Integrative Interpretation of Cardiopulmonary Exercise Tests for Cardiovascular Outcome Prediction: A Machine Learning Approach

Author:

Cauwenberghs Nicholas1ORCID,Sente Josephine1,Van Criekinge Hanne1,Sabovčik František1ORCID,Ntalianis Evangelos1,Haddad Francois2,Claes Jomme3ORCID,Claessen Guido45,Budts Werner6,Goetschalckx Kaatje7ORCID,Cornelissen Véronique3ORCID,Kuznetsova Tatiana1ORCID

Affiliation:

1. Hypertension and Cardiovascular Epidemiology, Department of Cardiovascular Sciences, University of Leuven, 3000 Leuven, Belgium

2. Stanford Cardiovascular Institute and Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA

3. Rehabilitation in Internal Disorders, Department of Rehabilitation Sciences, University of Leuven, 3001 Leuven, Belgium

4. Department of Cardiology, Hartcentrum, Virga Jessa Hospital, 3500 Hasselt, Belgium

5. Faculty of Medicine and Life Sciences, Hasselt University, 3500 Hasselt, Belgium

6. Cardiology, Department of Cardiovascular Sciences, University of Leuven, 3000 Leuven, Belgium

7. Cardiovascular Imaging and Dynamics, Department of Cardiovascular Sciences, University of Leuven, 3000 Leuven, Belgium

Abstract

Integrative interpretation of cardiopulmonary exercise tests (CPETs) may improve assessment of cardiovascular (CV) risk. Here, we identified patient phenogroups based on CPET summary metrics and evaluated their predictive value for CV events. We included 2280 patients with diverse CV risk who underwent maximal CPET by cycle ergometry. Key CPET indices and information on incident CV events (median follow-up time: 5.3 years) were derived. Next, we applied unsupervised clustering by Gaussian Mixture modeling to subdivide the cohort into four male and four female phenogroups solely based on differences in CPET metrics. Ten of 18 CPET metrics were used for clustering as eight were removed due to high collinearity. In males and females, the phenogroups differed significantly in age, BMI, blood pressure, disease prevalence, medication intake and spirometry. In males, phenogroups 3 and 4 presented a significantly higher risk for incident CV events than phenogroup 1 (multivariable-adjusted hazard ratio: 1.51 and 2.19; p ≤ 0.048). In females, differences in the risk for future CV events between the phenogroups were not significant after adjustment for clinical covariables. Integrative CPET-based phenogrouping, thus, adequately stratified male patients according to CV risk. CPET phenomapping may facilitate comprehensive evaluation of CPET results and steer CV risk stratification and management.

Funder

Research Foundation Flanders

Research Council KU Leuven

Publisher

MDPI AG

Subject

Clinical Biochemistry

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