Multiomics, virtual reality and artificial intelligence in heart failure

Author:

Gladding Patrick A1ORCID,Loader Suzanne1,Smith Kevin2,Zarate Erica3,Green Saras3,Villas-Boas Silas3,Shepherd Phillip4,Kakadiya Purvi4,Hewitt Will5,Thorstensen Eric6,Keven Christine6,Coe Margaret6,Nakisa Bahareh7,Vuong Tan7,Rastgoo Mohammad Naim8,Jüllig Mia9,Starc Vito10,Schlegel Todd T1112

Affiliation:

1. Department of Cardiology, Waitemata District Health Board, Auckland 0620, New Zealand

2. Clinical Laboratory, Waitemata District Health Board, Auckland 0620, New Zealand

3. School of Biological Science, University of Auckland, Auckland 1010, New Zealand

4. Grafton Genomics Ltd, Liggins Institute, University of Auckland, Auckland 1023, New Zealand

5. Auckland Bioengineering Institute, University of Auckland, Auckland 1010, New Zealand

6. Liggins Institute, University of Auckland, Auckland 1023, New Zealand

7. School of Information Technology, Deakin University, Victoria 3125, Australia

8. School of Electrical Engineering & Computer Science, Queensland University of Technology, Brisbane, QLD 4072, Australia

9. Paper Dog Limited, Waiheke Island, Auckland 1081, New Zealand

10. Faculty of Medicine, University of Ljubljana, Ljubljana 1000, Slovenia

11. Karolinska Institutet, Stockholm, Sweden 171 77, Switzerland

12. Nicollier-Schlegel Sàrl, Trélex, Karolinaka 1270, Switzerland

Abstract

Aim: Multiomics delivers more biological insight than targeted investigations. We applied multiomics to patients with heart failure (HF) and reduced ejection fraction (HFrEF), with machine learning applied to advanced ECG (AECG) and echocardiography artificial intelligence (Echo AI). Patients & methods: In total, 46 patients with HFrEF and 20 controls underwent metabolomic profiling, including liquid/gas chromatography–mass spectrometry and solid-phase microextraction volatilomics in plasma and urine. HFrEF was defined using left ventricular (LV) global longitudinal strain, EF and N-terminal pro hormone BNP. AECG and Echo AI were performed over 5 min, with a subset of patients undergoing a virtual reality mental stress test. Results: A-ECG had similar diagnostic accuracy as N-terminal pro hormone BNP for HFrEF (area under the curve = 0.95, 95% CI: 0.85–0.99), and correlated with global longitudinal strain (r = -0.77, p < 0.0001), while Echo AI-generated measurements correlated well with manually measured LV end diastolic volume r = 0.77, LV end systolic volume r = 0.8, LVEF r = 0.71, indexed left atrium volume r = 0.71 and indexed LV mass r = 0.6, p < 0.005. AI-LVEF and other HFrEF biomarkers had a similar discrimination for HFrEF (area under the curve AI-LVEF = 0.88; 95% CI: -0.03 to 0.15; p = 0.19). Virtual reality mental stress test elicited arrhythmic biomarkers on AECG and indicated blunted autonomic responsiveness (alpha 2 of RR interval variability, p = 1 × 10-4) in HFrEF. Conclusion: Multiomics-related machine learning shows promise for the assessment of HF.

Funder

Health Research Council of New Zealand

Publisher

Future Medicine Ltd

Subject

Cardiology and Cardiovascular Medicine,Molecular Medicine

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