Unraveling heterogeneity and treatment of asthma through integrating multi-omics data.

IF 3.3 Q2 ALLERGY Frontiers in allergy Pub Date : 2024-11-05 eCollection Date: 2024-01-01 DOI:10.3389/falgy.2024.1496392
Wei Zhang, Yu Zhang, Lifei Li, Rongchang Chen, Fei Shi
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Abstract

Asthma has become one of the most serious chronic respiratory diseases threatening people's lives worldwide. The pathogenesis of asthma is complex and driven by numerous cells and their interactions, which contribute to its genetic and phenotypic heterogeneity. The clinical characteristic is insufficient for the precision of patient classification and therapies; thus, a combination of the functional or pathophysiological mechanism and clinical phenotype proposes a new concept called "asthma endophenotype" representing various patient subtypes defined by distinct pathophysiological mechanisms. High-throughput omics approaches including genomics, epigenomics, transcriptomics, proteomics, metabolomics and microbiome enable us to investigate the pathogenetic heterogeneity of diverse endophenotypes and the underlying mechanisms from different angles. In this review, we provide a comprehensive overview of the roles of diverse cell types in the pathophysiology and heterogeneity of asthma and present a current perspective on their contribution into the bidirectional interaction between airway inflammation and airway remodeling. We next discussed how integrated analysis of multi-omics data via machine learning can systematically characterize the molecular and biological profiles of genetic heterogeneity of asthma phenotype. The current application of multi-omics approaches on patient stratification and therapies will be described. Integrating multi-omics and clinical data will provide more insights into the key pathogenic mechanism in asthma heterogeneity and reshape the strategies for asthma management and treatment.

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通过整合多组学数据揭示哮喘的异质性和治疗方法。
哮喘已成为威胁全世界人民生命的最严重慢性呼吸道疾病之一。哮喘的发病机制十分复杂,由众多细胞及其相互作用驱动,这导致了其遗传和表型的异质性。临床特征不足以对患者进行精确分类和治疗;因此,将功能或病理生理学机制与临床表型相结合,提出了 "哮喘内表型 "这一新概念,代表了由不同病理生理学机制定义的各种患者亚型。包括基因组学、表观基因组学、转录组学、蛋白质组学、代谢组学和微生物组在内的高通量全局组学方法使我们能够从不同角度研究不同内表型的致病异质性及其内在机制。在这篇综述中,我们全面概述了各种细胞类型在哮喘的病理生理学和异质性中的作用,并从目前的角度阐述了它们在气道炎症和气道重塑之间的双向互动中所起的作用。接下来,我们讨论了通过机器学习对多组学数据进行综合分析如何系统地描述哮喘表型遗传异质性的分子和生物学特征。我们还将介绍多组学方法在患者分层和治疗中的应用。多组学与临床数据的整合将为哮喘异质性的关键致病机制提供更多见解,并重塑哮喘管理和治疗策略。
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CiteScore
2.80
自引率
0.00%
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0
审稿时长
12 weeks
期刊最新文献
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