Induced Sputum Transcriptomics Profile and Serum C3 are Associated with Asthma Severity.

IF 3.7 3区 医学 Q2 ALLERGY
Journal of Asthma and Allergy Pub Date : 2025-06-24 eCollection Date: 2025-01-01 DOI:10.2147/JAA.S517140
Fawang Du, Hanchao Wang, Zhihong Chen, Wei Xiong, Qin Wang, Bo Li, Rong Li, Li Li, Yongchun Shen, Tao Zhu
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引用次数: 0

Abstract

Rational: Asthma severity assessment is essential for asthma management. Transcriptomics contributes substantially to asthma pathogenesis. Then, this study aimed to explore asthma severity-associated transcriptomics profile and promising biomarkers for asthma severity prediction.

Methods: In discovery cohort, induced sputum cells from 3 non-severe and 3 severe asthma patients were collected and analyzed using RNA-seq. Multivariate analysis was performed to explore asthma severity-associated transcriptomics profile and differential expressed genes (DEGs). The Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) were used for pathway enrichment analysis. Subsequently, based on the previous study and clinical experience, the mRNA expressions of 6 overlapped asthma severity-associated DEGs and C3 in induced sputum cells and serum C3 were verified in validation cohort.

Results: Distinct asthma severity-associated transcriptomics profile was identified in induced sputum cells in discovery cohort. Then, 345 DEGs were found, of which 38 terms and 32 pathways were enriched using GO and KEGG, respectively. In validation cohort, the mRNA expressions of ZNF331, CD163, MACC1, ADAMTS2, and C3 were increased, and RYR1 and NRXN3 were decreased in induced sputum cells in severe asthma. Meanwhile, the AUC of ROC was 0.890 for serum C3 in asthma severity prediction, with the best cut-off of 1.272 g/L.

Conclusion: Collectively, this study provides the first identification of the association between induced sputum cells transcriptomics profile and asthma severity, indicating the potential value of transcriptomics for asthma management. The study also reveals the promising value of serum C3 for predicting asthma severity in clinical practice.

诱导痰转录组学特征和血清C3与哮喘严重程度相关。
理性:哮喘严重程度评估对哮喘管理至关重要。转录组学在哮喘发病机制中起重要作用。然后,本研究旨在探索哮喘严重程度相关的转录组学特征和有希望的哮喘严重程度预测生物标志物。方法:在发现队列中,分别收集3例非重度哮喘患者和3例重度哮喘患者的诱导痰细胞,采用RNA-seq方法进行分析。进行多变量分析以探索哮喘严重程度相关的转录组学特征和差异表达基因(DEGs)。利用京都基因与基因组百科全书(KEGG)和基因本体(GO)进行途径富集分析。随后,在既往研究和临床经验的基础上,在验证队列中验证了诱导痰细胞和血清C3中6个重叠的哮喘严重程度相关DEGs和C3的mRNA表达。结果:在发现队列中,在诱导痰细胞中发现了不同的哮喘严重程度相关的转录组学谱。共发现345个基因片段,其中GO富集38个,KEGG富集32个。在验证队列中,重度哮喘患者诱导痰细胞中ZNF331、CD163、MACC1、ADAMTS2和C3 mRNA表达升高,RYR1和NRXN3 mRNA表达降低。同时,血清C3预测哮喘严重程度的ROC AUC为0.890,最佳临界值为1.272 g/L。结论:总的来说,本研究首次确定了诱导痰细胞转录组学特征与哮喘严重程度之间的关联,表明转录组学在哮喘管理中的潜在价值。该研究还揭示了血清C3在预测哮喘严重程度方面的临床应用价值。
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来源期刊
Journal of Asthma and Allergy
Journal of Asthma and Allergy Medicine-Immunology and Allergy
CiteScore
5.30
自引率
6.20%
发文量
185
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal publishing original research, reports, editorials and commentaries on the following topics: Asthma; Pulmonary physiology; Asthma related clinical health; Clinical immunology and the immunological basis of disease; Pharmacological interventions and new therapies. Although the main focus of the journal will be to publish research and clinical results in humans, preclinical, animal and in vitro studies will be published where they shed light on disease processes and potential new therapies.
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