4.2 Article

Could a Multi-Marker and Machine Learning Approach Help Stratify Patients with Heart Failure?

期刊

MEDICINA-LITHUANIA
卷 57, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/medicina57100996

关键词

Machine Learning strategy; HFpEF; blood signature; HF patient stratification; multi-marker approach

资金

  1. French Society of Cardiology
  2. NOVARTIS

向作者/读者索取更多资源

This study aimed to stratify HFpEF and HFrEF patients using biochemical markers and clinical data, developing a Machine Learning strategy to distinguish the two groups based on blood signature. Results showed that combining biochemical and clinical markers can be an excellent entry to develop a computer classification tool to diagnose HFpEF.
Half of the patients with heart failure (HF) have preserved ejection fraction (HFpEF). To date, there are no specific markers to distinguish this subgroup. The main objective of this work was to stratify HF patients using current biochemical markers coupled with clinical data. The cohort study included HFpEF (n = 24) and heart failure with reduced ejection fraction (HFrEF) (n = 34) patients as usually considered in clinical practice based on cardiac imaging (EF >= 50% for HFpEF; EF < 50% for HFrEF). Routine blood tests consisted of measuring biomarkers of renal and heart functions, inflammation, and iron metabolism. A multi-test approach and analysis of peripheral blood samples aimed to establish a computerized Machine Learning strategy to provide a blood signature to distinguish HFpEF and HFrEF. Based on logistic regression, demographic characteristics and clinical biomarkers showed no statistical significance to differentiate the HFpEF and HFrEF patient subgroups. Hence a multivariate factorial discriminant analysis, performed blindly using the data set, allowed us to stratify the two HF groups. Consequently, a Machine Learning (ML) strategy was developed using the same variables in a genetic algorithm approach. ML provided very encouraging explorative results when considering the small size of the samples applied. The accuracy and the sensitivity were high for both validation and test groups (69% and 100%, 64% and 75%, respectively). Sensitivity was 100% for the validation and 75% for the test group, whereas specificity was 44% and 55% for the validation and test groups because of the small number of samples. Lastly, the precision was acceptable, with 58% in the validation and 60% in the test group. Combining biochemical and clinical markers is an excellent entry to develop a computer classification tool to diagnose HFpEF. This translational approach is a springboard for improving new personalized treatment methods and identifying high-yield populations for clinical trials.

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