• Sarah Gregory, James H Cole, Ruth E Farmer, Elin M Rees, Raymund A C Roos, Reiner Sprengelmeyer, Alexandra Durr, Bernhard Landwehrmeyer, Hui Zhang, Rachael I Scahill, Sarah J Tabrizi, Chris Frost, and Nicola Z Hobbs.
• Wellcome Trust Centre for Neuroimaging, UCL, London, WC1N 3BG, UK.
• J Huntingtons Dis. 2015 Jan 1; 4 (4): 333-46.

BackgroundHuntington's disease is marked by progressive neuroanatomical changes, assumed to underlie the development of the disease's characteristic symptoms. Previous work has demonstrated longitudinal macrostructural white-matter atrophy, with some evidence of microstructural change focused in the corpus callosum.ObjectiveTo more accurately characterise longitudinal patterns, we examined white matter microstructural change using Diffusion Tensor Imaging (DTI) data from three timepoints over a 15 month period.MethodsIn 48 early-stage HD patients and 36 controls from the multi-site PADDINGTON project, diffusion tensor imaging (DTI) was employed to measure changes in fractional anisotropy (FA) and axial (AD) and radial diffusivity (RD) in 24 white matter regions-of-interest (ROIs).ResultsCross-sectional analysis indicated widespread baseline between-group differences, with significantly decreased FA and increased AD and RD found in HD patients across multiple ROIs. Longitudinal rates of change differed significantly between HD patients and controls in the genu and body of corpus callosum, corona radiata and anterior limb of internal capsule. Change in RD in the body of the corpus callosum was significantly associated with baseline disease burden, but other clinical associations were not significant.ConclusionsWe detected subtle longitudinal white matter changes in early HD patients. Progressive white matter abnormalities in HD may not be uniform throughout the brain, with some areas remaining static in the early symptomatic phase. Longer assessment periods across disease stages will help map this progressive trajectory.

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