Magnetization transfer ratio: a quantitative imaging biomarker for 5q spinal muscular atrophy

In this exploratory study, we used magnetization transfer contrast (MTC) imaging, an MRI technique that provides information about protons bound to macromolecular structures such as myelin lipids or collagen, to quantify sciatic nerve lesions in patients with spinal muscular atrophy (SMA) 3a and 3b....

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Veröffentlicht in:European journal of neurology 2021-01, Vol.28 (1), p.331-340
Hauptverfasser: Kollmer, J., Kessler, T., Sam, G., Hayes, J. M., Lentz, S. I., Heiland, S., Bendszus, M., Wick, W., Weiler, M.
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container_title European journal of neurology
container_volume 28
creator Kollmer, J.
Kessler, T.
Sam, G.
Hayes, J. M.
Lentz, S. I.
Heiland, S.
Bendszus, M.
Wick, W.
Weiler, M.
description In this exploratory study, we used magnetization transfer contrast (MTC) imaging, an MRI technique that provides information about protons bound to macromolecular structures such as myelin lipids or collagen, to quantify sciatic nerve lesions in patients with spinal muscular atrophy (SMA) 3a and 3b. Our results show that the calculated magnetization transfer ratio (MTR) reliably differentiated between healthy controls, SMA 3a, and SMA 3b, while correlating well with clinical scores and compound motor action potentials. MTR might become a new imaging biomarker that potentially helps to better monitor SMA patients on causative pharmacotherapies in the future. Background and purpose We quantified peripheral nerve lesions in adults with 5q‐linked spinal muscular atrophy (SMA) type 3 by analysing the magnetization transfer ratio (MTR) of the sciatic nerve, and tested its potential as a novel biomarker for macromolecular changes. Methods Eighteen adults with SMA 3 (50% SMA 3a, 50% SMA 3b) and 18 age‐/sex‐matched healthy controls prospectively underwent magnetization transfer contrast imaging in a 3‐Tesla magnetic resonance scanner. Two axial three‐dimensional gradient echo sequences, with and without an off‐resonance saturation rapid frequency pulse, were performed at the right distal thigh. Sciatic nerve regions of interest were manually traced on 10 consecutive axial slices in the images generated without off‐resonance saturation, and then transferred to corresponding slices generated by the sequence with the off‐resonance saturation pulse. Subsequently, MTR and cross‐sectional areas (CSAs) of the sciatic nerve were analysed. In addition, detailed neurologic, physiotherapeutic and electrophysiologic examinations were conducted in all patients. Results Sciatic nerve MTR and CSA reliably differentiated between healthy controls and SMA 3, 3a or 3b. MTR was lower in the SMA 3 (P 
doi_str_mv 10.1111/ene.14528
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M. ; Lentz, S. I. ; Heiland, S. ; Bendszus, M. ; Wick, W. ; Weiler, M.</creator><creatorcontrib>Kollmer, J. ; Kessler, T. ; Sam, G. ; Hayes, J. M. ; Lentz, S. I. ; Heiland, S. ; Bendszus, M. ; Wick, W. ; Weiler, M.</creatorcontrib><description>In this exploratory study, we used magnetization transfer contrast (MTC) imaging, an MRI technique that provides information about protons bound to macromolecular structures such as myelin lipids or collagen, to quantify sciatic nerve lesions in patients with spinal muscular atrophy (SMA) 3a and 3b. Our results show that the calculated magnetization transfer ratio (MTR) reliably differentiated between healthy controls, SMA 3a, and SMA 3b, while correlating well with clinical scores and compound motor action potentials. MTR might become a new imaging biomarker that potentially helps to better monitor SMA patients on causative pharmacotherapies in the future. Background and purpose We quantified peripheral nerve lesions in adults with 5q‐linked spinal muscular atrophy (SMA) type 3 by analysing the magnetization transfer ratio (MTR) of the sciatic nerve, and tested its potential as a novel biomarker for macromolecular changes. Methods Eighteen adults with SMA 3 (50% SMA 3a, 50% SMA 3b) and 18 age‐/sex‐matched healthy controls prospectively underwent magnetization transfer contrast imaging in a 3‐Tesla magnetic resonance scanner. Two axial three‐dimensional gradient echo sequences, with and without an off‐resonance saturation rapid frequency pulse, were performed at the right distal thigh. Sciatic nerve regions of interest were manually traced on 10 consecutive axial slices in the images generated without off‐resonance saturation, and then transferred to corresponding slices generated by the sequence with the off‐resonance saturation pulse. Subsequently, MTR and cross‐sectional areas (CSAs) of the sciatic nerve were analysed. In addition, detailed neurologic, physiotherapeutic and electrophysiologic examinations were conducted in all patients. Results Sciatic nerve MTR and CSA reliably differentiated between healthy controls and SMA 3, 3a or 3b. MTR was lower in the SMA 3 (P &lt; 0.0001), SMA 3a (P &lt; 0.0001) and SMA 3b groups (P = 0.0020) than in respective controls. In patients with SMA 3, MTR correlated with all clinical scores, and arm nerve compound motor action potentials (CMAPs). CSA was lower in the SMA 3 (P &lt; 0.0001), SMA 3a (P &lt; 0.0001) and SMA 3b groups (P = 0.0006) than in controls, but did not correlate with clinical scores or electrophysiologic results. Conclusions Magnetization transfer ratio is a novel imaging marker that quantifies macromolecular nerve changes in SMA 3, and positively correlates with clinical scores and CMAPs.</description><identifier>ISSN: 1351-5101</identifier><identifier>EISSN: 1468-1331</identifier><identifier>DOI: 10.1111/ene.14528</identifier><identifier>PMID: 32918834</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>Adults ; Atrophy ; Biomarkers ; Correlation analysis ; electrophysiology ; Imaging ; Macromolecules ; Magnetic resonance ; Magnetization ; magnetization transfer contrast (MTC) imaging ; magnetization transfer ratio (MTR) ; neurodegeneration ; Neuromuscular diseases ; Peripheral nerves ; Resonance ; Saturation ; Sciatic nerve ; Spinal muscular atrophy ; spinal muscular atrophy (SMA) ; Thigh</subject><ispartof>European journal of neurology, 2021-01, Vol.28 (1), p.331-340</ispartof><rights>2020 The Authors. published by John Wiley &amp; Sons Ltd on behalf of European Academy of Neurology</rights><rights>2020 The Authors. European Journal of Neurology published by John Wiley &amp; Sons Ltd on behalf of European Academy of Neurology.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3888-ab87ffebb3515de2eda3ab3405054703cffc5285735da1905f434cf17239ef943</citedby><cites>FETCH-LOGICAL-c3888-ab87ffebb3515de2eda3ab3405054703cffc5285735da1905f434cf17239ef943</cites><orcidid>0000-0002-8942-7662 ; 0000-0002-6254-9192</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fene.14528$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fene.14528$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32918834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kollmer, J.</creatorcontrib><creatorcontrib>Kessler, T.</creatorcontrib><creatorcontrib>Sam, G.</creatorcontrib><creatorcontrib>Hayes, J. M.</creatorcontrib><creatorcontrib>Lentz, S. I.</creatorcontrib><creatorcontrib>Heiland, S.</creatorcontrib><creatorcontrib>Bendszus, M.</creatorcontrib><creatorcontrib>Wick, W.</creatorcontrib><creatorcontrib>Weiler, M.</creatorcontrib><title>Magnetization transfer ratio: a quantitative imaging biomarker for 5q spinal muscular atrophy</title><title>European journal of neurology</title><addtitle>Eur J Neurol</addtitle><description>In this exploratory study, we used magnetization transfer contrast (MTC) imaging, an MRI technique that provides information about protons bound to macromolecular structures such as myelin lipids or collagen, to quantify sciatic nerve lesions in patients with spinal muscular atrophy (SMA) 3a and 3b. Our results show that the calculated magnetization transfer ratio (MTR) reliably differentiated between healthy controls, SMA 3a, and SMA 3b, while correlating well with clinical scores and compound motor action potentials. MTR might become a new imaging biomarker that potentially helps to better monitor SMA patients on causative pharmacotherapies in the future. Background and purpose We quantified peripheral nerve lesions in adults with 5q‐linked spinal muscular atrophy (SMA) type 3 by analysing the magnetization transfer ratio (MTR) of the sciatic nerve, and tested its potential as a novel biomarker for macromolecular changes. Methods Eighteen adults with SMA 3 (50% SMA 3a, 50% SMA 3b) and 18 age‐/sex‐matched healthy controls prospectively underwent magnetization transfer contrast imaging in a 3‐Tesla magnetic resonance scanner. Two axial three‐dimensional gradient echo sequences, with and without an off‐resonance saturation rapid frequency pulse, were performed at the right distal thigh. Sciatic nerve regions of interest were manually traced on 10 consecutive axial slices in the images generated without off‐resonance saturation, and then transferred to corresponding slices generated by the sequence with the off‐resonance saturation pulse. Subsequently, MTR and cross‐sectional areas (CSAs) of the sciatic nerve were analysed. In addition, detailed neurologic, physiotherapeutic and electrophysiologic examinations were conducted in all patients. Results Sciatic nerve MTR and CSA reliably differentiated between healthy controls and SMA 3, 3a or 3b. MTR was lower in the SMA 3 (P &lt; 0.0001), SMA 3a (P &lt; 0.0001) and SMA 3b groups (P = 0.0020) than in respective controls. In patients with SMA 3, MTR correlated with all clinical scores, and arm nerve compound motor action potentials (CMAPs). CSA was lower in the SMA 3 (P &lt; 0.0001), SMA 3a (P &lt; 0.0001) and SMA 3b groups (P = 0.0006) than in controls, but did not correlate with clinical scores or electrophysiologic results. Conclusions Magnetization transfer ratio is a novel imaging marker that quantifies macromolecular nerve changes in SMA 3, and positively correlates with clinical scores and CMAPs.</description><subject>Adults</subject><subject>Atrophy</subject><subject>Biomarkers</subject><subject>Correlation analysis</subject><subject>electrophysiology</subject><subject>Imaging</subject><subject>Macromolecules</subject><subject>Magnetic resonance</subject><subject>Magnetization</subject><subject>magnetization transfer contrast (MTC) imaging</subject><subject>magnetization transfer ratio (MTR)</subject><subject>neurodegeneration</subject><subject>Neuromuscular diseases</subject><subject>Peripheral nerves</subject><subject>Resonance</subject><subject>Saturation</subject><subject>Sciatic nerve</subject><subject>Spinal muscular atrophy</subject><subject>spinal muscular atrophy (SMA)</subject><subject>Thigh</subject><issn>1351-5101</issn><issn>1468-1331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNp10E1LwzAYB_AgitPpwS8gAS966JbXNvUmY77A1IsepaRtMjPbZktaZX56Mzs9COaSPPDjT54_ACcYjXA4Y9WoEWaciB1wgFksIkwp3g1vynHEMcIDcOj9AiFEEoL2wYCSFAtB2QF4uZfzRrXmU7bGNrB1svFaOeg28yWUcNXJpjVtGN8VNLWcm2YOc2Nr6d6C09ZBvoJ-aRpZwbrzRVdJB2Xr7PJ1fQT2tKy8Ot7eQ_B8PX2a3Eazx5u7ydUsKqgQIpK5SLRWeR7-y0tFVCmpzClDHHGWIFpoXYTteEJ5KXGKuGaUFRonhKZKp4wOwXmfu3R21SnfZrXxhaoq2Sjb-YwwRghBaSwCPftDF7Zz4fMbleCU85jGQV30qnDWe6d0tnRhebfOMMo2nWeh8-y782BPt4ldXqvyV_6UHMC4Bx-mUuv_k7Lpw7SP_ALH5osn</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Kollmer, J.</creator><creator>Kessler, T.</creator><creator>Sam, G.</creator><creator>Hayes, J. M.</creator><creator>Lentz, S. I.</creator><creator>Heiland, S.</creator><creator>Bendszus, M.</creator><creator>Wick, W.</creator><creator>Weiler, M.</creator><general>John Wiley &amp; Sons, Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8942-7662</orcidid><orcidid>https://orcid.org/0000-0002-6254-9192</orcidid></search><sort><creationdate>202101</creationdate><title>Magnetization transfer ratio: a quantitative imaging biomarker for 5q spinal muscular atrophy</title><author>Kollmer, J. ; Kessler, T. ; Sam, G. ; Hayes, J. M. ; Lentz, S. 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M.</creatorcontrib><creatorcontrib>Lentz, S. I.</creatorcontrib><creatorcontrib>Heiland, S.</creatorcontrib><creatorcontrib>Bendszus, M.</creatorcontrib><creatorcontrib>Wick, W.</creatorcontrib><creatorcontrib>Weiler, M.</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kollmer, J.</au><au>Kessler, T.</au><au>Sam, G.</au><au>Hayes, J. M.</au><au>Lentz, S. I.</au><au>Heiland, S.</au><au>Bendszus, M.</au><au>Wick, W.</au><au>Weiler, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnetization transfer ratio: a quantitative imaging biomarker for 5q spinal muscular atrophy</atitle><jtitle>European journal of neurology</jtitle><addtitle>Eur J Neurol</addtitle><date>2021-01</date><risdate>2021</risdate><volume>28</volume><issue>1</issue><spage>331</spage><epage>340</epage><pages>331-340</pages><issn>1351-5101</issn><eissn>1468-1331</eissn><abstract>In this exploratory study, we used magnetization transfer contrast (MTC) imaging, an MRI technique that provides information about protons bound to macromolecular structures such as myelin lipids or collagen, to quantify sciatic nerve lesions in patients with spinal muscular atrophy (SMA) 3a and 3b. Our results show that the calculated magnetization transfer ratio (MTR) reliably differentiated between healthy controls, SMA 3a, and SMA 3b, while correlating well with clinical scores and compound motor action potentials. MTR might become a new imaging biomarker that potentially helps to better monitor SMA patients on causative pharmacotherapies in the future. Background and purpose We quantified peripheral nerve lesions in adults with 5q‐linked spinal muscular atrophy (SMA) type 3 by analysing the magnetization transfer ratio (MTR) of the sciatic nerve, and tested its potential as a novel biomarker for macromolecular changes. Methods Eighteen adults with SMA 3 (50% SMA 3a, 50% SMA 3b) and 18 age‐/sex‐matched healthy controls prospectively underwent magnetization transfer contrast imaging in a 3‐Tesla magnetic resonance scanner. Two axial three‐dimensional gradient echo sequences, with and without an off‐resonance saturation rapid frequency pulse, were performed at the right distal thigh. Sciatic nerve regions of interest were manually traced on 10 consecutive axial slices in the images generated without off‐resonance saturation, and then transferred to corresponding slices generated by the sequence with the off‐resonance saturation pulse. Subsequently, MTR and cross‐sectional areas (CSAs) of the sciatic nerve were analysed. In addition, detailed neurologic, physiotherapeutic and electrophysiologic examinations were conducted in all patients. Results Sciatic nerve MTR and CSA reliably differentiated between healthy controls and SMA 3, 3a or 3b. MTR was lower in the SMA 3 (P &lt; 0.0001), SMA 3a (P &lt; 0.0001) and SMA 3b groups (P = 0.0020) than in respective controls. In patients with SMA 3, MTR correlated with all clinical scores, and arm nerve compound motor action potentials (CMAPs). CSA was lower in the SMA 3 (P &lt; 0.0001), SMA 3a (P &lt; 0.0001) and SMA 3b groups (P = 0.0006) than in controls, but did not correlate with clinical scores or electrophysiologic results. Conclusions Magnetization transfer ratio is a novel imaging marker that quantifies macromolecular nerve changes in SMA 3, and positively correlates with clinical scores and CMAPs.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>32918834</pmid><doi>10.1111/ene.14528</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-8942-7662</orcidid><orcidid>https://orcid.org/0000-0002-6254-9192</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adults
Atrophy
Biomarkers
Correlation analysis
electrophysiology
Imaging
Macromolecules
Magnetic resonance
Magnetization
magnetization transfer contrast (MTC) imaging
magnetization transfer ratio (MTR)
neurodegeneration
Neuromuscular diseases
Peripheral nerves
Resonance
Saturation
Sciatic nerve
Spinal muscular atrophy
spinal muscular atrophy (SMA)
Thigh
title Magnetization transfer ratio: a quantitative imaging biomarker for 5q spinal muscular atrophy
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