Causal Effects of Asthma on Upper Airway Diseases and Allergic Diseases: A Two-Sample Mendelian Randomization.

IF 2.5 4区 医学 Q3 ALLERGY
International Archives of Allergy and Immunology Pub Date : 2025-01-01 Epub Date: 2024-08-06 DOI:10.1159/000540358
Zengxiao Zhang, Gongfei Li, Shizhe Zhou, Minghui Wang, Longgang Yu, Yan Jiang
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引用次数: 0

Abstract

Introduction: Asthma is associated with upper airway diseases and allergic diseases; however, the causal effects need to be investigated further. Thus, we performed this two-sample Mendelian randomization (MR) analysis to explore and measure the causal effects of asthma on allergic rhinitis (AR), vasomotor rhinitis (VMR), allergic conjunctivitis (AC), atopic dermatitis (AD), and allergic urticaria (AU).

Methods: The data for asthma, AR, VMR, AC, AD, and AU were obtained from large-scale genome-wide association studies summarized recently. We defined single-nucleotide polymorphisms satisfying the MR assumptions as instrumental variables. Inverse-variance weighted (IVW) approach under random-effects was applied as the dominant method for causal estimation. The weighted median approach, MR-Egger regression analysis, MR pleiotropy residual sum and outlier test, and leave-one-out sensitivity analysis were performed as sensitivity analysis. Horizontal pleiotropy was measured using MR-Egger regression analysis. Significant causal effects were attempted for replication and meta-analysis.

Results: We revealed that asthma had causal effects on AR (IVW, odds ratio [OR] = 1.93; 95% confidence interval [CI], 1.74-2.14; p < 0.001), VMR (IVW, OR = 1.40; 95% CI, 1.15-1.71; p < 0.001), AC (IVW, OR = 1.65; 95% CI, 1.49-1.82; p < 0.001), and AD (IVW, OR = 2.13; 95% CI, 1.82-2.49; p < 0.001). No causal effect of asthma on AU was observed. Sensitivity analysis further assured the robustness of these results. The evaluation of the replication stage and meta-analysis further confirmed the causal effect of asthma on AR (IVW OR = 1.81, 95% CI 1.62-2.02, p < 0.001), AC (IVW OR = 1.44, 95% CI 1.11-1.87, p < 0.001), and AD (IVW OR = 1.85, 95% CI 1.42-2.41, p < 0.001).

Conclusions: We revealed and quantified the causal effects of asthma on AR, VMR, AC, and AD. These findings can provide powerful causal evidence of asthma on upper airway diseases and allergic diseases, suggesting that the treatment of asthma should be a preventive and therapeutic strategy for AR, VMR, AC, and AD.

哮喘对上呼吸道疾病和过敏性疾病的因果效应:双样本孟德尔随机试验
导言:哮喘与上呼吸道疾病和过敏性疾病有关,但其因果效应还需要进一步研究。因此,我们进行了这项双样本孟德尔随机化(MR)分析,以探讨和测量哮喘对过敏性鼻炎(AR)、血管运动性鼻炎(VMR)、过敏性结膜炎(AC)、特应性皮炎(AD)和过敏性荨麻疹(AU)的因果效应:哮喘、AR、VMR、AC、AD 和 AU 的数据来自最近总结的大规模全基因组关联研究。我们将符合 MR 假设的单核苷酸多态性定义为工具变量。随机效应下的逆方差加权(IVW)法被用作因果关系估计的主要方法。加权中值法、MR-Egger 回归分析、MR 多向性残差总和和离群检验以及撇一敏感性分析作为敏感性分析方法进行。使用 MR-Egger 回归分析测量了水平多向性。结果显示,哮喘具有因果效应:我们发现哮喘对 AR(IVW,几率比 [OR] = 1.93;95% 置信区间 [CI],1.74-2.14;p <;0.001)、VMR(IVW,OR = 1.40;95% CI,1.15-1.71;p <;0.001)、AC(IVW,OR = 1.65;95% CI,1.49-1.82;p <;0.001)和 AD(IVW,OR = 2.13;95% CI,1.82-2.49;p <;0.001)。没有观察到哮喘对AU的因果效应。敏感性分析进一步确保了这些结果的稳健性。对复制阶段和荟萃分析的评估进一步证实了哮喘对AR(IVW OR = 1.81,95% CI 1.62-2.02,p <0.001)、AC(IVW OR = 1.44,95% CI 1.11-1.87,p <0.001)和AD(IVW OR = 1.85,95% CI 1.42-2.41,p <0.001)的因果效应:我们揭示并量化了哮喘对AR、VMR、AC和AD的因果效应。这些发现为哮喘对上呼吸道疾病和过敏性疾病的影响提供了有力的因果证据,表明哮喘的治疗应成为AR、VMR、AC和AD的预防和治疗策略。
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来源期刊
CiteScore
5.60
自引率
3.60%
发文量
105
审稿时长
2 months
期刊介绍: ''International Archives of Allergy and Immunology'' provides a forum for basic and clinical research in modern molecular and cellular allergology and immunology. Appearing monthly, the journal publishes original work in the fields of allergy, immunopathology, immunogenetics, immunopharmacology, immunoendocrinology, tumor immunology, mucosal immunity, transplantation and immunology of infectious and connective tissue diseases.
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