Systemic inflammation, polygenic risk score, and risk of incident abdominal aortic aneurysm in the UK biobank

There remains clinical uncertainty concerning the relationship between systemic inflammation and subsequent abdominal aortic aneurysm (AAA) risk. To investigate the association between chronic systematic inflammation markers (C-reactive protein (CRP), peripheral immune cell counts, and their derived ratios) and risk of AAA incidence, and identify potential effect modifiers. We included 271,068 individuals from the UK Biobank, who were free of aortic aneurysm and other conditions impacting their inflammatory states at baseline. Cox proportional-hazards model was used to analyze associations between inflammatory biomarkers and AAA, adjusting for AAA polygenetic risk score (PRS) and major risk factors. Restricted cubic splines were plotted to visualize non-linear relationship. Subgroup analyses by age, sex, hypertension, smoking and PRS were performed to identify any interaction. Over a median follow-up of 13·9 years, 629 incident AAAs were recorded. For each 1-SD increase in baseline CRP, lymphocyte, monocyte, and neutrophil counts, the risk of AAA increased by 46%, 17%, 27% and 27%, respectively (all p < 0·001). The cubic splines showed the CRP-AAA association to be monotonic. The highest tertile of PRS was associated with an 80% increased AAA risk compared with the lowest tertile. The association between CRP and AAA was significant and comparable across PRS tertile groups. Sex and smoking status modified the CRP-AAA association, with the strongest association observed in males and current smokers. Our study found a significant association between chronic systemic inflammation and risk of AAA incidence. CRP compliments PRS and other AAA risk factors in better identifying high-risk populations. Current indexes for identifying patients to screen for AAA are family history, age, sex and smoking. This study revealed that a healthy public with a high level of CRP and one of the above traditional high-risk factors of AAA (high genetic risk, ≥ 65 years old, male, or current smoker) had a high risk of incident AAA and is recommended to screen for AAA.

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Publication Details

Journal
BMC Public Health
Published
2025-12-24
DOI
https://doi.org/10.1186/s12889-025-25123-8
Primary Topic
Aortic aneurysm repair treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Systemic inflammation, polygenic risk score, and risk of incident abdominal aortic aneurysm in the UK biobank

Jinbao Qin, Jiahao Lei, Zhijue Xu, Weiqing Wei et al.
BMC Public Health
Aortic aneurysm repair treatments
article

Systemic inflammation, polygenic risk score, and risk of incident abdominal aortic aneurysm in the UK biobank

Jinbao Qin, Jiahao Lei, Zhijue Xu, Weiqing Wei, Jiateng Hu, Ying Liu, Wang Rui-hua, Xinwu Lu, Hongji Pu, Hongbin Guo, Zhen Zhou, Zhaoyu Wu, Kaihuang Ye, Peng Qiu
article en

Abstract

There remains clinical uncertainty concerning the relationship between systemic inflammation and subsequent abdominal aortic aneurysm (AAA) risk. To investigate the association between chronic systematic inflammation markers (C-reactive protein (CRP), peripheral immune cell counts, and their derived ratios) and risk of AAA incidence, and identify potential effect modifiers. We included 271,068 individuals from the UK Biobank, who were free of aortic aneurysm and other conditions impacting their inflammatory states at baseline. Cox proportional-hazards model was used to analyze associations between inflammatory biomarkers and AAA, adjusting for AAA polygenetic risk score (PRS) and major risk factors. Restricted cubic splines were plotted to visualize non-linear relationship. Subgroup analyses by age, sex, hypertension, smoking and PRS were performed to identify any interaction. Over a median follow-up of 13·9 years, 629 incident AAAs were recorded. For each 1-SD increase in baseline CRP, lymphocyte, monocyte, and neutrophil counts, the risk of AAA increased by 46%, 17%, 27% and 27%, respectively (all p < 0·001). The cubic splines showed the CRP-AAA association to be monotonic. The highest tertile of PRS was associated with an 80% increased AAA risk compared with the lowest tertile. The association between CRP and AAA was significant and comparable across PRS tertile groups. Sex and smoking status modified the CRP-AAA association, with the strongest association observed in males and current smokers. Our study found a significant association between chronic systemic inflammation and risk of AAA incidence. CRP compliments PRS and other AAA risk factors in better identifying high-risk populations. Current indexes for identifying patients to screen for AAA are family history, age, sex and smoking. This study revealed that a healthy public with a high level of CRP and one of the above traditional high-risk factors of AAA (high genetic risk, ≥ 65 years old, male, or current smoker) had a high risk of incident AAA and is recommended to screen for AAA.

BMC Public HealthVol. 25(1)
Shanghai Jiao Tong University (CN), Shanghai Ninth People's Hospital (CN), Monash University (AU)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Science and Technology Commission of Shanghai Municipality, Shanghai Municipal Health Bureau, Fundamental Research Funds for the Central Universities, Science and Technology Innovation Plan Of Shanghai Science and Technology Commission
Good health and well-being
Openalex Percentile: Top 28%
Aortic aneurysm repair treatments
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