Cargando…

Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach

BACKGROUND: Genomic conditions can be associated with developmental delay, intellectual disability, autism spectrum disorder, and physical and mental health symptoms. They are individually rare and highly variable in presentation, which limits the use of standard clinical guidelines for diagnosis an...

Descripción completa

Detalles Bibliográficos
Autores principales: Donnelly, Nicholas, Cunningham, Adam, Salas, Sergio Marco, Bracher-Smith, Matthew, Chawner, Samuel, Stochl, Jan, Ford, Tamsin, Raymond, F. Lucy, Escott-Price, Valentina, van den Bree, Marianne B. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207854/
https://www.ncbi.nlm.nih.gov/pubmed/37221545
http://dx.doi.org/10.1186/s13229-023-00549-2
_version_ 1785046545715953664
author Donnelly, Nicholas
Cunningham, Adam
Salas, Sergio Marco
Bracher-Smith, Matthew
Chawner, Samuel
Stochl, Jan
Ford, Tamsin
Raymond, F. Lucy
Escott-Price, Valentina
van den Bree, Marianne B. M.
author_facet Donnelly, Nicholas
Cunningham, Adam
Salas, Sergio Marco
Bracher-Smith, Matthew
Chawner, Samuel
Stochl, Jan
Ford, Tamsin
Raymond, F. Lucy
Escott-Price, Valentina
van den Bree, Marianne B. M.
author_sort Donnelly, Nicholas
collection PubMed
description BACKGROUND: Genomic conditions can be associated with developmental delay, intellectual disability, autism spectrum disorder, and physical and mental health symptoms. They are individually rare and highly variable in presentation, which limits the use of standard clinical guidelines for diagnosis and treatment. A simple screening tool to identify young people with genomic conditions associated with neurodevelopmental disorders (ND-GCs) who could benefit from further support would be of considerable value. We used machine learning approaches to address this question. METHOD: A total of 493 individuals were included: 389 with a ND-GC, mean age = 9.01, 66% male) and 104 siblings without known genomic conditions (controls, mean age = 10.23, 53% male). Primary carers completed assessments of behavioural, neurodevelopmental and psychiatric symptoms and physical health and development. Machine learning techniques (penalised logistic regression, random forests, support vector machines and artificial neural networks) were used to develop classifiers of ND-GC status and identified limited sets of variables that gave the best classification performance. Exploratory graph analysis was used to understand associations within the final variable set. RESULTS: All machine learning methods identified variable sets giving high classification accuracy (AUROC between 0.883 and 0.915). We identified a subset of 30 variables best discriminating between individuals with ND-GCs and controls which formed 5 dimensions: conduct, separation anxiety, situational anxiety, communication and motor development. LIMITATIONS: This study used cross-sectional data from a cohort study which was imbalanced with respect to ND-GC status. Our model requires validation in independent datasets and with longitudinal follow-up data for validation before clinical application. CONCLUSIONS: In this study, we developed models that identified a compact set of psychiatric and physical health measures that differentiate individuals with a ND-GC from controls and highlight higher-order structure within these measures. This work is a step towards developing a screening instrument to identify young people with ND-GCs who might benefit from further specialist assessment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13229-023-00549-2.
format Online
Article
Text
id pubmed-10207854
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-102078542023-05-25 Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach Donnelly, Nicholas Cunningham, Adam Salas, Sergio Marco Bracher-Smith, Matthew Chawner, Samuel Stochl, Jan Ford, Tamsin Raymond, F. Lucy Escott-Price, Valentina van den Bree, Marianne B. M. Mol Autism Research BACKGROUND: Genomic conditions can be associated with developmental delay, intellectual disability, autism spectrum disorder, and physical and mental health symptoms. They are individually rare and highly variable in presentation, which limits the use of standard clinical guidelines for diagnosis and treatment. A simple screening tool to identify young people with genomic conditions associated with neurodevelopmental disorders (ND-GCs) who could benefit from further support would be of considerable value. We used machine learning approaches to address this question. METHOD: A total of 493 individuals were included: 389 with a ND-GC, mean age = 9.01, 66% male) and 104 siblings without known genomic conditions (controls, mean age = 10.23, 53% male). Primary carers completed assessments of behavioural, neurodevelopmental and psychiatric symptoms and physical health and development. Machine learning techniques (penalised logistic regression, random forests, support vector machines and artificial neural networks) were used to develop classifiers of ND-GC status and identified limited sets of variables that gave the best classification performance. Exploratory graph analysis was used to understand associations within the final variable set. RESULTS: All machine learning methods identified variable sets giving high classification accuracy (AUROC between 0.883 and 0.915). We identified a subset of 30 variables best discriminating between individuals with ND-GCs and controls which formed 5 dimensions: conduct, separation anxiety, situational anxiety, communication and motor development. LIMITATIONS: This study used cross-sectional data from a cohort study which was imbalanced with respect to ND-GC status. Our model requires validation in independent datasets and with longitudinal follow-up data for validation before clinical application. CONCLUSIONS: In this study, we developed models that identified a compact set of psychiatric and physical health measures that differentiate individuals with a ND-GC from controls and highlight higher-order structure within these measures. This work is a step towards developing a screening instrument to identify young people with ND-GCs who might benefit from further specialist assessment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13229-023-00549-2. BioMed Central 2023-05-23 /pmc/articles/PMC10207854/ /pubmed/37221545 http://dx.doi.org/10.1186/s13229-023-00549-2 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Donnelly, Nicholas
Cunningham, Adam
Salas, Sergio Marco
Bracher-Smith, Matthew
Chawner, Samuel
Stochl, Jan
Ford, Tamsin
Raymond, F. Lucy
Escott-Price, Valentina
van den Bree, Marianne B. M.
Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
title Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
title_full Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
title_fullStr Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
title_full_unstemmed Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
title_short Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
title_sort identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207854/
https://www.ncbi.nlm.nih.gov/pubmed/37221545
http://dx.doi.org/10.1186/s13229-023-00549-2
work_keys_str_mv AT donnellynicholas identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT cunninghamadam identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT salassergiomarco identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT brachersmithmatthew identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT chawnersamuel identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT stochljan identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT fordtamsin identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT raymondflucy identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT escottpricevalentina identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach
AT vandenbreemariannebm identifyingtheneurodevelopmentalandpsychiatricsignaturesofgenomicdisordersassociatedwithintellectualdisabilityamachinelearningapproach