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American Heart Association

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Final ID: Mo3034

Aspirin Use and Cardiovascular Disease Incidence in Adults with High Lipoprotein(a): A Multi-Cohort Study

Abstract Body (Do not enter title and authors here): Introduction: There is an active debate about who may benefit from taking aspirin to reduce their incidence of cardiovascular disease (CVD). Some prior cohort studies with small sample size suggest that aspirin use may be associated with a lower incidence of CVD or coronary heart disease (CHD) in adults with Lp(a) ≥50 mg/dL but not in those with Lp(a) <50 mg/dL, a hypothesis that needs confirmation.
Research question: Does the association of aspirin use with incident CVD or CHD vary by Lp(a) among US adults?
Methods: We analyzed publicly available data from adults without CVD at baseline in the ARIC (n=13,085, mean age 54 years), CHS (n=3,956, mean age 72 years), and MESA (n=6,324, mean age 62 years) studies. Lp(a) ≥50 mg/dL was defined as high. Participants were followed for incident CVD (myocardial infarction, stroke, or CVD death) and CHD (myocardial infarction or CHD death; median follow-up: ARIC 26 years, CHS 12 years, MESA 14 years). Hazard ratios associated with aspirin use were calculated after propensity score matching (primary analysis) and in all participants using multivariable adjustment (secondary analysis). Mixed-effects models were used to obtain pooled hazard ratios.
Results: Aspirin use was 25.1% in ARIC, 29.6% in CHS, and 19.9% in MESA. In MESA, adults taking aspirin were older, had higher blood pressure, and were more likely to have diabetes and a low estimated glomerular filtration rate and to be taking antihypertensive medication and a statin versus those not taking aspirin. These differences were attenuated or not present in ARIC and CHS. The CVD incidence rate per 1,000 person-years (95%CI) was higher in adults with versus without high Lp(a): 16.3 (15.3-17.4) and 12.5 (12.1-13.0), respectively, in ARIC, 35.8 (31.5-40.1) and 32.3 (30.6-34.0) in CHS, and 10.8 (9.1-12.4) and 8.2 (7.5-8.9) in MESA. Aspirin use was not associated with CVD or CHD incidence in adults with or without high Lp(a) in the primary analysis (Figure). No association between aspirin use and CVD or CHD incidence was present in the secondary analysis using multivariable adjustment (data not shown).
Conclusion: The association of aspirin use with CVD and CHD incidence did not differ by Lp(a) in this multi-cohort study.
  • Colantonio, Lisandro  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Bittner, Vera  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Wang, Zhixin  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Ghazi, Lama  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Alanaeme, Chibuike  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Christenson, Ashley  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Dubal, Medha  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Malick, Waqas  ( Mount Sinai Fuster Heart Hospital , New York , New York , United States )
  • Levitan, Emily  ( University of Alabama at Birmingham , Birmingham , Alabama , United States )
  • Rosenson, Robert  ( Mount Sinai Fuster Heart Hospital , New York , New York , United States )
  • Author Disclosures:
    Lisandro Colantonio: DO have relevant financial relationships ; Research Funding (PI or named investigator):Amgen:Past (completed) | Vera Bittner: DO have relevant financial relationships ; Research Funding (PI or named investigator):Sanofi and Regeneron:Past (completed) ; Research Funding (PI or named investigator):Novartis:Active (exists now) ; Research Funding (PI or named investigator):Amgen:Active (exists now) ; Other (please indicate in the box next to the company name):Esperion - National Coordinator:Past (completed) ; Other (please indicate in the box next to the company name):Verve Therapeutics - DSMB:Active (exists now) ; Other (please indicate in the box next to the company name):Eli Lilly - DSMB:Active (exists now) | Zhixin Wang: DO NOT have relevant financial relationships | Lama Ghazi: DO NOT have relevant financial relationships | Chibuike Alanaeme: DO NOT have relevant financial relationships | Ashley Christenson: DO NOT have relevant financial relationships | Medha Dubal: DO NOT have relevant financial relationships | Waqas Malick: DO NOT have relevant financial relationships | Emily Levitan: DO have relevant financial relationships ; Research Funding (PI or named investigator):Amgen Inc:Past (completed) | Robert Rosenson: DO have relevant financial relationships ; Research Funding (PI or named investigator):Amgen:Active (exists now) ; Research Funding (PI or named investigator):verve:Active (exists now) ; Researcher:Regeneron:Past (completed) ; Consultant:Editas:Active (exists now) ; Consultant:Lipigon:Active (exists now) ; Consultant:Novartis:Active (exists now) ; Consultant:Lilly:Active (exists now) ; Consultant:Arrowhead:Active (exists now) ; Consultant:Amgen:Active (exists now) ; Royalties/Patent Beneficiary:Wolters Kluwer:Active (exists now) ; Research Funding (PI or named investigator):89 Bio:Active (exists now) ; Research Funding (PI or named investigator):Novo Nordisk:Active (exists now) ; Research Funding (PI or named investigator):Novartis:Active (exists now) ; Research Funding (PI or named investigator):Lilly:Active (exists now) ; Research Funding (PI or named investigator):Arrowhead:Active (exists now)
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Medications in Motion: Innovating Pharmacotherapy for Enhanced Treatment Outcomes

Monday, 11/18/2024 , 01:30PM - 02:30PM

Abstract Poster Session

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