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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...

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Autores principales: Sarica, Alessia, Aracri, Federica, Bianco, Maria Giovanna, Arcuri, Fulvia, Quattrone, Andrea, Quattrone, Aldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
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.
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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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