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Research ArticleBrain
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Impact of Methodologic Choice for Automatic Detection of Different Aspects of Brain Atrophy by Using Temporal Lobe Epilepsy as a Model

C. Scanlon, S.G. Mueller, D. Tosun, I. Cheong, P. Garcia, J. Barakos, M.W. Weiner and K.D. Laxer
American Journal of Neuroradiology October 2011, 32 (9) 1669-1676; DOI: https://doi.org/10.3174/ajnr.A2578
C. Scanlon
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S.G. Mueller
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D. Tosun
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I. Cheong
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P. Garcia
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J. Barakos
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M.W. Weiner
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K.D. Laxer
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    Fig 1.

    Controls versus TLE-mts. A, VBM-SPM GM differences. B, DBM Jacobian differences. C, FS-CT differences between groups. All results corrected for multiple comparisons by using permutation analysis (P < .05).

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    Fig 2.

    Controls versus TLE-no. A, VBM-SPM GM differences. B, DBM Jacobian differences. C, FS-CT differences between groups. All results corrected for multiple comparisons by using permutation analysis (P < .05).

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    Fig 3.

    Controls versus TLE-mts and controls versus TLE-no after FDR < .05 correction for multiple comparisons. A, VBM-SPM GM differences. B, DBM Jacobian differences. C, FS-CT differences between controls and TLE-mts. D, VBM-SPM GM differences. E, DBM Jacobian differences. F, FS-CT differences between controls and TLE-no.

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    Table 1:

    TLE-mts versus controls

    MethodRegionCluster SizeCluster t-Statistic
    FreesurferIpsilateral temporo-occipital20 414.11 mm2 (70 691 vertices)6.139
    DBMBilateral mesial temporal lobe, bilateral thalamus, basal ganglia, subcortical white matter, cerebellum, and brain stem259 230 mm2 (259 230 vertices)7.529
    VBMIpsilateral mesial temporal lobe, bilateral thalamus, and ipsilateral basal ganglia282 288 mm3 (282 288 voxels)5.693
    Ipsilateral temporal and bilateral occipital cortex
    Cerebellum and brain stem
    • Note:—Clusters representing significant differences between controls and TLE-mts for each method after correction for multiple comparisons by using permutation testing.

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    Table 2:

    TLE-no versus controls

    MethodRegionCluster SizeCluster t-Statistic
    FreesurferIpsilateral inferior and lateral temporal lobe; insula, posterior, and superior frontal lobe; and lateral and medial occipital region62 071 mm2 (70 691 vertices)7.679
    Contralateral inferior and lateral temporal lobe; insula, posterior, and superior frontal lobe; and lateral and medial occipital region58 961 mm2 (66 554 vertices)4.883
    DBMCerebellum, brain stem, and ipsilateral temporal lobe74 453 mm3 (74 453 voxels)5.281
    Bilateral superior frontal cortex, pre- and postcentral cortex, and superior pariental cortex54 397 mm3 (54 397 voxels)4.572
    • Note:—Clusters representing significant differences between controls and TLE-no for each method after correction for multiple comparisons by using permutation testing. No significant clusters were found using the VBM method.

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American Journal of Neuroradiology: 32 (9)
American Journal of Neuroradiology
Vol. 32, Issue 9
1 Oct 2011
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C. Scanlon, S.G. Mueller, D. Tosun, I. Cheong, P. Garcia, J. Barakos, M.W. Weiner, K.D. Laxer
Impact of Methodologic Choice for Automatic Detection of Different Aspects of Brain Atrophy by Using Temporal Lobe Epilepsy as a Model
American Journal of Neuroradiology Oct 2011, 32 (9) 1669-1676; DOI: 10.3174/ajnr.A2578

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Impact of Methodologic Choice for Automatic Detection of Different Aspects of Brain Atrophy by Using Temporal Lobe Epilepsy as a Model
C. Scanlon, S.G. Mueller, D. Tosun, I. Cheong, P. Garcia, J. Barakos, M.W. Weiner, K.D. Laxer
American Journal of Neuroradiology Oct 2011, 32 (9) 1669-1676; DOI: 10.3174/ajnr.A2578
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