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Deep neural networks learn by using human-selected electrocardiogram features and novel features
AIMS: We sought to investigate whether artificial intelligence (AI) and specifically deep neural networks (NNs) for electrocardiogram (ECG) signal analysis can be explained using human-selected features. We also sought to quantify such explainability and test if the AI model learns features that are...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707937/ https://www.ncbi.nlm.nih.gov/pubmed/36713603 http://dx.doi.org/10.1093/ehjdh/ztab060 |
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author | Attia, Zachi I Lerman, Gilad Friedman, Paul A |
author_facet | Attia, Zachi I Lerman, Gilad Friedman, Paul A |
author_sort | Attia, Zachi I |
collection | PubMed |
description | AIMS: We sought to investigate whether artificial intelligence (AI) and specifically deep neural networks (NNs) for electrocardiogram (ECG) signal analysis can be explained using human-selected features. We also sought to quantify such explainability and test if the AI model learns features that are similar to a human expert. METHODS AND RESULTS: We used a set of 100 000 ECGs that were annotated by human explainable features. We applied both linear and non-linear models to predict published ECG AI models output for the detection of patients’ age and sex. We further used canonical correlation analysis to quantify the amount of shared information between the NN features and human-selected features. We reconstructed single human-selected ECG features from the unexplained NN features using a simple linear model. We noticed a strong correlation between the simple models and the AI output ([Formula: see text] of 0.49–0.57 for the linear models and [Formula: see text] of 0.69–0.70 for the non-linear models). We found that the correlation of the human explainable features with either 13 of the strongest age AI features or 15 of the strongest sex AI features was above 0.85 (for comparison, the first 14 principal components explain 90% of the human feature variance). We linearly reconstructed single human-selected ECG features from the AI features with [Formula: see text] up to 0.86. CONCLUSION: This work shows that NNs for ECG signals extract features in a similar manner to human experts and that they also generate additional novel features that help achieve superior performance. |
format | Online Article Text |
id | pubmed-9707937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97079372023-01-27 Deep neural networks learn by using human-selected electrocardiogram features and novel features Attia, Zachi I Lerman, Gilad Friedman, Paul A Eur Heart J Digit Health Original Articles AIMS: We sought to investigate whether artificial intelligence (AI) and specifically deep neural networks (NNs) for electrocardiogram (ECG) signal analysis can be explained using human-selected features. We also sought to quantify such explainability and test if the AI model learns features that are similar to a human expert. METHODS AND RESULTS: We used a set of 100 000 ECGs that were annotated by human explainable features. We applied both linear and non-linear models to predict published ECG AI models output for the detection of patients’ age and sex. We further used canonical correlation analysis to quantify the amount of shared information between the NN features and human-selected features. We reconstructed single human-selected ECG features from the unexplained NN features using a simple linear model. We noticed a strong correlation between the simple models and the AI output ([Formula: see text] of 0.49–0.57 for the linear models and [Formula: see text] of 0.69–0.70 for the non-linear models). We found that the correlation of the human explainable features with either 13 of the strongest age AI features or 15 of the strongest sex AI features was above 0.85 (for comparison, the first 14 principal components explain 90% of the human feature variance). We linearly reconstructed single human-selected ECG features from the AI features with [Formula: see text] up to 0.86. CONCLUSION: This work shows that NNs for ECG signals extract features in a similar manner to human experts and that they also generate additional novel features that help achieve superior performance. Oxford University Press 2021-07-17 /pmc/articles/PMC9707937/ /pubmed/36713603 http://dx.doi.org/10.1093/ehjdh/ztab060 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Attia, Zachi I Lerman, Gilad Friedman, Paul A Deep neural networks learn by using human-selected electrocardiogram features and novel features |
title | Deep neural networks learn by using human-selected electrocardiogram features and novel features |
title_full | Deep neural networks learn by using human-selected electrocardiogram features and novel features |
title_fullStr | Deep neural networks learn by using human-selected electrocardiogram features and novel features |
title_full_unstemmed | Deep neural networks learn by using human-selected electrocardiogram features and novel features |
title_short | Deep neural networks learn by using human-selected electrocardiogram features and novel features |
title_sort | deep neural networks learn by using human-selected electrocardiogram features and novel features |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707937/ https://www.ncbi.nlm.nih.gov/pubmed/36713603 http://dx.doi.org/10.1093/ehjdh/ztab060 |
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