Abstract
Background and aims: Aortic aneurysms, including abdominal (AAA) and thoracic (TAA), pose significant challenges due to their rupture risk and complex pathophysiology. While aspirin has been proposed to manage aneurysm progression, evidence remains limited. This retrospective, single-center study used AI-driven methods to examine the association between aspirin therapy and aneurysm growth. Methods: The study, at the University of Kentucky Healthcare, utilized de-identified electronic health record data from 2010 to 2023. To evaluate platelet count changes, Cohort 1 included patients with AAA or TAA and matched healthy controls. To evaluate aortic diameter, Cohort 2 included AAA or TAA patients who had at least two imaging studies. Extraction of aortic diameters utilized an advanced AI-based natural language processing (NLP) algorithm to identify and extract relevant text strings related to aortic dimensions. Multivariable-adjusted linear regression analyses assessed the impact of aspirin on aneurysm progression. Results: Cohort 1 included 11,538 participants: 5774 controls, 3439 with AAA, and 2325 with TAA. Platelet counts were significantly lower in patients with aortic aneurysms compared to controls, though they were not considered thrombocytopenic. Cohort 2 included 302 AAA and 141 TAA patients. Subgroup analysis revealed that aspirin use was associated with increased AAA progression in females with small aneurysms (<50 mm). Further, aspirin therapy showed no significant impact on the annualized change in aneurysm diameter for TAA or for males with AAA. Conclusions: Our findings suggest aspirin's effectiveness varies by sex and potentially aneurysm size, underscoring the need for further research to refine antiplatelet therapy guidelines for aortic aneurysms.
| Original language | English |
|---|---|
| Article number | 119224 |
| Journal | Atherosclerosis |
| Volume | 407 |
| DOIs | |
| State | Published - Aug 2025 |
Bibliographical note
Publisher Copyright:© 2025 Elsevier B.V.
Funding
In abdominal aortic aneurysms (AAA), platelets contribute to intraluminal thrombus (ILT) formation and release inflammatory mediators and proteolytic enzymes that degrade the extracellular matrix and weaken the aortic wall [2,8,9,11]. Thoracic aortic aneurysms (TAA), although involving minimal ILT, exhibit significant platelet activation, which directly impairs endothelial integrity and amplifies inflammation [12]. Antiplatelet therapies, traditionally used for their antithrombotic effects, may also target these pathological pathways, potentially affecting aneurysm growth [2,13,14]. The 2022 American College of Cardiology and American Heart Association guidelines recommend aspirin with a class 2b indication (level of evidence: C), highlighting the limited strength of evidence, for patients with AAA and intramural thrombus [5]. Similarly, the European Society for Vascular Surgery advises the use of antiplatelet agents in patients undergoing AAA surgery, though evidence supporting their impact on sac volume remains limited [6].The authors' research was supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health R35HL150818 to S.W.W. Additional support was provided by the NIH National Center for Advancing Translational Sciences through grant numbers UL1TR000117 and UL1TR001998. SM is supported by the American Heart Association Postdoctoral Fellowship (25POST1378684). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH or American Heart Association. The authors wish to thank the members of the Whiteheart lab for their comments on the manuscript and their careful editing of the final version. The authors' research was supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health R35HL150818 to S.W.W. Additional support was provided by the NIH National Center for Advancing Translational Sciences through grant numbers UL1TR000117 and UL1TR001998 . SM is supported by the American Heart Association Postdoctoral Fellowship ( 25POST1378684 ). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH or American Heart Association. The authors wish to thank the members of the Whiteheart lab for their comments on the manuscript and their careful editing of the final version.
| Funders | Funder number |
|---|---|
| American College of Cardiology Foundation | |
| National Heart, Lung, and Blood Institute (NHLBI) | |
| National Center for Advancing Translational Sciences (NCATS) | 25POST1378684, UL1TR001998, UL1TR000117 |
| American the American Heart Association | 25POST1378684 |
| National Institutes of Health (NIH) | R35HL150818 |
Keywords
- Aneurysm
- Anti-thrombotic
- Platelets
- Salicylic acid
- Thrombosis
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
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Stowe, A. (Manager), Chen, M. (Operator), Hubbard, W. (Operator), Gipson-Reichardt, C. (Operator), Sullivan, P. (Operator), Roberts, J. (Operator), Trout, A. (Operator), Whiteheart, S. (Operator) & Wood, J. (Operator)
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