Corpus callosum biometry in children born very preterm with and without cerebral palsy

IF 2.3 3区 医学 Q3 CLINICAL NEUROLOGY
Manuel Lubián-Gutiérrez , Monica Crotti , Isabel Benavente-Fernández , Simón Pedro Lubián-López , Nofar Ben Itzhak , Lisa Mailleux , Els Ortibus
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引用次数: 0

Abstract

Background

Corpus callosum (CC) measurements are used as a biomarker of white matter volume in infants born very preterm (VPT; gestational age≤32 weeks). Although smaller CC measurements are found in both children born VPT and those with cerebral palsy (CP) compared to neurotypical children born at term, there is a lack of research specifically comparing CC measurements in VPT children with and without CP at different ages.

Participants and methods

We compared five CC measurements (total length, and thickness of genu, body, isthmus, and splenium) calculated on the midsagittal plane of T1 magnetic resonance imaging (MRI) in a retrospective case-control study between VPT children with (case) and without CP (control) matched 1:1 by age at MRI at different ages (<12 months age; 5-11 years-old).

Results

Seventy-four VPT children were included (median age 5.8 months [2.1–89.3], 34 females). Children with CP showed shorter length (45.3 mm [40.9–66.2] vs 50.9 mm [44.5–69]; p = 0.01), smaller isthmus thickness (1.8 mm [1.2–2.2] vs 2.2 mm [1.8–4.1]; p = 0.03), and smaller splenium thickness (3.5 [2.7–7.9] vs 5 mm [3.7–9.8]; p = 0.04) compared to children without CP. Comparison of the two groups by age at MRI, showed significantly smaller splenium thickness in both infants (<12 months age) and children (5-11 years-old) with CP than in controls.

Conclusion

Infants and children born VPT with CP had smaller CC measurements than those without CP, with the posterior region being the most affected. Splenium thickness in VPT infants could serve as a biomarker for white matter damage, potentially leading to CP.
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来源期刊
CiteScore
6.30
自引率
3.20%
发文量
115
审稿时长
81 days
期刊介绍: The European Journal of Paediatric Neurology is the Official Journal of the European Paediatric Neurology Society, successor to the long-established European Federation of Child Neurology Societies. Under the guidance of a prestigious International editorial board, this multi-disciplinary journal publishes exciting clinical and experimental research in this rapidly expanding field. High quality papers written by leading experts encompass all the major diseases including epilepsy, movement disorders, neuromuscular disorders, neurodegenerative disorders and intellectual disability. Other exciting highlights include articles on brain imaging and neonatal neurology, and the publication of regularly updated tables relating to the main groups of disorders.
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