Magnetic resonance imaging pattern variability in dysferlinopathy
The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy. Twenty-five patients with the clin...
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Veröffentlicht in: | Acta myologica 2021-12, Vol.40 (4), p.158-171 |
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creator | Bardakov, Sergey N Tsargush, Vadim A Carlier, Pierre G Nikitin, Sergey S Kurbatov, Sergey A Titova, Angelina A Umakhanova, Zoya R Akhmedova, Patimat G Magomedova, Raisat M Zheleznyak, Igor S Emelyantsev, Alexander A Berezhnaya, Ekaterina N A Yakovlev, Ivan Isaev, Artur A Deev, Roman V |
description | The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy.
Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken.
Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished.
Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations. |
doi_str_mv | 10.36185/2532-1900-059 |
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Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken.
Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished.
Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations.</description><identifier>ISSN: 1128-2460</identifier><identifier>EISSN: 2532-1900</identifier><identifier>DOI: 10.36185/2532-1900-059</identifier><identifier>PMID: 35047756</identifier><language>eng</language><publisher>Italy: Pacini Editore Srl</publisher><subject>Humans ; Magnetic Resonance Imaging ; Muscle, Skeletal - diagnostic imaging ; Muscular Diseases ; Muscular Dystrophies, Limb-Girdle - diagnostic imaging ; Muscular Dystrophies, Limb-Girdle - genetics ; Original</subject><ispartof>Acta myologica, 2021-12, Vol.40 (4), p.158-171</ispartof><rights>2021 Gaetano Conte Academy - Mediterranean Society of Myology, Naples, Italy.</rights><rights>2021 Gaetano Conte Academy - Mediterranean Society of Myology, Naples, Italy 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c226t-ca2ec78cfac1aacf4269d791d66c47f60c5509eb09a8aa9de8151df0bd670fb33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744010/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744010/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35047756$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bardakov, Sergey N</creatorcontrib><creatorcontrib>Tsargush, Vadim A</creatorcontrib><creatorcontrib>Carlier, Pierre G</creatorcontrib><creatorcontrib>Nikitin, Sergey S</creatorcontrib><creatorcontrib>Kurbatov, Sergey A</creatorcontrib><creatorcontrib>Titova, Angelina A</creatorcontrib><creatorcontrib>Umakhanova, Zoya R</creatorcontrib><creatorcontrib>Akhmedova, Patimat G</creatorcontrib><creatorcontrib>Magomedova, Raisat M</creatorcontrib><creatorcontrib>Zheleznyak, Igor S</creatorcontrib><creatorcontrib>Emelyantsev, Alexander A</creatorcontrib><creatorcontrib>Berezhnaya, Ekaterina N</creatorcontrib><creatorcontrib>A Yakovlev, Ivan</creatorcontrib><creatorcontrib>Isaev, Artur A</creatorcontrib><creatorcontrib>Deev, Roman V</creatorcontrib><title>Magnetic resonance imaging pattern variability in dysferlinopathy</title><title>Acta myologica</title><addtitle>Acta Myol</addtitle><description>The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy.
Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken.
Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished.
Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations.</description><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Muscle, Skeletal - diagnostic imaging</subject><subject>Muscular Diseases</subject><subject>Muscular Dystrophies, Limb-Girdle - diagnostic imaging</subject><subject>Muscular Dystrophies, Limb-Girdle - genetics</subject><subject>Original</subject><issn>1128-2460</issn><issn>2532-1900</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkM1Lw0AQxRdRbKm9epT8A9HZzX5kL0IpWoWKFz2HyX6kK-mmbGIh_70Btehchsd78-MxhFxTuC0kLcUdEwXLqQbIQegzMj_pczKnlJU54xJmZNn3HzAN51ILdklmhQCulJBzsnrBJrohmCy5vosYjcvCHpsQm-yAw-BSzI6YAtahDcOYhZjZsfcutSF2U2A3XpELj23vlj97Qd4fH97WT_n2dfO8Xm1zw5gccoPMGVUaj4YiGs-Z1FZpaqU0XHkJRgjQrgaNJaK2rqSCWg-1lQp8XRQLcv_NPXzWe2eNi0PCtjqkqW4aqw5D9d-JYVc13bEqFedAYQLc_AWcLn-fUXwBudpktA</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Bardakov, Sergey N</creator><creator>Tsargush, Vadim A</creator><creator>Carlier, Pierre G</creator><creator>Nikitin, Sergey S</creator><creator>Kurbatov, Sergey A</creator><creator>Titova, Angelina A</creator><creator>Umakhanova, Zoya R</creator><creator>Akhmedova, Patimat G</creator><creator>Magomedova, Raisat M</creator><creator>Zheleznyak, Igor S</creator><creator>Emelyantsev, Alexander A</creator><creator>Berezhnaya, Ekaterina N</creator><creator>A Yakovlev, Ivan</creator><creator>Isaev, Artur A</creator><creator>Deev, Roman V</creator><general>Pacini Editore Srl</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>5PM</scope></search><sort><creationdate>20211201</creationdate><title>Magnetic resonance imaging pattern variability in dysferlinopathy</title><author>Bardakov, Sergey N ; Tsargush, Vadim A ; Carlier, Pierre G ; Nikitin, Sergey S ; Kurbatov, Sergey A ; Titova, Angelina A ; Umakhanova, Zoya R ; Akhmedova, Patimat G ; Magomedova, Raisat M ; Zheleznyak, Igor S ; Emelyantsev, Alexander A ; Berezhnaya, Ekaterina N ; A Yakovlev, Ivan ; Isaev, Artur A ; Deev, Roman V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c226t-ca2ec78cfac1aacf4269d791d66c47f60c5509eb09a8aa9de8151df0bd670fb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Muscle, Skeletal - diagnostic imaging</topic><topic>Muscular Diseases</topic><topic>Muscular Dystrophies, Limb-Girdle - diagnostic imaging</topic><topic>Muscular Dystrophies, Limb-Girdle - genetics</topic><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bardakov, Sergey N</creatorcontrib><creatorcontrib>Tsargush, Vadim A</creatorcontrib><creatorcontrib>Carlier, Pierre G</creatorcontrib><creatorcontrib>Nikitin, Sergey S</creatorcontrib><creatorcontrib>Kurbatov, Sergey A</creatorcontrib><creatorcontrib>Titova, Angelina A</creatorcontrib><creatorcontrib>Umakhanova, Zoya R</creatorcontrib><creatorcontrib>Akhmedova, Patimat G</creatorcontrib><creatorcontrib>Magomedova, Raisat M</creatorcontrib><creatorcontrib>Zheleznyak, Igor S</creatorcontrib><creatorcontrib>Emelyantsev, Alexander A</creatorcontrib><creatorcontrib>Berezhnaya, Ekaterina N</creatorcontrib><creatorcontrib>A Yakovlev, Ivan</creatorcontrib><creatorcontrib>Isaev, Artur A</creatorcontrib><creatorcontrib>Deev, Roman V</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Acta myologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bardakov, Sergey N</au><au>Tsargush, Vadim A</au><au>Carlier, Pierre G</au><au>Nikitin, Sergey S</au><au>Kurbatov, Sergey A</au><au>Titova, Angelina A</au><au>Umakhanova, Zoya R</au><au>Akhmedova, Patimat G</au><au>Magomedova, Raisat M</au><au>Zheleznyak, Igor S</au><au>Emelyantsev, Alexander A</au><au>Berezhnaya, Ekaterina N</au><au>A Yakovlev, Ivan</au><au>Isaev, Artur A</au><au>Deev, Roman V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnetic resonance imaging pattern variability in dysferlinopathy</atitle><jtitle>Acta myologica</jtitle><addtitle>Acta Myol</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>40</volume><issue>4</issue><spage>158</spage><epage>171</epage><pages>158-171</pages><issn>1128-2460</issn><eissn>2532-1900</eissn><abstract>The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy.
Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken.
Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished.
Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations.</abstract><cop>Italy</cop><pub>Pacini Editore Srl</pub><pmid>35047756</pmid><doi>10.36185/2532-1900-059</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Humans Magnetic Resonance Imaging Muscle, Skeletal - diagnostic imaging Muscular Diseases Muscular Dystrophies, Limb-Girdle - diagnostic imaging Muscular Dystrophies, Limb-Girdle - genetics Original |
title | Magnetic resonance imaging pattern variability in dysferlinopathy |
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