Longitudinal Diffusion Tensor Imaging Shows Progressive Changes in White Matter in Huntington's Disease

被引:29
作者
Gregory, Sarah [1 ]
Cole, James H. [2 ,3 ]
Farmer, Ruth E. [4 ]
Rees, Elin M. [2 ]
Roos, Raymund A. C. [5 ]
Sprengelmeyer, Reiner [6 ]
Durr, Alexandra [7 ]
Landwehrmeyer, Bernhard [6 ]
Zhang, Hui [8 ]
Scahill, Rachael I. [2 ]
Tabrizi, Sarah J. [2 ]
Frost, Chris [4 ]
Hobbs, Nicola Z. [2 ,9 ]
机构
[1] UCL, Wellcome Trust Ctr Neuroimaging, 12 Queen Sq, London WC1N 3BG, England
[2] UCL, UCL Inst Neurol, London WC1N 3BG, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Med, Computat Cognit & Clin Neuroimaging Lab, London SW7 2AZ, England
[4] London Sch Hyg & Trop Med, Dept Med Stat, London WC1, England
[5] Leiden Univ, Med Ctr, Dept Neurol, NL-2300 RC Leiden, Netherlands
[6] Univ Ulm, Dept Neurol, D-89069 Ulm, Germany
[7] Hop La Pitie Salpetriere, APHP, INSERM, Dept Genet & Cytogenet,UMR S679, Paris, France
[8] UCL, Ctr Med Image Comp, London WC1N 3BG, England
[9] IXICO Plc, London, England
基金
英国医学研究理事会;
关键词
Huntington's disease; diffusion tensor imaging; longitudinal; symptomatic;
D O I
10.3233/JHD-150173
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Huntington'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. Objective: To 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. Methods: In 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). Results: Cross-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. Conclusions: We 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.
引用
收藏
页码:333 / 346
页数:14
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