心房颤动
高尿酸血症
蛋白质组学
内科学
医学
心脏病学
生物信息学
尿酸
生物
遗传学
基因
作者
Meiwei Zhang,Lei Shi,Cong Qin,Mengling Peng,Zhiguo Zhang
标识
DOI:10.3389/fendo.2025.1429465
摘要
Background Atrial fibrillation (AF), the most common cardiac arrhythmia, is associated with high incidence and mortality rates. Recent studies have confirmed a close correlation between hyperuricemia and the onset of AF, though the mechanisms remain unclear. Consequently, this study employs Mendelian randomization based on proteomics and mediation analysis to investigate the potential mechanisms by which hyperuricemia induces AF. Methods A two-step mediation MR analysis was conducted to determine whether plasma proteins mediate atrial fibrillation induced by serum urate. The Reactome database was subsequently utilized to analyze the list of significant mediating plasma proteins to identify enriched pathways. Results Mediation Mendelian randomization analysis suggested that hyperuricemia may promote the development of atrial fibrillation (AF) through 17 plasma proteins, includeing hepatocyte nuclear factor 4-alpha (HNF4α), identified as key mediators. Subsequent enrichment analysis of these proteins revealed 9 metabolic or signaling pathways potentially involved in this pathological process. Central mediator proteins such as HNF4α appear to drive AF through metabolic and inflammatory pathways. Conclusion There is a close correlation between hyperuricemia and the onset of atrial fibrillation.
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