Literature DB >> 23269598

Clinically feasible MTR is sensitive to cortical demyelination in MS.

Jacqueline Tien-Hsiang Chen1, 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.   

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 (MM(ctx)), mostly demyelinated (MD(ctx)), or intermediately demyelinated (ID(ctx)). 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 (ID(ctx) or MD(ctx)) compared to MM(ctx) (demyelinated cortex: least-squares mean [LSM] = 0.797, SE = 0.007; MM(ctx): 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.

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Year:  2012        PMID: 23269598      PMCID: PMC3589181          DOI: 10.1212/WNL.0b013e31827deb99

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  21 in total

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2.  A global optimisation method for robust affine registration of brain images.

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3.  Imaging the tip of the iceberg: visualization of cortical lesions in multiple sclerosis.

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4.  Postmortem verification of MS cortical lesion detection with 3D DIR.

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5.  Inflammatory cortical demyelination in early multiple sclerosis.

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8.  Subpial demyelination in the cerebral cortex of multiple sclerosis patients.

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3.  Comparison of Multiple Sclerosis Cortical Lesion Types Detected by Multicontrast 3T and 7T MRI.

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4.  MR Imaging-based Estimation of Upper Motor Neuron Density in Patients with Amyotrophic Lateral Sclerosis: A Feasibility Study.

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5.  Multisite reliability and repeatability of an advanced brain MRI protocol.

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6.  HLA-DRB1*15 influences the development of brain tissue damage in early PPMS.

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Review 8.  Imaging as an Outcome Measure in Multiple Sclerosis.

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10.  Hippocampal volume is related to cognitive decline and fornicial diffusion measures in multiple sclerosis.

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