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Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia
Negative symptoms are a transdiagnostic feature of serious mental illness (SMI) that can be potentially “digitally phenotyped” using objective vocal analysis. In prior studies, vocal measures show low convergence with clinical ratings, potentially because analysis has used small, constrained acousti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519104/ https://www.ncbi.nlm.nih.gov/pubmed/32978400 http://dx.doi.org/10.1038/s41537-020-00115-2 |
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author | Cohen, Alex S. Cox, Christopher R. Le, Thanh P. Cowan, Tovah Masucci, Michael D. Strauss, Gregory P. Kirkpatrick, Brian |
author_facet | Cohen, Alex S. Cox, Christopher R. Le, Thanh P. Cowan, Tovah Masucci, Michael D. Strauss, Gregory P. Kirkpatrick, Brian |
author_sort | Cohen, Alex S. |
collection | PubMed |
description | Negative symptoms are a transdiagnostic feature of serious mental illness (SMI) that can be potentially “digitally phenotyped” using objective vocal analysis. In prior studies, vocal measures show low convergence with clinical ratings, potentially because analysis has used small, constrained acoustic feature sets. We sought to evaluate (1) whether clinically rated blunted vocal affect (BvA)/alogia could be accurately modelled using machine learning (ML) with a large feature set from two separate tasks (i.e., a 20-s “picture” and a 60-s “free-recall” task), (2) whether “Predicted” BvA/alogia (computed from the ML model) are associated with demographics, diagnosis, psychiatric symptoms, and cognitive/social functioning, and (3) which key vocal features are central to BvA/Alogia ratings. Accuracy was high (>90%) and was improved when computed separately by speaking task. ML scores were associated with poor cognitive performance and social functioning and were higher in patients with schizophrenia versus depression or mania diagnoses. However, the features identified as most predictive of BvA/Alogia were generally not considered critical to their operational definitions. Implications for validating and implementing digital phenotyping to reduce SMI burden are discussed. |
format | Online Article Text |
id | pubmed-7519104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75191042020-10-14 Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia Cohen, Alex S. Cox, Christopher R. Le, Thanh P. Cowan, Tovah Masucci, Michael D. Strauss, Gregory P. Kirkpatrick, Brian NPJ Schizophr Article Negative symptoms are a transdiagnostic feature of serious mental illness (SMI) that can be potentially “digitally phenotyped” using objective vocal analysis. In prior studies, vocal measures show low convergence with clinical ratings, potentially because analysis has used small, constrained acoustic feature sets. We sought to evaluate (1) whether clinically rated blunted vocal affect (BvA)/alogia could be accurately modelled using machine learning (ML) with a large feature set from two separate tasks (i.e., a 20-s “picture” and a 60-s “free-recall” task), (2) whether “Predicted” BvA/alogia (computed from the ML model) are associated with demographics, diagnosis, psychiatric symptoms, and cognitive/social functioning, and (3) which key vocal features are central to BvA/Alogia ratings. Accuracy was high (>90%) and was improved when computed separately by speaking task. ML scores were associated with poor cognitive performance and social functioning and were higher in patients with schizophrenia versus depression or mania diagnoses. However, the features identified as most predictive of BvA/Alogia were generally not considered critical to their operational definitions. Implications for validating and implementing digital phenotyping to reduce SMI burden are discussed. Nature Publishing Group UK 2020-09-25 /pmc/articles/PMC7519104/ /pubmed/32978400 http://dx.doi.org/10.1038/s41537-020-00115-2 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cohen, Alex S. Cox, Christopher R. Le, Thanh P. Cowan, Tovah Masucci, Michael D. Strauss, Gregory P. Kirkpatrick, Brian Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia |
title | Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia |
title_full | Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia |
title_fullStr | Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia |
title_full_unstemmed | Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia |
title_short | Using machine learning of computerized vocal expression to measure blunted vocal affect and alogia |
title_sort | using machine learning of computerized vocal expression to measure blunted vocal affect and alogia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519104/ https://www.ncbi.nlm.nih.gov/pubmed/32978400 http://dx.doi.org/10.1038/s41537-020-00115-2 |
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