The impact of body mass index on antiplatelet monotherapy strategy for secondary prevention after percutaneous coronary intervention: A substudy of the HOST-EXAM trial
- PMID: 40623657
- DOI: 10.1016/j.ahj.2025.07.005
The impact of body mass index on antiplatelet monotherapy strategy for secondary prevention after percutaneous coronary intervention: A substudy of the HOST-EXAM trial
Abstract
Background: Body mass index (BMI) may influence both clinical risk and pharmacologic response after percutaneous coronary intervention (PCI). We aimed to evaluate the association between BMI and long-term outcomes in a stabilized post-PCI population and to determine whether the effects of clopidogrel versus aspirin as single antiplatelet therapy (SAPT) differ across BMI strata.
Methods: This secondary analysis of the HOST-EXAM Extended study (median follow-up 5.8 years) included 4,549 per-protocol patients randomized to aspirin or clopidogrel after uneventful dual antiplatelet therapy. The primary endpoint was a composite of all-cause death, myocardial infarction, stroke, acute coronary syndrome readmission, or major bleeding (BARC ≥3). BMI was analyzed both categorically and continuously using multivariable Cox regression and restricted cubic spline models.
Results: There was a decreasing trend in adverse outcomes across increasing BMI categories (p for trend < .001), although most differences were attenuated after adjustment. Clopidogrel was associated with a significantly lower risk of the primary endpoint compared to aspirin in overweight and obese patients (adjusted HRs: 0.51 for overweight, 0.69 for obese), with similar reductions for thrombotic events (HRs: 0.43 and 0.59, respectively). These findings were consistent in both categorical and spline-based analyses. No significant differences were observed between treatment groups for bleeding outcomes.
Conclusions: In stabilized post-PCI patients, clopidogrel was associated with improved long-term outcomes compared to aspirin in overweight and obese patients. Further studies are warranted to explore BMI-guided antiplatelet strategies.
Trial registration: This trial was registered at ClinicalTrials.gov (Registration number: NCT02044250). URL: https://clinicaltrials.gov/study/NCT02044250.
Copyright © 2025 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest Dr. KW Park reports grants from the Ministry of Health and Welfare, Republic of Korea, Chong Kun Dang, Samjin Pharmaceutical, Hanmi Pharmaceutical, and Daewoong Pharmaceutical during the conduct of the study; speaker’s fees from Daiichi Sankyo, Sanofi, Bristol Myers Squibb, Bayer, Pfizer, inno.N Pharmaceutical, Daewoong Pharmaceutical, and JW Pharmaceutical outside of the submitted work. Dr. H Kim has received research grants or speaker’s fees from Daiichi Sankyo, Boston Scientific, Terumo, Biotronik, Dio, Medtronic, Abbott Vascular, Edwards Life Science, Amgen, and Boehringer Ingelheim outside of the submitted work. No other disclosures were reported.
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