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

Yi Deng, Naomi J. Goodrich-Hunsaker, Margarita Cabaral, David G Amaral, Michael H. Buonocore, Danielle J Harvey, Kristopher Kalish, Owen T. Carmichael, Cynthia Schumann, Aaron Lee, Robert F. Dougherty, Lee M. Perry, Brian A. Wandell, Tony J Simon

Research output: Contribution to journalArticle

8 Citations (Scopus)

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[U+05F3]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.

Original languageEnglish (US)
Pages (from-to)106-114
Number of pages9
JournalPsychiatry Research - Neuroimaging
Volume232
Issue number1
DOIs
StatePublished - Apr 30 2015

Fingerprint

DiGeorge Syndrome
Chromosome Deletion
Hippocampus
Anisotropy
Diffusion Tensor Imaging
Schizophrenia
Brain

Keywords

  • Chromosome 22q11.2 deletion
  • Connectivity
  • Hippocampal formation
  • Tractography
  • Velo-cardio-facial Syndrome

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Radiology Nuclear Medicine and imaging
  • Neuroscience (miscellaneous)

Cite this

Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome. / Deng, Yi; Goodrich-Hunsaker, Naomi J.; Cabaral, Margarita; Amaral, David G; Buonocore, Michael H.; Harvey, Danielle J; Kalish, Kristopher; Carmichael, Owen T.; Schumann, Cynthia; Lee, Aaron; Dougherty, Robert F.; Perry, Lee M.; Wandell, Brian A.; Simon, Tony J.

In: Psychiatry Research - Neuroimaging, Vol. 232, No. 1, 30.04.2015, p. 106-114.

Research output: Contribution to journalArticle

Deng, Y, Goodrich-Hunsaker, NJ, Cabaral, M, Amaral, DG, Buonocore, MH, Harvey, DJ, Kalish, K, Carmichael, OT, Schumann, C, Lee, A, Dougherty, RF, Perry, LM, Wandell, BA & Simon, TJ 2015, 'Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome', Psychiatry Research - Neuroimaging, vol. 232, no. 1, pp. 106-114. https://doi.org/10.1016/j.pscychresns.2015.02.002
Deng, Yi ; Goodrich-Hunsaker, Naomi J. ; Cabaral, Margarita ; Amaral, David G ; Buonocore, Michael H. ; Harvey, Danielle J ; Kalish, Kristopher ; Carmichael, Owen T. ; Schumann, Cynthia ; Lee, Aaron ; Dougherty, Robert F. ; Perry, Lee M. ; Wandell, Brian A. ; Simon, Tony J. / Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome. In: Psychiatry Research - Neuroimaging. 2015 ; Vol. 232, No. 1. pp. 106-114.
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