Clusters of multidimensional exercise response patterns and estimated heart failure risk in the Framingham Heart Study

Author:

Miller Patricia E.1,Gajjar Priya2,Mitchell Gary F.3,Khan Sadiya S.4,Vasan Ramachandran S.5678,Larson Martin G.15,Lewis Gregory D.9,Shah Ravi V.10,Nayor Matthew2511ORCID

Affiliation:

1. Department of Biostatistics Boston University School of Public Health Boston MA USA

2. Section of Cardiovascular Medicine, Department of Medicine Boston University School of Medicine Boston MA USA

3. Cardiovascular Engineering, Inc. Norwood MA USA

4. Division of Cardiology, Department of Medicine and Preventive Medicine Northwestern University Feinberg School of Medicine Chicago IL USA

5. Boston University's and NHLBI's Framingham Heart Study Framingham MA USA

6. University of Texas School of Public Health San Antonio San Antonio TX USA

7. Department of Medicine University of Texas Health Science Center San Antonio TX USA

8. Department of Population Health Sciences University of Texas Health Science Center San Antonio TX USA

9. Division of Cardiology, Cardiovascular Research Center, and Pulmonary Critical Care Unit, Department of Medicine Massachusetts General Hospital, Harvard Medical School Boston MA USA

10. Division of Cardiology, Vanderbilt Translational and Clinical Research Center Vanderbilt University Medical Center Nashville TN USA

11. Section of Preventive Medicine and Epidemiology, Department of Medicine Boston University School of Medicine 72 E Concord Street, Suite L‐516 Boston MA 02118 USA

Abstract

AbstractAimsNew tools are needed to identify heart failure (HF) risk earlier in its course. We evaluated the association of multidimensional cardiopulmonary exercise testing (CPET) phenotypes with subclinical risk markers and predicted long‐term HF risk in a large community‐based cohort.Methods and resultsWe studied 2532 Framingham Heart Study participants [age 53 ± 9 years, 52% women, body mass index (BMI) 28.0 ± 5.3 kg/m2, peak oxygen uptake (VO2) 21.1 ± 5.9 kg/m2 in women, 26.4 ± 6.7 kg/m2 in men] who underwent maximum effort CPET and were not taking atrioventricular nodal blocking agents. Higher peak VO2 was associated with a lower estimated HF risk score (Spearman correlation r: −0.60 in men and −0.55 in women, P < 0.0001), with an observed overlap of estimated risk across peak VO2 categories. Hierarchical clustering of 26 separate CPET phenotypes (values residualized on age, sex, and BMI to provide uniformity across these variables) identified three clusters with distinct exercise physiologies: Cluster 1—impaired oxygen kinetics; Cluster 2—impaired vascular; and Cluster 3—favourable exercise response. These clusters were similar in age, sex distribution, and BMI but displayed distinct associations with relevant subclinical phenotypes [Cluster 1—higher subcutaneous and visceral fat and lower pulmonary function; Cluster 2—higher carotid‐femoral pulse wave velocity (CFPWV); and Cluster 3—lower CFPWV, C‐reactive protein, fat volumes, and higher lung function; all false discovery rate < 5%]. Cluster membership provided incremental variance explained (adjusted R2 increment of 0.10 in women and men, P < 0.0001 for both) when compared with peak VO2 alone in association with predicted HF risk.ConclusionsIntegrated CPET response patterns identify physiologically relevant profiles with distinct associations to subclinical phenotypes that are largely independent of standard risk factor‐based assessment, which may suggest alternate pathways for prevention.

Funder

National Heart, Lung, and Blood Institute

National Institutes of Health

American Heart Association

Department of Orthopaedic Surgery, Boston University School of Medicine

Publisher

Wiley

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