全身炎症调节因子与慢加急性肝衰竭风险:一项双向孟德尔随机化研究。

Systemic inflammatory regulators and risk of acute-on-chronic liver failure: A bidirectional mendelian-randomization study.

作者信息

Wang Shengnan, Zhu Hao, Pan Lin, Zhang Mengyuan, Wan Xiaoqiang, Xu Hongqin, Hua Rui, Zhu Mingqin, Gao Pujun

机构信息

Department of Neurology, The First Hospital of Jilin University, Changchun, China.

Department of Hepatology, The First Hospital of Jilin University, Changchun, China.

出版信息

Front Cell Dev Biol. 2023 Jan 19;11:1125233. doi: 10.3389/fcell.2023.1125233. eCollection 2023.

Abstract

Inflammation plays a role in the pathogenesis of acute-on-chronic liver failure (ACLF), however, whether there is a causal relationship between inflammation and ACLF remains unclear. A two-sample Mendelian randomization (MR) approach was used to investigate the causal relationship between systemic inflammatory regulators and ACLF. The study analyzed 41 cytokines and growth factors from 8,293 individuals extracted from a genome-wide association study (GWAS) meta-analysis database involving 253 ACLF cases and 456,095 controls. Our results showed that lower stem cell factor (SCF) levels, lower basic fibroblast growth factor (bFGF) levels and higher Interleukin-13 (IL-13) levels were associated with an increased risk of ACLF (OR = 0.486, 95% CI = 0.264-0.892, = 0.020; OR = 0.323, 95% CI = 0.107-0.972, = 0.044; OR = 1.492, 95% CI = 1.111-2.004, = 0.008, respectively). In addition, genetically predicted ACLF did not affect the expression of systemic inflammatory regulators. Our results indicate that cytokines play a crucial role in the pathogenesis of ACLF. Further studies are needed to determine whether these biomarkers can be used to prevent and treat ACLF.

摘要

炎症在慢加急性肝衰竭(ACLF)的发病机制中起作用,然而,炎症与ACLF之间是否存在因果关系仍不清楚。采用两样本孟德尔随机化(MR)方法研究全身炎症调节因子与ACLF之间的因果关系。该研究分析了从一项全基因组关联研究(GWAS)荟萃分析数据库中提取的8293名个体的41种细胞因子和生长因子,该数据库涉及253例ACLF病例和456,095名对照。我们的结果表明,较低的干细胞因子(SCF)水平、较低的碱性成纤维细胞生长因子(bFGF)水平和较高的白细胞介素-13(IL-13)水平与ACLF风险增加相关(OR = 0.486,95%CI = 0.264 - 0.892,P = 0.020;OR = 0.323,95%CI = 0.107 - 0.972,P = 0.044;OR = 1.492,95%CI = 1.111 - 2.004,P = 0.008,分别)。此外,基因预测ACLF不影响全身炎症调节因子的表达。我们的结果表明细胞因子在ACLF的发病机制中起关键作用。需要进一步研究以确定这些生物标志物是否可用于预防和治疗ACLF。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cd4/9892464/b20c9db6107a/fcell-11-1125233-g001.jpg

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