Neuroreport 2003 Mar 3;14(3):335-9
Bermel RA, Innus MD, Tjoa CW, Bakshi R.
Buffalo Neuroimaging Analysis Center The Jacobs Neurological Institute, 100 High St, Buffalo, NY 14203 Department of Neurology, School of Medicine and Biomedical Sciences.
Deep gray matter damage may be an important component of the multiple sclerosis (MS) disease process.
We tested whether caudate atrophy occurs in MS, and whether it correlates with conventional MRI or clinical markers of disease progression.
Caudate nuclei of 24 MS patients and 10 age-matched healthy controls were traced, normalized, reconstructed and visualized from MRI scans.
Normalized bicaudate volume was 19% lower in MS controls ( < 0.001), an effect that persisted after adjusting for whole-brain atrophy ( < 0.008).
Caudate volume did not correlate with disease duration, physical disability score, whole-brain atrophy, or total T2 hyperintense or T1 hypointense lesion load (all > 0.05).
We conclude that selective caudate atrophy is associated with MS and may occur through direct mechanisms.