Modelling brain development to detect white matter injury in term and preterm born neonates

Author:

O'Muircheartaigh Jonathan123ORCID,Robinson Emma C24,Pietsch Maximillian2,Wolfers Thomas56,Aljabar Paul2,Grande Lucilio Cordero2,Teixeira Rui P A G2,Bozek Jelena7,Schuh Andreas8ORCID,Makropoulos Antonios8,Batalle Dafnis12ORCID,Hutter Jana2,Vecchiato Katy2,Steinweg Johannes K2,Fitzgibbon Sean9,Hughes Emer2,Price Anthony N2,Marquand Andre5610,Reuckert Daniel8,Rutherford Mary2,Hajnal Joseph V2,Counsell Serena J2,Edwards A David23

Affiliation:

1. Department of Forensic and Neurodevelopmental Sciences, Sackler Institute for Translational Neurodevelopment, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK

2. Centre for the Developing Brain, School Biomedical Engineering and Imaging Sciences, King’s College London, St Thomas’ Hospital, London, UK

3. MRC Centre for Neurodevelopmental Disorders, King’s College London, London, UK

4. Department of Bioengineering, Imperial College London, London, UK

5. Donders Centre for Cognitive Neuroimaging, Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands

6. Department of Cognitive Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands

7. Faculty of Electrical Engineering and Computing, University of Zagreb, Zagreb, Croatia

8. Biomedical Image Analysis Group, Department of Computing, Imperial College London, London, UK

9. Centre for Functional MRI of the Brain (FMRIB), Wellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK

10. Department of Neuroimaging, Centre for Neuroimaging Sciences, Institute of Psychiatry, King’s College London, London, UK

Abstract

Abstract Premature birth occurs during a period of rapid brain growth. In this context, interpreting clinical neuroimaging can be complicated by the typical changes in brain contrast, size and gyrification occurring in the background to any pathology. To model and describe this evolving background in brain shape and contrast, we used a Bayesian regression technique, Gaussian process regression, adapted to multiple correlated outputs. Using MRI, we simultaneously estimated brain tissue intensity on T1- and T2-weighted scans as well as local tissue shape in a large cohort of 408 neonates scanned cross-sectionally across the perinatal period. The resulting model provided a continuous estimate of brain shape and intensity, appropriate to age at scan, degree of prematurity and sex. Next, we investigated the clinical utility of this model to detect focal white matter injury. In individual neonates, we calculated deviations of a neonate’s observed MRI from that predicted by the model to detect punctate white matter lesions with very good accuracy (area under the curve > 0.95). To investigate longitudinal consistency of the model, we calculated model deviations in 46 neonates who were scanned on a second occasion. These infants’ voxelwise deviations from the model could be used to identify them from the other 408 images in 83% (T2-weighted) and 76% (T1-weighted) of cases, indicating an anatomical fingerprint. Our approach provides accurate estimates of non-linear changes in brain tissue intensity and shape with clear potential for radiological use.

Funder

European Research Council

European Union Seventh Framework Programme

National Institute for Health Research Mental Health Biomedical Research Centre at South London

NHS Foundation Trust

King's College London

National Institute for Health Research Mental Health Biomedical Research Centre

St Thomas’ Hospitals NHS Foundation Trust

Wellcome Engineering and Physical Sciences Research Council Centre for Medical Engineering at King’s College London

Medical Research Council

Wellcome Trust

Royal Society

Medical Research Council Centre for Neurodevelopmental Disorders, King’s College London

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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