TY - JOUR
T1 - Thalamic lesions in multiple sclerosis by 7T MRI
T2 - Clinical implications and relationship to cortical pathology
AU - Harrison, Daniel M.
AU - Oh, Jiwon
AU - Roy, Snehashis
AU - Wood, Emily T.
AU - Whetstone, Anna
AU - Seigo, Michaela A.
AU - Jones, Craig K.
AU - Pham, Dzung
AU - Van Zijl, Peter
AU - Reich, Daniel S.
AU - Calabresi, Peter A.
N1 - Publisher Copyright:
© The Author(s), 2015.
PY - 2015/8/25
Y1 - 2015/8/25
N2 - 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 relapsingremitting (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.
AB - 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 relapsingremitting (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.
KW - MRI
KW - multiple sclerosis
UR - http://www.scopus.com/inward/record.url?scp=84937691980&partnerID=8YFLogxK
U2 - 10.1177/1352458514558134
DO - 10.1177/1352458514558134
M3 - Article
C2 - 25583851
AN - SCOPUS:84937691980
SN - 1352-4585
VL - 21
SP - 1139
EP - 1150
JO - Multiple Sclerosis Journal
JF - Multiple Sclerosis Journal
IS - 9
ER -