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Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome
Fragile X syndrome (FXS) and Rett syndrome (RTT) are developmental disorders currently not diagnosed before toddlerhood. Even though speech-language deficits are among the key symptoms of both conditions, little is known about infant vocalisation acoustics for an automatic earlier identification of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349308/ https://www.ncbi.nlm.nih.gov/pubmed/35922535 http://dx.doi.org/10.1038/s41598-022-17203-1 |
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author | Pokorny, Florian B. Schmitt, Maximilian Egger, Mathias Bartl-Pokorny, Katrin D. Zhang, Dajie Schuller, Björn W. Marschik, Peter B. |
author_facet | Pokorny, Florian B. Schmitt, Maximilian Egger, Mathias Bartl-Pokorny, Katrin D. Zhang, Dajie Schuller, Björn W. Marschik, Peter B. |
author_sort | Pokorny, Florian B. |
collection | PubMed |
description | Fragile X syndrome (FXS) and Rett syndrome (RTT) are developmental disorders currently not diagnosed before toddlerhood. Even though speech-language deficits are among the key symptoms of both conditions, little is known about infant vocalisation acoustics for an automatic earlier identification of affected individuals. To bridge this gap, we applied intelligent audio analysis methodology to a compact dataset of 4454 home-recorded vocalisations of 3 individuals with FXS and 3 individuals with RTT aged 6 to 11 months, as well as 6 age- and gender-matched typically developing controls (TD). On the basis of a standardised set of 88 acoustic features, we trained linear kernel support vector machines to evaluate the feasibility of automatic classification of (a) FXS vs TD, (b) RTT vs TD, (c) atypical development (FXS+RTT) vs TD, and (d) FXS vs RTT vs TD. In paradigms (a)–(c), all infants were correctly classified; in paradigm (d), 9 of 12 were so. Spectral/cepstral and energy-related features were most relevant for classification across all paradigms. Despite the small sample size, this study reveals new insights into early vocalisation characteristics in FXS and RTT, and provides technical underpinnings for a future earlier identification of affected individuals, enabling earlier intervention and family counselling. |
format | Online Article Text |
id | pubmed-9349308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93493082022-08-05 Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome Pokorny, Florian B. Schmitt, Maximilian Egger, Mathias Bartl-Pokorny, Katrin D. Zhang, Dajie Schuller, Björn W. Marschik, Peter B. Sci Rep Article Fragile X syndrome (FXS) and Rett syndrome (RTT) are developmental disorders currently not diagnosed before toddlerhood. Even though speech-language deficits are among the key symptoms of both conditions, little is known about infant vocalisation acoustics for an automatic earlier identification of affected individuals. To bridge this gap, we applied intelligent audio analysis methodology to a compact dataset of 4454 home-recorded vocalisations of 3 individuals with FXS and 3 individuals with RTT aged 6 to 11 months, as well as 6 age- and gender-matched typically developing controls (TD). On the basis of a standardised set of 88 acoustic features, we trained linear kernel support vector machines to evaluate the feasibility of automatic classification of (a) FXS vs TD, (b) RTT vs TD, (c) atypical development (FXS+RTT) vs TD, and (d) FXS vs RTT vs TD. In paradigms (a)–(c), all infants were correctly classified; in paradigm (d), 9 of 12 were so. Spectral/cepstral and energy-related features were most relevant for classification across all paradigms. Despite the small sample size, this study reveals new insights into early vocalisation characteristics in FXS and RTT, and provides technical underpinnings for a future earlier identification of affected individuals, enabling earlier intervention and family counselling. Nature Publishing Group UK 2022-08-03 /pmc/articles/PMC9349308/ /pubmed/35922535 http://dx.doi.org/10.1038/s41598-022-17203-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Article Pokorny, Florian B. Schmitt, Maximilian Egger, Mathias Bartl-Pokorny, Katrin D. Zhang, Dajie Schuller, Björn W. Marschik, Peter B. Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome |
title | Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome |
title_full | Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome |
title_fullStr | Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome |
title_full_unstemmed | Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome |
title_short | Automatic vocalisation-based detection of fragile X syndrome and Rett syndrome |
title_sort | automatic vocalisation-based detection of fragile x syndrome and rett syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349308/ https://www.ncbi.nlm.nih.gov/pubmed/35922535 http://dx.doi.org/10.1038/s41598-022-17203-1 |
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