Clinical Implications of Echocardiographic Phenotypes of Patients With Diabetes Mellitus.
Identifieur interne : 000279 ( PubMed/Corpus ); précédent : 000278; suivant : 000280Clinical Implications of Echocardiographic Phenotypes of Patients With Diabetes Mellitus.
Auteurs : Laura Ernande ; Etienne Audureau ; Christine L. Jellis ; Cyrille Bergerot ; Corneliu Henegar ; Daigo Sawaki ; Gabor Czibik ; Chiara Volpi ; Florence Canoui-Poitrine ; Hélène Thibault ; Julien Ternacle ; Philippe Moulin ; Thomas H. Marwick ; Geneviève DerumeauxSource :
- Journal of the American College of Cardiology [ 1558-3597 ] ; 2017.
English descriptors
- KwdEn :
- Aged, Asymptomatic Diseases, Cardiovascular Diseases (mortality), Cluster Analysis, Diabetes Mellitus, Type 2 (epidemiology), Diabetes Mellitus, Type 2 (physiopathology), Echocardiography (methods), Female, France (epidemiology), Humans, Male, Middle Aged, Prognosis, Risk Assessment, Risk Factors, Statistics as Topic, Stroke Volume, Ventricular Dysfunction, Left (diagnosis), Ventricular Dysfunction, Left (physiopathology), Ventricular Function, Left, Ventricular Remodeling.
- MESH :
- diagnosis : Ventricular Dysfunction, Left.
- epidemiology : Diabetes Mellitus, Type 2, France.
- methods : Echocardiography.
- mortality : Cardiovascular Diseases.
- physiopathology : Diabetes Mellitus, Type 2, Ventricular Dysfunction, Left.
- Aged, Asymptomatic Diseases, Cluster Analysis, Female, Humans, Male, Middle Aged, Prognosis, Risk Assessment, Risk Factors, Statistics as Topic, Stroke Volume, Ventricular Function, Left, Ventricular Remodeling.
Abstract
Type 2 diabetes mellitus (T2DM) may alter cardiac structure and function, but obesity, hypertension (HTN), or aging can induce similar abnormalities.
DOI: 10.1016/j.jacc.2017.07.792
PubMed: 28958326
Links to Exploration step
pubmed:28958326Le document en format XML
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<author><name sortKey="Marwick, Thomas H" sort="Marwick, Thomas H" uniqKey="Marwick T" first="Thomas H" last="Marwick">Thomas H. Marwick</name>
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<author><name sortKey="Canoui Poitrine, Florence" sort="Canoui Poitrine, Florence" uniqKey="Canoui Poitrine F" first="Florence" last="Canoui-Poitrine">Florence Canoui-Poitrine</name>
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<author><name sortKey="Thibault, Helene" sort="Thibault, Helene" uniqKey="Thibault H" first="Hélène" last="Thibault">Hélène Thibault</name>
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<author><name sortKey="Ternacle, Julien" sort="Ternacle, Julien" uniqKey="Ternacle J" first="Julien" last="Ternacle">Julien Ternacle</name>
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<author><name sortKey="Moulin, Philippe" sort="Moulin, Philippe" uniqKey="Moulin P" first="Philippe" last="Moulin">Philippe Moulin</name>
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<author><name sortKey="Marwick, Thomas H" sort="Marwick, Thomas H" uniqKey="Marwick T" first="Thomas H" last="Marwick">Thomas H. Marwick</name>
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<author><name sortKey="Derumeaux, Genevieve" sort="Derumeaux, Genevieve" uniqKey="Derumeaux G" first="Geneviève" last="Derumeaux">Geneviève Derumeaux</name>
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<series><title level="j">Journal of the American College of Cardiology</title>
<idno type="eISSN">1558-3597</idno>
<imprint><date when="2017" type="published">2017</date>
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<term>Asymptomatic Diseases</term>
<term>Cardiovascular Diseases (mortality)</term>
<term>Cluster Analysis</term>
<term>Diabetes Mellitus, Type 2 (epidemiology)</term>
<term>Diabetes Mellitus, Type 2 (physiopathology)</term>
<term>Echocardiography (methods)</term>
<term>Female</term>
<term>France (epidemiology)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Prognosis</term>
<term>Risk Assessment</term>
<term>Risk Factors</term>
<term>Statistics as Topic</term>
<term>Stroke Volume</term>
<term>Ventricular Dysfunction, Left (diagnosis)</term>
<term>Ventricular Dysfunction, Left (physiopathology)</term>
<term>Ventricular Function, Left</term>
<term>Ventricular Remodeling</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Ventricular Dysfunction, Left</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Diabetes Mellitus, Type 2</term>
<term>France</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Echocardiography</term>
</keywords>
<keywords scheme="MESH" qualifier="mortality" xml:lang="en"><term>Cardiovascular Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Diabetes Mellitus, Type 2</term>
<term>Ventricular Dysfunction, Left</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Asymptomatic Diseases</term>
<term>Cluster Analysis</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Prognosis</term>
<term>Risk Assessment</term>
<term>Risk Factors</term>
<term>Statistics as Topic</term>
<term>Stroke Volume</term>
<term>Ventricular Function, Left</term>
<term>Ventricular Remodeling</term>
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<front><div type="abstract" xml:lang="en">Type 2 diabetes mellitus (T2DM) may alter cardiac structure and function, but obesity, hypertension (HTN), or aging can induce similar abnormalities.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">28958326</PMID>
<DateCreated><Year>2017</Year>
<Month>09</Month>
<Day>29</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>10</Month>
<Day>05</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>10</Month>
<Day>05</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1558-3597</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>70</Volume>
<Issue>14</Issue>
<PubDate><Year>2017</Year>
<Month>Oct</Month>
<Day>03</Day>
</PubDate>
</JournalIssue>
<Title>Journal of the American College of Cardiology</Title>
<ISOAbbreviation>J. Am. Coll. Cardiol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Clinical Implications of Echocardiographic Phenotypes of Patients With Diabetes Mellitus.</ArticleTitle>
<Pagination><MedlinePgn>1704-1716</MedlinePgn>
</Pagination>
<ELocationID EIdType="pii" ValidYN="Y">S0735-1097(17)39262-8</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.jacc.2017.07.792</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Type 2 diabetes mellitus (T2DM) may alter cardiac structure and function, but obesity, hypertension (HTN), or aging can induce similar abnormalities.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">This study sought to link cardiac phenotypes in T2DM patients with clinical profiles and outcomes using cluster analysis.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Baseline echocardiography and a composite endpoint (cardiovascular mortality and hospitalization) were evaluated in 842 T2DM patients from 2 prospective cohorts. A cluster analysis was performed on echocardiographic variables, and the association between clusters and clinical profiles and outcomes was assessed.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Three clusters were identified. Cluster 1 patients had the lowest left ventricular (LV) mass index and ratio between early mitral inflow velocity and mitral annular early diastolic velocity (E/e') ratio, had the highest left ventricular ejection fraction (LVEF), and were predominantly male with the lowest rate of obesity or HTN. Cluster 2 patients had the highest strain and highest E/e' ratio, were the oldest, were predominantly female, and had the lowest rate of isolated T2DM (without HTN or obesity). Cluster 3 patients had the highest LV mass index and volumes and the lowest LVEF and strain, were predominantly male, and shared similar age and rate of obesity and HTN as cluster 1 patients. After follow-up of 67 months (interquartile range: 40 to 87), the composite endpoint occurred in 56 of 521 patients (10.8%). Clusters 2 (hazard ratio: 2.37; 95% confidence interval: 1.15 to 4.88) and 3 (hazard ratio: 2.19; 95% confidence interval: 1.00 to 4.82) had a similar outcome, which was worse than cluster 1.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Cluster analysis of echocardiographic variables identified 3 different echocardiographic phenotypes of T2DM patients that were associated with distinct clinical profiles and highlighted the prognostic value of LV remodeling and subclinical dysfunction.</AbstractText>
<CopyrightInformation>Copyright © 2017 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ernande</LastName>
<ForeName>Laura</ForeName>
<Initials>L</Initials>
<AffiliationInfo><Affiliation>Physiology Department, DHU Ageing-Thorax-Vessel-Blood, Henri Mondor Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France; INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Audureau</LastName>
<ForeName>Etienne</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Biostatistics Department, Henri Mondor Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France; CEpiA EA7376, DHU Ageing-Thorax-Vessel-Blood, Université Paris Est (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Jellis</LastName>
<ForeName>Christine L</ForeName>
<Initials>CL</Initials>
<AffiliationInfo><Affiliation>Cardiology Department, Cleveland Clinic, Cleveland, Ohio.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bergerot</LastName>
<ForeName>Cyrille</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Centre d'Investigation Clinique INSERM 1407 Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Henegar</LastName>
<ForeName>Corneliu</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Sawaki</LastName>
<ForeName>Daigo</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Czibik</LastName>
<ForeName>Gabor</ForeName>
<Initials>G</Initials>
<AffiliationInfo><Affiliation>INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Volpi</LastName>
<ForeName>Chiara</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Physiology Department, DHU Ageing-Thorax-Vessel-Blood, Henri Mondor Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Canoui-Poitrine</LastName>
<ForeName>Florence</ForeName>
<Initials>F</Initials>
<AffiliationInfo><Affiliation>Biostatistics Department, Henri Mondor Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France; CEpiA EA7376, DHU Ageing-Thorax-Vessel-Blood, Université Paris Est (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Thibault</LastName>
<ForeName>Hélène</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Service d'Explorations Fonctionnelles Cardiovasculaires, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France; INSERM UMR-1060, CarMeN Laboratory, Université Claude Bernard Lyon, Lyon, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Ternacle</LastName>
<ForeName>Julien</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Physiology Department, DHU Ageing-Thorax-Vessel-Blood, Henri Mondor Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France; INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Moulin</LastName>
<ForeName>Philippe</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>INSERM UMR-1060, CarMeN Laboratory, Université Claude Bernard Lyon, Lyon, France; Fédération d'endocrinologie, Hospices Civils de Lyon, Bron, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Marwick</LastName>
<ForeName>Thomas H</ForeName>
<Initials>TH</Initials>
<AffiliationInfo><Affiliation>Baker Heart and Diabetes Institute, Melbourne, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Derumeaux</LastName>
<ForeName>Geneviève</ForeName>
<Initials>G</Initials>
<AffiliationInfo><Affiliation>Physiology Department, DHU Ageing-Thorax-Vessel-Blood, Henri Mondor Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France; INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France. Electronic address: gderumeaux@gmail.com.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>J Am Coll Cardiol</MedlineTA>
<NlmUniqueID>8301365</NlmUniqueID>
<ISSNLinking>0735-1097</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>AIM</CitationSubset>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D058070" MajorTopicYN="N">Asymptomatic Diseases</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002318" MajorTopicYN="N">Cardiovascular Diseases</DescriptorName>
<QualifierName UI="Q000401" MajorTopicYN="Y">mortality</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D016000" MajorTopicYN="N">Cluster Analysis</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003924" MajorTopicYN="Y">Diabetes Mellitus, Type 2</DescriptorName>
<QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName>
<QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004452" MajorTopicYN="N">Echocardiography</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
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