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Growth Differentiation Factor 15 Predicts All-Cause Morbidity and Mortality in Stable Coronary Heart Disease.

Identifieur interne : 003E22 ( Ncbi/Merge ); précédent : 003E21; suivant : 003E23

Growth Differentiation Factor 15 Predicts All-Cause Morbidity and Mortality in Stable Coronary Heart Disease.

Auteurs : Emil Hagström [Suède] ; Claes Held [Suède] ; Ralph A H. Stewart [Nouvelle-Zélande] ; Philip E. Aylward [Australie] ; Andrzej Budaj [Pologne] ; Christopher P. Cannon [États-Unis] ; Wolfgang Koenig [Allemagne] ; Sue Krug-Gourley [États-Unis] ; Emile R. Mohler [États-Unis] ; Philippe Gabriel Steg [France] ; Elizabeth Tarka [États-Unis] ; Ollie Östlund [Suède] ; Harvey D. White [Nouvelle-Zélande] ; Agneta Siegbahn [Suède] ; Lars Wallentin [Suède]

Source :

RBID : pubmed:27811204

Descripteurs français

English descriptors

Abstract

Higher growth differentiation factor 15 (GDF-15) concentrations are associated with cardiovascular (CV) and non-CV morbidity and mortality. However, information on associations between GDF-15 and the risk of specific CV and non-CV events in stable coronary heart disease (CHD) patients is limited.

DOI: 10.1373/clinchem.2016.260570
PubMed: 27811204

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pubmed:27811204

Le document en format XML

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<term>Facteur-15 de croissance et de différenciation</term>
<term>Maladie coronarienne</term>
<term>Marqueurs biologiques</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Morbidity</term>
<term>Prospective Studies</term>
<term>Risk Factors</term>
<term>Survival Rate</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Humains</term>
<term>Morbidité</term>
<term>Mâle</term>
<term>Sujet âgé</term>
<term>Taux de survie</term>
<term>Études prospectives</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">Higher growth differentiation factor 15 (GDF-15) concentrations are associated with cardiovascular (CV) and non-CV morbidity and mortality. However, information on associations between GDF-15 and the risk of specific CV and non-CV events in stable coronary heart disease (CHD) patients is limited.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">27811204</PMID>
<DateCreated>
<Year>2016</Year>
<Month>11</Month>
<Day>04</Day>
</DateCreated>
<DateCompleted>
<Year>2017</Year>
<Month>06</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>06</Month>
<Day>06</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1530-8561</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>63</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2017</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Clinical chemistry</Title>
<ISOAbbreviation>Clin. Chem.</ISOAbbreviation>
</Journal>
<ArticleTitle>Growth Differentiation Factor 15 Predicts All-Cause Morbidity and Mortality in Stable Coronary Heart Disease.</ArticleTitle>
<Pagination>
<MedlinePgn>325-333</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1373/clinchem.2016.260570</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Higher growth differentiation factor 15 (GDF-15) concentrations are associated with cardiovascular (CV) and non-CV morbidity and mortality. However, information on associations between GDF-15 and the risk of specific CV and non-CV events in stable coronary heart disease (CHD) patients is limited.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">In 14 577 patients with stable CHD participating in the Stabilization of Atherosclerotic Plaque by Initiation of Darapladib Therapy Trial (STABILITY), GDF-15 and other prognostic biomarkers (N-terminal pro-B-type natriuretic peptide, high-sensitivity troponin T, cystatin C, and high-sensitivity C-reactive protein) were measured. In adjusted Cox regression models, the associations between GDF-15 and the composite CV end point [CV death, myocardial infarction (MI), and stroke], as well as other CV and non-CV events, were assessed.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The median concentration (interquartile range) of GDF-15 at baseline was 1253 (915-1827) ng/L. The hazard ratio for the composite end point for the highest compared to the lowest quartile of GDF-15 was 1.8 (95% CI, 1.5-2.2); for CV death, 2.63 (1.9-3.6); for sudden death, 3.06 (1.9-4.8); for heart failure (HF) death, 4.3 (1.3-14); for cancer death, 2.5 (1.3-4.7); for hospitalization for HF, 5.8 (3.2-10); for MI 1.4 (95% CI, 1.1-1.9); and for stroke, 1.8 (95% CI, 1.1-2.8). After adjustment for other prognostic biomarkers, GDF-15 remained significantly associated with all outcomes except for MI.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">In stable CHD, GDF-15 was independently associated with CV, non-CV, and cancer mortality, as well as with MI and stroke. When also adjusting for other prognostic biomarkers, the associations to all fatal and nonfatal events were maintained except for MI. Information on GDF-15, therefore, might be helpful when assessing the risk of adverse outcomes in patients with stable CHD. ClinicalTrials.gov Identifier: NCT00799903.</AbstractText>
<CopyrightInformation>© 2016 American Association for Clinical Chemistry.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Hagström</LastName>
<ForeName>Emil</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden; emil.hagstrom@ucr.uu.se.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Uppsala Clinical Research Center (UCR), Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Held</LastName>
<ForeName>Claes</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Uppsala Clinical Research Center (UCR), Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Stewart</LastName>
<ForeName>Ralph A H</ForeName>
<Initials>RA</Initials>
<AffiliationInfo>
<Affiliation>Green Lane Cardiovascular Service, Auckland City Hospital, and University of Auckland, Auckland, New Zealand.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Aylward</LastName>
<ForeName>Philip E</ForeName>
<Initials>PE</Initials>
<AffiliationInfo>
<Affiliation>South Australian Health and Medical Research Institute, Flinders University and Medical Centre, Adelaide, Australia.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Budaj</LastName>
<ForeName>Andrzej</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Postgraduate Medical School, Grochowski Hospital, Warsaw, Poland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Cannon</LastName>
<ForeName>Christopher P</ForeName>
<Initials>CP</Initials>
<AffiliationInfo>
<Affiliation>Cardiovascular Division, Brigham and Women's Hospital, and Harvard Clinical Research Institute, Boston, MA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Koenig</LastName>
<ForeName>Wolfgang</ForeName>
<Initials>W</Initials>
<AffiliationInfo>
<Affiliation>Department of Internal Medicine II-Cardiology, University of Ulm Medical Center, Ulm, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>DZHK (German Centre for Cardiovascular Research), partner site Munich Heart Alliance, Munich, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Krug-Gourley</LastName>
<ForeName>Sue</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKline, King of Prussia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mohler</LastName>
<ForeName>Emile R</ForeName>
<Initials>ER</Initials>
<Suffix>3rd</Suffix>
<AffiliationInfo>
<Affiliation>University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Steg</LastName>
<ForeName>Philippe Gabriel</ForeName>
<Initials>PG</Initials>
<AffiliationInfo>
<Affiliation>Département Hospitalo-Universitaire FIRE, AP-HP, Hôpital Bichat, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Paris Diderot University, Sorbonne Paris Cité, Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>NHLI Imperial College, ICMS, Royal Brompton Hospital, London, UK.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>FACT (French Alliance for Cardiovascular Trials), an F-CRIN network, INSERM U1148, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tarka</LastName>
<ForeName>Elizabeth</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>former employee of Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKline, King of Prussia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Östlund</LastName>
<ForeName>Ollie</ForeName>
<Initials>O</Initials>
<AffiliationInfo>
<Affiliation>Uppsala Clinical Research Center (UCR), Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>White</LastName>
<ForeName>Harvey D</ForeName>
<Initials>HD</Initials>
<AffiliationInfo>
<Affiliation>Green Lane Cardiovascular Service, Auckland City Hospital, and University of Auckland, Auckland, New Zealand.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Siegbahn</LastName>
<ForeName>Agneta</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Uppsala Clinical Research Center (UCR), Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Medical Sciences, Clinical Chemistry, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wallentin</LastName>
<ForeName>Lars</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Uppsala Clinical Research Center (UCR), Uppsala University, Uppsala, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<CollectiveName>STABILITY Investigators</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
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<DataBank>
<DataBankName>ClinicalTrials.gov</DataBankName>
<AccessionNumberList>
<AccessionNumber>NCT00799903</AccessionNumber>
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<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016449">Randomized Controlled Trial</PublicationType>
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<ArticleDate DateType="Electronic">
<Year>2016</Year>
<Month>11</Month>
<Day>03</Day>
</ArticleDate>
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<Country>United States</Country>
<MedlineTA>Clin Chem</MedlineTA>
<NlmUniqueID>9421549</NlmUniqueID>
<ISSNLinking>0009-9147</ISSNLinking>
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<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D015415">Biomarkers</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C526140">GDF15 protein, human</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D055436">Growth Differentiation Factor 15</NameOfSubstance>
</Chemical>
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<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015415" MajorTopicYN="N">Biomarkers</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D003327" MajorTopicYN="N">Coronary Disease</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="Y">blood</QualifierName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000401" MajorTopicYN="Y">mortality</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D055436" MajorTopicYN="N">Growth Differentiation Factor 15</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="Y">blood</QualifierName>
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<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D009017" MajorTopicYN="N">Morbidity</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D011446" MajorTopicYN="N">Prospective Studies</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D012307" MajorTopicYN="N">Risk Factors</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D015996" MajorTopicYN="N">Survival Rate</DescriptorName>
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<PubMedPubDate PubStatus="received">
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</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2016</Year>
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<li>Allemagne</li>
<li>Australie</li>
<li>France</li>
<li>Nouvelle-Zélande</li>
<li>Pologne</li>
<li>Suède</li>
<li>États-Unis</li>
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<li>Bade-Wurtemberg</li>
<li>District de Tübingen</li>
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<li>Massachusetts</li>
<li>Pennsylvanie</li>
<li>Svealand</li>
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<name sortKey="Cannon, Christopher P" sort="Cannon, Christopher P" uniqKey="Cannon C" first="Christopher P" last="Cannon">Christopher P. Cannon</name>
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<name sortKey="Krug Gourley, Sue" sort="Krug Gourley, Sue" uniqKey="Krug Gourley S" first="Sue" last="Krug-Gourley">Sue Krug-Gourley</name>
<name sortKey="Mohler, Emile R" sort="Mohler, Emile R" uniqKey="Mohler E" first="Emile R" last="Mohler">Emile R. Mohler</name>
<name sortKey="Tarka, Elizabeth" sort="Tarka, Elizabeth" uniqKey="Tarka E" first="Elizabeth" last="Tarka">Elizabeth Tarka</name>
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<region name="Bade-Wurtemberg">
<name sortKey="Koenig, Wolfgang" sort="Koenig, Wolfgang" uniqKey="Koenig W" first="Wolfgang" last="Koenig">Wolfgang Koenig</name>
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<name sortKey="Steg, Philippe Gabriel" sort="Steg, Philippe Gabriel" uniqKey="Steg P" first="Philippe Gabriel" last="Steg">Philippe Gabriel Steg</name>
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