Journal Article

Alterations in white matter pathways in Angelman syndrome

CHU, ZILI, TRAIPE, ELFRIDES, WILDE, ELISABETH A, HUNTER, JILL V, BACINO, CARLOS A, ANDERSON, ADAM W, YALLAMPALLI, RAGINI, KAUFMANN, WALTER E, PETERS, SARIKA U, ADAPA, PAVANI

2011

Overview

Aim  Angelman syndrome is a neurogenetic disorder characterized by severe intellectual disability, absent speech, seizures, and outbursts of laughter. The aim of this study was to utilize diffusion tensor imaging (DTI) to examine alterations in white matter pathways in Angelman syndrome, with an emphasis on correlations with clinical severity. Method  DTI was used to examine the arcuate fasciculus (AF), uncinate fasciculus (UF), inferior longitudinal fasciculus (ILF), inferior fronto‐occipital fasciculus (IFOF), and the corpus callosum (CC). We enrolled 14 children aged 8 to 17 years (mean age 10y 8mo; SD 2y 7mo) with Angelman syndrome (seven male; seven female) and 13 typically developing children, aged 8 to 17 years, for comparison (five male; eight female; mean age 12y; SD 2y 9mo). Individuals with Angelman syndrome were assessed using standardized measures of development, language, and behaviour. Results  The children with Angelman syndrome exhibited lower fractional anisotropy and increased radial diffusivity values than the comparison group for the AF, UF, ILF, and CC (p<0.006 corrected for multiple comparisons). They also had lower fractional anisotropy values for the IFOF and higher radial diffusivity values for the left IFOF (p<0.006). Additionally, children with Angelman syndrome had significantly higher apparent diffusion coefficient values in the AF, CC, ILF, and the left IFOF (p<0.006). Significant correlations were noted between DTI parameters and some of the clinical assessment outcomes (e.g. language, socialization, cognition) for three of the temporal pathways (AF, UF, ILF; p<0.05). Interpretation  Changes in DTI parameters in individuals with Angelman syndrome suggest decreased/delayed myelination, decreased axonal density or diameter, or aberrant axonal organization. Our findings suggest a generalized white matter alteration throughout the brain in those with Angelman syndrome; however, only the alterations in temporal white matter pathways were associated with language and cognitive and social functioning.

• Publisher: Blackwell Publishing Ltd,Mac Keith Press
• Subject: Adolescent / Analysis of Variance / Angelman Syndrome - genetics / Angelman Syndrome - pathology / Anisotropy / Brain - pathology / Child / Chromosomes, Human, Pair 15 - genetics / Corpus Callosum - pathology / Diffusion Tensor Imaging - methods / Female / Functional Laterality / Humans / Magnetic Resonance Imaging - methods / Male / Nerve Fibers, Myelinated - pathology / Neural Pathways - pathology / Psychological Tests / Statistics as Topic