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Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial

BACKGROUND: There are limited data on how the combination of diabetes mellitus (DM) and chronic kidney disease (CKD) affects cardiovascular outcomes as well as response to different P2Y(12) receptor antagonists, which represented the aim of the present investigation. METHODS AND RESULTS: In this pos...

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Autores principales: Franchi, Francesco, James, Stefan K., Ghukasyan Lakic, Tatevik, Budaj, Andrzej J., Cornel, Jan H., Katus, Hugo A., Keltai, Matyas, Kontny, Frederic, Lewis, Basil S., Storey, Robert F., Himmelmann, Anders, Wallentin, Lars, Angiolillo, Dominick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475041/
https://www.ncbi.nlm.nih.gov/pubmed/30857464
http://dx.doi.org/10.1161/JAHA.118.011139
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author Franchi, Francesco
James, Stefan K.
Ghukasyan Lakic, Tatevik
Budaj, Andrzej J.
Cornel, Jan H.
Katus, Hugo A.
Keltai, Matyas
Kontny, Frederic
Lewis, Basil S.
Storey, Robert F.
Himmelmann, Anders
Wallentin, Lars
Angiolillo, Dominick J.
author_facet Franchi, Francesco
James, Stefan K.
Ghukasyan Lakic, Tatevik
Budaj, Andrzej J.
Cornel, Jan H.
Katus, Hugo A.
Keltai, Matyas
Kontny, Frederic
Lewis, Basil S.
Storey, Robert F.
Himmelmann, Anders
Wallentin, Lars
Angiolillo, Dominick J.
author_sort Franchi, Francesco
collection PubMed
description BACKGROUND: There are limited data on how the combination of diabetes mellitus (DM) and chronic kidney disease (CKD) affects cardiovascular outcomes as well as response to different P2Y(12) receptor antagonists, which represented the aim of the present investigation. METHODS AND RESULTS: In this post hoc analysis of the PLATO (Platelet Inhibition and Patient Outcomes) trial, which randomized acute coronary syndrome patients to ticagrelor versus clopidogrel, patients (n=15 108) with available DM and CKD status were classified into 4 groups: DM+/CKD+ (n=1058), DM+/CKD− (n=2748), DM−/CKD+ (n=2160), and DM−/CKD− (n=9142). The primary efficacy end point was a composite of cardiovascular death, myocardial infarction, or stroke at 12 months. The primary safety end point was PLATO major bleeding. DM+/CKD+ patients had a higher incidence of the primary end point compared with DM−/CKD− patients (23.3% versus 7.1%; adjusted hazard ratio 2.22; 95% CI 1.88–2.63; P<0.001). Patients with DM+/CKD− and DM−/CKD+ had an intermediate risk profile. The same trend was shown for the individual components of the primary end point and for major bleeding. Compared with clopidogrel, ticagrelor reduced the incidence of the primary end point consistently across subgroups (P‐interaction=0.264), but with an increased absolute risk reduction in DM+/CKD+. The effects on major bleeding were also consistent across subgroups (P‐interaction=0.288). CONCLUSIONS: In acute coronary syndrome patients, a gradient of risk was observed according to the presence or absence of DM and CKD, with patients having both risk factors at the highest risk. Although the ischemic benefit of ticagrelor over clopidogrel was consistent in all subgroups, the absolute risk reduction was greatest in patients with both DM and CKD. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicatrials.gov. Unique identifier: NCT00391872.
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spelling pubmed-64750412019-04-24 Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial Franchi, Francesco James, Stefan K. Ghukasyan Lakic, Tatevik Budaj, Andrzej J. Cornel, Jan H. Katus, Hugo A. Keltai, Matyas Kontny, Frederic Lewis, Basil S. Storey, Robert F. Himmelmann, Anders Wallentin, Lars Angiolillo, Dominick J. J Am Heart Assoc Original Research BACKGROUND: There are limited data on how the combination of diabetes mellitus (DM) and chronic kidney disease (CKD) affects cardiovascular outcomes as well as response to different P2Y(12) receptor antagonists, which represented the aim of the present investigation. METHODS AND RESULTS: In this post hoc analysis of the PLATO (Platelet Inhibition and Patient Outcomes) trial, which randomized acute coronary syndrome patients to ticagrelor versus clopidogrel, patients (n=15 108) with available DM and CKD status were classified into 4 groups: DM+/CKD+ (n=1058), DM+/CKD− (n=2748), DM−/CKD+ (n=2160), and DM−/CKD− (n=9142). The primary efficacy end point was a composite of cardiovascular death, myocardial infarction, or stroke at 12 months. The primary safety end point was PLATO major bleeding. DM+/CKD+ patients had a higher incidence of the primary end point compared with DM−/CKD− patients (23.3% versus 7.1%; adjusted hazard ratio 2.22; 95% CI 1.88–2.63; P<0.001). Patients with DM+/CKD− and DM−/CKD+ had an intermediate risk profile. The same trend was shown for the individual components of the primary end point and for major bleeding. Compared with clopidogrel, ticagrelor reduced the incidence of the primary end point consistently across subgroups (P‐interaction=0.264), but with an increased absolute risk reduction in DM+/CKD+. The effects on major bleeding were also consistent across subgroups (P‐interaction=0.288). CONCLUSIONS: In acute coronary syndrome patients, a gradient of risk was observed according to the presence or absence of DM and CKD, with patients having both risk factors at the highest risk. Although the ischemic benefit of ticagrelor over clopidogrel was consistent in all subgroups, the absolute risk reduction was greatest in patients with both DM and CKD. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicatrials.gov. Unique identifier: NCT00391872. John Wiley and Sons Inc. 2019-03-12 /pmc/articles/PMC6475041/ /pubmed/30857464 http://dx.doi.org/10.1161/JAHA.118.011139 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Franchi, Francesco
James, Stefan K.
Ghukasyan Lakic, Tatevik
Budaj, Andrzej J.
Cornel, Jan H.
Katus, Hugo A.
Keltai, Matyas
Kontny, Frederic
Lewis, Basil S.
Storey, Robert F.
Himmelmann, Anders
Wallentin, Lars
Angiolillo, Dominick J.
Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial
title Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial
title_full Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial
title_fullStr Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial
title_full_unstemmed Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial
title_short Impact of Diabetes Mellitus and Chronic Kidney Disease on Cardiovascular Outcomes and Platelet P2Y(12) Receptor Antagonist Effects in Patients With Acute Coronary Syndromes: Insights From the PLATO Trial
title_sort impact of diabetes mellitus and chronic kidney disease on cardiovascular outcomes and platelet p2y(12) receptor antagonist effects in patients with acute coronary syndromes: insights from the plato trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475041/
https://www.ncbi.nlm.nih.gov/pubmed/30857464
http://dx.doi.org/10.1161/JAHA.118.011139
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