Advanced MRI technique detects cellular damage in living Huntington’s patients
Researchers showed that the diffusion-MRI method Sandi can identify cellular-level abnormalities in the brains of Huntington’s disease patients, mirroring post-mortem findings.
Scientists applied soma and neurite density imaging (Sandi), a diffusion-MRI approach, to compare scans of 56 individuals with Huntington’s disease against 57 healthy controls. Targeting the basal ganglia, the scans revealed reduced apparent cell-body density, enlarged cell bodies and increased inter-cellular space in patients, while the thalamus showed no such changes. These alterations echo post-mortem studies that document loss of specific striatal neurons and reactive glial enlargement.
Sandi measurements were linked to clinical severity scores and poorer finger-tapping results, and together with one outlet explained up to 63 % of regional brain shrinkage. Although promising as a non-invasive biomarker for monitoring disease-modifying treatments, the method still needs longitudinal validation and adaptation for routine clinical MRI systems. Its capacity to probe cellular damage may also be useful for other neurodegenerative diseases.
Why it matters
The new scan could provide a way to monitor whether experimental therapies are protecting brain cells in Huntington’s disease.
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