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Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlations
•MUNIX is a feasible biomarker in SMA types 3 and 4 patients with mild phenotype.•MUNIX variability is higher in SMA patients compared to healthy controls.•MUNIX in TA correlates with disease severity by functional scales in patients with mild motor impairment. Spinal muscular atrophy (SMA) is a mot...
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Published in: | Neuromuscular disorders : NMD 2021-06, Vol.31 (6), p.498-504 |
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creator | Mendonça, Rodrigo Holanda Machado, Ligia Maria Sotero Heise, Carlos Otto Polido, Graziela Jorge Matsui, Ciro Silva, André Macedo Serafim Reed, Umbertina Conti Zanoteli, Edmar |
description | •MUNIX is a feasible biomarker in SMA types 3 and 4 patients with mild phenotype.•MUNIX variability is higher in SMA patients compared to healthy controls.•MUNIX in TA correlates with disease severity by functional scales in patients with mild motor impairment.
Spinal muscular atrophy (SMA) is a motor neuron disease associated with progressive muscle weakness and motor disability. The motor unit number index (MUNIX) is a biomarker used to assess loss of motor units in later-onset SMA patients. Twenty SMA patients (SMA types 3 and 4), aged between 7 and 41 years, were clinically evaluated through the Hammersmith Motor Functional Scale Expanded and the Spinal Muscular Atrophy-Functional Rating Scale. The patients underwent compound motor action potential (CMAP) and MUNIX studies of the right abductor pollicis brevis, abductor digiti minimi and tibialis anterior (TA) muscles. Age-matched healthy controls (n = 20) were enrolled to obtain normative CMAP and MUNIX values from the same muscles. Compared to healthy controls, SMA patients showed significant reductions in MUNIX values among all muscles studied, whereas CMAP showed reductions only in the weaker muscles (abductor digiti minimi and TA). MUNIX variability was significantly higher in the SMA group than in the control group. MUNIX variability in TA correlated with CMAP variability. Motor functional scores correlated with TA MUNIX. The MUNIX study is feasible in later-onset SMA patients, and TA MUNIX values correlate with disease severity in patients with mild motor impairment. |
doi_str_mv | 10.1016/j.nmd.2021.02.019 |
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Spinal muscular atrophy (SMA) is a motor neuron disease associated with progressive muscle weakness and motor disability. The motor unit number index (MUNIX) is a biomarker used to assess loss of motor units in later-onset SMA patients. Twenty SMA patients (SMA types 3 and 4), aged between 7 and 41 years, were clinically evaluated through the Hammersmith Motor Functional Scale Expanded and the Spinal Muscular Atrophy-Functional Rating Scale. The patients underwent compound motor action potential (CMAP) and MUNIX studies of the right abductor pollicis brevis, abductor digiti minimi and tibialis anterior (TA) muscles. Age-matched healthy controls (n = 20) were enrolled to obtain normative CMAP and MUNIX values from the same muscles. Compared to healthy controls, SMA patients showed significant reductions in MUNIX values among all muscles studied, whereas CMAP showed reductions only in the weaker muscles (abductor digiti minimi and TA). MUNIX variability was significantly higher in the SMA group than in the control group. MUNIX variability in TA correlated with CMAP variability. Motor functional scores correlated with TA MUNIX. The MUNIX study is feasible in later-onset SMA patients, and TA MUNIX values correlate with disease severity in patients with mild motor impairment.</description><identifier>ISSN: 0960-8966</identifier><identifier>EISSN: 1873-2364</identifier><identifier>DOI: 10.1016/j.nmd.2021.02.019</identifier><identifier>PMID: 33824074</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>CMAP ; Hammersmith functional motor scale expanded ; MUNIX ; Spinal muscular atrophy</subject><ispartof>Neuromuscular disorders : NMD, 2021-06, Vol.31 (6), p.498-504</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-16b31e2c9f155b1011c8d91e08b29152f839fb7c2bdca40378825a7edfd634d23</citedby><cites>FETCH-LOGICAL-c353t-16b31e2c9f155b1011c8d91e08b29152f839fb7c2bdca40378825a7edfd634d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33824074$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mendonça, Rodrigo Holanda</creatorcontrib><creatorcontrib>Machado, Ligia Maria Sotero</creatorcontrib><creatorcontrib>Heise, Carlos Otto</creatorcontrib><creatorcontrib>Polido, Graziela Jorge</creatorcontrib><creatorcontrib>Matsui, Ciro</creatorcontrib><creatorcontrib>Silva, André Macedo Serafim</creatorcontrib><creatorcontrib>Reed, Umbertina Conti</creatorcontrib><creatorcontrib>Zanoteli, Edmar</creatorcontrib><title>Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlations</title><title>Neuromuscular disorders : NMD</title><addtitle>Neuromuscul Disord</addtitle><description>•MUNIX is a feasible biomarker in SMA types 3 and 4 patients with mild phenotype.•MUNIX variability is higher in SMA patients compared to healthy controls.•MUNIX in TA correlates with disease severity by functional scales in patients with mild motor impairment.
Spinal muscular atrophy (SMA) is a motor neuron disease associated with progressive muscle weakness and motor disability. The motor unit number index (MUNIX) is a biomarker used to assess loss of motor units in later-onset SMA patients. Twenty SMA patients (SMA types 3 and 4), aged between 7 and 41 years, were clinically evaluated through the Hammersmith Motor Functional Scale Expanded and the Spinal Muscular Atrophy-Functional Rating Scale. The patients underwent compound motor action potential (CMAP) and MUNIX studies of the right abductor pollicis brevis, abductor digiti minimi and tibialis anterior (TA) muscles. Age-matched healthy controls (n = 20) were enrolled to obtain normative CMAP and MUNIX values from the same muscles. Compared to healthy controls, SMA patients showed significant reductions in MUNIX values among all muscles studied, whereas CMAP showed reductions only in the weaker muscles (abductor digiti minimi and TA). MUNIX variability was significantly higher in the SMA group than in the control group. MUNIX variability in TA correlated with CMAP variability. Motor functional scores correlated with TA MUNIX. The MUNIX study is feasible in later-onset SMA patients, and TA MUNIX values correlate with disease severity in patients with mild motor impairment.</description><subject>CMAP</subject><subject>Hammersmith functional motor scale expanded</subject><subject>MUNIX</subject><subject>Spinal muscular atrophy</subject><issn>0960-8966</issn><issn>1873-2364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kDtvFDEUhS0EIkvgB9Agl6GYwY95QoUiHpESaAiiszz2He1deeyN7QG24L_jZQMl1dWVvnOk8xHynLOaM9692tV-sbVggtdM1IyPD8iGD72shOyah2TDxo5Vw9h1Z-RJSjvGeNt3_WNyJuUgGtY3G_LrJuQQ6eoxU78uE0SK3sJPenFz--nq28vyUbNFZyN4qr2l2q4uJ_oD85a2d1Xao9eOLmsyq9OR6hzDfnt4Tb_qiHpCh_nwJ2ccejQFNSFGcDpj8OkpeTRrl-DZ_T0nt-_ffbn8WF1__nB1-fa6MrKVueLdJDkIM868bacynZvBjhzYMImRt2Ie5DhPvRGTNbphsh8G0eoe7Gw72Vghz8nFqXcfw90KKasFkwHntIewJiXao6pjVUH5CTUxpBRhVvuIi44HxZk6Wlc7Vayro3XFhCrWS-bFff06LWD_Jf5qLsCbEwBl5HeEqJJB8AYsRjBZ2YD_qf8NFBKTZg</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Mendonça, Rodrigo Holanda</creator><creator>Machado, Ligia Maria Sotero</creator><creator>Heise, Carlos Otto</creator><creator>Polido, Graziela Jorge</creator><creator>Matsui, Ciro</creator><creator>Silva, André Macedo Serafim</creator><creator>Reed, Umbertina Conti</creator><creator>Zanoteli, Edmar</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210601</creationdate><title>Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlations</title><author>Mendonça, Rodrigo Holanda ; Machado, Ligia Maria Sotero ; Heise, Carlos Otto ; Polido, Graziela Jorge ; Matsui, Ciro ; Silva, André Macedo Serafim ; Reed, Umbertina Conti ; Zanoteli, Edmar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-16b31e2c9f155b1011c8d91e08b29152f839fb7c2bdca40378825a7edfd634d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>CMAP</topic><topic>Hammersmith functional motor scale expanded</topic><topic>MUNIX</topic><topic>Spinal muscular atrophy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mendonça, Rodrigo Holanda</creatorcontrib><creatorcontrib>Machado, Ligia Maria Sotero</creatorcontrib><creatorcontrib>Heise, Carlos Otto</creatorcontrib><creatorcontrib>Polido, Graziela Jorge</creatorcontrib><creatorcontrib>Matsui, Ciro</creatorcontrib><creatorcontrib>Silva, André Macedo Serafim</creatorcontrib><creatorcontrib>Reed, Umbertina Conti</creatorcontrib><creatorcontrib>Zanoteli, Edmar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neuromuscular disorders : NMD</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mendonça, Rodrigo Holanda</au><au>Machado, Ligia Maria Sotero</au><au>Heise, Carlos Otto</au><au>Polido, Graziela Jorge</au><au>Matsui, Ciro</au><au>Silva, André Macedo Serafim</au><au>Reed, Umbertina Conti</au><au>Zanoteli, Edmar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlations</atitle><jtitle>Neuromuscular disorders : NMD</jtitle><addtitle>Neuromuscul Disord</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>31</volume><issue>6</issue><spage>498</spage><epage>504</epage><pages>498-504</pages><issn>0960-8966</issn><eissn>1873-2364</eissn><abstract>•MUNIX is a feasible biomarker in SMA types 3 and 4 patients with mild phenotype.•MUNIX variability is higher in SMA patients compared to healthy controls.•MUNIX in TA correlates with disease severity by functional scales in patients with mild motor impairment.
Spinal muscular atrophy (SMA) is a motor neuron disease associated with progressive muscle weakness and motor disability. The motor unit number index (MUNIX) is a biomarker used to assess loss of motor units in later-onset SMA patients. Twenty SMA patients (SMA types 3 and 4), aged between 7 and 41 years, were clinically evaluated through the Hammersmith Motor Functional Scale Expanded and the Spinal Muscular Atrophy-Functional Rating Scale. The patients underwent compound motor action potential (CMAP) and MUNIX studies of the right abductor pollicis brevis, abductor digiti minimi and tibialis anterior (TA) muscles. Age-matched healthy controls (n = 20) were enrolled to obtain normative CMAP and MUNIX values from the same muscles. Compared to healthy controls, SMA patients showed significant reductions in MUNIX values among all muscles studied, whereas CMAP showed reductions only in the weaker muscles (abductor digiti minimi and TA). MUNIX variability was significantly higher in the SMA group than in the control group. MUNIX variability in TA correlated with CMAP variability. Motor functional scores correlated with TA MUNIX. The MUNIX study is feasible in later-onset SMA patients, and TA MUNIX values correlate with disease severity in patients with mild motor impairment.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>33824074</pmid><doi>10.1016/j.nmd.2021.02.019</doi><tpages>7</tpages></addata></record> |
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title | Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlations |
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