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January 15, 2013; 80 (3) Article

Clinically feasible MTR is sensitive to cortical demyelination in MS

Jacqueline Tien-Hsiang Chen, Kathryn Easley, Colleen Schneider, Kunio Nakamura, Grahame J. Kidd, Ansi Chang, Susan M. Staugaitis, Robert J. Fox, Elizabeth Fisher, Douglas L. Arnold, Bruce D. Trapp
First published December 26, 2012, DOI: https://doi.org/10.1212/WNL.0b013e31827deb99
Jacqueline Tien-Hsiang Chen
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Kathryn Easley
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Colleen Schneider
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Kunio Nakamura
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Grahame J. Kidd
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Ansi Chang
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Susan M. Staugaitis
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Robert J. Fox
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Elizabeth Fisher
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Douglas L. Arnold
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Bruce D. Trapp
From the Departments of Neurosciences (J.T.-H.C., K.E., C.S., G.J.K., A.C., S.M.S., B.D.T.) and Biomedical Engineering (K.N., E.F.), Lerner Research Institute, Department of Anatomic Pathology, Pathology and Laboratory Medicine Institute (S.M.S.), and Mellen Center for Multiple Sclerosis Treatment and Research (R.J.F.), Cleveland Clinic, Cleveland, OH; and McConnell Brain Imaging Centre (J.T.-H.C., D.L.A.), Montreal Neurological Institute, McGill University, Montreal, Canada.
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Full PDF
Citation
Clinically feasible MTR is sensitive to cortical demyelination in MS
Jacqueline Tien-Hsiang Chen, Kathryn Easley, Colleen Schneider, Kunio Nakamura, Grahame J. Kidd, Ansi Chang, Susan M. Staugaitis, Robert J. Fox, Elizabeth Fisher, Douglas L. Arnold, Bruce D. Trapp
Neurology Jan 2013, 80 (3) 246-252; DOI: 10.1212/WNL.0b013e31827deb99

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Abstract

Objective: Presently there is no clinically feasible imaging modality that can effectively detect cortical demyelination in patients with multiple sclerosis (MS). The objective of this study is to determine if clinically feasible magnetization transfer ratio (MTR) imaging is sensitive to cortical demyelination in MS.

Methods: MRI were acquired in situ on 7 recently deceased patients with MS using clinically feasible sequences at 3 T, including relatively high-resolution T1-weighted and proton density–weighted images with/without a magnetization transfer pulse for calculation of MTR. The brains were rapidly removed and placed in fixative. Multiple cortical regions from each brain were immunostained for myelin proteolipid protein and classified as mostly myelinated (MMctx), mostly demyelinated (MDctx), or intermediately demyelinated (IDctx). MRIs were registered with the cortical sections so that the cortex corresponding to each cortical section could be identified, along with adjacent subcortical white matter (WM). Mean cortical MTR normalized to mean WM MTR was calculated for each cortical region. Linear mixed-effects models were used to test if mean normalized cortical MTR was significantly lower in demyelinated cortex.

Results: We found that mean normalized cortical MTR was significantly lower in cortical tissue with any demyelination (IDctx or MDctx) compared to MMctx (demyelinated cortex: least-squares mean [LSM] = 0.797, SE = 0.007; MMctx: LSM = 0.837, SE = 0.006; p = 0.01, n = 89).

Conclusions: This result demonstrates that clinically feasible MTR imaging is sensitive to cortical demyelination and suggests that MTR will be a useful tool to help detect MS cortical lesions in living patients with MS.

GLOSSARY

CL=
cortical demyelinated lesions;
HSD=
honestly significant difference;
IDctx=
intermediately demyelinated;
LSM=
least-squares mean;
MDctx=
mostly demyelinated;
MMctx=
mostly myelinated;
MR=
magnetic resonance;
MS=
multiple sclerosis;
MTR=
magnetization transfer ratio;
MTRctx=
mean cortical magnetization transfer ratio;
normMTRctx=
normalized cortical magnetization transfer ratio;
PLP=
proteolipid protein;
TE=
echo time;
TR=
repetition time;
T1W=
T1-weighted;
WM=
white matter

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Received May 14, 2012.
  • Accepted September 4, 2012.
  • © 2012 American Academy of Neurology
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