Prevalence and relevance of abnormal glucose metabolism in acute coronary syndromes: insights from the PLATelet inhibition and patient Outcomes (PLATO) trial.


Journal

Journal of thrombosis and thrombolysis
ISSN: 1573-742X
Titre abrégé: J Thromb Thrombolysis
Pays: Netherlands
ID NLM: 9502018

Informations de publication

Date de publication:
Nov 2019
Historique:
pubmed: 13 9 2019
medline: 11 3 2020
entrez: 13 9 2019
Statut: ppublish

Résumé

Diabetes mellitus (DM) and abnormal glucose metabolism are associated with cardiovascular (CV) disease. We investigated the prevalence and prognostic importance of dysglycaemia in patients with acute coronary syndromes (ACS) in the PLATelet inhibition and patient Outcomes (PLATO) trial. Diabetes was defined as known diabetes or HbA1c ≥ 6.5% or non-fasting glucose ≥ 11.1 mmol/L on admission, prediabetes as HbA1c ≥ 5.7% but < 6.5%, and no diabetes as HbA1c < 5.7%. The primary endpoint was the composite of CV death, spontaneous myocardial infarction type 1 (sMI) or stroke at 12 months. Multivariable Cox regression models, adjusting for baseline characteristics, and biomarkers NT-proBNP and troponin I, were used to explore the association between glycaemia and outcome. On admission, 16,007 (86.1%) patients had HbA1c and/or glucose levels available and were subdivided into DM 38.5% (6160) (1501 patients had no previous DM diagnosis), prediabetes 38.8% (6210), and no DM 22.7% (3637). Kaplan Meier event rates at 12 months for CV death, sMI or stroke per subgroups were 14.5% (832), 9.0% (522), and 8.5% (293), respectively with multivariable adjusted HRs, versus no diabetes, for diabetes: 1.71 (1.50-1.95) and for prediabetes 1.03 (0.90-1.19). Corresponding event rates for CV death were 6.9% (391), 3.4% (195) and 3.0% (102), respectively, with adjusted HRs for patients with DM of: 1.92 (1.42-2.60) and for prediabetes 1.02 (0.79-1.32). Abnormal glucose metabolism is common in ACS patients, but only patients with definite DM have an increased CV risk, indicating that prediabetes is not immediately associated with worse CV outcomes.

Identifiants

pubmed: 31512201
doi: 10.1007/s11239-019-01938-2
pii: 10.1007/s11239-019-01938-2
pmc: PMC6800838
doi:

Substances chimiques

Glucose IY9XDZ35W2

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

563-569

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Auteurs

Axel Åkerblom (A)

Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden. Axel.Akerblom@ucr.uu.se.
Uppsala Clinical Research Center UCR, Uppsala University, Uppsala, Sweden. Axel.Akerblom@ucr.uu.se.
Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA. Axel.Akerblom@ucr.uu.se.
Uppsala Clinical Research Center, Dag Hammarskjölds väg 38, 751 85, Uppsala, Sweden. Axel.Akerblom@ucr.uu.se.

Daniel Wojdyla (D)

Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA.

Philippe Gabriel Steg (PG)

INSERM-Unité 1148, Paris, France.
Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat, Paris, France.
Université Paris-Diderot, Sorbonne-Paris Cité, Paris, France.
NHLI Imperial College, ICMS, Royal Brompton Hospital, London, UK.

Lars Wallentin (L)

Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden.
Uppsala Clinical Research Center UCR, Uppsala University, Uppsala, Sweden.

Stefan K James (SK)

Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden.
Uppsala Clinical Research Center UCR, Uppsala University, Uppsala, Sweden.

Andrzej Budaj (A)

Postgraduate Medical School, Grochowski Hospital, Warsaw, Poland.

Hugo A Katus (HA)

Medizinishe Klinik, Universitätsklinikum Heidelberg, Heidelberg, Germany.

Anders Himmelmann (A)

AstraZeneca Research and Development, Mölndal, Sweden.

Kurt Huber (K)

Department of Cardiology and Intensive Care Medicine, Wilhelminen Hospital, Vienna, Austria.
Medical School, Sigmund Freud University, Vienna, Austria.

Agneta Siegbahn (A)

Uppsala Clinical Research Center UCR, Uppsala University, Uppsala, Sweden.
Department of Medical Sciences, Clinical Chemistry, Uppsala University, Uppsala, Sweden.

Robert F Storey (RF)

Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.

Richard C Becker (RC)

Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA.
Division of Cardiovascular Health and Disease, Heart, Lung and Vascular Institute, Academic Health Center, Cincinnati, OH, USA.

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Classifications MeSH