Causal Effects of Inflammatory Cytokines on Urethral Stricture Disease: A Bidirectional Mendelian Randomization Study.

IF 1 4区 生物学 Q4 GENETICS & HEREDITY
Yue Chong, Li Xue, Zihe Peng, Zhenlong Wang, Delai Fu, Zhixin Huang, Tie Chong
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引用次数: 0

Abstract

Background: Inflammation has been reported to be associated with urethral stricture, whereas rarely any studies have reported the causal relationship between inflammatory cytokines and urethral stricture. We investigated the causal effects between inflammatory cytokines and urethral stricture with Mendelian randomization (MR).

Methods: Genome-wide association study (GWAS) summary statistics on 41 inflammatory cytokines from 8293 Finns and 787 patients with urethral stricture were included for bidirectional MR analysis. The causality between inflammatory cytokines and urethral stricture was estimated using inverse variance weighting (IVW), weighted median, and model selection. Multiple sensitivity analyses (including pleiotropy, heterogeneity, and leave-one-out tests) were performed to evaluate the robustness and dependability of the MR results, followed by Bayesian colocalization, phenotype scanning, and protein-protein interaction (PPI) analysis.

Results: We identified a significant causal relationship between three inflammatory cytokines (granulocyte colony-stimulating factor [GCSF], stem cell growth factor beta [SCGFb], and interleukin-5 [IL5]) and urethral stricture. GCSF (odds ratio [OR] = 4.722, 95% confidence interval [CI] = 1.367-16.303, p = 0.014) and SCGFb (OR = 1.209, 95% CI = 1.06-1.379, p = 0.004) increased the risk of urethral stricture, whereas IL5 decreased the risk of urethral stricture (OR = 0.782, 95% CI = 0.626-0.976, p = 0.029). Reverse MR showed no reverse causality between inflammatory cytokines, with significant causality and urethral stricture. PPI analysis showed that the three inflammatory cytokines interacted with multiple fibrosis-related genes: transforming growth factor beta 1, nitric oxide synthase 2, and C-X-C motif chemokine receptor 3.

Conclusion: Our study demonstrated that the inflammatory cytokines GCSF, SCGFb, and IL5 are significantly associated with urethral stricture, providing valuable insights for the prevention and diagnosis of urethral stricture.

炎症细胞因子对尿道狭窄疾病的因果影响:一项双向孟德尔随机研究。
背景:炎症已被报道与尿道狭窄相关,但很少有研究报道炎症细胞因子与尿道狭窄之间的因果关系。我们用孟德尔随机化(MR)研究了炎症细胞因子与尿道狭窄之间的因果关系。方法:采用全基因组关联研究(GWAS)对8293名芬兰人和787例尿道狭窄患者41种炎症因子进行双向MR分析。使用逆方差加权(IVW)、加权中位数和模型选择来估计炎症细胞因子与尿道狭窄之间的因果关系。进行多重敏感性分析(包括多效性、异质性和留一检验)来评估MR结果的稳健性和可靠性,随后进行贝叶斯共定位、表型扫描和蛋白质-蛋白质相互作用(PPI)分析。结果:我们发现三种炎症细胞因子(粒细胞集落刺激因子[GCSF]、干细胞生长因子β [SCGFb]和白细胞介素-5 [IL5])与尿道狭窄之间存在显著的因果关系。GCSF(比值比[OR] = 4.722, 95%可信区间[CI] = 1.367 ~ 16.303, p = 0.014)和SCGFb (OR = 1.209, 95% CI = 1.06 ~ 1.379, p = 0.004)增加尿道狭窄的风险,而IL5降低尿道狭窄的风险(OR = 0.782, 95% CI = 0.626 ~ 0.976, p = 0.029)。反向MR显示炎症因子与尿道狭窄无反向因果关系,与尿道狭窄有显著的因果关系。PPI分析显示,这三种炎症因子与多种纤维化相关基因相互作用:转化生长因子β 1、一氧化氮合酶2和C-X-C基序趋化因子受体3。结论:我们的研究表明炎性细胞因子GCSF、SCGFb和IL5与尿道狭窄有显著相关性,为尿道狭窄的预防和诊断提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Human Genetics
Annals of Human Genetics 生物-遗传学
CiteScore
4.20
自引率
0.00%
发文量
34
审稿时长
3 months
期刊介绍: Annals of Human Genetics publishes material directly concerned with human genetics or the application of scientific principles and techniques to any aspect of human inheritance. Papers that describe work on other species that may be relevant to human genetics will also be considered. Mathematical models should include examples of application to data where possible. Authors are welcome to submit Supporting Information, such as data sets or additional figures or tables, that will not be published in the print edition of the journal, but which will be viewable via the online edition and stored on the website.
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