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Improved Turnaround Times | Median time to first decision: 12 days

Research ArticleBrain

Combined 3T Diffusion Tensor Tractography and 1H-MR Spectroscopy in Motor Neuron Disease

M. Nelles, W. Block, F. Träber, U. Wüllner, H.H. Schild and H. Urbach
American Journal of Neuroradiology October 2008, 29 (9) 1708-1714; DOI: https://doi.org/10.3174/ajnr.A1201
M. Nelles
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W. Block
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F. Träber
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U. Wüllner
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H.H. Schild
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H. Urbach
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    Fig 1.

    A, Illustration of spectroscopic VOI in the central region in axial (left hemisphere) and coronal (right hemisphere) T2-weighted planscan images (left, upper and lower row). Sample spectra (TR/TE, 2000/140 ms; H2O-suppressed) of a healthy control (right, upper row) and patient IV/7 (Table 1) (right, lower row). B, 3D DTT (left) with intersection lines (yellow) shown at the level of FA/MD measurements (precentral gyrus, corona radiata, internal capsule, cerebral peduncles, pons, and pyramid). Fibers are projected onto axial FA (right/upper row, precentral gyrus) and MD maps (right/lower row, internal capsule) to allow a guided region-of-interest placement along the corticospinal tract. FA and MD statistics were additionally averaged on the CSTs as a whole to account for a region-independent analysis.

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    Fig 2.

    A, NAA/Cho and NAA/PCr metabolite ratios for patient subgroups and controls. Both parameters are lowest in group IV (EE probable/definite [prob./def.]). B, FA boxplots of the central region for groups I–IV. Mean FA values of groups III (EE clinically possible [clin. poss.]) and IV (prob./def.) were markedly lower in the upper 3 regions of measurements (Table 3).

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    Table 1:

    Results of the combination MR Spectroscopy/DTI*

    Patient No.UMN†MRSDTIMRS/DTITMS‡DENERV§
    Group IV
        1+++++true pos.NA+
        2+++true pos.–+
        3+++++true pos.––
        4+++++true pos.+–
        5+++++true pos.++
        6+++true pos.–+
        7+++++true pos.++
    Group III
        1+++++true pos.+–
        2–++++false pos.NA+
        3–––true neg.––
        4–––true neg.++
        5–+–true neg.–+
        6–––true neg.++
        7––+true neg.NA+
    Group II
        1–––true neg.+–
        2–––true neg.––
        3–++–true neg.–+
        4–––true neg.––
    • Note:—MRS indicates MR spectroscopy; UMN, upper motor neuron; TMS, transcranial magnetic stimulation; DENERV, denervation; true pos., true-positive; false pos., false positive; true neg., true negative; NA, not applicable; DTI, diffusion tensor imaging.

    • * ++ for MRS indicates NAA/Cho reduction beyond double SD; + beyond single SD. For DTI, ++ indicates 2 or more regions with FA below double SD; + just 1 region, respectively. −indicates a negative result. Reduction beyond the single SD threshold for MRS and beyond the double SD threshold in 1 region for DTI is regarded as a pathologic result of the MRS/DTI combination; discordance is graded as negative. Note that patient III/1 had primary lateral sclerosis but was subgrouped into the “clinically possible” group (III) due to his initial EE rating. DTI and MRS concurrently are false-positive in 1 patient with lower motor neuron involvement only (patient III/2).

    • † Clinical evidence for upper motor neuron involvement.

    • ‡ Pathologic central conduction times in transcranial magnetic stimulation.

    • § Presence or absence of generalized denervation.

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    Table 2:

    NAA/Cho and NAA/PCr metabolite ratios and absolute molar concentrations of NAA, Cho, and PCr (mmol/L brain tissue, mM) for patient subgroups and healthy controls (group Ia)

    GroupNAA/ChoNAA/PCrNAA (mM)Cho (mM)PCr (mM)
    IV* mean1.721.629.791.888.19
        SD0.200.110.700.210.70
    III mean2.081.8310.361.647.61
        SD0.360.181.920.211.03
    II mean2.101.7810.261.607.78
        SD0.250.091.770.231.16
    Ia mean2.111.8212.642.009.15
        SD0.140.121.160.211.24
    • Note:—NAA indicates N-acetylaspartate; Cho, choline; PCr, phosphocreatine.

    • * Both metabolite ratios are lowest in group IV.

    • View popup
    Table 3:

    DTI group results and Mann-Whitney–Wilcoxon test for comparison of mean FA with healthy controls (group Ib)*

    FAPyramidPonsPeduncleCapsuleCent. Semi.Precent. Gyr.FA CSTMD CST
    Group IV
        Mean456.07489.71593.93570.93426.21356.21510.64901.14
        SD64.98111.8662.6255.0184.6948.5036.1031.99
        MWW(P = .062)(P = .001)(P = .001)(P < .001)(P > .05)(P > .05)
    Group III
        Mean508.71553.64617.86612.64435.93417.86510.71932.93
        SD71.2060.8764.3430.8267.2885.6713.82110.01
        MWW(P > .05)(P = .022)(P < .001)(P = .116)(P > .05)(P > .05)
    Group II
        Mean498.75531.00582.38643.75475.75449.75525.13888.63
        SD64.2545.7697.7051.2463.2934.0217.0450.71
    Group Ib (controls)
        Mean495.32577.29592.06648.34531.66475.09524.25897.10
        SD63.4766.9765.8048.9753.9750.4124.5834.92
    • Note:—MWW indicates Mann-Whitney–Wilcoxon test; Cent. Semi., centrum semiovale; Precent. Gyr., precentral gyrus; DTI, diffusion tensor imaging; FA, fractional anisotropy.

    • * The lowest mean FA in comparison with controls is found in the internal capsule, centrum semiovale, and the precentral gyrus of group IV (EE clinically probable/definite) and the internal capsule and centrum semiovale for patients of group III (EE clinically possible). The rightmost FA/MD CST columns illustrate diffusion characteristics averaged for the entire CST. FA ranges from 1000 (maximum anisotropy) to 0 (no anisotropy). MD exhibits statistically significant differences with elevation in the internal capsule in group IV compared with healthy controls (data not shown).

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American Journal of Neuroradiology: 29 (9)
American Journal of Neuroradiology
Vol. 29, Issue 9
October 2008
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M. Nelles, W. Block, F. Träber, U. Wüllner, H.H. Schild, H. Urbach
Combined 3T Diffusion Tensor Tractography and 1H-MR Spectroscopy in Motor Neuron Disease
American Journal of Neuroradiology Oct 2008, 29 (9) 1708-1714; DOI: 10.3174/ajnr.A1201

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Combined 3T Diffusion Tensor Tractography and 1H-MR Spectroscopy in Motor Neuron Disease
M. Nelles, W. Block, F. Träber, U. Wüllner, H.H. Schild, H. Urbach
American Journal of Neuroradiology Oct 2008, 29 (9) 1708-1714; DOI: 10.3174/ajnr.A1201
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