Language function following preterm birth: prediction using machine learning.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
08 2022
Historique:
received: 20 04 2021
accepted: 12 09 2021
revised: 04 08 2021
pubmed: 13 10 2021
medline: 4 10 2022
entrez: 12 10 2021
Statut: ppublish

Résumé

Preterm birth can lead to impaired language development. This study aimed to predict language outcomes at 2 years corrected gestational age (CGA) for children born preterm. We analysed data from 89 preterm neonates (median GA 29 weeks) who underwent diffusion MRI (dMRI) at term-equivalent age and language assessment at 2 years CGA using the Bayley-III. Feature selection and a random forests classifier were used to differentiate typical versus delayed (Bayley-III language composite score <85) language development. The model achieved balanced accuracy: 91%, sensitivity: 86%, and specificity: 96%. The probability of language delay at 2 years CGA is increased with: increasing values of peak width of skeletonized fractional anisotropy (PSFA), radial diffusivity (PSRD), and axial diffusivity (PSAD) derived from dMRI; among twins; and after an incomplete course of, or no exposure to, antenatal corticosteroids. Female sex and breastfeeding during the neonatal period reduced the risk of language delay. The combination of perinatal clinical information and MRI features leads to accurate prediction of preterm infants who are likely to develop language deficits in early childhood. This model could potentially enable stratification of preterm children at risk of language dysfunction who may benefit from targeted early interventions. A combination of clinical perinatal factors and neonatal DTI measures of white matter microstructure leads to accurate prediction of language outcome at 2 years corrected gestational age following preterm birth. A model that comprises clinical and MRI features that has potential to be scalable across centres. It offers a basis for enhancing the power and generalizability of diagnostic and prognostic studies of neurodevelopmental disorders associated with language impairment. Early identification of infants who are at risk of language delay, facilitating targeted early interventions and support services, which could improve the quality of life for children born preterm.

Sections du résumé

BACKGROUND
Preterm birth can lead to impaired language development. This study aimed to predict language outcomes at 2 years corrected gestational age (CGA) for children born preterm.
METHODS
We analysed data from 89 preterm neonates (median GA 29 weeks) who underwent diffusion MRI (dMRI) at term-equivalent age and language assessment at 2 years CGA using the Bayley-III. Feature selection and a random forests classifier were used to differentiate typical versus delayed (Bayley-III language composite score <85) language development.
RESULTS
The model achieved balanced accuracy: 91%, sensitivity: 86%, and specificity: 96%. The probability of language delay at 2 years CGA is increased with: increasing values of peak width of skeletonized fractional anisotropy (PSFA), radial diffusivity (PSRD), and axial diffusivity (PSAD) derived from dMRI; among twins; and after an incomplete course of, or no exposure to, antenatal corticosteroids. Female sex and breastfeeding during the neonatal period reduced the risk of language delay.
CONCLUSIONS
The combination of perinatal clinical information and MRI features leads to accurate prediction of preterm infants who are likely to develop language deficits in early childhood. This model could potentially enable stratification of preterm children at risk of language dysfunction who may benefit from targeted early interventions.
IMPACT
A combination of clinical perinatal factors and neonatal DTI measures of white matter microstructure leads to accurate prediction of language outcome at 2 years corrected gestational age following preterm birth. A model that comprises clinical and MRI features that has potential to be scalable across centres. It offers a basis for enhancing the power and generalizability of diagnostic and prognostic studies of neurodevelopmental disorders associated with language impairment. Early identification of infants who are at risk of language delay, facilitating targeted early interventions and support services, which could improve the quality of life for children born preterm.

Identifiants

pubmed: 34635792
doi: 10.1038/s41390-021-01779-x
pii: 10.1038/s41390-021-01779-x
pmc: PMC8503721
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

480-489

Subventions

Organisme : Medical Research Council
ID : G1002033
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom
Organisme : Chief Scientist Office
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© 2021. Crown.

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Auteurs

Evdoxia Valavani (E)

Usher Institute, Medical School, University of Edinburgh, Edinburgh, UK. evdoxia.valavani@ed.ac.uk.

Manuel Blesa (M)

MRC Centre for Reproductive Health, University of Edinburgh, Edinburgh, UK.

Paola Galdi (P)

MRC Centre for Reproductive Health, University of Edinburgh, Edinburgh, UK.

Gemma Sullivan (G)

MRC Centre for Reproductive Health, University of Edinburgh, Edinburgh, UK.

Bethan Dean (B)

MRC Centre for Reproductive Health, University of Edinburgh, Edinburgh, UK.

Hilary Cruickshank (H)

NHS Lothian-Neonatal Physiotherapy, Royal Infirmary of Edinburgh, Edinburgh, UK.

Magdalena Sitko-Rudnicka (M)

NHS Lothian-Neonatology, Royal Infirmary of Edinburgh, Edinburgh, UK.

Mark E Bastin (ME)

Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

Richard F M Chin (RFM)

Muir Maxwell Epilepsy Centre, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Royal Hospital for Sick Children, Edinburgh, UK.

Donald J MacIntyre (DJ)

Division of Psychiatry, Deanery of Clinical Sciences, Royal Edinburgh Hospital, University of Edinburgh, Edinburgh, UK.

Sue Fletcher-Watson (S)

Salvesen Mindroom Research Centre, University of Edinburgh, Edinburgh, UK.

James P Boardman (JP)

MRC Centre for Reproductive Health, University of Edinburgh, Edinburgh, UK.
Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

Athanasios Tsanas (A)

Usher Institute, Medical School, University of Edinburgh, Edinburgh, UK.

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