Literature DB >> 30144569

Altered functional network connectivity relates to motor development in children born very preterm.

M D Wheelock1, N C Austin2, S Bora3, A T Eggebrecht4, T R Melzer5, L J Woodward6, C D Smyser7.   

Abstract

Individuals born very preterm (<32 weeks gestation) are at increased risk for neuromotor impairments. The ability to characterize the structural and functional mechanisms underlying these impairments remains limited using existing neuroimaging techniques. Resting state-functional magnetic resonance imaging (rs-fMRI) holds promise for defining the functional network architecture of the developing brain in relation to typical and aberrant neurodevelopment. In 58 very preterm and 65 term-born children studied from birth to age 12 years, we examined relations between functional connectivity measures from low-motion rs-fMRI data and motor skills assessed using the Movement Assessment Battery for Children, 2nd edition. Across all subscales, motor performance was better in term than very preterm children. Examination of relations between functional connectivity and motor measures using enrichment analysis revealed between-group differences within cerebellar, frontoparietal, and default mode networks, and between basal ganglia-motor, thalamus-motor, basal ganglia-auditory, and dorsal attention-default mode networks. Specifically, very preterm children exhibited weaker associations between motor scores and thalamus-motor and basal ganglia-motor network connectivity. These findings highlight key functional brain systems underlying motor development. They also demonstrate persisting developmental effects of preterm birth on functional connectivity and motor performance in childhood, providing evidence for an alternative network architecture supporting motor function in preterm children.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Functional connectivity; Motor development; Neurodevelopmental outcome; Prematurity; Resting state functional MRI

Mesh:

Year:  2018        PMID: 30144569      PMCID: PMC6258200          DOI: 10.1016/j.neuroimage.2018.08.051

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


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