significantly lower than in asymptomatic subjects (0.54±0.20sec-1; P<.001 for all). However, although the former group also showed abnormal longitudinal deformation, ventricular-arterial coupling, and cardiac output responses to exercise, the latter group showed only reduced LV systolic reserve. The normal CR/DR group had a lower incidence of cardiovascular hospitalization or death (P=.003) and heart failure hospitalization (P=.002) than the abnormal CR/DR group during 2-year follow-up. Diminished LV systolic reserve may represent the major identifiable cardiac functional abnormality associated with exercise intolerance in some patients with HFpEF. Despite significant functional limitation, these patients are characterized by a better prognosis than subjects with HFpEF with more physiologic abnormalities.

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