Huntington Disease Clinical Trial
Official title:
Decoding Presymptomatic White Matter Changes in Huntington Disease
WIN-HD is a monocentric longitudinal study comparing premanifest Huntingtin (HTT) mutation
carriers and non HTT mutation carriers to determine that white-matter atrophy occurs far
earlier than clinical onset in HD using Diffusion-weighted Nuclear Magnetic Resonance (N
spectroscopy (DWS) and Diffusion Tensor Imaging (DTI).
The investigators will recruit up to 20 premanifest HTT mutation carriers (15 completed) and
up to 20 non HTT mutation carriers (15 completed). It is important to have those 2
populations in order to compare our results and determine if there are significant
white-matter changes far from the onset of HD. Therefore, non HTT mutation carriers will be
age and gender matched to premanifest HTT mutation carriers.
In order to test the hypothesis, the study has 2 visits with a year interval.
This study is based on 4 principal criteria:
1. Imaging criteria
2. Clinical and neurological criteria
3. Psychological criteria
4. Behavioral criteria
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