Liu Xinyi, Liu Hao, Chen Suwei, Gong Chen, Ge Yipeng, Qiao Zhiyu, Li Chengnan, Zhu Junming
Department of Cardiovascular Surgery, Beijing Aortic Disease Center, Beijing Anzhen Hospital of Capital Medical University, Beijing, China.
Department of Hematology, Beijing Anzhen Hospital of Capital Medical University, Beijing, China.
Front Endocrinol (Lausanne). 2025 Jul 4;16:1612975. doi: 10.3389/fendo.2025.1612975. eCollection 2025.
CONTEXT/OBJECTIVES: Metabolic syndrome (MetS) is associated with various diseases, yet its connection with aortic aneurysm (AA) is not well understood. The role of chronic inflammation as a mediator in this relationship also remains unclear. This study explores the combined effects of MetS and inflammation on AA risk.
Data from 312,505 UK Biobank participants were analyzed to assess the relationship between MetS and AA. Cox proportional hazards regression models evaluated the association, while restricted cubic splines, mediation analyses, interaction assessments, and joint analyses explored the impact of inflammatory indicators, including the low-grade chronic inflammation (INFLA) score.
Over a mean follow-up of 14.6 years, 2,382 participants developed AA. MetS was associated with a higher AA risk (HR: 1.27; 95% CI: 1.16-1.39) in fully adjusted models. Each additional MetS component increased AA risk by 16%. Inflammatory markers, including the INFLA score, significantly mediated this relationship. Joint analyses revealed a stronger association in MetS patients with high INFLA scores (HR: 1.68; 95% CI: 1.45-1.95).
MetS and its components notably elevate AA risk, with inflammation playing a key mediating role. These findings underscore the importance of targeted prevention strategies, particularly for MetS populations with high chronic inflammation.
背景/目的:代谢综合征(MetS)与多种疾病相关,但其与主动脉瘤(AA)的联系尚未完全明确。慢性炎症作为这种关系的介导因素,其作用也仍不清楚。本研究探讨了MetS和炎症对AA风险的联合影响。
分析了来自312,505名英国生物银行参与者的数据,以评估MetS与AA之间的关系。Cox比例风险回归模型评估了这种关联,而受限立方样条、中介分析、交互作用评估和联合分析则探讨了炎症指标的影响,包括低度慢性炎症(INFLA)评分。
在平均14.6年的随访中,2382名参与者发生了AA。在完全调整的模型中,MetS与较高的AA风险相关(HR:1.27;95%CI:1.16-1.39)。每增加一个MetS组分,AA风险增加16%。包括INFLA评分在内的炎症标志物显著介导了这种关系。联合分析显示,在INFLA评分高的MetS患者中关联更强(HR:1.68;95%CI:1.45-1.95)。
MetS及其组分显著提高AA风险,炎症起关键介导作用。这些发现强调了针对性预防策略的重要性,特别是对于慢性炎症程度高的MetS人群。