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Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease
Random Survival Forests (RSF) has recently showed better performance than statistical survival methods as Cox proportional hazard (CPH) in predicting conversion risk from mild cognitive impairment (MCI) to Alzheimer’s disease (AD). However, RSF application in real-world clinical setting is still lim...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657350/ https://www.ncbi.nlm.nih.gov/pubmed/37979033 http://dx.doi.org/10.1186/s40708-023-00211-w |
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author | Sarica, Alessia Aracri, Federica Bianco, Maria Giovanna Arcuri, Fulvia Quattrone, Andrea Quattrone, Aldo |
author_facet | Sarica, Alessia Aracri, Federica Bianco, Maria Giovanna Arcuri, Fulvia Quattrone, Andrea Quattrone, Aldo |
author_sort | Sarica, Alessia |
collection | PubMed |
description | Random Survival Forests (RSF) has recently showed better performance than statistical survival methods as Cox proportional hazard (CPH) in predicting conversion risk from mild cognitive impairment (MCI) to Alzheimer’s disease (AD). However, RSF application in real-world clinical setting is still limited due to its black-box nature. For this reason, we aimed at providing a comprehensive study of RSF explainability with SHapley Additive exPlanations (SHAP) on biomarkers of stable and progressive patients (sMCI and pMCI) from Alzheimer’s Disease Neuroimaging Initiative. We evaluated three global explanations—RSF feature importance, permutation importance and SHAP importance—and we quantitatively compared them with Rank-Biased Overlap (RBO). Moreover, we assessed whether multicollinearity among variables may perturb SHAP outcome. Lastly, we stratified pMCI test patients in high, medium and low risk grade, to investigate individual SHAP explanation of one pMCI patient per risk group. We confirmed that RSF had higher accuracy (0.890) than CPH (0.819), and its stability and robustness was demonstrated by high overlap (RBO > 90%) between feature rankings within first eight features. SHAP local explanations with and without correlated variables had no substantial difference, showing that multicollinearity did not alter the model. FDG, ABETA42 and HCI were the first important features in global explanations, with the highest contribution also in local explanation. FAQ, mPACCdigit, mPACCtrailsB and RAVLT immediate had the highest influence among all clinical and neuropsychological assessments in increasing progression risk, as particularly evident in pMCI patients’ individual explanation. In conclusion, our findings suggest that RSF represents a useful tool to support clinicians in estimating conversion-to-AD risk and that SHAP explainer boosts its clinical utility with intelligible and interpretable individual outcomes that highlights key features associated with AD prognosis. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40708-023-00211-w. |
format | Online Article Text |
id | pubmed-10657350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-106573502023-11-18 Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease Sarica, Alessia Aracri, Federica Bianco, Maria Giovanna Arcuri, Fulvia Quattrone, Andrea Quattrone, Aldo Brain Inform Research Random Survival Forests (RSF) has recently showed better performance than statistical survival methods as Cox proportional hazard (CPH) in predicting conversion risk from mild cognitive impairment (MCI) to Alzheimer’s disease (AD). However, RSF application in real-world clinical setting is still limited due to its black-box nature. For this reason, we aimed at providing a comprehensive study of RSF explainability with SHapley Additive exPlanations (SHAP) on biomarkers of stable and progressive patients (sMCI and pMCI) from Alzheimer’s Disease Neuroimaging Initiative. We evaluated three global explanations—RSF feature importance, permutation importance and SHAP importance—and we quantitatively compared them with Rank-Biased Overlap (RBO). Moreover, we assessed whether multicollinearity among variables may perturb SHAP outcome. Lastly, we stratified pMCI test patients in high, medium and low risk grade, to investigate individual SHAP explanation of one pMCI patient per risk group. We confirmed that RSF had higher accuracy (0.890) than CPH (0.819), and its stability and robustness was demonstrated by high overlap (RBO > 90%) between feature rankings within first eight features. SHAP local explanations with and without correlated variables had no substantial difference, showing that multicollinearity did not alter the model. FDG, ABETA42 and HCI were the first important features in global explanations, with the highest contribution also in local explanation. FAQ, mPACCdigit, mPACCtrailsB and RAVLT immediate had the highest influence among all clinical and neuropsychological assessments in increasing progression risk, as particularly evident in pMCI patients’ individual explanation. In conclusion, our findings suggest that RSF represents a useful tool to support clinicians in estimating conversion-to-AD risk and that SHAP explainer boosts its clinical utility with intelligible and interpretable individual outcomes that highlights key features associated with AD prognosis. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40708-023-00211-w. Springer Berlin Heidelberg 2023-11-18 /pmc/articles/PMC10657350/ /pubmed/37979033 http://dx.doi.org/10.1186/s40708-023-00211-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Sarica, Alessia Aracri, Federica Bianco, Maria Giovanna Arcuri, Fulvia Quattrone, Andrea Quattrone, Aldo Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease |
title | Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease |
title_full | Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease |
title_fullStr | Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease |
title_full_unstemmed | Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease |
title_short | Explainability of random survival forests in predicting conversion risk from mild cognitive impairment to Alzheimer’s disease |
title_sort | explainability of random survival forests in predicting conversion risk from mild cognitive impairment to alzheimer’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657350/ https://www.ncbi.nlm.nih.gov/pubmed/37979033 http://dx.doi.org/10.1186/s40708-023-00211-w |
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