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Motor predictors of cortical brain development and full-IQ in children born extremely preterm with and without discrete white matter abnormalities
Department of Psychology, Faculty of Health Sciences, University of Deusto, Bilbao, Bizkaia, Spain.
Department of Paediatrics, Örebro University Hospital, Örebro, Sweden.
Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden; Sachs' Children and Youth Hospital, Södersjukhuset, Stockholm, Sweden.
Vise andre og tillknytning
2024 (engelsk)Inngår i: Brain Structure and Function, ISSN 1863-2653, E-ISSN 1863-2661, Vol. 230, nr 1, artikkel-id 18Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

AIM: To describe the cortical brain development and full-IQ performance in middle school age children after extremely preterm (EPT) birth considering discrete white matter abnormalities (WMA). In addition, to assess possible early motor predictors of cortical brain development and full-IQ in children born EPT with and without discrete WMA diagnosed at 10 years. METHODS: T1-weighted MRI images from fifty-one children born before 27 weeks' gestation and 40 full-term born controls (Mage=10.09 years; SDage=0.77) were scored for discrete WMA and analyzed with Freesurfer (v7.2.0). The assessments included motor assessments (i.e., fine- and gross motor function) of Bayley Scales of Infant and Toddler Development - Third Edition (BSID-III) at a mean age of 2½ years. Full-IQ was also assessed with Wechsler Intelligence Scale for Children - Fifth Edition (WISC-V) at 12 years. RESULTS: No differences were displayed in motor function or full-IQ score between children born EPT with and without discrete WMA at 10 years. Moreover, no global differences were found in cortex volume. However, bilateral mean cortical thicknesses (CTh) were exhibited to be thicker in children born EPT with discrete WMA. Children born EPT with discrete WMA exhibited regional increases mainly in the frontal and temporal lobes apart from left caudal anterior cingulate gyrus (mean difference = -0.11 (-0.22, -0.01), p = 0.026). Full-IQ was predicted by impairments in fine motor skills in children born EPT with discrete WMA, explaining 42.9% of the variance. CONCLUSIONS: Bilateral mean and regional CTh were found to be greater in children born EPT with discrete WMA at 10 years compared to those without. Fine motor function at 2½ years was a strong predictor of full-IQ dependent in children with discrete WMA.

sted, utgiver, år, opplag, sider
Springer, 2024. Vol. 230, nr 1, artikkel-id 18
Emneord [en]
Cortical thickness, Discrete white matter abnormalities, Extremely preterm birth, Motor function and full-IQ
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-127336DOI: 10.1007/s00429-024-02874-5PubMedID: 39718655OAI: oai:DiVA.org:oru-127336DiVA, id: diva2:2038995
Tilgjengelig fra: 2026-02-16 Laget: 2026-02-16 Sist oppdatert: 2026-02-16bibliografisk kontrollert
Inngår i avhandling
1. Neuromotor outcomes, motor-related healthcare, and brain morphology in children born extremely preterm
Åpne denne publikasjonen i ny fane eller vindu >>Neuromotor outcomes, motor-related healthcare, and brain morphology in children born extremely preterm
2026 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Children born extremely preterm (EPT) are at increased risk for brain injury and developmental impairments. CP and non-CP motor difficulties are common. The overall aim of this thesis was to describe longitudinal motor development, deepen understanding of underpinning brain morphology, and study access to motor-related health care in this population.

Study I showed that the prevalence of a non-optimal neurological condition declined with age. Nevertheless, at 12 years, such conditions still remained significantly more frequent among children born EPT than among term-born peers, and were associated with reduced motor function.

Study II found that discrete white matter abnormalities were commonly observed at 8–11 years of age in children born EPT, but were not associated with neurodevelopmental outcomes.

Study III revealed a high prevalence of significant non-CP motor difficulties in children born EPT, although only a small proportion of affected children had received motor-related health care by 5.5 years of age. Access to motor-related health care was associated with bronchopulmonary dysplasia, hyperactivity, and involvement with additional health services beyond physiotherapy.

Study IV demonstrated that children born EPT with discrete white matter abnormalities exhibited greater mean and regional cortical thickness at 10 years of age compared with those without such abnormalities. Fine motorfunction at 2.5 years was a strong predictor of full-scale IQ in children born EPT with discrete white matter abnormalities.

A better understanding of the long-term consequences of EPT birth may, over time, inform strategies to improve clinical care and societal support for these children. Such knowledge can help create conditions that allow children born EPT to fully develop their abilities and reach their developmental potential.

sted, utgiver, år, opplag, sider
Örebro: Örebro universitet, 2026. s. 101
Serie
Örebro Studies in Medicine, ISSN 1652-4063 ; 349
Emneord
Extremely preterm, neurodevelopment, motor function, minor neurological dysfunction, magnetic resonance imaging, white matter abnormalities, cortical thickness, motor-related health care
HSV kategori
Identifikatorer
urn:nbn:se:oru:diva-125527 (URN)9789175297453 (ISBN)9789175297460 (ISBN)
Disputas
2026-03-13, Örebro universitet, Campus USÖ, Tidefeltsalen, Södra Grev Rosengatan 32, Örebro, 10:00 (svensk)
Opponent
Veileder
Tilgjengelig fra: 2025-12-10 Laget: 2025-12-10 Sist oppdatert: 2026-03-17bibliografisk kontrollert

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