Pharmacogenetics of childhood uncontrolled asthma.

IF 3.9 3区 医学 Q2 IMMUNOLOGY Expert Review of Clinical Immunology Pub Date : 2025-02-01 Epub Date: 2023-05-19 DOI:10.1080/1744666X.2023.2214363
Manaswitha Khare, Shraddha Piparia, Kelan G Tantisira
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Abstract

Introduction: Asthma is a heterogeneous, multifactorial disease with multiple genetic and environmental risk factors playing a role in pathogenesis and therapeutic response. Understanding of pharmacogenetics can help with matching individualized treatments to specific genotypes of asthma to improve therapeutic outcomes especially in uncontrolled or severe asthma.

Areas covered: In this review, we outline novel information about biology, pathways, and mechanisms related to interindividual variability in drug response (corticosteroids, bronchodilators, leukotriene modifiers, and biologics) for childhood asthma. We discuss candidate gene, genome-wide association studies and newer omics studies including epigenomics, transcriptomics, proteomics, and metabolomics as well as integrative genomics and systems biology methods related to childhood asthma. The articles were obtained after a series of searches, last updated November 2022, using database PubMed/CINAHL DB.

Expert opinion: Implementation of pharmacogenetic algorithms can improve therapeutic targeting in children with asthma, particularly with severe or uncontrolled asthma who typically have challenges in clinical management and carry considerable financial burden. Future studies focusing on potential biomarkers both clinical and pharmacogenetic can help formulate a prognostic test for asthma treatment response that would represent true bench to bedside clinical implementation.

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儿童哮喘失控的药物遗传学。
引言:哮喘是一种异质性、多因素的疾病,多种遗传和环境风险因素在发病机制和治疗反应中发挥作用。了解药物遗传学有助于将个性化治疗与哮喘的特定基因型相匹配,以改善治疗结果,尤其是在未控制或严重哮喘的情况下。涵盖领域:在这篇综述中,我们概述了与儿童哮喘药物反应(皮质类固醇、支气管扩张剂、白三烯调节剂和生物制品)个体间变异性相关的生物学、途径和机制的新信息。我们讨论了候选基因、全基因组关联研究和新的组学研究,包括表观基因组学、转录组学、蛋白质组学和代谢组学,以及与儿童哮喘相关的综合基因组学和系统生物学方法。这些文章是在一系列搜索后获得的,最后一次更新于2022年11月,使用数据库PubMed/CINAHL DB。专家意见:实施药物遗传学算法可以提高哮喘儿童的治疗靶向性,特别是严重或未控制的哮喘儿童,他们通常在临床管理方面面临挑战,并承担相当大的经济负担。未来专注于临床和药物遗传学潜在生物标志物的研究可以帮助制定哮喘治疗反应的预后测试,这将代表真正的床旁临床实施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.60
自引率
2.30%
发文量
221
审稿时长
6-12 weeks
期刊介绍: Expert Review of Clinical Immunology (ISSN 1744-666X) provides expert analysis and commentary regarding the performance of new therapeutic and diagnostic modalities in clinical immunology. Members of the International Editorial Advisory Panel of Expert Review of Clinical Immunology are the forefront of their area of expertise. This panel works with our dedicated editorial team to identify the most important and topical review themes and the corresponding expert(s) most appropriate to provide commentary and analysis. All articles are subject to rigorous peer-review, and the finished reviews provide an essential contribution to decision-making in clinical immunology. Articles focus on the following key areas: • Therapeutic overviews of specific immunologic disorders highlighting optimal therapy and prospects for new medicines • Performance and benefits of newly approved therapeutic agents • New diagnostic approaches • Screening and patient stratification • Pharmacoeconomic studies • New therapeutic indications for existing therapies • Adverse effects, occurrence and reduction • Prospects for medicines in late-stage trials approaching regulatory approval • Novel treatment strategies • Epidemiological studies • Commentary and comparison of treatment guidelines Topics include infection and immunity, inflammation, host defense mechanisms, congenital and acquired immunodeficiencies, anaphylaxis and allergy, systemic immune diseases, organ-specific inflammatory diseases, transplantation immunology, endocrinology and diabetes, cancer immunology, neuroimmunology and hematological diseases.
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