Journal
JACC-CARDIOVASCULAR INTERVENTIONS
Volume 15, Issue 19, Pages 1948-1960Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcin.2022.07.039
Keywords
body mass index; coronary artery disease; dual antiplatelet therapy; percutaneous coronary intervention; ticagrelor; aspirin
Categories
Funding
- AstraZeneca
- Medtronic
- Abbott Vascular
- Boston Scientific
- Abbott
- Amgen
- Aralez
- Bayer
- Biosensors
- Boehringer Ingelheim
- Bristol Myers Squibb
- Chiesi
- Daiichi Sankyo
- Eli Lilly
- Haemonetics
- Janssen
- Merck
- PhaseBio
- PLx Pharma
- Pfizer
- Sanofi
- Medicines Company
- CeloNova
- CSL Behring
- Eisai
- Gilead
- Matsutani Chemical Industry
- Novartis
- Osprey Medical
- Renal Guard Solutions
- Scott R. MacKenzie Foundation
- Philips
- Abiomed
- Terumo
- Medicure
- US World Meds
- Instrumentation Laboratory
- Idorsia
- Ionis
- 3D Communications
- ACI Clinical
- Biotie
- Cara Therapeutics
- Cardinal Health
- Faculty Connection
- Imbria
- Impulse Medical
- Janssen Pharmaceuticals
- Medscape
- Milestone Pharmaceuticals
- XyloCor
- Portola
- Bayer/Janssen
- Amarin
- Regeneron
- Novo Nordisk
- Servier
- Angel Medical
- Johnson Johnson
- Portola Pharmaceuticals
- Gilead Sciences
- WebMD
- UpToDate Cardiovascular Medicine
- Amarin Pharma
- PharmaMar
- Somahlution
- Verreseon
- Impact Bio
- MedImmume
- Medtelligence
- MicroPort
- PERT Consortium
- GE Healthcare
- Applied Therapeutics
- Arena
- Cardia-Wave
- Cell Aegis
- CERC
- Concept Medical
- Insel Gruppe
- Novartis Pharmaceuticals
- Orbus-Neich
- Transverse Medical
- Zoll
- American College of Cardiology
- California Institute for Regenerative Medicine
- Cine-Med Research
- Society for Cardiovascular Angiography and Interventions
- Duke University
- Idorsia Pharmaceuticals
Ask authors/readers for more resources
In this secondary analysis of the TWILIGHT trial, ticagrelor monotherapy was found to reduce bleeding events without increasing the risk of ischemia across different BMI categories.
BACKGROUND There is a paucity of data regarding the safety and efficacy of different antiplatelet regimens according to standardized body mass index (BMI) categories.OBJECTIVES The aim of this study was to investigate bleeding and ischemic outcomes according to BMI in the TWILIGHT (Ticagrelor With Aspirin or Alone in High-Risk Patients After Coronary Intervention) trial.METHODS The TWILIGHT trial randomized high-risk patients to ticagrelor plus aspirin or ticagrelor plus placebo at 3 months after percutaneous coronary intervention. In this secondary analysis, patients were stratified by standard BMI categories, as recommended by the European Society of Cardiology Working Group on Thrombosis (normal weight [BMI 18.5-24.99 kg/m2], overweight [BMI 25-29.99 kg/m2], and obese [BMI $30 kg/m2]) and by median BMI, as prespecified in the protocol.RESULTS Among 7,038 patients randomized and with available BMI, 1,807 (25.7%) were normal weight, 2,927 (41.6%) were overweight, and 2,304 (32.7%) were obese. In normal-weight, overweight, and obese patients, ticagrelor mono -therapy, compared with ticagrelor plus aspirin, reduced the primary endpoint of Bleeding Academic Research Consortium type 2, 3, or 5 bleeding (normal weight: HR: 0.48 [95% CI: 0.32-0.73]; overweight: HR: 0.57 [95% CI: 0.41-0.78]; obese: HR: 0.63 [95% CI: 0.44-0.91]; P for interaction = 0.627), without any increase in the composite ischemic endpoint of all -cause death, myocardial infarction, or stroke (normal weight: HR: 1.36 [95% CI: 0.84-2.19]; overweight: HR: 0.92 [95% CI: 0.63-1.35]; obese: HR: 0.84 [95% CI: 0.56-1.25]; P for interaction = 0.290). These findings were consistent with the prespecified analysis by median BMI.CONCLUSIONS Among high-risk patients undergoing percutaneous coronary intervention, ticagrelor monotherapy, compared with ticagrelor plus aspirin, reduced bleeding events without any increase in ischemic risk across different BMI categories. (J Am Coll Cardiol Intv 2022;15:1948-1960) (c) 2022 by the American College of Cardiology Foundation.
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