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川崎病患者循环炎症因子与双向孟德尔随机化分析

Circulating Inflammatory Factors and Bidirectional Mendelian Randomization Analysis in Patients with Kawasaki Disease.

作者信息

Niu Muqing, Pan Jinyong, Wang Kui, Zhang Li, Lin Zhaotang, Zhang Fengling

机构信息

The First Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, People's Republic of China.

Department of Pediatrics, The First Affiliated Hospital of Shihezi University, Shihezi, Xinjiang, People's Republic of China.

出版信息

Vasc Health Risk Manag. 2025 Mar 12;21:99-108. doi: 10.2147/VHRM.S509753. eCollection 2025.

Abstract

BACKGROUND

Kawasaki disease (KD), also known as mucocutaneous lymph node syndrome, is a systemic immune vasculitis with an unclear etiology. It is often complicated by coronary artery disease. This study uses bidirectional Mendelian randomization (MR) to investigate the interaction between KD and circulating inflammatory factors, providing insights into their causal relationships.

METHODS

We conducted a two-way pooled MR analysis to examine the causal links between 41 circulating inflammatory regulators and the risk of KD. Genetic data related to inflammation were sourced from three genome-wide association studies (GWASs) involving CRP, PCT, and cytokines, while KD data were derived from other studies. Inverse-variance weighting (IVW) was the primary MR method, with sensitivity analyses performed using MR‒Egger, weighted median, weighted mode, and MR-PRESSO to ensure robustness.

RESULTS

Forward MR analyses showed no significant relationship between inflammatory factors and KD outcomes. In contrast, reverse MR, with KD as the exposure factor, revealed that interleukin-2 (IL-2) and interleukin-8 (IL-8) were significantly associated with KD (IL-2: OR=1.0085, P=0.037; IL-8: OR=1.0099, P=0.014). Borderline significant associations were observed for factors such as B_NGF, EOTAXIN, HGF, and IL_12_P70 in MR‒Egger and weighted median analyses.

CONCLUSION

This bidirectional MR study highlights the role of circulating inflammatory modulators in KD risk, offering insights into KD pathogenesis and potential therapeutic targets.

摘要

背景

川崎病(KD),又称皮肤黏膜淋巴结综合征,是一种病因不明的全身性免疫性血管炎。它常并发冠状动脉疾病。本研究采用双向孟德尔随机化(MR)方法来研究KD与循环炎症因子之间的相互作用,以深入了解它们之间的因果关系。

方法

我们进行了一项双向汇总MR分析,以检验41种循环炎症调节因子与KD风险之间的因果联系。与炎症相关的基因数据来自三项全基因组关联研究(GWAS),涉及C反应蛋白(CRP)、降钙素原(PCT)和细胞因子,而KD数据则来自其他研究。逆方差加权(IVW)是主要的MR方法,并使用MR-Egger、加权中位数、加权模式和MR-PRESSO进行敏感性分析,以确保结果的稳健性。

结果

正向MR分析显示炎症因子与KD结局之间无显著关系。相比之下,以KD作为暴露因素的反向MR分析显示,白细胞介素-2(IL-2)和白细胞介素-8(IL-8)与KD显著相关(IL-2:比值比[OR]=1.0085,P=0.037;IL-8:OR=1.0099,P=0.014)。在MR-Egger和加权中位数分析中,观察到B_NGF、嗜酸性粒细胞趋化因子(EOTAXIN)、肝细胞生长因子(HGF)和IL_12_P70等因素存在边缘显著关联。

结论

这项双向MR研究突出了循环炎症调节因子在KD风险中的作用,为KD的发病机制和潜在治疗靶点提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f19/11910938/aca5eb816d3d/VHRM-21-99-g0001.jpg

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