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免疫细胞与哮喘之间的因果联系:孟德尔随机化分析的见解

Causal links between immune cells and asthma: Insights from a Mendelian Randomization analysis.

作者信息

Xu Shengshan, Liang Jiahua, Shen Tao, Zhang Dongxi, Lu Zhuming

机构信息

Department of Thoracic Surgery, Jiangmen Central Hospital, Jiangmen, Guangdong, China.

Department of Pancreato-Biliary Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

J Asthma. 2025 Feb;62(2):346-353. doi: 10.1080/02770903.2024.2403740. Epub 2024 Sep 17.

Abstract

OBJECTIVES

Recent studies suggest immunophenotypes may play a role in asthma, but their causal relationship has not been thoroughly examined.

METHODS

We used single nucleotide polymorphism (SNP)-derived instrumental variables. Summary data from 731 immune cell profiles and asthma cases were analyzed from genome-wide association studies (GWAS) of European populations. Mendelian Randomization (MR) analyses included inverse variance weighted (IVW), weighted median, and MR-Egger methods. Pleiotropy was assessed using the MR-Egger intercept and MR pleiotropy residual sum and outlier (MR-PRESSO) tests. Reverse MR analysis explored bidirectional causation between asthma and immunophenotypes. All statistical analyses were conducted using R software.

RESULTS

MR analysis identified 108 immune signatures potentially contributing to asthma. Two immunophenotypes were significantly associated with asthma risk: CD4+ secreting Treg cells in allergic asthma (OR = 1.078; 95% CI: 1.036-1.122; P = 0.0002) and IgD + CD38- %lymphocyte cells in non-allergic asthma (OR = 1.123; 95% CI: 1.057-1.194; P = 0.0002).

CONCLUSIONS

This study highlights the causal associations between specific immunophenotypes and asthma risk, providing new insights into asthma pathogenesis.

摘要

目的

近期研究表明免疫表型可能在哮喘中发挥作用,但其因果关系尚未得到充分研究。

方法

我们使用单核苷酸多态性(SNP)衍生的工具变量。从欧洲人群的全基因组关联研究(GWAS)中分析了731个免疫细胞谱和哮喘病例的汇总数据。孟德尔随机化(MR)分析包括逆方差加权(IVW)、加权中位数和MR-Egger方法。使用MR-Egger截距和MR多效性残差和离群值(MR-PRESSO)检验评估多效性。反向MR分析探讨了哮喘与免疫表型之间的双向因果关系。所有统计分析均使用R软件进行。

结果

MR分析确定了108个可能导致哮喘的免疫特征。两种免疫表型与哮喘风险显著相关:过敏性哮喘中分泌CD4+的调节性T细胞(OR = 1.078;95%CI:1.036-1.122;P = 0.0002)和非过敏性哮喘中IgD+CD38-%淋巴细胞(OR = 1.123;95%CI:1.057-1.194;P = 0.0002)。

结论

本研究突出了特定免疫表型与哮喘风险之间的因果关联,为哮喘发病机制提供了新的见解。

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