Combined Magnetization Transfer and Proton Spectroscopic Imaging in the Assessment of Pathologic Brain Lesions in Multiple Sclerosis
G. Bruce Pike
,a,
Nicola de Stefanoa,
Sridar Narayanana,
Gordon S. Francisa,
Jack P. Antela and
Douglas L. Arnolda
a From the McConnell Brain Imaging Center, Montreal Neurological Institute, McGill University, Canada (G.B.P., S.N., G.F., J.P.A., D.L.A.); and the Department of Neurology, University of Siena, Italy (N.D.S.).

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FIG 1. AF, T1-weighted (A), T2-weighted (B), proton densityweighted (C), MTR (D), and NAA/Cr (E) spectroscopic images of a patient with MS acquired using the protocol presented in the Table; also shown is the classified lesion map for this section (F).
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FIG 2. A and B, Mean (per patient) lesional MTR versus NAA/Cr for the entire cohort of patients with MS (A) and the relapsing-remitting subgroup (B) (circles indicate relapsing-remitting group; plus signs, primary progressive; diamonds, secondary progressive). Linear regression lines are plotted for both data sets, but the correlation was significant only for the relapsing-remitting subgroup (solid line in B; rS = .70; P = .016)
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FIG 3. A and B, Mean (per patient) MTR versus NAA/Cr in new lesions (<6 months old) for the entire cohort of patients with MS (A) and the relapsing-remitting subgroup (B) (circles indicate relapsing-remitting group; plus signs, primary progressive; diamonds, secondary progressive). The solid lines represent the linear regressions, and the corresponding rank correlations were rS = .44, P = .015 (A) and rS = .81, P = .002 (B)
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FIG 4. A and B, Mean (per MRSI voxel) MTR versus NAA/Cr in all MRSI voxels containing more than 25% lesion and less than 10% ventricle for the entire cohort of patients with MS (A) and the relapsing-remitting subgroup (B) (circles indicate relapsing-remitting group; plus signs, primary progressive; diamonds, secondary progressive). The solid lines represent the linear regressions corresponding to linear correlations of rP = .27, P < .0001 (A) and rP = .45, P < .0001 (B)
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