• Yudiyang Ma, Jianing Wang, Linxi Tang, Feipeng Cui, Yaohua Tian, Jing Zhang, and Jian Yang.
• Hubei Key Laboratory of Ischemic Cardiovascular Disease, Yichang, China.
• Ann. Surg. 2025 Jan 23.

ObjectiveThe aim of this study is to explore the risk profiles associated with Abdominal aortic aneurysm (AAA) incidence in both the general population and diverse subpopulations.Summary Background DataAAA is a life-threatening arterial disease, and there is limited understanding of its etiological spectrum across the age, sex, and genetic risk subgroups, making early prevention efforts more complicated.MethodsThis study encompassed a sample size of 364399 participants from the UK. Utilizing the Cox proportional hazards model, we estimated the hazard ratios (HRs) and population attributable fraction (PAF) for 24 risk factors and 5 weighted risk scores associated with AAA incidence. Subsequently, this study investigated the relationships between AAA onset and various risk factors based on age, sex, and genetic susceptibility subgroups, and assessed the two- and three-way interactions.ResultsAfter a median follow-up of 12.62 years, 1684 participants developed AAA. Among the 24 risk factors from 5 different aspects, 12 exhibited significant associations with AAA development. Socio-demographic factors (age and sex) and genetic factors accounted for the majority of AAA cases in both the general population and diverse subpopulations. For lifestyle factors, AAA cases attributable to smoking are larger in the older group (PAF: 15.45% vs. 11.25%) and women (PAF: 23.79% vs. 16.75%). Similarly, physical inactivity had a greater effect on AAA risk in women (4.84% vs. 1.95%), but no age and genetic risk differences were observed. PAF of high C-reactive protein was the most prominent of all cardiometabolic factors across different age, sex, and genetic risk strata, with 18.92% (< 60 years) and 13.71% (≥ 60 years) in age groups, 18.18% (women) and 13.31% (men) in sex groups, and 17.64% (intermediate genetic risk) and 13.01% (high genetic risk) in genetic risk groups. Clinical comorbidities, such as cardiovascular diseases, dyslipidemia, and hypertension significantly associated with the risk of incident AAA, and these factors exerted a greater influence on AAA risk in younger group, women, and those with low genetic risk (P for interaction < 0.05).ConclusionsThis study depicted specific risk profiles that influence AAA incidence among general population and diverse subpopulations, thereby aiding in the formulation of precise and effective strategies for AAA prevention.Copyright © 2025 Wolters Kluwer Health, Inc. All rights reserved.

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