Fractional anisotropy distributions in 2‐ to 6‐year‐old children with autism. (24th September 2012)

• Record Type: Journal Article
• Authors: Cascio, C.; Gribbin, M.; Gouttard, S.; Smith, R. G.; Jomier, M.; Field, S.; Graves, M.; Hazlett, H. C.; Muller, K.; Gerig, G.; Piven, J.
• Is Part Of: Journal of intellectual disability research. Volume 57:Part 11(2013:Nov.)
• Page Start: 1037
• Page End: 1049
• Publication Date: 2012-09-24
• Subjects: Mental retardation -- Research -- Periodicals; 362.2
• DOI: 10.1111/j.1365-2788.2012.01599.x
• Languages: English
• ISSNs: 0964-2633

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p> <bold>Background </bold> Increasing evidence suggests that autism is a disorder of distributed neural networks that may exhibit abnormal developmental trajectories. Characterisation of white matter early in the developmental course of the disorder is critical to understanding these aberrant trajectories.</p> <p> <bold>Methods </bold> A cross‐sectional study of 2‐ to 6‐year‐old children with autism was conducted using diffusion tensor imaging combined with a novel statistical approach employing fractional anisotropy distributions. Fifty‐eight children aged 18–79 months were imaged: 33 were diagnosed with autism, 8 with general developmental delay, and 17 were typically developing. Fractional anisotropy values within global white matter, cortical lobes and the cerebellum were measured and transformed to random <italic>F</italic> distributions for each subject. Each distribution of values for a region was summarised by estimating δ, the estimated mean and standard deviation of the approximating <italic>F</italic> for each distribution.</p> <p> <bold>Results </bold> The estimated δ parameter, <inline-graphic xlink:href="ark:/27927/pgg3g3bzcx5" mimetype="image" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />, was significantly decreased in individuals with autism compared to the combined control group. This was true in all cortical lobes, as well as in the cerebellum, but differences were most robust in the temporal lobe. Predicted developmental trajectories of <inline-graphic xlink:href="ark:/27927/pgg3g3bzczq" mimetype="image" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />across the age range in the sample showed patterns that partially distinguished the groups. Exploratory analyses suggested that the variability, rather than the central tendency, component of <inline-graphic xlink:href="ark:/27927/pgg3g3bzd1b" mimetype="image" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />was the driving force behind these results.</p> <p> <bold>Conclusions </bold> While preliminary, our results suggest white matter in young children with autism may be abnormally homogeneous, which may reflect poorly organised or differentiated pathways, particularly in the temporal lobe, which is important for social and emotional cognition.</p> </abstract>