The value of external anal sphincter electromyography for the diagnosis of multiple system atrophy
Identifieur interne : 003134 ( Istex/Checkpoint ); précédent : 003133; suivant : 003135The value of external anal sphincter electromyography for the diagnosis of multiple system atrophy
Auteurs : François Tison [France] ; Pierre Arne [France] ; Chrystophe Sourgen [France] ; Virginie Chrysostome [France] ; Farid Yeklef [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2000-11.
English descriptors
Abstract
OBJECTIVE: To assess the value of external anal sphincter electromyography (ASEMG) for the diagnosis of multiple system atrophy (MSA) among various causes of parkinsonism. ASEMG denervation profiles have previously been proposed as a diagnosis test for MSA, but their specificity is disputed. METHODS: ASEMG variables of 52 parkinsonian patients were analyzed according to the clinical diagnosis: MSA (n = 31) or no MSA (n = 21). Mean motor unit potential duration, percentage of polyphasicity, and the electromyographer's interpretation were analyzed according to clinical diagnosis, disease duration, genitourinary symptoms, gender, parity, and history of pelvic surgery. RESULTS: All patients with MSA showed ASEMG denervation. Mean motor unit potential duration was the most discriminant variable. No patient with MSA had a mean duration less than 12 ms and no patient without MSA had one greater than 16 ms. ASEMG discriminates between patients with MSA and Parkinson's disease. Using a threshold of 13 ms, the sensitivity was 80% and specificity was almost 70% (positive predictive value, 80%) for the diagnosis of MSA. Age, history of pelvic surgery, and to a lesser extent, female gender, parity, disease duration, and presence of urinary symptoms increased the likelihood of abnormal ASEMG. CONCLUSION: ASEMG was highly sensitive and rather specific for the diagnosis of MSA.
Url:
DOI: 10.1002/1531-8257(200011)15:6<1148::AID-MDS1014>3.0.CO;2-6
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
ISTEX:EAD057B06884149A2897C290EE4A708A943B2CECLe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">The value of external anal sphincter electromyography for the diagnosis of multiple system atrophy</title>
<author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name>
</author>
<author><name sortKey="Arne, Pierre" sort="Arne, Pierre" uniqKey="Arne P" first="Pierre" last="Arne">Pierre Arne</name>
</author>
<author><name sortKey="Sourgen, Chrystophe" sort="Sourgen, Chrystophe" uniqKey="Sourgen C" first="Chrystophe" last="Sourgen">Chrystophe Sourgen</name>
</author>
<author><name sortKey="Chrysostome, Virginie" sort="Chrysostome, Virginie" uniqKey="Chrysostome V" first="Virginie" last="Chrysostome">Virginie Chrysostome</name>
</author>
<author><name sortKey="Yeklef, Farid" sort="Yeklef, Farid" uniqKey="Yeklef F" first="Farid" last="Yeklef">Farid Yeklef</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:EAD057B06884149A2897C290EE4A708A943B2CEC</idno>
<date when="2000" year="2000">2000</date>
<idno type="doi">10.1002/1531-8257(200011)15:6<1148::AID-MDS1014>3.0.CO;2-6</idno>
<idno type="url">https://api.istex.fr/document/EAD057B06884149A2897C290EE4A708A943B2CEC/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000496</idno>
<idno type="wicri:Area/Istex/Curation">000496</idno>
<idno type="wicri:Area/Istex/Checkpoint">003134</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">The value of external anal sphincter electromyography for the diagnosis of multiple system atrophy</title>
<author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Service de Neurologie, INSERM U‐330, Centre Hospitalier Universitaire, Bordeaux</wicri:regionArea>
<placeName><settlement type="city">Bordeaux</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Arne, Pierre" sort="Arne, Pierre" uniqKey="Arne P" first="Pierre" last="Arne">Pierre Arne</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire d'Explorations Fonctionnelles du Système Nerveux, INSERM U‐330, Centre Hospitalier Universitaire, Bordeaux</wicri:regionArea>
<placeName><settlement type="city">Bordeaux</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Sourgen, Chrystophe" sort="Sourgen, Chrystophe" uniqKey="Sourgen C" first="Chrystophe" last="Sourgen">Chrystophe Sourgen</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Département d'Informatique Médicale, INSERM U‐330, Centre Hospitalier Universitaire, Bordeaux</wicri:regionArea>
<placeName><settlement type="city">Bordeaux</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Chrysostome, Virginie" sort="Chrysostome, Virginie" uniqKey="Chrysostome V" first="Virginie" last="Chrysostome">Virginie Chrysostome</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Service de Neurologie, INSERM U‐330, Centre Hospitalier Universitaire, Bordeaux</wicri:regionArea>
<placeName><settlement type="city">Bordeaux</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Yeklef, Farid" sort="Yeklef, Farid" uniqKey="Yeklef F" first="Farid" last="Yeklef">Farid Yeklef</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Service de Neurologie, INSERM U‐330, Centre Hospitalier Universitaire, Bordeaux</wicri:regionArea>
<placeName><settlement type="city">Bordeaux</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>John Wiley & Sons, Inc.</publisher>
<pubPlace>New York</pubPlace>
<date type="published" when="2000-11">2000-11</date>
<biblScope unit="vol">15</biblScope>
<biblScope unit="issue">6</biblScope>
<biblScope unit="page" from="1148">1148</biblScope>
<biblScope unit="page" to="1157">1157</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">EAD057B06884149A2897C290EE4A708A943B2CEC</idno>
<idno type="DOI">10.1002/1531-8257(200011)15:6<1148::AID-MDS1014>3.0.CO;2-6</idno>
<idno type="ArticleID">MDS1014</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Anal sphincter electromyography</term>
<term>Multiple system atrophy</term>
<term>Parkinsonism</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">OBJECTIVE: To assess the value of external anal sphincter electromyography (ASEMG) for the diagnosis of multiple system atrophy (MSA) among various causes of parkinsonism. ASEMG denervation profiles have previously been proposed as a diagnosis test for MSA, but their specificity is disputed. METHODS: ASEMG variables of 52 parkinsonian patients were analyzed according to the clinical diagnosis: MSA (n = 31) or no MSA (n = 21). Mean motor unit potential duration, percentage of polyphasicity, and the electromyographer's interpretation were analyzed according to clinical diagnosis, disease duration, genitourinary symptoms, gender, parity, and history of pelvic surgery. RESULTS: All patients with MSA showed ASEMG denervation. Mean motor unit potential duration was the most discriminant variable. No patient with MSA had a mean duration less than 12 ms and no patient without MSA had one greater than 16 ms. ASEMG discriminates between patients with MSA and Parkinson's disease. Using a threshold of 13 ms, the sensitivity was 80% and specificity was almost 70% (positive predictive value, 80%) for the diagnosis of MSA. Age, history of pelvic surgery, and to a lesser extent, female gender, parity, disease duration, and presence of urinary symptoms increased the likelihood of abnormal ASEMG. CONCLUSION: ASEMG was highly sensitive and rather specific for the diagnosis of MSA.</div>
</front>
</TEI>
<affiliations><list><country><li>France</li>
</country>
<settlement><li>Bordeaux</li>
</settlement>
</list>
<tree><country name="France"><noRegion><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name>
</noRegion>
<name sortKey="Arne, Pierre" sort="Arne, Pierre" uniqKey="Arne P" first="Pierre" last="Arne">Pierre Arne</name>
<name sortKey="Chrysostome, Virginie" sort="Chrysostome, Virginie" uniqKey="Chrysostome V" first="Virginie" last="Chrysostome">Virginie Chrysostome</name>
<name sortKey="Sourgen, Chrystophe" sort="Sourgen, Chrystophe" uniqKey="Sourgen C" first="Chrystophe" last="Sourgen">Chrystophe Sourgen</name>
<name sortKey="Yeklef, Farid" sort="Yeklef, Farid" uniqKey="Yeklef F" first="Farid" last="Yeklef">Farid Yeklef</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Istex/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003134 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Checkpoint/biblio.hfd -nk 003134 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Istex |étape= Checkpoint |type= RBID |clé= ISTEX:EAD057B06884149A2897C290EE4A708A943B2CEC |texte= The value of external anal sphincter electromyography for the diagnosis of multiple system atrophy }}
This area was generated with Dilib version V0.6.23. |