Ticagrelor vs. clopidogrel in patients with acute coronary syndromes and diabetes: a substudy from the PLATelet inhibition and patient Outcomes (PLATO) trial


Autoria(s): JAMES, Stefan; ANGIOLILLO, Dominick J.; CORNEL, Jan H.; ERLINGE, David; HUSTED, Steen; KONTNY, Frederic; MAYA, Juan; NICOLAU, Jose C.; SPINAR, Jindrich; STOREY, Robert F.; STEVENS, Susanna R.; WALLENTIN, Lars; PLATO Study Grp
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Patients with diabetes mellitus (DM) have high platelet reactivity and are at increased risk of ischaemic events and bleeding post-acute coronary syndromes (ACS). In the PLATelet inhibition and patient Outcomes (PLATO) trial, ticagrelor reduced the primary composite endpoint of cardiovascular death, myocardial infarction, or stroke, but with similar rates of major bleeding compared with clopidogrel. We aimed to investigate the outcome with ticagrelor vs. clopidogrel in patients with DM or poor glycaemic control. We analysed patients with pre-existing DM (n = 4662), including 1036 patients on insulin, those without DM (n = 13 951), and subgroups based on admission levels of haemoglobin A1c (HbA1c; n = 15 150). In patients with DM, the reduction in the primary composite endpoint (HR: 0.88, 95% CI: 0.76-1.03), all-cause mortality (HR: 0.82, 95% CI: 0.66-1.01), and stent thrombosis (HR: 0.65, 95% CI: 0.36-1.17) with no increase in major bleeding (HR: 0.95, 95% CI: 0.81-1.12) with ticagrelor was consistent with the overall cohort and without significant diabetes status-by-treatment interactions. There was no heterogeneity between patients with or without ongoing insulin treatment. Ticagrelor reduced the primary endpoint, all-cause mortality, and stent thrombosis in patients with HbA1c above the median (HR: 0.80, 95% CI: 0.70-0.91; HR: 0.78, 95% CI: 0.65-0.93; and HR: 0.62, 95% CI: 0.39-1.00, respectively) with similar bleeding rates (HR: 0.98, 95% CI: 0.86-1.12). Ticagrelor, when compared with clopidogrel, reduced ischaemic events in ACS patients irrespective of diabetic status and glycaemic control, without an increase in major bleeding events.

AstraZeneca

Uppsala Clinical Research Center

GlaxoSmithKline

Otsuka

Accumetrics

Eli Lilly and Company

Daiichi Sankyo, Inc.

Medicines Company

Eisai

Portola Pharmaceutical

Schering-Plough

Johnson and Johnson

Bristol-Myers Squibb

sanofi-aventis

Pfizer

Bayer

Merck Sharp Dohme (MSD)

Perseus Proteomics Inc.

Dynabyte

Eli Lilly/Daiichi Sankyo alliance

Teva

Novartis

sanofi-aventis/Bristol-Myers Squibb

Regado Biotechnologies

Athera Biotechnologies

Identificador

EUROPEAN HEART JOURNAL, v.31, n.24, p.3006-3016, 2010

0195-668X

http://producao.usp.br/handle/BDPI/21781

10.1093/eurheartj/ehq325

http://dx.doi.org/10.1093/eurheartj/ehq325

Idioma(s)

eng

Publicador

OXFORD UNIV PRESS

Relação

European Heart Journal

Direitos

restrictedAccess

Copyright OXFORD UNIV PRESS

Palavras-Chave #Acute coronary syndromes #Diabetes #Ticagrelor #Clopidogrel #Mortality #Myocardial infarction #ST-SEGMENT ELEVATION #ARTERY-DISEASE #ANTIPLATELET THERAPY #RISK-FACTOR #MELLITUS #ASPIRIN #RESPONSIVENESS #MANAGEMENT #PRASUGREL #RESPOND #Cardiac & Cardiovascular Systems
Tipo

article

original article

publishedVersion