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循环细胞因子与脓毒症的因果关系:一项孟德尔随机化研究。

Causal association of circulating cytokines with sepsis: a Mendelian randomization study.

机构信息

Department of Respiratory and Critical Care Medicine, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.

Department of Medical Intensive Care Unit, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.

出版信息

Front Immunol. 2023 Oct 17;14:1281845. doi: 10.3389/fimmu.2023.1281845. eCollection 2023.

Abstract

BACKGROUND

Observational studies have reported an association between circulating cytokines and sepsis. However, the precise causal relationship between these factors remains unclear. The objective of this study was to explore the causal link between circulating cytokines and sepsis using genetic data within the framework of Mendelian Randomization (MR).

METHODS

We performed a two-sample MR analysis to investigate this causality relationship in individuals of European ancestry. The publicly available genome-wide association studies (GWAS) statistics were used. We selected eligible instrumental single nucleotide polymorphisms (SNPs) that were significantly related to the circulating cytokines. Multiple MR analysis approaches were carried out, which included inverse variance weighted (IVW), Weighted Median, MR-Egger, Weighted Mode, Simple Mode, and MR pleiotropy residual sum and outlier (MR-PRESSO) methods.

RESULTS

We found evidence to support the causal role of genetically predicted circulating levels on decreased risk of sepsis, including RANTES (OR = 0.920, 95% CI: 0.849-0.997, = 0.041) and basic fibroblast growth factor (basic-FGF) (OR = 0.869, 95% CI: 0.766-0.986, = 0.029). Additionally, MR analysis positive causal association of between beta-nerve growth factor (β-NGF) and sepsis (OR = 1.120, 95% CI: 1.037-1.211, = 0.004). The results of MR-Egger, Weighted Median, Weighted Mode, and Simple Mode methods were consistent with the IVW estimates. Sensitivity analysis showed no horizontal pleiotropy to bias the causal estimates.

CONCLUSION

This MR study provides first novel evidence that genetically predicted causal association of circulating levels of RANTES, basic-FGF, and β-NGF with altered sepsis risk. The findings shed light on the potential involvement of these cytokines in sepsis pathogenesis. Although requiring additional confirmation, the results contribute new insights into cytokine mediators in sepsis and suggest promising future research directions.

摘要

背景

观察性研究报告称,循环细胞因子与败血症之间存在关联。然而,这些因素之间的确切因果关系尚不清楚。本研究旨在使用孟德尔随机化(MR)框架内的遗传数据探讨循环细胞因子与败血症之间的因果关系。

方法

我们进行了两样本 MR 分析,以在欧洲血统个体中研究这种因果关系。使用了公开的全基因组关联研究(GWAS)统计数据。我们选择了与循环细胞因子显著相关的合格工具单核苷酸多态性(SNP)。进行了多种 MR 分析方法,包括逆方差加权(IVW)、加权中位数、MR-Egger、加权模式、简单模式和 MR 多效性残差和异常值(MR-PRESSO)方法。

结果

我们有证据支持遗传预测的循环水平与败血症风险降低之间存在因果关系,包括 RANTES(OR=0.920,95%CI:0.849-0.997, = 0.041)和碱性成纤维细胞生长因子(碱性-FGF)(OR=0.869,95%CI:0.766-0.986, = 0.029)。此外,MR 分析还显示β-神经生长因子(β-NGF)与败血症之间存在正因果关联(OR=1.120,95%CI:1.037-1.211, = 0.004)。MR-Egger、加权中位数、加权模式和简单模式的结果与 IVW 估计一致。敏感性分析表明没有水平异质性偏倚因果估计。

结论

本 MR 研究首次提供了新的证据,证明 RANTES、碱性-FGF 和 β-NGF 的循环水平与败血症风险改变之间存在遗传预测的因果关系。这些发现揭示了这些细胞因子在败血症发病机制中的潜在作用。尽管需要进一步证实,但结果为败血症中的细胞因子介质提供了新的见解,并为未来的研究方向提供了有希望的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f67d/10616607/d8389ba393b3/fimmu-14-1281845-g001.jpg

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