A longitudinal diffusion tensor imaging study in symptomatic Huntington's disease
Adult
Male
Psychopharmacology
Statistics as Topic
610
Corpus Callosum
03 medical and health sciences
C1
0302 clinical medicine
Thalamus
Reference Values
Image Processing, Computer-Assisted
Humans
Physiological Psychology)
Longitudinal Studies
Dominance, Cerebral
Neurologic Examination
970117 Expanding Knowledge in Psychology and Cognitive Sciences
Putamen
Huntington's disease
Middle Aged
Corpus Striatum
Diffusion Tensor Imaging
Huntington Disease
Nerve Degeneration
Female
Caudate Nucleus
170101 Biological Psychology (Neuropsychology
DOI:
10.1136/jnnp.2007.142786
Publication Date:
2009-02-24T01:12:39Z
AUTHORS (12)
ABSTRACT
The striatum and its projections are thought to be the earliest sites of Huntington's disease (HD) pathology. This study aimed to investigate progression of striatal pathology in symptomatic HD using diffusion tensor imaging.Diffusion weighted images were acquired in 18 HD patients and in 17 healthy controls twice, 1 year apart. Mean diffusivity (MD) was calculated in the caudate, putamen, thalamus and corpus callosum, and compared between groups. In addition, caudate width was measured using T1 high resolution images and correlated with caudate MD. Correlation analyses were also performed in HD between caudate/putamen MD and clinical measures.MD was significantly higher in the caudate and putamen bilaterally for patients compared with controls at both time points although there were no significant MD differences in the thalamus or corpus callosum. For both groups, MD did not change significantly in any region from baseline to year 1. There was a significant negative correlation between caudate width and MD in patients at baseline but no correlation between these parameters in controls. There was also a significant negative correlation between Mini-Mental State Examination scores and caudate MD and putamen MD at both time points in HD.It appears that microstructural changes influence cognitive status in HD. Although MD was significantly higher in HD compared with controls at both time points, there were no longitudinal changes in either group. This finding does not rule out the possibility that MD could be a sensitive biomarker for detecting early change in preclinical HD.
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