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白细胞介素-6信号通路下调对慢性疼痛治疗的潜在疗效:一项孟德尔随机化研究

Therapeutic Potential of Downregulated Interleukin-6 Signaling for the Treatment of Chronic Pain: A Mendelian Randomization Study.

作者信息

Bi Yaodan, Zhu Yingchao, Tang Shuai

机构信息

Department of Anesthesiology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, People's Republic of China.

Department of Anesthesiology, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.

出版信息

J Pain Res. 2023 Dec 18;16:4317-4328. doi: 10.2147/JPR.S424086. eCollection 2023.

Abstract

INTRODUCTION

While numerous studies have emphasized the pivotal involvement of the Interleukin 6 (IL-6) pathway in the development of chronic pain, the causal nature of this relationship remains uncertain.

METHODS

In this study, we opted to include genetic variants situated within the locus of the IL-6 receptor (IL-6R) that exhibited associations with C-reactive protein (CRP) levels. CRP serves as a downstream effector in the IL-6 pathway. Utilizing these variants as genetic proxies, we aimed to modulate IL-6 signaling. Employing a two-sample Mendelian randomization (MR) approach, we investigated the potential link between the genetic proxy and seven distinct subtypes of chronic pain, categorized based on their corresponding body locations. Moreover, we examined the relationship between chronic pain and an alternative instrument of IL-6 signaling that was weighted based on s-IL-6R levels. Furthermore, we conducted exploratory analyses to estimate the plausible causal association between CRP, gp130, and the subtypes of chronic pain.

RESULTS

Our analysis showed that genetic proxied downregulation of IL-6 signaling, weighted on CRP levels, was linked to a reduced risk of chronic back and knee pain. The sensitivity analyses across various MR methods confirmed the consistency of the findings and showed no evidence of horizontal pleiotropy or heterogeneity. Moreover, the results remained robust with different sets of instrument variables. A genetically increased level of s-IL-6R was also negatively associated with chronic back and knee pain. However, there was no causal relationship between CRP and gp130 with chronic pain.

CONCLUSION

Based on our findings, there is evidence to suggest a potential causal relationship between IL-6 signaling and chronic back and knee pain. Consequently, the downregulation of IL-6 signaling holds promise as a potential therapeutic target for addressing chronic back and knee pain.

摘要

引言

尽管众多研究强调白细胞介素6(IL-6)通路在慢性疼痛发展中起关键作用,但这种关系的因果性质仍不确定。

方法

在本研究中,我们选择纳入位于IL-6受体(IL-6R)基因座内且与C反应蛋白(CRP)水平相关的基因变异。CRP是IL-6通路中的下游效应物。利用这些变异作为基因替代指标,我们旨在调节IL-6信号传导。采用两样本孟德尔随机化(MR)方法,我们研究了基因替代指标与七种不同类型慢性疼痛之间的潜在联系,这些慢性疼痛根据其相应身体部位进行分类。此外,我们还研究了慢性疼痛与基于可溶性IL-6受体(s-IL-6R)水平加权的IL-6信号传导替代指标之间的关系。此外,我们进行了探索性分析,以估计CRP、gp130与慢性疼痛亚型之间可能的因果关联。

结果

我们的分析表明,基于CRP水平加权的IL-6信号传导基因替代下调与慢性背痛和膝痛风险降低有关。各种MR方法的敏感性分析证实了研究结果的一致性,且未发现水平多效性或异质性的证据。此外,使用不同的工具变量集时,结果仍然稳健。s-IL-6R基因水平升高也与慢性背痛和膝痛呈负相关。然而,CRP和gp130与慢性疼痛之间没有因果关系。

结论

基于我们的研究结果,有证据表明IL-6信号传导与慢性背痛和膝痛之间存在潜在因果关系。因此,下调IL-6信号传导有望成为治疗慢性背痛和膝痛的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee16/10743722/2fa4b9c2f081/JPR-16-4317-g0001.jpg

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