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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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    Fig 1.

    A representative case depicting the T2WI FLAIR precontrast, T2WI FLAIR postcontrast, and T2WI FLAIR pre-/postcontrast subtraction images. The FreeSurfer-derived white and pial surfaces are shown in yellow and red, respectively. The white arrow shows a focus of leptomeningeal contrast enhancement.

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    Fig 2.

    A representative cortical reconstruction from FreeSurfer is shown with dilated ROIs overlaid on the cortical surface. Gyri are shown in green, while sulci are shown in red. The red circle corresponds to the position of the mapped focus of leptomeningeal contrast enhancement. Different-sized ROIs are shown in varying colors.

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    Table 1:

    Demographic, clinical, and MR imaging characteristics of the cohort

    RRMS (n = 43)SPMS (n = 15)P Valuea
    Women (No.) (%)38 (88.4)11 (73.3).658
    Age (mean) (SD) (yr)52.8 (12.1)60.5 (6.7).023b
    Disease duration (mean) (SD) (yr)15.2 (8.9)21.9 (8.3).014b
    EDSS (median) (IQR)3.0 (2.0–3.5)6.0 (3.6–6.5).003b
    Age at onset (mean) (SD) (yr)37.6 (12.0)38.7 (8.5).428
    Disease-modifying therapy (No.) (%)
        Interferon β-1a I.M.14 (32.6)2 (13.3).111
        Interferon β-1a S.C.3 (9.3)0 (0)
        Glatiramer acetate8 (18.6)2 (13.3)
        Natalizumab4 (9.3)1 (6.7)
        Dimethyl fumarate2 (4.7)0 (0)
        Fingolimod3 (7.0)0 (0)
        Teriflunomide1 (2.3)3 (20.0)
        Rituximab1 (2.3)0 (0)
        Ocrelizumab0 (0)1 (6.7)
        IVIG1 (2.3)1 (6.7)
        No therapy6 (14.0)5 (33.3)
    No. of LMCE foci1 (n = 33)1 (n = 8).292
    2 (n = 8)2 (n = 4)
    3 (n = 2)3 (n = 3)
    LMCE shape (No.).637
        Nodular3616
        Linear75
        Plate-like124
    T2 lesion volume (mean) (SD) (mL)16.0 (16.2)15.8 (11.4).965
    Gd lesion volume (median) (IQR) (mL)0 (0–0)0 (0–0).097
    • Note:—EDSS indicates Expanded Disability Status Scale; I.M., intramuscular; S.C., subcutaneous; IVIG, intravenous immunoglobulin; Gd, gadolinium.

    • ↵a P value represents differences between the patients with RRMS and SPMS. The differences between the groups were analyzed using the Fisher exact, Student t, Mann-Whitney U, or χ2 test.

    • ↵b P values < .05.

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    Table 2:

    Cortical thickness measurements in the ipsilateral region surrounding focal areas of leptomeningeal contrast enhancement and in the contralateral regiona

    Entire Cohort (80 LMCE Foci)Patients with RRMS (55 LMCE Foci)Patients with SPMS (25 LMCE Foci)
    DilationsIpsilateralContralateralPct. Diff.P/FDR-PIpsilateralContralateralPct. Diff.P/FDR-PIpsilateralContralateralPct. Diff.P/FDR-P
    52.043 (.515)2.149 (.556)−5.06.07/.1872.031 (.534)2.212 (.567)−8.53.005/.04b2.070 (.480)2.000 (.510)3.44.562/.823
    102.063 (.437)2.160 (.476)−4.59.016/.1282.099 (.455)2.211 (.501)−5.20.011/.044b1.979 (.387)2.039 (.396)−2.99.493/.823
    152.088 (.411)2.153 (.413)−3.07.039/.1562.141 (.414)2.208 (.432)−3.08.055/.1471.964 (.383)2.023 (.339)−2.96.384/.823
    202.114 (.286)2.136 (.385)−1.04.409/.5542.167 (.394)2.196 (.395)−1.33.365/.4171.989 (.342)2.000 (.325)−.55.895/.895
    252.116 (.362)2.131 (.368)−.71.485/.5542.167 (.376)2.194 (.377)−1.24.306/.4081.996 (.301)1.983 (.306)0.65.749/.856
    302.113 (.348)2.131 (.354)−.85.342/.5542.162 (.363)2.195 (.361)−1.51.137/.2741.997 (.284)1.980 (.291)0.85.617/.823
    352.115 (.338)2.127 (.342)−.57.483/.5542.165 (.353)2.190 (.347)−1.15.191/.3061.998 (.273)1.977 (.284)1.06.509/.823
    402.117 (.327)2.120 (.332)−.14.882/.8822.168 (.341)2.180 (.336)−.55.529/.5291.998 (.261)1.979 (.282)0.95.485/.823
    • Note:—Pct. Diff. indicates percentage difference; FDR, false discovery rate.

    • Ipsilateral and contralateral columns represent mean (standard deviation) cortical thickness measures in millimeters.

    • ↵a Paired t tests comparing the ipsilateral and contralateral regions were used to calculate P values. The Benjamini-Hochberg procedure was used to control the false discovery rate.

    • ↵b Corrected P values < .05.

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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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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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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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