Shang Hui, Liu Xianqiang, Bai Mengying, Li Xiao, Lan Yuhang, Bai Bingbing, Yang Shuyun, Wu Xianlin, Li Guocai
Department of Anesthesiology, Shenzhen Hospital (Fu Tian) of Guangzhou University of Chinese Medicine, Shenzhen, People's Republic of China.
Graduate School, Medical School of Chinese PLA, Beijing, People's Republic of China.
Brain Behav. 2025 Apr;15(4):e70463. doi: 10.1002/brb3.70463.
Inflammatory regulators play a fundamental role in the development of trigeminal neuralgia (TN). However, the precise mechanisms and causal relationship with the risk of TN remain poorly understood.
This study aimed to assess the causal relationship between 41 inflammatory cytokines and TN using Mendelian randomization (MR) analysis. A two-sample MR approach was utilized, employing genetic variation data on TN from a large publicly available genome-wide association study (GWAS) comprising 1777 cases of European ancestry and 360,538 controls. Additionally, summary data from a GWAS on inflammatory cytokines, comprising 8293 healthy participants, were utilized. The causal relationship between exposure and outcome was primarily assessed using the inverse variance weighted (IVW) method, accompanied by sensitivity analyses.
The study revealed an association between increased risk of TN and cutaneous T cell-attracting chemokine(CTACK) (odds ratio [OR] = 1.187; 95% confidence interval [CI], 1.041-1.35; p = 0.01) and interferon (IFN)-gamma(MIG) (OR = 1.232; 95% CI, 1.080-1.449; p = 0.01), while interleukin (IL)-16 (OR = 0.823; 95% CI, 0.685-0.989; p = 0.03) and interferon (IFN)-G (OR = 0.779; 95% CI, 0.612-0.992; p = 0.04) were associated with decreased risk of TN. Notably, no potential effect of TN on inflammatory factors was observed.
This study provides novel insights into the pathogenesis of TN, highlighting the crucial role of inflammatory cytokines in TN risk.
This study advances our understanding of TN by using MR to identify the causal roles of specific inflammatory cytokines. These results underscore the importance of inflammation in TN development and suggest potential targets for new treatments.
炎症调节因子在三叉神经痛(TN)的发生发展中起重要作用。然而,其确切机制以及与TN风险的因果关系仍知之甚少。
本研究旨在采用孟德尔随机化(MR)分析评估41种炎症细胞因子与TN之间的因果关系。采用两样本MR方法,利用来自一项大型公开全基因组关联研究(GWAS)的TN遗传变异数据,该研究包括1777例欧洲血统病例和360538例对照。此外,还利用了一项关于炎症细胞因子的GWAS的汇总数据,该数据包括8293名健康参与者。主要采用逆方差加权(IVW)方法评估暴露与结局之间的因果关系,并进行敏感性分析。
研究发现TN风险增加与皮肤T细胞趋化因子(CTACK)(优势比[OR]=1.187;95%置信区间[CI],1.041 - 1.35;p = 0.01)和干扰素(IFN)-γ(MIG)(OR = 1.232;95%CI,1.080 - 1.449;p = 0.01)有关,而白细胞介素(IL)-16(OR = 0.823;95%CI,0.685 - 0.989;p = 0.03)和干扰素(IFN)-G(OR = 0.779;95%CI,0.612 - 0.992;p = 0.04)与TN风险降低有关。值得注意的是,未观察到TN对炎症因子的潜在影响。
本研究为TN的发病机制提供了新的见解,突出了炎症细胞因子在TN风险中的关键作用。
本研究通过使用MR来确定特定炎症细胞因子的因果作用,推进了我们对TN的理解。这些结果强调了炎症在TN发展中的重要性,并为新的治疗方法提出了潜在靶点。