Zhong Cheng, Wang Li-Hua, Zhang Hao-Peng, Ji Lin, Guo Yu
Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Department of Otolaryngology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Indian J Otolaryngol Head Neck Surg. 2025 Apr;77(4):1823-1830. doi: 10.1007/s12070-025-05413-8. Epub 2025 Mar 17.
This study investigates the potential causal relationships among immune cells, plasma liposomes, and plasma metabolites in allergic rhinitis (AR) using a two-sample bidirectional multivariate and mediated Mendelian Randomization (MR) approach. Genetic data from five GWAS datasets covering traits linked to immune cells, plasma liposomes, plasma metabolites, and AR were used. Instrumental variables were selected based on strict criteria to ensure independence and exclude confounders. The primary MR analysis employed the Inverse Variance Weighted method, supplemented by sensitivity analyses using the Weighted Median and MR-Egger methods. The MR analyses suggest a genetic correlation among immune cells, plasma liposomes, and plasma metabolites, influencing the risk of AR. Findings were robust across various sensitivity analyses, supporting the absence of pleiotropy and outliers. No reverse causality was found, indicating a unidirectional influence. Genetic predispositions to immune cells, plasma liposomes, and plasma metabolites significantly change the risk of developing AR. Further studies are needed to explore these associations in diverse populations and refine the underlying mechanisms.
The online version contains supplementary material available at 10.1007/s12070-025-05413-8.
本研究采用两样本双向多变量中介孟德尔随机化(MR)方法,研究变应性鼻炎(AR)中免疫细胞、血浆脂质体和血浆代谢物之间的潜在因果关系。使用了来自五个全基因组关联研究(GWAS)数据集的遗传数据,这些数据集涵盖了与免疫细胞、血浆脂质体、血浆代谢物和AR相关的性状。基于严格标准选择工具变量,以确保独立性并排除混杂因素。主要的MR分析采用逆方差加权法,并辅以使用加权中位数和MR-Egger方法的敏感性分析。MR分析表明免疫细胞、血浆脂质体和血浆代谢物之间存在遗传相关性,影响AR的风险。在各种敏感性分析中结果都很稳健,支持不存在多效性和异常值。未发现反向因果关系,表明存在单向影响。免疫细胞、血浆脂质体和血浆代谢物的遗传易感性显著改变患AR的风险。需要进一步研究以在不同人群中探索这些关联并完善潜在机制。
在线版本包含可在10.1007/s12070-025-05413-8获取的补充材料。