MRI shows thickening and altered diffusion in the median and ulnar nerves in multifocal motor neuropathy

Objectives To study disease mechanisms in multifocal motor neuropathy (MMN) with magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) of the median and ulnar nerves. Methods We enrolled ten MMN patients, ten patients with amyotrophic lateral sclerosis (ALS) and ten healthy controls (H...

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Veröffentlicht in:European radiology 2017-05, Vol.27 (5), p.2216-2224
Hauptverfasser: Haakma, Wieke, Jongbloed, Bas A., Froeling, Martijn, Goedee, H. Stephan, Bos, Clemens, Leemans, Alexander, van den Berg, Leonard H., Hendrikse, Jeroen, van der Pol, W. Ludo
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container_issue 5
container_start_page 2216
container_title European radiology
container_volume 27
creator Haakma, Wieke
Jongbloed, Bas A.
Froeling, Martijn
Goedee, H. Stephan
Bos, Clemens
Leemans, Alexander
van den Berg, Leonard H.
Hendrikse, Jeroen
van der Pol, W. Ludo
description Objectives To study disease mechanisms in multifocal motor neuropathy (MMN) with magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) of the median and ulnar nerves. Methods We enrolled ten MMN patients, ten patients with amyotrophic lateral sclerosis (ALS) and ten healthy controls (HCs). Patients underwent MRI (in a prone position) and nerve conduction studies. DTI and fat-suppressed T2-weighted scans of the forearms were performed on a 3.0T MRI scanner. Fibre tractography of the median and ulnar nerves was performed to extract diffusion parameters: fractional anisotropy (FA), mean (MD), axial (AD) and radial (RD) diffusivity. Cross-sectional areas (CSA) were measured on T2-weighted scans. Results Forty-five out of 60 arms were included in the analysis. AD was significantly lower in MMN patients (2.20 ± 0.12 × 10 -3  mm 2 /s) compared to ALS patients (2.31 ± 0.17 × 10 -3  mm 2 /s; p  
doi_str_mv 10.1007/s00330-016-4575-0
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Stephan ; Bos, Clemens ; Leemans, Alexander ; van den Berg, Leonard H. ; Hendrikse, Jeroen ; van der Pol, W. Ludo</creator><creatorcontrib>Haakma, Wieke ; Jongbloed, Bas A. ; Froeling, Martijn ; Goedee, H. Stephan ; Bos, Clemens ; Leemans, Alexander ; van den Berg, Leonard H. ; Hendrikse, Jeroen ; van der Pol, W. Ludo</creatorcontrib><description>Objectives To study disease mechanisms in multifocal motor neuropathy (MMN) with magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) of the median and ulnar nerves. Methods We enrolled ten MMN patients, ten patients with amyotrophic lateral sclerosis (ALS) and ten healthy controls (HCs). Patients underwent MRI (in a prone position) and nerve conduction studies. DTI and fat-suppressed T2-weighted scans of the forearms were performed on a 3.0T MRI scanner. Fibre tractography of the median and ulnar nerves was performed to extract diffusion parameters: fractional anisotropy (FA), mean (MD), axial (AD) and radial (RD) diffusivity. Cross-sectional areas (CSA) were measured on T2-weighted scans. Results Forty-five out of 60 arms were included in the analysis. AD was significantly lower in MMN patients (2.20 ± 0.12 × 10 -3  mm 2 /s) compared to ALS patients (2.31 ± 0.17 × 10 -3  mm 2 /s; p  &lt; 0.05) and HCs (2.31± 0.17 × 10 -3  mm 2 /s; p  &lt; 0.05). Segmental analysis showed significant restriction of AD, RD and MD ( p  &lt; 0.005) in the proximal third of the nerves. CSA was significantly larger in MMN patients compared to ALS patients and HCs ( p  &lt; 0.01). Conclusions Thickening of nerves is compatible with changes in the myelin sheath structure, whereas lowered AD values suggest axonal dysfunction. These findings suggest that myelin and axons are diffusely involved in MMN pathogenesis. Key Points • Diffusion magnetic resonance imaging provides quantitative information about multifocal motor neuropathy (MMN). • Diffusion tensor imaging allows non-invasive evaluation of the forearm nerves in MMN. • Nerve thickening and lowered diffusion parameters suggests myelin and axonal changes. • This study can help to provide insight into pathological mechanisms of MMN.</description><identifier>ISSN: 0938-7994</identifier><identifier>EISSN: 1432-1084</identifier><identifier>DOI: 10.1007/s00330-016-4575-0</identifier><identifier>PMID: 27655303</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adult ; Aged ; Amyotrophic lateral sclerosis ; Amyotrophic Lateral Sclerosis - diagnostic imaging ; Amyotrophic Lateral Sclerosis - physiopathology ; Anisotropy ; Case-Control Studies ; Diagnostic Radiology ; Diffusion Magnetic Resonance Imaging - methods ; Diffusion Tensor Imaging - methods ; Female ; Forearm - innervation ; Humans ; Imaging ; Internal Medicine ; Interventional Radiology ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Median Nerve - diagnostic imaging ; Median Nerve - physiopathology ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Motor Neuron Disease - diagnostic imaging ; Motor Neuron Disease - physiopathology ; Nervous system ; Neural Conduction - physiology ; Neuro ; Neuroradiology ; Pathogenesis ; Radiology ; Ulnar Nerve - diagnostic imaging ; Ulnar Nerve - physiopathology ; Ultrasound</subject><ispartof>European radiology, 2017-05, Vol.27 (5), p.2216-2224</ispartof><rights>The Author(s) 2016</rights><rights>European Radiology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-5c5eca923e8c5c29362531157ab4920f29094685e73ed0a218d180296d6dccab3</citedby><cites>FETCH-LOGICAL-c503t-5c5eca923e8c5c29362531157ab4920f29094685e73ed0a218d180296d6dccab3</cites><orcidid>0000-0003-1586-885X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00330-016-4575-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00330-016-4575-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27655303$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haakma, Wieke</creatorcontrib><creatorcontrib>Jongbloed, Bas A.</creatorcontrib><creatorcontrib>Froeling, Martijn</creatorcontrib><creatorcontrib>Goedee, H. Stephan</creatorcontrib><creatorcontrib>Bos, Clemens</creatorcontrib><creatorcontrib>Leemans, Alexander</creatorcontrib><creatorcontrib>van den Berg, Leonard H.</creatorcontrib><creatorcontrib>Hendrikse, Jeroen</creatorcontrib><creatorcontrib>van der Pol, W. Ludo</creatorcontrib><title>MRI shows thickening and altered diffusion in the median and ulnar nerves in multifocal motor neuropathy</title><title>European radiology</title><addtitle>Eur Radiol</addtitle><addtitle>Eur Radiol</addtitle><description>Objectives To study disease mechanisms in multifocal motor neuropathy (MMN) with magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) of the median and ulnar nerves. Methods We enrolled ten MMN patients, ten patients with amyotrophic lateral sclerosis (ALS) and ten healthy controls (HCs). Patients underwent MRI (in a prone position) and nerve conduction studies. DTI and fat-suppressed T2-weighted scans of the forearms were performed on a 3.0T MRI scanner. Fibre tractography of the median and ulnar nerves was performed to extract diffusion parameters: fractional anisotropy (FA), mean (MD), axial (AD) and radial (RD) diffusivity. Cross-sectional areas (CSA) were measured on T2-weighted scans. Results Forty-five out of 60 arms were included in the analysis. AD was significantly lower in MMN patients (2.20 ± 0.12 × 10 -3  mm 2 /s) compared to ALS patients (2.31 ± 0.17 × 10 -3  mm 2 /s; p  &lt; 0.05) and HCs (2.31± 0.17 × 10 -3  mm 2 /s; p  &lt; 0.05). Segmental analysis showed significant restriction of AD, RD and MD ( p  &lt; 0.005) in the proximal third of the nerves. CSA was significantly larger in MMN patients compared to ALS patients and HCs ( p  &lt; 0.01). Conclusions Thickening of nerves is compatible with changes in the myelin sheath structure, whereas lowered AD values suggest axonal dysfunction. These findings suggest that myelin and axons are diffusely involved in MMN pathogenesis. Key Points • Diffusion magnetic resonance imaging provides quantitative information about multifocal motor neuropathy (MMN). • Diffusion tensor imaging allows non-invasive evaluation of the forearm nerves in MMN. • Nerve thickening and lowered diffusion parameters suggests myelin and axonal changes. • This study can help to provide insight into pathological mechanisms of MMN.</description><subject>Adult</subject><subject>Aged</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Amyotrophic Lateral Sclerosis - diagnostic imaging</subject><subject>Amyotrophic Lateral Sclerosis - physiopathology</subject><subject>Anisotropy</subject><subject>Case-Control Studies</subject><subject>Diagnostic Radiology</subject><subject>Diffusion Magnetic Resonance Imaging - methods</subject><subject>Diffusion Tensor Imaging - methods</subject><subject>Female</subject><subject>Forearm - innervation</subject><subject>Humans</subject><subject>Imaging</subject><subject>Internal Medicine</subject><subject>Interventional Radiology</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Median Nerve - diagnostic imaging</subject><subject>Median Nerve - physiopathology</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Motor Neuron Disease - diagnostic imaging</subject><subject>Motor Neuron Disease - physiopathology</subject><subject>Nervous system</subject><subject>Neural Conduction - physiology</subject><subject>Neuro</subject><subject>Neuroradiology</subject><subject>Pathogenesis</subject><subject>Radiology</subject><subject>Ulnar Nerve - diagnostic imaging</subject><subject>Ulnar Nerve - physiopathology</subject><subject>Ultrasound</subject><issn>0938-7994</issn><issn>1432-1084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkU1rFTEUhoMo9lr9AW4k4MbN6MnXJNkIUvwoVAqlrkNuJnMndSa5JjOV_nszvbVUQXB1Fu9z3vPxIvSSwFsCIN8VAMagAdI2XEjRwCO0IZzRhoDij9EGNFON1JofoWelXAGAJlw-RUdUtkIwYBs0fL04xWVIPwueh-C--xjiDtvYYTvOPvsOd6HvlxJSxCFWxuPJd8HGW2YZo804-nztyypPyziHPjk74inNaZWWnPZ2Hm6eoye9HYt_cVeP0bdPHy9PvjRn559PTz6cNU4AmxvhhHdWU-aVE45q1lLBCBHSbrmm0FMNmrdKeMl8B5YS1REFVLdd2zlnt-wYvT_47pdt3dT5OGc7mn0Ok803Jtlg_lRiGMwuXRvBJCeSV4M3dwY5_Vh8mc0UivPjaKNPSzFEaaJarbX6D1RoSeoFpKKv_0Kv0pJj_USlFGVCCVgNyYFyOZWSfX-_NwGzRm4OkZsauVkjN1B7Xj08-L7jd8YVoAegVCnufH4w-p-uvwBjuLci</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Haakma, Wieke</creator><creator>Jongbloed, Bas A.</creator><creator>Froeling, Martijn</creator><creator>Goedee, H. 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Stephan</au><au>Bos, Clemens</au><au>Leemans, Alexander</au><au>van den Berg, Leonard H.</au><au>Hendrikse, Jeroen</au><au>van der Pol, W. Ludo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MRI shows thickening and altered diffusion in the median and ulnar nerves in multifocal motor neuropathy</atitle><jtitle>European radiology</jtitle><stitle>Eur Radiol</stitle><addtitle>Eur Radiol</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>27</volume><issue>5</issue><spage>2216</spage><epage>2224</epage><pages>2216-2224</pages><issn>0938-7994</issn><eissn>1432-1084</eissn><abstract>Objectives To study disease mechanisms in multifocal motor neuropathy (MMN) with magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) of the median and ulnar nerves. Methods We enrolled ten MMN patients, ten patients with amyotrophic lateral sclerosis (ALS) and ten healthy controls (HCs). Patients underwent MRI (in a prone position) and nerve conduction studies. DTI and fat-suppressed T2-weighted scans of the forearms were performed on a 3.0T MRI scanner. Fibre tractography of the median and ulnar nerves was performed to extract diffusion parameters: fractional anisotropy (FA), mean (MD), axial (AD) and radial (RD) diffusivity. Cross-sectional areas (CSA) were measured on T2-weighted scans. Results Forty-five out of 60 arms were included in the analysis. AD was significantly lower in MMN patients (2.20 ± 0.12 × 10 -3  mm 2 /s) compared to ALS patients (2.31 ± 0.17 × 10 -3  mm 2 /s; p  &lt; 0.05) and HCs (2.31± 0.17 × 10 -3  mm 2 /s; p  &lt; 0.05). Segmental analysis showed significant restriction of AD, RD and MD ( p  &lt; 0.005) in the proximal third of the nerves. CSA was significantly larger in MMN patients compared to ALS patients and HCs ( p  &lt; 0.01). Conclusions Thickening of nerves is compatible with changes in the myelin sheath structure, whereas lowered AD values suggest axonal dysfunction. These findings suggest that myelin and axons are diffusely involved in MMN pathogenesis. Key Points • Diffusion magnetic resonance imaging provides quantitative information about multifocal motor neuropathy (MMN). • Diffusion tensor imaging allows non-invasive evaluation of the forearm nerves in MMN. • Nerve thickening and lowered diffusion parameters suggests myelin and axonal changes. • This study can help to provide insight into pathological mechanisms of MMN.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>27655303</pmid><doi>10.1007/s00330-016-4575-0</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1586-885X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis - diagnostic imaging
Amyotrophic Lateral Sclerosis - physiopathology
Anisotropy
Case-Control Studies
Diagnostic Radiology
Diffusion Magnetic Resonance Imaging - methods
Diffusion Tensor Imaging - methods
Female
Forearm - innervation
Humans
Imaging
Internal Medicine
Interventional Radiology
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Male
Median Nerve - diagnostic imaging
Median Nerve - physiopathology
Medicine
Medicine & Public Health
Middle Aged
Motor Neuron Disease - diagnostic imaging
Motor Neuron Disease - physiopathology
Nervous system
Neural Conduction - physiology
Neuro
Neuroradiology
Pathogenesis
Radiology
Ulnar Nerve - diagnostic imaging
Ulnar Nerve - physiopathology
Ultrasound
title MRI shows thickening and altered diffusion in the median and ulnar nerves in multifocal motor neuropathy
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