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脐带血中与过敏性鼻炎和哮喘发展相关的早期生命期微小RNA特征。

Early-life microRNA signatures in cord blood associated with allergic rhinitis and asthma development.

作者信息

Mirzakhani Hooman, Wang Alberta L, Sharma Rinku, Sun Maoyun, Panganiban Ronald, Lu Quan, McGeachie Michael, Lu Zheng, Litonjua Augusto A, Tantisira Kelan G, Weiss Scott T

机构信息

Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Mass.

Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Mass; Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Mass.

出版信息

J Allergy Clin Immunol. 2024 Dec 25. doi: 10.1016/j.jaci.2024.12.1077.

Abstract

BACKGROUND

MicroRNAs (miRNAs) are involved in the biological regulation of asthma and allergies.

OBJECTIVE

We sought to investigate the association between cord blood miRNAs and the development of allergic rhinitis and early childhood asthma.

METHODS

miRNAs were sequenced from cord blood of subjects participating in the Vitamin D Antenatal Asthma Reduction Trial. Multivariable miRNA differential expression analyses were performed to examine their association with physician-diagnosed asthma and allergic rhinitis by age 3 years as well as active asthma status at age 6 years. miRNA signatures were further investigated for their ability to induce human airway smooth muscle cell proliferation in vitro.

RESULTS

In a cohort of 389 subjects, elevated cord blood expression of miR-149-5p was associated with both allergic rhinitis and asthma at age 3 years (log fold change [logFC], 1.87 and 1.42, respectively; false-discovery rate [FDR] < 0.001) as well as active asthma status at age 6 years (logFC, 2.26; FDR < 0.001). Higher expressions of miR-99b-5p, miR-125a-5p, and miR-200c-3p were also associated with both diagnosis of allergic rhinitis at age 3 years and active asthma status at age 6 years (allergic rhinitis: logFC, 0.6, 0.62, and 1.06, respectively; FDR < 0.001; active asthma: logFC, 0.55, 0.60, and 1.10, respectively; FDR < 0.001). Higher expression of miR-145-5p was associated with both new-onset asthma after age 3 years and active asthma status at age 6 years (logFC, 0.73 and 0.40, respectively; FDR < 0.001). These 5 miRNA signatures target key hubs in the interactome module of 71 genes associated with allergic rhinitis and asthma. Transfection of miR-125a-5p and miR-145-5p into human airway smooth muscle cells induced cell proliferation.

CONCLUSIONS

The dysregulation of cord blood miRNAs at birth is associated with allergic rhinitis and early childhood asthma. The miRNAs that regulate postembryonic development and immune response may serve as potential biomarkers and preventive targets for asthma.

摘要

背景

微小RNA(miRNA)参与哮喘和过敏的生物学调节。

目的

我们试图研究脐血miRNA与变应性鼻炎及儿童早期哮喘发生之间的关联。

方法

对参与维生素D产前哮喘减少试验的受试者的脐血进行miRNA测序。进行多变量miRNA差异表达分析,以检查其与3岁时医生诊断的哮喘和变应性鼻炎以及6岁时的活动性哮喘状态之间的关联。进一步研究miRNA特征在体外诱导人气道平滑肌细胞增殖的能力。

结果

在389名受试者的队列中,脐血中miR-149-5p表达升高与3岁时的变应性鼻炎和哮喘均相关(对数倍变化[logFC]分别为1.87和1.42;错误发现率[FDR]<0.001)以及6岁时的活动性哮喘状态(logFC,2.26;FDR<0.001)。miR-99b-5p、miR-125a-5p和miR-200c-3p的较高表达也与3岁时变应性鼻炎的诊断和6岁时的活动性哮喘状态相关(变应性鼻炎:logFC分别为0.6、0.62和1.06;FDR<0.001;活动性哮喘:logFC分别为0.55、0.60和1.10;FDR<0.001)。miR-145-5p的较高表达与3岁后新发哮喘和6岁时的活动性哮喘状态均相关(logFC分别为0.73和0.40;FDR<\u00a00.001)。这5种miRNA特征靶向与变应性鼻炎和哮喘相关的71个基因的相互作用组模块中的关键节点。将miR-125a-5p和miR-145-5p转染到人气道平滑肌细胞中可诱导细胞增殖。

结论

出生时脐血miRNA失调与变应性鼻炎和儿童早期哮喘相关。调节胚胎后发育和免疫反应的miRNA可能作为哮喘的潜在生物标志物和预防靶点。

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