Artificial intelligence to improve ischemia prediction in Rubidium Positron Emission Tomography-a validation study.

Artificial intelligence Coronary artery disease (CAD) Gatekeeper Improved individual outcome Ischemia Patient stratification Positron emission tomography (PET) Predictive preventive personalised medicine (PPPM/3PM) Pretest probability (PTP) Risk stratification

Journal

The EPMA journal
ISSN: 1878-5077
Titre abrégé: EPMA J
Pays: Switzerland
ID NLM: 101517307

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 22 07 2023
accepted: 14 10 2023
medline: 14 12 2023
pubmed: 14 12 2023
entrez: 14 12 2023
Statut: epublish

Résumé

Patients are referred to functional coronary artery disease (CAD) testing based on their pre-test probability (PTP) to search for myocardial ischemia. The recommended prediction tools incorporate three variables (symptoms, age, sex) and are easy to use, but have a limited diagnostic accuracy. Hence, a substantial proportion of non-invasive functional tests reveal no myocardial ischemia, leading to unnecessary radiation exposure and costs. Therefore, preselection of patients before ischemia testing needs to be improved using a more predictive and personalised approach. Using multiple variables (symptoms, vitals, ECG, biomarkers), artificial intelligence-based tools can provide a detailed and individualised profile of each patient. This could improve PTP assessment and provide a more personalised diagnostic approach in the framework of predictive, preventive and personalised medicine (PPPM). Consecutive patients ( Ischemia was present in 37.1%. The MPA model was most accurate to predict ischemia (AUC: 0.758, The MPA model enhanced ischemia testing according to the PPPM framework:The MPA model improved individual prediction of ischemia significantly and could safely exclude ischemia based on readily available variables without advanced testing ("predictive").It reduced the proportion of patients in the intermediate PTP range. Therefore, it could be used as a gatekeeper to prevent patients from further unnecessary downstream testing, radiation exposure and costs ("preventive").Consequently, the MPA model could transform ischemia testing towards a more personalised diagnostic algorithm ("personalised"). The online version contains supplementary material available at 10.1007/s13167-023-00341-5.

Sections du résumé

Background UNASSIGNED
Patients are referred to functional coronary artery disease (CAD) testing based on their pre-test probability (PTP) to search for myocardial ischemia. The recommended prediction tools incorporate three variables (symptoms, age, sex) and are easy to use, but have a limited diagnostic accuracy. Hence, a substantial proportion of non-invasive functional tests reveal no myocardial ischemia, leading to unnecessary radiation exposure and costs. Therefore, preselection of patients before ischemia testing needs to be improved using a more predictive and personalised approach.
Aims UNASSIGNED
Using multiple variables (symptoms, vitals, ECG, biomarkers), artificial intelligence-based tools can provide a detailed and individualised profile of each patient. This could improve PTP assessment and provide a more personalised diagnostic approach in the framework of predictive, preventive and personalised medicine (PPPM).
Methods UNASSIGNED
Consecutive patients (
Results UNASSIGNED
Ischemia was present in 37.1%. The MPA model was most accurate to predict ischemia (AUC: 0.758,
Conclusion UNASSIGNED
The MPA model enhanced ischemia testing according to the PPPM framework:The MPA model improved individual prediction of ischemia significantly and could safely exclude ischemia based on readily available variables without advanced testing ("predictive").It reduced the proportion of patients in the intermediate PTP range. Therefore, it could be used as a gatekeeper to prevent patients from further unnecessary downstream testing, radiation exposure and costs ("preventive").Consequently, the MPA model could transform ischemia testing towards a more personalised diagnostic algorithm ("personalised").
Supplementary Information UNASSIGNED
The online version contains supplementary material available at 10.1007/s13167-023-00341-5.

Identifiants

pubmed: 38094578
doi: 10.1007/s13167-023-00341-5
pii: 341
pmc: PMC10713509
doi:

Types de publication

Journal Article

Langues

eng

Pagination

631-643

Informations de copyright

© The Author(s) 2023.

Déclaration de conflit d'intérêts

Competing interestsSimon M. Frey: nothing to declare. Adam Bakula: nothing to declare. Andrew Tsirkin: head modeling and development of Exploris Health. Vasily Vasilchenko: developer of MPA model at Exploris Health. Peter Ruff: CEO of Exploris Health, stock owner Exploris Health. Caroline Oehri: chief operating officer at Exploris Health, stock owner Exploris Health. Melissa F. Amrein: nothing to declare. Gabrielle Huré: nothing to declare. Klara Rumora: nothing to declare. Ibrahim Schäfer: nothing to declare. Federico Caobelli: nothing to declare. Philip Haaf: nothing to declare. Christian E. Mueller: no conflict of interest to declare regarding this project. Dr. Mueller has received research support from the Swiss National Science Foundation, the Swiss Heart Foundation, the KTI, the University Hospital Basel, the University of Basel, Abbott, Astra Zeneca, Beckman Coulter, Idorsia, Novartis, Ortho Diagnostics, Quidel, Roche, Siemens, Singulex, SpinChip and Sphingotec, as well as speaker honoraria/consulting honoraria from Amgen, Astra Zeneca, Bayer, Boehringer Ingelheim, BMS, Idorsia, Novartis, Osler, Roche, Sanofi and SpinChip. Bjoern Andrew Remppis: advisory board member Exploris Health. Hans-Peter Brunner-La Rocca: advisory board member Exploris Health, stock owner Exploris Health, unrestricted research grant by and advisor to Roche Diagnostics. Michael J. Zellweger: advisory board member Exploris Health, stock owner Exploris Health.

Auteurs

Simon M Frey (SM)

Department of Cardiology, University Hospital Basel, University of Basel, Petersgraben 4, CH-4031 Basel, Switzerland.
Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Adam Bakula (A)

Department of Cardiology, University Hospital Basel, University of Basel, Petersgraben 4, CH-4031 Basel, Switzerland.
University Hospital Bern, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Andrew Tsirkin (A)

Exploris Health AG, Industriestrasse 44, CH-8304 Wallisellen, Switzerland.

Vasily Vasilchenko (V)

Exploris Health AG, Industriestrasse 44, CH-8304 Wallisellen, Switzerland.

Peter Ruff (P)

Exploris Health AG, Industriestrasse 44, CH-8304 Wallisellen, Switzerland.

Caroline Oehri (C)

Exploris Health AG, Industriestrasse 44, CH-8304 Wallisellen, Switzerland.

Melissa Fee Amrein (MF)

Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Gabrielle Huré (G)

Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Klara Rumora (K)

Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Ibrahim Schäfer (I)

Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Federico Caobelli (F)

Department of Cardiology, University Hospital Basel, University of Basel, Petersgraben 4, CH-4031 Basel, Switzerland.
University Hospital Bern, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.

Philip Haaf (P)

Department of Cardiology, University Hospital Basel, University of Basel, Petersgraben 4, CH-4031 Basel, Switzerland.
Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Christian E Mueller (CE)

Department of Cardiology, University Hospital Basel, University of Basel, Petersgraben 4, CH-4031 Basel, Switzerland.
Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Bjoern Andrew Remppis (BA)

Department of Cardiology, Herz- Und Gefässzentrum Bad Bevensen, Römstedter Straße 25, 29549 Bad Bevensen, Germany.

Hans-Peter Brunner-La Rocca (HB)

Department of Cardiology, Maastricht UMC+, Minderbroedersberg 4-6, Maastricht, 6211 LK The Netherlands.

Michael J Zellweger (MJ)

Department of Cardiology, University Hospital Basel, University of Basel, Petersgraben 4, CH-4031 Basel, Switzerland.
Cardiovascular Research Institute Basel (CRIB), University Hospital Basel, University of Basel, Spitalstrasse 2, CH-4056 Basel, Switzerland.

Classifications MeSH