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Research ArticleBrain
Open Access

Tissue-Specific Imaging Is a Robust Methodology to Differentiate In Vivo T1 Black Holes with Advanced Multiple Sclerosis–Induced Damage

M. Riva, V.N. Ikonomidou, J.J. Ostuni, P. van Gelderen, S. Auh, J.M. Ohayon, F. Tovar-Moll, N.D. Richert, J.H. Duyn and F. Bagnato
American Journal of Neuroradiology August 2009, 30 (7) 1394-1401; DOI: https://doi.org/10.3174/ajnr.A1573
M. Riva
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V.N. Ikonomidou
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J.J. Ostuni
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P. van Gelderen
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S. Auh
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J.M. Ohayon
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F. Tovar-Moll
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N.D. Richert
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J.H. Duyn
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F. Bagnato
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    Fig 1.

    A, Axial view of IR-FSPGR image. B, Axial view of 3D-TSI-CSF image. C, Axial view of T1-weighted image acquired at the time of the 3T MR imaging. D, Axial view of T1-weighted image acquired 24 months before images reported in A–C. A–D shows a group-A lesion (arrowheads). Only one of the lesions identified on MR imaging is discussed as an example. It can be seen that the BH in A corresponds to a hyperintense area on the relative TSI volume (B). The BH marked here is defined as CBH because it was present 24 months before the 3T study (D).

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    Fig 2.

    A, Axial view of IR-FSPGR image. B, Axial view of 3D-TSI-CSF image. C, Axial view of T1-weighted image acquired at the time of the 3T MR imaging. D, Axial view of T1-weighted image acquired 24 months before images reported in A–C. A–D reports a group-B lesion (arrowheads). Compared with group A, group-B chronic BHs do not have a corresponding hyperintense area on the 3D-TSI-CSF image (B), thought to be present as an area of hypointensity on IR-FSPGR and T1-weighted images (A,C).

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    Fig 3.

    The figure represents the box plot distribution of mean MTR values of NAWM, the BG, group-B lesions, group-A lesions, and CSF. Although group-B and group-A lesions show a wider distribution, it is possible to note a separation among all observed groups.

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    Fig 4.

    The white bars represent group-A lesions; the gray bars represent group-B lesions. Patients with SPMS are marked with dotted columns. The graph reports the distribution of the mean MTR of group-A and group-B lesions per patient. The data refer to 15 patients. Of the 18 examined, 1 was excluded from the MTR evaluation because of the poor image quality and 1 because of presenting with no T2W image. Of the remaining 16 patients, all except 1 patient had at least 1 CBH.

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  • Demographic, clinical, and MR imaging characteristics of patients at the time of 3T MR imaging

    Patients with RRMS (n = 9)Patients with SPMS (n = 7)P value*
    Age (y)41.3 ± 6.3 (range, 32–53)50.2 ± 6.0 (range, 41–56).012
    Sex5 women, 4 men6 women, 1 manNS
    Years since MS onset10.4 ± 6.2 (range, 3–20)18.4 ± 5.2 (range, 13–28).016
    EDSS1.9 ± 1.1 (range, 0–4)6.0 ± 0.6 (range, 5–6.5)<.0001
    PASAT48.7 ± 12.8 (range, 22–60)31.2 ± 8.1 (range, 21–45).008
    BPF0.81 ± 0.05 (range, 0.76–0.92)0.75 ± 0.04 (range, 0.71–0.81).014
    T2-LV (cm3)11.5 ± 8.8 (range, 0.78–25.5)12.6 ± 8.4 (range, 4.6–30.1)NS
    Number of patients with CELs1†0N/A
    CBHs (number)48.9 ± 51.5 (range, 0–126)37.4 ± 19.7 (range, 19–76)NS
    CBHs (volume in cm3)2.8 ± 3.3 (range, 0.1–9.6)3.2 ± 2.7 (range, 0.8–8.4)NS
    CBHs-LV/T2-LV (%)16.9 ± 11.7 (range, 3–34)24.1 ± 10.3 (range, 14–48)NS
    Undergoing therapies
        Interferon beta33
        Daclizumab4−
        Other treatments−2
        None22
    • Note:—RRMS indicates relapsing-remitting multiple sclerosis; SPMS, secondary-progressive multiple sclerosis; EDSS, Expanded Disability Status Scale; PASAT, Paced Auditory Serial Addition Test; BPF, brain parenchyma fraction; T2-LV, T2 lesion volume; CELs, contrast-enhancing lesions; CBHs, chronic black holes; N/A, not applicable; NS, not significant.

    • * P values are significant if P ≤ .05.

    • † A single patient had 1 CEL in the corpus callosum (see text in the Results section).

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American Journal of Neuroradiology: 30 (7)
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M. Riva, V.N. Ikonomidou, J.J. Ostuni, P. van Gelderen, S. Auh, J.M. Ohayon, F. Tovar-Moll, N.D. Richert, J.H. Duyn, F. Bagnato
Tissue-Specific Imaging Is a Robust Methodology to Differentiate In Vivo T1 Black Holes with Advanced Multiple Sclerosis–Induced Damage
American Journal of Neuroradiology Aug 2009, 30 (7) 1394-1401; DOI: 10.3174/ajnr.A1573

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Tissue-Specific Imaging Is a Robust Methodology to Differentiate In Vivo T1 Black Holes with Advanced Multiple Sclerosis–Induced Damage
M. Riva, V.N. Ikonomidou, J.J. Ostuni, P. van Gelderen, S. Auh, J.M. Ohayon, F. Tovar-Moll, N.D. Richert, J.H. Duyn, F. Bagnato
American Journal of Neuroradiology Aug 2009, 30 (7) 1394-1401; DOI: 10.3174/ajnr.A1573
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