New insights on contraction efficiency in patients with Duchenne muscular dystrophy.
Identifieur interne : 003350 ( PubMed/Curation ); précédent : 003349; suivant : 003351New insights on contraction efficiency in patients with Duchenne muscular dystrophy.
Auteurs : Lilian Lacourpaille [France] ; François Hug [France] ; Arnaud Guével [France] ; Yann Péréon ; Armelle Magot ; Jean-Yves Hogrel [France] ; Antoine Nordez [France]Source :
- Journal of applied physiology (Bethesda, Md. : 1985) [ 1522-1601 ] ; 2014.
Descripteurs français
- KwdFr :
- Adolescent, Bras (physiopathologie), Contraction musculaire, Enfant, Enfant d'âge préscolaire, Femelle, Force musculaire, Humains, Imagerie d'élasticité tissulaire, Jeune adulte, Muscles squelettiques (imagerie diagnostique), Muscles squelettiques (physiopathologie), Myopathie de Duchenne (imagerie diagnostique), Myopathie de Duchenne (physiopathologie), Mâle, Nourrisson, Stimulation électrique, Transmission synaptique.
- MESH :
- imagerie diagnostique : Muscles squelettiques, Myopathie de Duchenne.
- physiopathologie : Bras, Muscles squelettiques, Myopathie de Duchenne.
- Adolescent, Contraction musculaire, Enfant, Enfant d'âge préscolaire, Femelle, Force musculaire, Humains, Imagerie d'élasticité tissulaire, Jeune adulte, Mâle, Nourrisson, Stimulation électrique, Transmission synaptique.
English descriptors
- KwdEn :
- Adolescent, Arm (physiopathology), Child, Child, Preschool, Elasticity Imaging Techniques, Electric Stimulation, Female, Humans, Infant, Male, Muscle Contraction, Muscle Strength, Muscle, Skeletal (diagnostic imaging), Muscle, Skeletal (physiopathology), Muscular Dystrophy, Duchenne (diagnostic imaging), Muscular Dystrophy, Duchenne (physiopathology), Synaptic Transmission, Young Adult.
- MESH :
- diagnostic imaging : Muscle, Skeletal, Muscular Dystrophy, Duchenne.
- physiopathology : Arm, Muscle, Skeletal, Muscular Dystrophy, Duchenne.
- Adolescent, Child, Child, Preschool, Elasticity Imaging Techniques, Electric Stimulation, Female, Humans, Infant, Male, Muscle Contraction, Muscle Strength, Synaptic Transmission, Young Adult.
Abstract
The decrease in muscle strength in patients with Duchenne muscular dystrophy (DMD) is mainly explained by a decrease in the number of active contractile elements. Nevertheless, it is possible that other electrochemical and force transmission processes may contribute. The present study aimed to quantify the effect of DMD on the relative contribution of electrochemical and force transmission components of the electromechanical delay (i.e., time lag between the onset of muscle activation and force production) in humans using very high frame rate ultrasound. Fourteen patients with DMD and thirteen control subjects underwent two electrically evoked contractions of the biceps brachii with the ultrasound probe over the muscle belly. The electromechanical delay was significantly longer in DMD patients compared with controls (18.5 ± 3.9 vs. 12.5 ± 1.4 ms, P < 0.0001). More precisely, DMD patients exhibited a longer delay between the onset of muscle fascicles motion and force production (13.6 ± 3.1 vs. 7.9 ± 2.0 ms, P < 0.0001). This delay was correlated to the chronological age of the DMD patients (r = 0.66; P = 0.01), but not of the controls (r = -0.45; P = 0.10). No significant difference was found for the delay between the onset of muscle stimulation and the onset of muscle fascicle motion. These results highlight the role of the alteration of muscle force transmission (delay between the onset of fascicle motion and force production) in the impairments of the contraction efficiency in patients with DMD.
DOI: 10.1152/japplphysiol.00544.2014
PubMed: 25103971
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Yann Péréon<affiliation><nlm:affiliation>Centre de Référence Maladies Neuromusculaires Nantes-Angers, University of Nantes, Centre Hospitalier Universitaire, Nantes, France; Atlantic Gene Therapies, Nantes, France; and.</nlm:affiliation><wicri:noCountry code="subField">France; and</wicri:noCountry></affiliation><affiliation><nlm:affiliation>Centre de Référence Maladies Neuromusculaires Nantes-Angers, University of Nantes, Centre Hospitalier Universitaire, Nantes, France; Atlantic Gene Therapies, Nantes, France; and.</nlm:affiliation><wicri:noCountry code="subField">France; and</wicri:noCountry></affiliation>Le document en format XML
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National Health and Medical Research Council, Centre of Clinical Research Excellence in Spinal Pain, Injury and Health, School of Health and Rehabilitation Sciences, University of Queensland, Brisbane, Queensland, Australia; francois.hug@univ-nantes.fr.</nlm:affiliation><country wicri:rule="url">France</country><wicri:regionArea>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes, France; National Health and Medical Research Council, Centre of Clinical Research Excellence in Spinal Pain, Injury and Health, School of Health and Rehabilitation Sciences, University of Queensland, Brisbane, Queensland</wicri:regionArea></affiliation></author><author><name sortKey="Guevel, Arnaud" sort="Guevel, Arnaud" uniqKey="Guevel A" first="Arnaud" last="Guével">Arnaud Guével</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes, France;</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes</wicri:regionArea></affiliation></author><author><name sortKey="Pereon, Yann" sort="Pereon, Yann" uniqKey="Pereon Y" first="Yann" last="Péréon">Yann Péréon</name><affiliation><nlm:affiliation>Centre de Référence Maladies Neuromusculaires Nantes-Angers, University of Nantes, Centre Hospitalier Universitaire, Nantes, France; Atlantic Gene Therapies, Nantes, France; and.</nlm:affiliation><wicri:noCountry code="subField">France; and</wicri:noCountry></affiliation></author><author><name sortKey="Magot, Armelle" sort="Magot, Armelle" uniqKey="Magot A" first="Armelle" last="Magot">Armelle Magot</name><affiliation><nlm:affiliation>Centre de Référence Maladies Neuromusculaires Nantes-Angers, University of Nantes, Centre Hospitalier Universitaire, Nantes, France; Atlantic Gene Therapies, Nantes, France; and.</nlm:affiliation><wicri:noCountry code="subField">France; and</wicri:noCountry></affiliation></author><author><name sortKey="Hogrel, Jean Yves" sort="Hogrel, Jean Yves" uniqKey="Hogrel J" first="Jean-Yves" last="Hogrel">Jean-Yves Hogrel</name><affiliation wicri:level="1"><nlm:affiliation>Institut de Myologie, GH Pitié-Salpêtrière, Paris, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Institut de Myologie, GH Pitié-Salpêtrière, Paris</wicri:regionArea></affiliation></author><author><name sortKey="Nordez, Antoine" sort="Nordez, Antoine" uniqKey="Nordez A" first="Antoine" last="Nordez">Antoine Nordez</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes, France;</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes</wicri:regionArea></affiliation></author></analytic><series><title level="j">Journal of applied physiology (Bethesda, Md. : 1985)</title><idno type="eISSN">1522-1601</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term><term>Arm (physiopathology)</term><term>Child</term><term>Child, Preschool</term><term>Elasticity Imaging Techniques</term><term>Electric Stimulation</term><term>Female</term><term>Humans</term><term>Infant</term><term>Male</term><term>Muscle Contraction</term><term>Muscle Strength</term><term>Muscle, Skeletal (diagnostic imaging)</term><term>Muscle, Skeletal (physiopathology)</term><term>Muscular Dystrophy, Duchenne (diagnostic imaging)</term><term>Muscular Dystrophy, Duchenne (physiopathology)</term><term>Synaptic Transmission</term><term>Young Adult</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term><term>Bras (physiopathologie)</term><term>Contraction musculaire</term><term>Enfant</term><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Force musculaire</term><term>Humains</term><term>Imagerie d'élasticité tissulaire</term><term>Jeune adulte</term><term>Muscles squelettiques (imagerie diagnostique)</term><term>Muscles squelettiques (physiopathologie)</term><term>Myopathie de Duchenne (imagerie diagnostique)</term><term>Myopathie de Duchenne (physiopathologie)</term><term>Mâle</term><term>Nourrisson</term><term>Stimulation électrique</term><term>Transmission synaptique</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Muscle, Skeletal</term><term>Muscular Dystrophy, Duchenne</term></keywords><keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Muscles squelettiques</term><term>Myopathie de Duchenne</term></keywords><keywords scheme="MESH" qualifier="physiopathologie" xml:lang="fr"><term>Bras</term><term>Muscles squelettiques</term><term>Myopathie de Duchenne</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Arm</term><term>Muscle, Skeletal</term><term>Muscular Dystrophy, Duchenne</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Child</term><term>Child, Preschool</term><term>Elasticity Imaging Techniques</term><term>Electric Stimulation</term><term>Female</term><term>Humans</term><term>Infant</term><term>Male</term><term>Muscle Contraction</term><term>Muscle Strength</term><term>Synaptic Transmission</term><term>Young Adult</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term><term>Contraction musculaire</term><term>Enfant</term><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Force musculaire</term><term>Humains</term><term>Imagerie d'élasticité tissulaire</term><term>Jeune adulte</term><term>Mâle</term><term>Nourrisson</term><term>Stimulation électrique</term><term>Transmission synaptique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The decrease in muscle strength in patients with Duchenne muscular dystrophy (DMD) is mainly explained by a decrease in the number of active contractile elements. Nevertheless, it is possible that other electrochemical and force transmission processes may contribute. The present study aimed to quantify the effect of DMD on the relative contribution of electrochemical and force transmission components of the electromechanical delay (i.e., time lag between the onset of muscle activation and force production) in humans using very high frame rate ultrasound. Fourteen patients with DMD and thirteen control subjects underwent two electrically evoked contractions of the biceps brachii with the ultrasound probe over the muscle belly. The electromechanical delay was significantly longer in DMD patients compared with controls (18.5 ± 3.9 vs. 12.5 ± 1.4 ms, P < 0.0001). More precisely, DMD patients exhibited a longer delay between the onset of muscle fascicles motion and force production (13.6 ± 3.1 vs. 7.9 ± 2.0 ms, P < 0.0001). This delay was correlated to the chronological age of the DMD patients (r = 0.66; P = 0.01), but not of the controls (r = -0.45; P = 0.10). No significant difference was found for the delay between the onset of muscle stimulation and the onset of muscle fascicle motion. These results highlight the role of the alteration of muscle force transmission (delay between the onset of fascicle motion and force production) in the impairments of the contraction efficiency in patients with DMD.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25103971</PMID><DateCreated><Year>2014</Year><Month>09</Month><Day>16</Day></DateCreated><DateCompleted><Year>2015</Year><Month>05</Month><Day>26</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>20</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1522-1601</ISSN><JournalIssue CitedMedium="Internet"><Volume>117</Volume><Issue>6</Issue><PubDate><Year>2014</Year><Month>Sep</Month><Day>15</Day></PubDate></JournalIssue><Title>Journal of applied physiology (Bethesda, Md. : 1985)</Title><ISOAbbreviation>J. Appl. Physiol.</ISOAbbreviation></Journal><ArticleTitle>New insights on contraction efficiency in patients with Duchenne muscular dystrophy.</ArticleTitle><Pagination><MedlinePgn>658-62</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1152/japplphysiol.00544.2014</ELocationID><Abstract><AbstractText>The decrease in muscle strength in patients with Duchenne muscular dystrophy (DMD) is mainly explained by a decrease in the number of active contractile elements. Nevertheless, it is possible that other electrochemical and force transmission processes may contribute. The present study aimed to quantify the effect of DMD on the relative contribution of electrochemical and force transmission components of the electromechanical delay (i.e., time lag between the onset of muscle activation and force production) in humans using very high frame rate ultrasound. Fourteen patients with DMD and thirteen control subjects underwent two electrically evoked contractions of the biceps brachii with the ultrasound probe over the muscle belly. The electromechanical delay was significantly longer in DMD patients compared with controls (18.5 ± 3.9 vs. 12.5 ± 1.4 ms, P < 0.0001). More precisely, DMD patients exhibited a longer delay between the onset of muscle fascicles motion and force production (13.6 ± 3.1 vs. 7.9 ± 2.0 ms, P < 0.0001). This delay was correlated to the chronological age of the DMD patients (r = 0.66; P = 0.01), but not of the controls (r = -0.45; P = 0.10). No significant difference was found for the delay between the onset of muscle stimulation and the onset of muscle fascicle motion. These results highlight the role of the alteration of muscle force transmission (delay between the onset of fascicle motion and force production) in the impairments of the contraction efficiency in patients with DMD.</AbstractText><CopyrightInformation>Copyright © 2014 the American Physiological Society.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Lacourpaille</LastName><ForeName>Lilian</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes, France;</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hug</LastName><ForeName>François</ForeName><Initials>F</Initials><AffiliationInfo><Affiliation>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes, France; National Health and Medical Research Council, Centre of Clinical Research Excellence in Spinal Pain, Injury and Health, School of Health and Rehabilitation Sciences, University of Queensland, Brisbane, Queensland, Australia; francois.hug@univ-nantes.fr.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Guével</LastName><ForeName>Arnaud</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes, France;</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Péréon</LastName><ForeName>Yann</ForeName><Initials>Y</Initials><AffiliationInfo><Affiliation>Centre de Référence Maladies Neuromusculaires Nantes-Angers, University of Nantes, Centre Hospitalier Universitaire, Nantes, France; Atlantic Gene Therapies, Nantes, France; and.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Magot</LastName><ForeName>Armelle</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Centre de Référence Maladies Neuromusculaires Nantes-Angers, University of Nantes, Centre Hospitalier Universitaire, Nantes, France; Atlantic Gene Therapies, Nantes, France; and.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hogrel</LastName><ForeName>Jean-Yves</ForeName><Initials>JY</Initials><AffiliationInfo><Affiliation>Institut de Myologie, GH Pitié-Salpêtrière, Paris, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Nordez</LastName><ForeName>Antoine</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Laboratory Motricité, Interactions, Performance (EA 4334), Unite de Formation et de Recherche Sciences et Techniques des Activités Physiques et Sportives, University of Nantes, Nantes, France;</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>08</Month><Day>07</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Appl Physiol (1985)</MedlineTA><NlmUniqueID>8502536</NlmUniqueID><ISSNLinking>0161-7567</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Acta Physiol (Oxf). 2014 May;211(1):82-96</RefSource><PMID Version="1">24319999</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Physiol Rev. 2002 Apr;82(2):291-329</RefSource><PMID Version="1">11917091</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Biochim Biophys Acta. 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