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Early Alterations in Cortical and Cerebellar Regional Brain Growth in Down Syndrome: An in Vivo Fetal and Neonatal MRI Assessment

Overview
Journal Neuroimage Clin
Publisher Elsevier
Specialties Neurology
Radiology
Date 2019 Dec 31
PMID 31887718
Citations 32
Authors
Affiliations
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Abstract

Down Syndrome (DS) is the most frequent genetic cause of intellectual disability with a wide spectrum of neurodevelopmental outcomes. At present, the relationship between structural brain morphology and the spectrum of cognitive phenotypes in DS, is not well understood. This study aimed to quantify the development of the fetal and neonatal brain in DS participants, with and without a congenital cardiac defect compared with a control population using dedicated, optimised and motion-corrected in vivo magnetic resonance imaging (MRI). We detected deviations in development and altered regional brain growth in the fetus with DS from 21 weeks' gestation, when compared to age-matched controls. Reduced cerebellar volume was apparent in the second trimester with significant alteration in cortical growth becoming evident during the third trimester. Developmental abnormalities in the cortex and cerebellum are likely substrates for later neurocognitive impairment, and ongoing studies will allow us to confirm the role of antenatal MRI as an early biomarker for subsequent cognitive ability in DS. In the era of rapidly developing technologies, we believe that the results of this study will assist counselling for prospective parents.

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References
1.
Bartesaghi R, Guidi S, Ciani E . Is it possible to improve neurodevelopmental abnormalities in Down syndrome?. Rev Neurosci. 2011; 22(4):419-55. DOI: 10.1515/RNS.2011.037. View

2.
Cignini P, Giorlandino M, Brutti P, Mangiafico L, Aloisi A, Giorlandino C . Reference Charts for Fetal Cerebellar Vermis Height: A Prospective Cross-Sectional Study of 10605 Fetuses. PLoS One. 2016; 11(1):e0147528. PMC: 4727931. DOI: 10.1371/journal.pone.0147528. View

3.
Raveau M, Nakahari T, Asada S, Ishihara K, Amano K, Shimohata A . Brain ventriculomegaly in Down syndrome mice is caused by Pcp4 dose-dependent cilia dysfunction. Hum Mol Genet. 2017; 26(5):923-931. DOI: 10.1093/hmg/ddx007. View

4.
Lanfranchi S, Mammarella I, Carretti B . Spatial-simultaneous working memory and selective interference in Down syndrome. Child Neuropsychol. 2014; 21(4):481-9. DOI: 10.1080/09297049.2014.913557. View

5.
Shiohama T, Levman J, Baumer N, Takahashi E . Structural Magnetic Resonance Imaging-Based Brain Morphology Study in Infants and Toddlers With Down Syndrome: The Effect of Comorbidities. Pediatr Neurol. 2019; 100:67-73. PMC: 6755072. DOI: 10.1016/j.pediatrneurol.2019.03.015. View