Impact of body mass index on clinical outcome among elderly patients with acute coronary syndrome treated with percutaneous coronary intervention: Insights from the ELDERLY ACS 2 trial.


Journal

Nutrition, metabolism, and cardiovascular diseases : NMCD
ISSN: 1590-3729
Titre abrégé: Nutr Metab Cardiovasc Dis
Pays: Netherlands
ID NLM: 9111474

Informations de publication

Date de publication:
07 05 2020
Historique:
received: 07 08 2019
revised: 26 12 2019
accepted: 12 01 2020
pubmed: 5 3 2020
medline: 21 7 2020
entrez: 5 3 2020
Statut: ppublish

Résumé

Elderly patients are at increased risk of hemorrhagic and thrombotic complications after an acute coronary syndrome (ACS). Frailty, comorbidities and low body weight have emerged as conditioning the prognostic impact of dual antiplatelet therapy (DAPT). The aim of the present study was to investigate the prognostic impact of body mass index (BMI) on clinical outcome among patients included in the Elderly-ACS 2 trial, a randomized, open-label, blinded endpoint study comparing low-dose (5 mg) prasugrel vs clopidogrel among elderly patients with ACS. Our population is represented by 1408 patients enrolled in the Elderly-ACS 2 trial. BMI was calculated at admission. The primary endpoint of this analysis was cardiovascular (CV) mortality. Secondary endpoints were all-cause death, recurrent MI, Bleeding Academic Research Consortium (BARC) type 2 or 3 bleeding, and re-hospitalization for cardiovascular reasons or stent thrombosis within 12 months after index admission. Patients were grouped according to median values of BMI (<or ≥ 25.7 kg/m2). BMI was associated with hypertension, diabetes, hypercholesterolemia, estimated glomerular filtration rate and hemoglobin (p < 0.001), and inversely with age (p = 0.005). Overweight patients displayed larger use of diuretics at admission (p = 0.03), aspirin pre-randomization (p = 0.01) and radial access (p = 0.04). At a median follow-up of 367 [337-378] days, BMI did not affect CV mortality in the overall population 4% vs 3.8%; adjusted HR [95%CI] = 2.3 [0.8-6.5], p = 0.12. Similar findings were observed for our secondary efficacy and safety endpoints. Results did not change when considering separately higher risk subsets of patients, (female gender, diabetics, ST-segment elevation myocardial infarction or the type of DAPT treatment allocation), with no significant interaction between these population characteristics and BMI. Among elderly patients with ACS, BMI did not condition the survival or the risk of major cardiovascular and bleeding complications. The results were consistent across several patient risk categories.

Sections du résumé

BACKGROUND AND AIM
Elderly patients are at increased risk of hemorrhagic and thrombotic complications after an acute coronary syndrome (ACS). Frailty, comorbidities and low body weight have emerged as conditioning the prognostic impact of dual antiplatelet therapy (DAPT). The aim of the present study was to investigate the prognostic impact of body mass index (BMI) on clinical outcome among patients included in the Elderly-ACS 2 trial, a randomized, open-label, blinded endpoint study comparing low-dose (5 mg) prasugrel vs clopidogrel among elderly patients with ACS.
METHODS AND RESULTS
Our population is represented by 1408 patients enrolled in the Elderly-ACS 2 trial. BMI was calculated at admission. The primary endpoint of this analysis was cardiovascular (CV) mortality. Secondary endpoints were all-cause death, recurrent MI, Bleeding Academic Research Consortium (BARC) type 2 or 3 bleeding, and re-hospitalization for cardiovascular reasons or stent thrombosis within 12 months after index admission. Patients were grouped according to median values of BMI (<or ≥ 25.7 kg/m2). BMI was associated with hypertension, diabetes, hypercholesterolemia, estimated glomerular filtration rate and hemoglobin (p < 0.001), and inversely with age (p = 0.005). Overweight patients displayed larger use of diuretics at admission (p = 0.03), aspirin pre-randomization (p = 0.01) and radial access (p = 0.04). At a median follow-up of 367 [337-378] days, BMI did not affect CV mortality in the overall population 4% vs 3.8%; adjusted HR [95%CI] = 2.3 [0.8-6.5], p = 0.12. Similar findings were observed for our secondary efficacy and safety endpoints. Results did not change when considering separately higher risk subsets of patients, (female gender, diabetics, ST-segment elevation myocardial infarction or the type of DAPT treatment allocation), with no significant interaction between these population characteristics and BMI.
CONCLUSIONS
Among elderly patients with ACS, BMI did not condition the survival or the risk of major cardiovascular and bleeding complications. The results were consistent across several patient risk categories.

Identifiants

pubmed: 32127336
pii: S0939-4753(20)30017-X
doi: 10.1016/j.numecd.2020.01.001
pii:
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0
Clopidogrel A74586SNO7
Prasugrel Hydrochloride G89JQ59I13

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

730-737

Informations de copyright

Copyright © 2020 The Italian Society of Diabetology, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition, and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Giuseppe De Luca (G)

Azienda Ospedaliera-Universitaria "Maggiore della Carità", Eastern Piedmont University, Novara, Italy. Electronic address: giuseppe.deluca@maggioreosp.novara.it.

Monica Verdoia (M)

Azienda Ospedaliera-Universitaria "Maggiore della Carità", Eastern Piedmont University, Novara, Italy.

Stefano Savonitto (S)

Ospedale Manzoni, Lecco, Italy.

Luca A Ferri (LA)

Ospedale Manzoni, Lecco, Italy.

Luigi Piatti (L)

Ospedale Manzoni, Lecco, Italy.

Daniele Grosseto (D)

Ospedale Infermi, Rimini, Italy.

Nuccia Morici (N)

ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Irene Bossi (I)

ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Paolo Sganzerla (P)

Ospedale Treviglio-Caravaggio, Treviglio, Italy.

Giovanni Tortorella (G)

S.C. Cardiologia-UTIC, Ospedale Vaio, Fidenza (PR), Italy.

Michele Cacucci (M)

Ospedale Maggiore, Crema, Italy.

Maurizio Ferrario (M)

IRCCS Fondazione Policlinico S. Matteo, Pavia, Italy.

Ernesto Murena (E)

Ospedale S. Maria delle Grazie, Pozzuoli, Italy.

Girolamo Sibilio (G)

Ospedale S. Maria delle Grazie, Pozzuoli, Italy.

Stefano Tondi (S)

Ospedale Baggiovara, Modena, Italy.

Anna Toso (A)

Ospedale S. Stefano, Prato, Italy.

Sergio Bongioanni (S)

Ospedale Mauriziano, Torino, Italy.

Amelia Ravera (A)

OspedaleRuggi D' Aragona, Salerno, Italy.

Elena Corrada (E)

HumanitasClinical and Research Center, Rozzano, Italy.

Matteo Mariani (M)

Ospedale Civile, Legnano, Italy.

Leonardo Di Ascenzo (L)

Ospedale di San Donà di Piave-Portogruaro, Portogruaro, Italy.

A Sonia Petronio (AS)

Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.

Claudio Cavallini (C)

Ospedale S. Maria della Misericordia, Perugia, Italy.

Giancarlo Vitrella (G)

Ospedali Riuniti di Trieste, Trieste, Italy.

Roberto Antonicelli (R)

Istituto Nazionale di Ricerca e Cura per l' Anziano, Ancona, Italy.

Renata Rogacka (R)

Azienda Ospedaliera di Desio e Vimercate, Desio, Italy.

Stefano De Servi (S)

Multimedica IRCSS, Milan, Italy.

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Classifications MeSH