Ono, Masafumi; Chichareon, Ply; Tomaniak, Mariusz; Kawashima, Hideyuki; Takahashi, Kuniaki; Kogame, Norihiro; Modolo, Rodrigo; Hara, Hironori; Gao, Chao; Wang, Rutao; Walsh, Simon; Suryapranata, Harry; da Silva, Pedro Canas; Cotton, James; Koning, René; Akin, Ibrahim; Rensing, Benno J W M; Garg, Scot; Wykrzykowska, Joanna J; Piek, Jan J; ... (2020). The association of body mass index with long-term clinical outcomes after ticagrelor monotherapy following abbreviated dual antiplatelet therapy in patients undergoing percutaneous coronary intervention: a prespecified sub-analysis of the GLOBAL LEADERS Trial. Clinical research in cardiology, 109(9), pp. 1125-1139. Springer-Verlag 10.1007/s00392-020-01604-1
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The association of body mass index with long-term clinical outcomes after ticagrelor monotherapy following abbreviated dual antiplatelet therapy in patients undergoing percutaneous coronary intervention.pdf - Published Version Available under License Creative Commons: Attribution (CC-BY). Download (3MB) | Preview |
BACKGROUND
The efficacy of antiplatelet therapies following percutaneous coronary intervention (PCI) may be affected by body mass index (BMI).
METHODS AND RESULTS
This is a prespecified subgroup analysis of the GLOBAL LEADERS trial, a prospective, multicenter, open-label, randomized controlled trial in an all-comer population undergoing PCI, comparing the experimental strategy (23-month ticagrelor monotherapy following 1-month dual antiplatelet therapy [DAPT]) with a reference regimen (12-month aspirin monotherapy following 12-month DAPT). A total of 15,968 patients were stratified by baseline BMI with prespecified threshold of 27 kg/m2. Of those, 6973 (43.7%) patients with a BMI < 27 kg/m2 had a higher risk of all-cause mortality at 2 years than those with BMI ≥ 27 kg/m2 (adjusted HR 1.24, 95% CI 1.02-1.49). At 2 years, the rates of the primary endpoint (all-cause mortality or new Q-wave myocardial infarction) were similar between treatment strategies in either BMI group (pinteraction = 0.51). In acute coronary syndrome, however, the experimental strategy was associated with significant reduction of the primary endpoint compared to the reference strategy in patients with BMI < 27 kg/m2 (HR 0.69, 95% CI 0.51-0.94), but not in the ones with BMI ≥ 27 kg/m2 (pinteraction = 0.047). In chronic coronary syndrome, there was no between-group difference in the efficacy and safety of the two antiplatelet strategies.
CONCLUSIONS
Overall, BMI did not influence the treatment effect seen with ticagrelor monotherapy; however, a beneficial effect of ticagrelor monotherapy was seen in ACS patients with BMI < 27 kg/m2.
TRIAL REGISTRATION
The trial has been registered with ClinicalTrials.gov, Number NCT01813435.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Department of Cardiovascular Disorders (DHGE) > Clinic of Cardiology |
UniBE Contributor: |
Windecker, Stephan |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
1861-0684 |
Publisher: |
Springer-Verlag |
Language: |
English |
Submitter: |
Nadia Biscozzo |
Date Deposited: |
29 Nov 2020 15:07 |
Last Modified: |
05 Dec 2022 15:41 |
Publisher DOI: |
10.1007/s00392-020-01604-1 |
PubMed ID: |
32006156 |
Uncontrolled Keywords: |
Acute coronary syndrome Body mass index Drug-eluting stent Dual antiplatelet therapy Percutaneous coronary intervention Ticagrelor monotherapy |
BORIS DOI: |
10.7892/boris.147488 |
URI: |
https://boris.unibe.ch/id/eprint/147488 |