Motor callosal disconnection in early relapsing-remitting multiple sclerosis

In relapsing‐remitting multiple sclerosis (RRMS) the corpus callosum (CC) is often and early affected by macroscopic lesions when investigated by conventional MRI. We sought to determine to which extent microstructural and effective disconnection of the CC are already present in RRMS patients at the...

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Veröffentlicht in:Human brain mapping 2011-06, Vol.32 (6), p.846-855
Hauptverfasser: Wahl, Mathias, Hübers, Annemarie, Lauterbach-Soon, Birgit, Hattingen, Elke, Jung, Patrick, Cohen, Leonardo G., Ziemann, Ulf
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container_issue 6
container_start_page 846
container_title Human brain mapping
container_volume 32
creator Wahl, Mathias
Hübers, Annemarie
Lauterbach-Soon, Birgit
Hattingen, Elke
Jung, Patrick
Cohen, Leonardo G.
Ziemann, Ulf
description In relapsing‐remitting multiple sclerosis (RRMS) the corpus callosum (CC) is often and early affected by macroscopic lesions when investigated by conventional MRI. We sought to determine to which extent microstructural and effective disconnection of the CC are already present in RRMS patients at the earliest stages of the disease prior to evidence of macroscopic CC lesion. We compared 16 very early RRMS patients (median expanded disability status scale (EDSS), 1.5; range, 0–2.0) to an age‐matched group of healthy controls and focused analysis to the motor CC, i.e. that part of the CC relaying interhemispheric motor information. A combined functional magnetic resonance imaging/diffusion tensor imaging fiber‐tracking procedure was applied to identify the callosal motor fibers (CMFs) connecting the hand areas of the primary motor cortices of the two hemispheres. Fractional anisotropy (FA) within the motor CC (FA‐CC) assessed the CMF microstructural integrity. Bifocal paired transcranial magnetic stimulation (TMS) tested short‐interval interhemispheric inhibition (S‐IHI), an established measure of CMF effective connectivity. FA‐CC and S‐IHI were significantly reduced in early RRMS compared to healthy controls. Furthermore, a significant linear correlation between microstructure (FA‐CC) and function (S‐IHI) in the controls was broken down in the patients. These abnormalities were obtained in the absence of macroscopic CMF lesion in conventional MRI, and whilst motor hand/arm function in the nine‐hole‐peg test and corticospinal conduction time were normal. Findings suggest that reductions in FA and S‐IHI may serve as surrogate markers of motor callosal disconnection at the earliest stages of RRMS prior to development of macroscopic lesion. Hum Brain Mapp, 2011. © 2010 Wiley‐Liss, Inc.
doi_str_mv 10.1002/hbm.21071
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We sought to determine to which extent microstructural and effective disconnection of the CC are already present in RRMS patients at the earliest stages of the disease prior to evidence of macroscopic CC lesion. We compared 16 very early RRMS patients (median expanded disability status scale (EDSS), 1.5; range, 0–2.0) to an age‐matched group of healthy controls and focused analysis to the motor CC, i.e. that part of the CC relaying interhemispheric motor information. A combined functional magnetic resonance imaging/diffusion tensor imaging fiber‐tracking procedure was applied to identify the callosal motor fibers (CMFs) connecting the hand areas of the primary motor cortices of the two hemispheres. Fractional anisotropy (FA) within the motor CC (FA‐CC) assessed the CMF microstructural integrity. Bifocal paired transcranial magnetic stimulation (TMS) tested short‐interval interhemispheric inhibition (S‐IHI), an established measure of CMF effective connectivity. FA‐CC and S‐IHI were significantly reduced in early RRMS compared to healthy controls. Furthermore, a significant linear correlation between microstructure (FA‐CC) and function (S‐IHI) in the controls was broken down in the patients. These abnormalities were obtained in the absence of macroscopic CMF lesion in conventional MRI, and whilst motor hand/arm function in the nine‐hole‐peg test and corticospinal conduction time were normal. Findings suggest that reductions in FA and S‐IHI may serve as surrogate markers of motor callosal disconnection at the earliest stages of RRMS prior to development of macroscopic lesion. 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Brain Mapp</addtitle><date>2011-06</date><risdate>2011</risdate><volume>32</volume><issue>6</issue><spage>846</spage><epage>855</epage><pages>846-855</pages><issn>1065-9471</issn><issn>1097-0193</issn><eissn>1097-0193</eissn><abstract>In relapsing‐remitting multiple sclerosis (RRMS) the corpus callosum (CC) is often and early affected by macroscopic lesions when investigated by conventional MRI. We sought to determine to which extent microstructural and effective disconnection of the CC are already present in RRMS patients at the earliest stages of the disease prior to evidence of macroscopic CC lesion. We compared 16 very early RRMS patients (median expanded disability status scale (EDSS), 1.5; range, 0–2.0) to an age‐matched group of healthy controls and focused analysis to the motor CC, i.e. that part of the CC relaying interhemispheric motor information. 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source Wiley Online Library Core Title; MEDLINE; PubMed Central; EZB Electronic Journals Library
subjects Adult
bifocal transcranial magnetic stimulation
Biological and medical sciences
Brain Mapping
Cerebrospinal fluid. Spinal cord. Spinal roots. Spinal nerves
Child
Corpus Callosum - pathology
Diffusion Tensor Imaging
effective connectivity
Humans
Image Interpretation, Computer-Assisted
Infant
interhemispheric inhibition
Investigative techniques, diagnostic techniques (general aspects)
Medical sciences
Middle Aged
motor corpus callosum
Motor Cortex - pathology
multiple sclerosis
Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
Multiple Sclerosis, Relapsing-Remitting - pathology
Nervous system
Neurology
Neurosurgery
Radiodiagnosis. Nmr imagery. Nmr spectrometry
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Transcranial Magnetic Stimulation
Young Adult
title Motor callosal disconnection in early relapsing-remitting multiple sclerosis
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