Investigating longitudinal changes to frontal cortico-striatal tracts in Huntington’s disease: the IMAGE-HD study

• Published in: Brain imaging and behavior 2022-12, Vol.16 (6), p.2457-2466
• Main Authors: Tan, Brendan, Shishegar, Rosita, Oldham, Stuart, Fornito, Alex, Poudel, Govinda, Georgiou-Karistianis, Nellie
• Format: Article
• Language: English
• Subjects: Abnormalities; Alzheimer's disease; Anisotropy; Biomedical and Life Sciences; Biomedicine; Brain; Brain - pathology; Brain research; Diffusion Tensor Imaging - methods; Diffusivity; Humans; Huntington Disease - diagnostic imaging; Huntington Disease - pathology; Huntington's disease; Huntingtons disease; Integrity; Magnetic Resonance Imaging; Medical imaging; Medical research; Microstructure; Neostriatum; Neuroimaging; Neuropsychology; Neuroradiology; Neurosciences; Original Research; Psychiatry; Signs and symptoms; Substantia alba; Time measurement; White Matter - diagnostic imaging; White Matter - pathology
• ISSN: 1931-7557; 1931-7565; 1931-7565
• DOI: 10.1007/s11682-022-00699-6

The striatum is the principal site of disease pathology in Huntington’s disease and contains neural connections to numerous cortical brain regions. Studies examining abnormalities to neural connections find that white matter integrity is compromised in HD; however, further regional, and longitudinal investigation is required. This paper is the first longitudinal investigation into region-based white-matter integrity changes in Huntington’s Disease. The aim of this study was to better understand how disease progression impacts white matter tracts connecting the striatum to the prefrontal and motor cortical regions in HD. We used existing neuroimaging data from IMAGE-HD, comprised of 25 pre-symptomatic, 27 symptomatic, and 25 healthy controls at three separate time points (baseline, 18-months, 30-months). Fractional anisotropy, axial diffusivity and radial diffusivity were derived as measures of white matter microstructure. The anatomical regions of interest were identified using the Desikan-Killiany brain atlas. A Group by Time repeated measures ANCOVA was conducted for each tract of interest and for each measure. We found significantly lower fractional anisotropy and significantly higher radial diffusivity in the symptomatic group, compared to both the pre-symptomatic group and controls (the latter two groups did not differ from each other), in the rostral middle frontal and superior frontal tracts; as well as significantly higher axial diffusivity in the rostral middle tracts only. We did not find a Group by Time interaction for any of the white matter integrity measures. These findings demonstrate that whilst the microstructure of white matter tracts, extending from the striatum to these regions of interest, are compromised during the symptomatic stages of Huntington’s disease, 36-month follow-up did not show progressive changes in these measures. Additionally, no correlations were found between clinical measures and tractography changes, indicating further investigations into the relationship between tractography changes and clinical symptoms in Huntington’s disease are required.