Literature DB >> 25748884

Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome.

Yi Deng1, Naomi J Goodrich-Hunsaker1, Margarita Cabaral1, David G Amaral1, Michael H Buonocore2, Danielle Harvey3, Kristopher Kalish4, Owen T Carmichael5, Cynthia M Schumann1, Aaron Lee1, Robert F Dougherty6, Lee M Perry6, Brian A Wandell6, Tony J Simon7.   

Abstract

The fornix is the primary subcortical output fiber system of the hippocampal formation. In children with 22q11.2 deletion syndrome (22q11.2DS), hippocampal volume reduction has been commonly reported, but few studies as yet have evaluated the integrity of the fornix. Therefore, we investigated the fornix of 45 school-aged children with 22q11.2DS and 38 matched typically developing (TD) children. Probabilistic diffusion tensor imaging (DTI) tractography was used to reconstruct the body of the fornix in each child׳s brain native space. Compared with children, significantly lower fractional anisotropy (FA) and higher radial diffusivity (RD) was observed bilaterally in the body of the fornix in children with 22q11.2DS. Irregularities were especially prominent in the posterior aspect of the fornix where it emerges from the hippocampus. Smaller volumes of the hippocampal formations were also found in the 22q11.2DS group. The reduced hippocampal volumes were correlated with lower fornix FA and higher fornix RD in the right hemisphere. Our findings provide neuroanatomical evidence of disrupted hippocampal connectivity in children with 22q11.2DS, which may help to further understand the biological basis of spatial impairments, affective regulation, and other factors related to the ultra-high risk for schizophrenia in this population.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Chromosome 22q11.2 deletion; Connectivity; Hippocampal formation; Tractography; Velo-cardio-facial Syndrome

Mesh:

Year:  2015        PMID: 25748884      PMCID: PMC4404209          DOI: 10.1016/j.pscychresns.2015.02.002

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


  83 in total

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4.  Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study.

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2.  DWI Hyperintensity in the Fornix Fimbria on MRI in Children.

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3.  White matter microstructural deficits in 22q11.2 deletion syndrome.

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Review 4.  Long-range dysconnectivity in frontal and midline structures is associated to psychosis in 22q11.2 deletion syndrome.

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6.  A typical 22q11.2 deletion syndrome and pseudohypoparathyroidism: A CARE compliant case report.

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7.  Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome.

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8.  Structural and functional connectivity in the default mode network in 22q11.2 deletion syndrome.

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9.  Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study.

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10.  Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.

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Journal:  Mol Psychiatry       Date:  2019-07-29       Impact factor: 15.992

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