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Clinical Implications of Echocardiographic Phenotypes of Patients With Diabetes Mellitus.

Identifieur interne : 000279 ( PubMed/Corpus ); précédent : 000278; suivant : 000280

Clinical 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 Derumeaux

Source :

RBID : pubmed:28958326

English descriptors

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:28958326

Le document en format XML

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<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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<name sortKey="Derumeaux, Genevieve" sort="Derumeaux, Genevieve" uniqKey="Derumeaux G" first="Geneviève" last="Derumeaux">Geneviève Derumeaux</name>
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<term>Aged</term>
<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>
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<term>Echocardiography</term>
</keywords>
<keywords scheme="MESH" qualifier="mortality" xml:lang="en">
<term>Cardiovascular Diseases</term>
</keywords>
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<term>Diabetes Mellitus, Type 2</term>
<term>Ventricular Dysfunction, Left</term>
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<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>
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<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>
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<DateCreated>
<Year>2017</Year>
<Month>09</Month>
<Day>29</Day>
</DateCreated>
<DateCompleted>
<Year>2017</Year>
<Month>10</Month>
<Day>05</Day>
</DateCompleted>
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<Year>2017</Year>
<Month>10</Month>
<Day>05</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1558-3597</ISSN>
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<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>
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<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>
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<ForeName>Laura</ForeName>
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<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>
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</AffiliationInfo>
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<Affiliation>Cardiology Department, Cleveland Clinic, Cleveland, Ohio.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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<Affiliation>INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
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<Affiliation>INSERM U955, Team08, Université Paris-Est Créteil (UPEC), Créteil, France.</Affiliation>
</AffiliationInfo>
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<Initials>C</Initials>
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<Affiliation>Physiology Department, DHU Ageing-Thorax-Vessel-Blood, Henri Mondor Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France.</Affiliation>
</AffiliationInfo>
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<LastName>Canoui-Poitrine</LastName>
<ForeName>Florence</ForeName>
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<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>
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<LastName>Thibault</LastName>
<ForeName>Hélène</ForeName>
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<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>
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<LastName>Ternacle</LastName>
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<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>
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</Author>
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<LastName>Moulin</LastName>
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<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>
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<Year>2017</Year>
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