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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Research ArticleAdult Brain
Open Access

Leptomeningeal Contrast Enhancement Is Related to Focal Cortical Thinning in Relapsing-Remitting Multiple Sclerosis: A Cross-Sectional MRI Study

N. Bergsland, D. Ramasamy, E. Tavazzi, D. Hojnacki, B. Weinstock-Guttman and R. Zivadinov
American Journal of Neuroradiology April 2019, 40 (4) 620-625; DOI: https://doi.org/10.3174/ajnr.A6011
N. Bergsland
aFrom the Buffalo Neuroimaging Analysis Center (N.B., D.R., E.T., R.Z.)
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D. Ramasamy
aFrom the Buffalo Neuroimaging Analysis Center (N.B., D.R., E.T., R.Z.)
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E. Tavazzi
aFrom the Buffalo Neuroimaging Analysis Center (N.B., D.R., E.T., R.Z.)
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D. Hojnacki
bJacobs Comprehensive MS Treatment and Research Center (D.H., B.W.-G.), Department of Neurology
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B. Weinstock-Guttman
bJacobs Comprehensive MS Treatment and Research Center (D.H., B.W.-G.), Department of Neurology
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R. Zivadinov
aFrom the Buffalo Neuroimaging Analysis Center (N.B., D.R., E.T., R.Z.)
cJacobs School of Medicine and Biomedical Sciences, Center for Biomedical Imaging at Clinical Translational Science Institute (R.Z.), University at Buffalo, State University of New York, Buffalo, New York.
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Abstract

BACKGROUND AND PURPOSE: Leptomeningeal inflammation is associated with the development of global cortical gray matter atrophy in multiple sclerosis. However, its association with localized loss of tissue remains unclear. The purpose of this study was to evaluate the relationship between leptomeningeal contrast enhancement, a putative marker of leptomeningeal inflammation, and focal cortical thinning in MS.

MATERIALS AND METHODS: Forty-three patients with relapsing-remitting MS and 15 with secondary-progressive MS were imaged on a 3T scanner. Cortical reconstruction was performed with FreeSurfer. Leptomeningeal contrast-enhancement foci were visually identified on 3D-FLAIR postcontrast images and confirmed using subtraction imaging. Leptomeningeal contrast-enhancement foci were mapped onto the cortex, and ROIs were obtained by dilating along the surface multiple times (n = 5, 10, 15, 20, 25, 30, 35, 40). Resulting ROIs were then mapped onto the homologous region of the contralateral hemisphere. Paired t tests compared the thickness of the cortex surrounding individual leptomeningeal contrast-enhancement foci and the corresponding contralateral region. Results were corrected for the false discovery rate.

RESULTS: Differences between ipsilateral and contralateral ROIs progressively decreased with larger ROIs, but no significant effects were detected when considering the entire MS sample. In patients with relapsing-remitting MS only, significantly reduced cortical thickness was found for 5 dilations (−8.53%, corrected P = .04) and 10 dilations (−5.20%, corrected P = .044).

CONCLUSIONS: Focal leptomeningeal contrast enhancement is associated with reduced thickness of the surrounding cortex in patients with relapsing-remitting MS, but not in those with secondary-progressive MS. Our results suggest that pathology associated with the presence of leptomeningeal contrast-enhancement foci has a stronger, localized effect on cortical tissue loss earlier in the disease.

ABBREVIATIONS:

LMCE
leptomeningeal contrast enhancement
RRMS
relapsing-remitting MS
SPMS
secondary-progressive MS
  • © 2019 by American Journal of Neuroradiology

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American Journal of Neuroradiology: 40 (4)
American Journal of Neuroradiology
Vol. 40, Issue 4
1 Apr 2019
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Cite this article
N. Bergsland, D. Ramasamy, E. Tavazzi, D. Hojnacki, B. Weinstock-Guttman, R. Zivadinov
Leptomeningeal Contrast Enhancement Is Related to Focal Cortical Thinning in Relapsing-Remitting Multiple Sclerosis: A Cross-Sectional MRI Study
American Journal of Neuroradiology Apr 2019, 40 (4) 620-625; DOI: 10.3174/ajnr.A6011

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Leptomeningeal Contrast Enhancement Is Related to Focal Cortical Thinning in Relapsing-Remitting Multiple Sclerosis: A Cross-Sectional MRI Study
N. Bergsland, D. Ramasamy, E. Tavazzi, D. Hojnacki, B. Weinstock-Guttman, R. Zivadinov
American Journal of Neuroradiology Apr 2019, 40 (4) 620-625; DOI: 10.3174/ajnr.A6011
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