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Research ArticleAdult Brain
Open Access

Systematic Assessment of Multispectral Voxel-Based Morphometry in Previously MRI-Negative Focal Epilepsy

R. Kotikalapudi, P. Martin, J. Marquetand, T. Lindig, B. Bender and N.K. Focke
American Journal of Neuroradiology November 2018, 39 (11) 2014-2021; DOI: https://doi.org/10.3174/ajnr.A5809
R. Kotikalapudi
aFrom the Departments of Diagnostic and Interventional Neuroradiology (R.K., T.L., B.B.)
bNeurology and Epileptology (R.K., P.M., J.M., N.K.F.), Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Tübingen, Germany
cDepartment of Clinical Neurophysiology (R.K., N.K.F.), University Hospital Göttingen, Göttingen, Germany.
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  • ORCID record for R. Kotikalapudi
P. Martin
bNeurology and Epileptology (R.K., P.M., J.M., N.K.F.), Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Tübingen, Germany
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J. Marquetand
bNeurology and Epileptology (R.K., P.M., J.M., N.K.F.), Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Tübingen, Germany
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T. Lindig
aFrom the Departments of Diagnostic and Interventional Neuroradiology (R.K., T.L., B.B.)
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B. Bender
aFrom the Departments of Diagnostic and Interventional Neuroradiology (R.K., T.L., B.B.)
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N.K. Focke
bNeurology and Epileptology (R.K., P.M., J.M., N.K.F.), Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Tübingen, Germany
cDepartment of Clinical Neurophysiology (R.K., N.K.F.), University Hospital Göttingen, Göttingen, Germany.
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  • Fig 1.
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    Fig 1.

    Diagnostic performance of different VBM models. A and B, The area under the curve for different smoothing kernels for gray matter concentration and volume. C, An example of an intersection plot for T1 VBM for the concordant rate and specificity against statistical cutoffs. D, An example of a receiver operating characteristic curve for T1 VBM at 12-mm smoothing for GMC. The Euclidean distance is calculated from the optimized T-threshold (3.7 in GMC analysis), where CR, SP = 38.5, 33.9 to CR, SP = 100, 100. False positive rate = 100-SP.

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    Fig 2.

    Sample case (patient 4). A and C, An overview in the native space T1, T2, and FLAIR images. B and D, Zoomed-in images focusing on a possible epileptogenic lesion. A subtle disruption of cortical morphology is visible in this figure, more prominent on FLAIR images. This finding is concordant with the clinical hypothesis supported by noninvasive and intracranial EEG, indicating seizure onset in the right frontal lobe. The possible lesion was detected as increased GM by all VBM models, but the extent and effect size were clearly better for the VBM models, including FLAIR (E).

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    Fig 3.

    Sample case (patient 13). A, A VBM finding detected only by T1+FLAIR in the left temporoinsular region overlaid on the native space FLAIR image. B, Magnified images of T1, T2, and FLAIR suggesting a blurred gray-white matter junction (arrow). This finding is concordant with the clinical hypothesis of seizure onset.

Tables

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    Table 1:

    GMC analysis for VBM models at 12 mm and a T-threshold of 3.7a

    ModelConcordant Rate (%)Specificity (%)Discordant Rate (%)Euclidean Distance (Range, 0–141.14)Concordant Rate/Discordant Rate
    T138.533.984.690.290.46
    T1+T246.240.353.880.370.86
    T1+FLAIR46.237.161.582.770.75
    T1+T2+FLAIR46.235.576.984.000.60
    • ↵a For VBM GMC automated analysis (prior to visual interpretation), values of concordant rate, specificity, discordant rate, Euclidean distance from CR = SP = 100, and concordant/discordant ratio are provided for all models: namely, T1, T1+T2, T1+FLAIR, and T1+T2+FLAIR. The smoothing level and T-threshold are 12 mm and 3.7, respectively.

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    Table 2:

    GMV analysis for VBM models at 12 mm and a T-threshold of 3.0a

    ModelConcordant Rate (%)Specificity (%)Discordant Rate (%)Euclidean Distance (Range, 0–141.14)Concordant Rate/Discordant Rate
    T123.121.084.6110.250.27
    T1+T27.717.776.9123.660.10
    T1+FLAIR38.59.784.6109.250.46
    T1+T2+FLAIR38.514.576.9105.320.50
    • ↵a For VBM GMV automated analysis (prior to visual interpretation), values of concordant rate, specificity, discordant rate, Euclidean distance from CR = SP = 100, and concordant/discordant ratio are provided for all models: namely, T1, T1+T2, T1+FLAIR, and T1+T2+FLAIR. The smoothing level and T-threshold are 12 mm and 3.0, respectively.

    • View popup
    Table 3:

    Patients—visual analysis results for GMCa

    ModelPotentially Epileptogenic (and Visible)Potentially Epileptogenic (and Not Visible)Potentially Epileptogenic (Combined)NonepileptogenicUnclearArtifacts
    Concordant lobe (%)
        T115.415.430.87.715.40
        T1+T215.4015.47.715.40
        T1+FLAIR15.430.846.27.723.10
        T1+T2+FLAIR15.415.430.87.723.10
    Discordant lobe (%)
        T17.738.546.27.730.815.4
        T1+T27.723.130.8023.10
        T1+FLAIR7.730.838.57.730.87.7
        T1+T2+FLAIR7.723.130.8030.87.7
    • ↵a Visual interpretation results of GMC analysis of patients are provided. The results contain percentages of patients scored by the reviewer as potentially epileptogenic and visible, potentially epileptogenic and not visible, potentially epileptogenic (number of patients with potentially epileptogenic and visible/not visible or both), nonepileptogenic, unclear, and artifacts. The results are reported for both concordant and discordant lobes.

    • View popup
    Table 4:

    Controls—visual analysis results for GMCa

    ModelsAll Lobes (%)
    NonepileptogenicUnclearArtifactsCorrected Specificity (Excluding Artifacts and Nonepileptogenic)
    T114.553.222.646.8
    T1+T221.045.217.754.8
    T1+FLAIR16.150.019.450.0
    T1+T2+FLAIR16.148.425.851.6
    • ↵a Visual interpretation results for GMC analysis for controls are presented. Results contain the percentage of controls scored by the reviewer as nonepileptogenic, unclear, and artifacts. Finally, corrected specificity is reported as the percentage of controls that did not have unclear findings—that is, all findings identified as artifacts/nonepileptogenic lesions and patients with no findings (VBM specificity prior to visual analysis).

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    Table 5:

    Nonvisible findings—visual analysis results for GMCa

    ModelsAll Lobes (%)
    ControlsPatients
    T153.261.5
    T1+T245.230.8
    T1+FLAIR50.061.5
    T1+T2+FLAIR48.446.2
    • ↵a Rates of findings not visible—that is, unclear findings in controls and unclear/potentially epileptogenic and not visible findings in patients across all models for all lobes (%) are reported.

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American Journal of Neuroradiology: 39 (11)
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Cite this article
R. Kotikalapudi, P. Martin, J. Marquetand, T. Lindig, B. Bender, N.K. Focke
Systematic Assessment of Multispectral Voxel-Based Morphometry in Previously MRI-Negative Focal Epilepsy
American Journal of Neuroradiology Nov 2018, 39 (11) 2014-2021; DOI: 10.3174/ajnr.A5809

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Systematic Assessment of Multispectral Voxel-Based Morphometry in Previously MRI-Negative Focal Epilepsy
R. Kotikalapudi, P. Martin, J. Marquetand, T. Lindig, B. Bender, N.K. Focke
American Journal of Neuroradiology Nov 2018, 39 (11) 2014-2021; DOI: 10.3174/ajnr.A5809
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