Zheng Yihan, Wang Hongmei, Zhang Huale, Wu Xizhu, Zhou Min, Denggui Wang
Department of Anesthesiology, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, Fujian, 350001, People's Republic of China.
Department of Breast Surgery, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, Fujian, 350001, People's Republic of China.
J Pain Res. 2025 Mar 24;18:1525-1544. doi: 10.2147/JPR.S495896. eCollection 2025.
Several recent observational studies have reported that the circulating inflammatory cytokine composition is associated with neuropathic pain. However, the causal effect of 41 circulating inflammatory cytokines on neuropathic pain is unknown.
A two-sample Mendelian randomization study was performed using summary statistics for a genome-wide association study (GWAS) of circulating inflammatory cytokines conducted within three Finnish cohorts (YFS and FINRISK 1997 and 2002, n=8,293). The summary statistics of neuropathic pain were obtained from the GWAS dataset (800 patients and 195,047 controls). Inverse variance weighting, weighted median weighting, MR‒Egger regression, simple weighting, and weighted weighting were used to examine the causal associations between inflammatory cytokines and neuropathic pain. Sensitivity analyses, including the Cochran Q test, Egger intercept test, and leave-one-out analysis, were performed to verify the robustness of the MR results.
Inverse variance weighted estimates suggested that (OR=0.57, 95% CI=0.39-0.83, =3.4e-03), (OR=0.73, 95% CI=0.55-0.96, =2.7e-02), and (OR=0.57, 95% CI=0.33-0.99, =4.4e-02) had protective effects on neuropathic pain. In addition, (OR=1.36, 95% CI=1.06-1.74, =1.5e-02) was suggested to be associated with neuropathic pain. No significant heterogeneity of instrumental variables or horizontal pleiotropy was found.
This two-sample Mendelian randomization study revealed that were causally associated with neuropathic pain. This knowledge could guide future research in developing more effective treatments for neuropathic pain, potentially leading to better pain management options for patients.
近期多项观察性研究报告称,循环炎症细胞因子组成与神经性疼痛有关。然而,41种循环炎症细胞因子对神经性疼痛的因果效应尚不清楚。
利用芬兰三个队列(YFS以及1997年和2002年的FINRISK,n = 8293)中进行的循环炎症细胞因子全基因组关联研究(GWAS)的汇总统计数据,开展了一项两样本孟德尔随机化研究。神经性疼痛的汇总统计数据来自GWAS数据集(800例患者和195,047例对照)。采用逆方差加权、加权中位数加权、MR-Egger回归、简单加权和加权加权法来检验炎症细胞因子与神经性疼痛之间的因果关联。进行了敏感性分析,包括 Cochr an Q检验、Egger截距检验和留一法分析,以验证孟德尔随机化结果的稳健性。
逆方差加权估计表明,[具体因子1](比值比=0.57,95%置信区间=0.39 - 0.83,P = 3.4×10⁻³)、[具体因子2](比值比=0.73,95%置信区间=0.55 - 0.96,P = 2.7×10⁻²)和[具体因子3](比值比=0.57,95%置信区间=0.33 - 0.99,P = 4.4×10⁻²)对神经性疼痛具有保护作用。此外,[具体因子4](比值比=1.36,95%置信区间=1.06 - 1.74,P = 1.5×10⁻²)被认为与神经性疼痛有关。未发现工具变量存在显著异质性或水平多效性。
这项两样本孟德尔随机化研究表明,[具体因子1、2、3、4]与神经性疼痛存在因果关联。这一认识可为未来开发更有效的神经性疼痛治疗方法的研究提供指导,有望为患者带来更好的疼痛管理选择。