Left ventricular myocardial dyssynchrony is already present in nondiabetic patients with metabolic syndrome.
Identifieur interne : 003762 ( Main/Exploration ); précédent : 003761; suivant : 003763Left ventricular myocardial dyssynchrony is already present in nondiabetic patients with metabolic syndrome.
Auteurs : Edward Crendal [Australie] ; Guillaume Walther [France] ; Fred Dutheil [France] ; Daniel Courteix [France] ; Bruno Lesourd [France] ; Robert Chapier [France] ; Geraldine Naughton [Australie] ; Agnès Vinet [France] ; Philippe Obert [Australie]Source :
- The Canadian journal of cardiology [ 1916-7075 ] ; 2014.
Descripteurs français
- KwdFr :
- Adulte d'âge moyen, Contraction myocardique, Dysfonction ventriculaire gauche (), Dysfonction ventriculaire gauche (imagerie diagnostique), Dysfonction ventriculaire gauche (physiopathologie), Débit systolique, Femelle, Fonction ventriculaire gauche (physiologie), Humains, Indice de gravité médicale, Marqueurs biologiques (sang), Mâle, Pronostic, Sujet âgé, Syndrome métabolique X (), Syndrome métabolique X (sang), Échocardiographie (), Évolution de la maladie.
- MESH :
- imagerie diagnostique : Dysfonction ventriculaire gauche.
- physiologie : Fonction ventriculaire gauche.
- physiopathologie : Dysfonction ventriculaire gauche.
- sang : Marqueurs biologiques, Syndrome métabolique X.
- Adulte d'âge moyen, Contraction myocardique, Dysfonction ventriculaire gauche, Débit systolique, Femelle, Humains, Indice de gravité médicale, Mâle, Pronostic, Sujet âgé, Syndrome métabolique X, Échocardiographie, Évolution de la maladie.
English descriptors
- KwdEn :
- Aged, Biomarkers (blood), Disease Progression, Echocardiography (methods), Female, Humans, Male, Metabolic Syndrome X (blood), Metabolic Syndrome X (complications), Middle Aged, Myocardial Contraction, Prognosis, Severity of Illness Index, Stroke Volume, Ventricular Dysfunction, Left (complications), Ventricular Dysfunction, Left (diagnostic imaging), Ventricular Dysfunction, Left (physiopathology), Ventricular Function, Left (physiology).
- MESH :
- chemical , blood : Biomarkers.
- blood : Metabolic Syndrome X.
- complications : Metabolic Syndrome X, Ventricular Dysfunction, Left.
- diagnostic imaging : Ventricular Dysfunction, Left.
- methods : Echocardiography.
- physiology : Ventricular Function, Left.
- physiopathology : Ventricular Dysfunction, Left.
- Aged, Disease Progression, Female, Humans, Male, Middle Aged, Myocardial Contraction, Prognosis, Severity of Illness Index, Stroke Volume.
Abstract
The presence of left ventricular (LV) dyssynchrony in individuals with metabolic syndrome (MetS), a predictor of type 2 diabetes (T2D), lacks clarity. We compared LV dyssynchrony in MetS individuals with and without T2D, and healthy control subjects using speckle-tracking imaging echocardiography. Ninety-two MetS participants (64 without, 28 with T2D) and 40 control subjects underwent echocardiographic and clinical/biological analyses. LV-dyssynchrony in the longitudinal axis only was present in all MetS individuals, but was not further exacerbated by T2D. Strong associations were found with systemic inflammation, abdominal obesity, and LV mass. Investigations of myocardial dyssynchrony in the nondiabetic MetS stage might facilitate timely and more effective prevention.
DOI: 10.1016/j.cjca.2013.10.019
PubMed: 24388804
Affiliations:
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School of Exercise Science, Australian Catholic University, Fitzroy, Australia. 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School of Exercise Science, Australian Catholic University, Fitzroy, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>EA4278, LAPEC, Avignon University, Avignon, France; School of Exercise Science, Australian Catholic University, Fitzroy</wicri:regionArea><wicri:noRegion>Fitzroy</wicri:noRegion></affiliation></author><author><name sortKey="Walther, Guillaume" sort="Walther, Guillaume" uniqKey="Walther G" first="Guillaume" last="Walther">Guillaume Walther</name><affiliation wicri:level="3"><nlm:affiliation>EA4278, LAPEC, Avignon University, Avignon, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>EA4278, LAPEC, Avignon University, Avignon</wicri:regionArea><placeName><region type="region">Provence-Alpes-Côte d'Azur</region><region type="old region">Provence-Alpes-Côte d'Azur</region><settlement type="city">Avignon</settlement></placeName></affiliation></author><author><name sortKey="Dutheil, Fred" sort="Dutheil, Fred" uniqKey="Dutheil F" first="Fred" last="Dutheil">Fred Dutheil</name><affiliation wicri:level="1"><nlm:affiliation>School of Exercise Science, Australian Catholic University, Fitzroy, Australia; EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand, France; Occupational Medicine, University Hospital CHU G, Montpied, Clermon-Ferrand, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>School of Exercise Science, Australian Catholic University, Fitzroy, Australia; EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand, France; Occupational Medicine, University Hospital CHU G, Montpied, Clermon-Ferrand</wicri:regionArea><wicri:noRegion>Clermon-Ferrand</wicri:noRegion><wicri:noRegion>Clermon-Ferrand</wicri:noRegion></affiliation></author><author><name sortKey="Courteix, Daniel" sort="Courteix, Daniel" uniqKey="Courteix D" first="Daniel" last="Courteix">Daniel Courteix</name><affiliation wicri:level="1"><nlm:affiliation>School of Exercise Science, Australian Catholic University, Fitzroy, Australia; EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>School of Exercise Science, Australian Catholic University, Fitzroy, Australia; EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand</wicri:regionArea><wicri:noRegion>Clermon-Ferrand</wicri:noRegion><wicri:noRegion>Clermon-Ferrand</wicri:noRegion></affiliation></author><author><name sortKey="Lesourd, Bruno" sort="Lesourd, Bruno" uniqKey="Lesourd B" first="Bruno" last="Lesourd">Bruno Lesourd</name><affiliation wicri:level="1"><nlm:affiliation>EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand, France; Geriatrics, PRES Clermont University of Auvergne, Clermon-Ferrand, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand, France; Geriatrics, PRES Clermont University of Auvergne, Clermon-Ferrand</wicri:regionArea><wicri:noRegion>Clermon-Ferrand</wicri:noRegion><wicri:noRegion>Clermon-Ferrand</wicri:noRegion></affiliation></author><author><name sortKey="Chapier, Robert" sort="Chapier, Robert" uniqKey="Chapier R" first="Robert" last="Chapier">Robert Chapier</name><affiliation wicri:level="1"><nlm:affiliation>EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>EA3533, Laboratory of Metabolic Adaptations to Exercise in Physiological and Pathological Conditions (AME2P), Blaise Pascal University, Clermon-Ferrand</wicri:regionArea><wicri:noRegion>Clermon-Ferrand</wicri:noRegion><wicri:noRegion>Clermon-Ferrand</wicri:noRegion></affiliation></author><author><name sortKey="Naughton, Geraldine" sort="Naughton, Geraldine" uniqKey="Naughton G" first="Geraldine" last="Naughton">Geraldine Naughton</name><affiliation wicri:level="1"><nlm:affiliation>School of Exercise Science, Australian Catholic University, Fitzroy, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>School of Exercise Science, Australian Catholic University, Fitzroy</wicri:regionArea><wicri:noRegion>Fitzroy</wicri:noRegion></affiliation></author><author><name sortKey="Vinet, Agnes" sort="Vinet, Agnes" uniqKey="Vinet A" first="Agnès" last="Vinet">Agnès Vinet</name><affiliation wicri:level="3"><nlm:affiliation>EA4278, LAPEC, Avignon University, Avignon, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>EA4278, LAPEC, Avignon University, Avignon</wicri:regionArea><placeName><region type="region">Provence-Alpes-Côte d'Azur</region><region type="old region">Provence-Alpes-Côte d'Azur</region><settlement type="city">Avignon</settlement></placeName></affiliation></author><author><name sortKey="Obert, Philippe" sort="Obert, Philippe" uniqKey="Obert P" first="Philippe" last="Obert">Philippe Obert</name><affiliation wicri:level="1"><nlm:affiliation>EA4278, LAPEC, Avignon University, Avignon, France; School of Exercise Science, Australian Catholic University, Fitzroy, Australia. Electronic address: philippe.obert@univ-avignon.fr.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>EA4278, LAPEC, Avignon University, Avignon, France; School of Exercise Science, Australian Catholic University, Fitzroy</wicri:regionArea><wicri:noRegion>Fitzroy</wicri:noRegion></affiliation></author></analytic><series><title level="j">The Canadian journal of cardiology</title><idno type="eISSN">1916-7075</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Biomarkers (blood)</term><term>Disease Progression</term><term>Echocardiography (methods)</term><term>Female</term><term>Humans</term><term>Male</term><term>Metabolic Syndrome X (blood)</term><term>Metabolic Syndrome X (complications)</term><term>Middle Aged</term><term>Myocardial Contraction</term><term>Prognosis</term><term>Severity of Illness Index</term><term>Stroke Volume</term><term>Ventricular Dysfunction, Left (complications)</term><term>Ventricular Dysfunction, Left (diagnostic imaging)</term><term>Ventricular Dysfunction, Left (physiopathology)</term><term>Ventricular Function, Left (physiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Contraction myocardique</term><term>Dysfonction ventriculaire gauche ()</term><term>Dysfonction ventriculaire gauche (imagerie diagnostique)</term><term>Dysfonction ventriculaire gauche (physiopathologie)</term><term>Débit systolique</term><term>Femelle</term><term>Fonction ventriculaire gauche (physiologie)</term><term>Humains</term><term>Indice de gravité médicale</term><term>Marqueurs biologiques (sang)</term><term>Mâle</term><term>Pronostic</term><term>Sujet âgé</term><term>Syndrome métabolique X ()</term><term>Syndrome métabolique X (sang)</term><term>Échocardiographie ()</term><term>Évolution de la maladie</term></keywords><keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Biomarkers</term></keywords><keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>Metabolic Syndrome X</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Metabolic Syndrome X</term><term>Ventricular Dysfunction, Left</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Ventricular Dysfunction, Left</term></keywords><keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Dysfonction ventriculaire gauche</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Echocardiography</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Fonction ventriculaire gauche</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Ventricular Function, Left</term></keywords><keywords scheme="MESH" qualifier="physiopathologie" xml:lang="fr"><term>Dysfonction ventriculaire gauche</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Ventricular Dysfunction, Left</term></keywords><keywords scheme="MESH" qualifier="sang" xml:lang="fr"><term>Marqueurs biologiques</term><term>Syndrome métabolique X</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Disease Progression</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Myocardial Contraction</term><term>Prognosis</term><term>Severity of Illness Index</term><term>Stroke Volume</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Contraction myocardique</term><term>Dysfonction ventriculaire gauche</term><term>Débit systolique</term><term>Femelle</term><term>Humains</term><term>Indice de gravité médicale</term><term>Mâle</term><term>Pronostic</term><term>Sujet âgé</term><term>Syndrome métabolique X</term><term>Échocardiographie</term><term>Évolution de la maladie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The presence of left ventricular (LV) dyssynchrony in individuals with metabolic syndrome (MetS), a predictor of type 2 diabetes (T2D), lacks clarity. We compared LV dyssynchrony in MetS individuals with and without T2D, and healthy control subjects using speckle-tracking imaging echocardiography. Ninety-two MetS participants (64 without, 28 with T2D) and 40 control subjects underwent echocardiographic and clinical/biological analyses. LV-dyssynchrony in the longitudinal axis only was present in all MetS individuals, but was not further exacerbated by T2D. Strong associations were found with systemic inflammation, abdominal obesity, and LV mass. Investigations of myocardial dyssynchrony in the nondiabetic MetS stage might facilitate timely and more effective prevention.</div></front></TEI><affiliations><list><country><li>Australie</li><li>France</li></country><region><li>Provence-Alpes-Côte d'Azur</li></region><settlement><li>Avignon</li></settlement></list><tree><country name="Australie"><noRegion><name sortKey="Crendal, Edward" sort="Crendal, Edward" uniqKey="Crendal E" first="Edward" last="Crendal">Edward Crendal</name></noRegion><name sortKey="Naughton, Geraldine" sort="Naughton, Geraldine" uniqKey="Naughton G" first="Geraldine" last="Naughton">Geraldine Naughton</name><name sortKey="Obert, Philippe" sort="Obert, Philippe" uniqKey="Obert P" first="Philippe" last="Obert">Philippe Obert</name></country><country name="France"><region name="Provence-Alpes-Côte d'Azur"><name sortKey="Walther, Guillaume" sort="Walther, Guillaume" uniqKey="Walther G" first="Guillaume" last="Walther">Guillaume Walther</name></region><name sortKey="Chapier, Robert" sort="Chapier, Robert" uniqKey="Chapier R" first="Robert" last="Chapier">Robert Chapier</name><name sortKey="Courteix, Daniel" sort="Courteix, Daniel" uniqKey="Courteix D" first="Daniel" last="Courteix">Daniel Courteix</name><name sortKey="Dutheil, Fred" sort="Dutheil, Fred" uniqKey="Dutheil F" first="Fred" last="Dutheil">Fred Dutheil</name><name sortKey="Lesourd, Bruno" sort="Lesourd, Bruno" uniqKey="Lesourd B" first="Bruno" last="Lesourd">Bruno Lesourd</name><name sortKey="Vinet, Agnes" sort="Vinet, Agnes" uniqKey="Vinet A" first="Agnès" last="Vinet">Agnès Vinet</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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