학술논문

Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome
Document Type
article
Source
Psychiatry Research. 232(1)
Subject
Biological Psychology
Psychology
Basic Behavioral and Social Science
Behavioral and Social Science
Mental Health
Biomedical Imaging
Clinical Research
Pediatric
Neurosciences
2.1 Biological and endogenous factors
Aetiology
Mental health
Adolescent
Anisotropy
Child
DiGeorge Syndrome
Diffusion Tensor Imaging
Female
Fornix
Brain
Hippocampus
Humans
Male
Organ Size
Schizophrenia
Chromosome 22q11.2 deletion
Connectivity
Hippocampal formation
Tractography
Velo-cardio-facial Syndrome
Medical and Health Sciences
Psychology and Cognitive Sciences
Psychiatry
Clinical sciences
Clinical and health psychology
Language
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.