Thalamic lesions in multiple sclerosis by 7T MRI: Clinical implications and relationship to cortical pathology.
Title | Thalamic lesions in multiple sclerosis by 7T MRI: Clinical implications and relationship to cortical pathology. |
Publication Type | Journal Article |
Year of Publication | 2015 |
Authors | Harrison DM, Oh J, Roy S, Wood ET, Whetstone A, Seigo MA, Jones CK, Pham D, van Zijl P, Reich DS, Calabresi PA |
Journal | Mult Scler |
Volume | 21 |
Issue | 9 |
Pagination | 1139-50 |
Date Published | 2015 Aug |
ISSN | 1477-0970 |
Keywords | Adult, Cerebral Cortex, Female, Gray Matter, Humans, Image Interpretation, Computer-Assisted, Magnetic Resonance Imaging, Male, Middle Aged, Multiple Sclerosis, Thalamus, White Matter |
Abstract | OBJECTIVE: Pathology in both cortex and deep gray matter contribute to disability in multiple sclerosis (MS). We used the increased signal-to-noise ratio of 7-tesla (7T) MRI to visualize small lesions within the thalamus and to relate this to clinical information and cortical lesions. METHODS: We obtained 7T MRI scans on 34 MS cases and 15 healthy volunteers. Thalamic lesion number and volume were related to demographic data, clinical disability measures, and lesions in cortical gray matter. RESULTS: Thalamic lesions were found in 24/34 of MS cases. Two lesion subtypes were noted: discrete, ovoid lesions, and more diffuse lesional areas lining the periventricular surface. The number of thalamic lesions was greater in progressive MS compared to relapsing-remitting (mean ±SD, 10.7 ±0.7 vs. 3.0 ±0.7, respectively, p < 0.001). Thalamic lesion burden (count and volume) correlated with EDSS score and measures of cortical lesion burden, but not with white matter lesion burden or white matter volume. CONCLUSIONS: Using 7T MRI allows identification of thalamic lesions in MS, which are associated with disability, progressive disease, and cortical lesions. Thalamic lesion analysis may be a simpler, more rapid estimate of overall gray matter lesion burden in MS. |
DOI | 10.1177/1352458514558134 |
Alternate Journal | Mult. Scler. |
PubMed ID | 25583851 |
PubMed Central ID | PMC4499502 |
Grant List | T32 GM007309 / GM / NIGMS NIH HHS / United States 5P41EB15909 / EB / NIBIB NIH HHS / United States 5P41 RR15241-09S1 / RR / NCRR NIH HHS / United States R01 NS070906 / NS / NINDS NIH HHS / United States K23 NS072366 / NS / NINDS NIH HHS / United States / / Intramural NIH HHS / United States K23NS072366 / NS / NINDS NIH HHS / United States P41 RR015241 / RR / NCRR NIH HHS / United States L30 NS088825 / NS / NINDS NIH HHS / United States P41 EB015909 / EB / NIBIB NIH HHS / United States |