Personalized asthma management in pediatric patients based on treatment response

N. Navanandan, S. Szefler
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Abstract

ABSTRACT Introduction Asthma is the most common chronic illness in the pediatric population and is characterized by substantial heterogeneity in phenotypes and treatment response. A precision medicine approach is required to advance asthma care and improve asthma morbidity in children. Areas covered We present a review of currently available biomarkers for the diagnosis and management of pediatric asthma. We discuss a core set of biomarkers recognized by the National Institute of Health Asthma Outcomes Task Force including eosinophil counts, IgE levels, and fraction of exhaled nitric oxide. We also review emerging biomarkers including periostin, thymic stromal lymphopoietin, and volatile organic compounds. These biomarkers have proven effective in differentiating asthma phenotypes and predicting and monitoring treatment response, and have led to the development of game-changing biologic therapies for pediatric asthma. Expert opinion Substantial progress has been made in the identification of key biomarkers to aid in the classification and management of pediatric asthma. However, for biomarkers to be used routinely in clinical practice, further investigations are needed to expand biomarker representation of additional asthma phenotypes. A systems biology approach is also required, combining the various ‘omic’ strategies, for precision medicine to reach its full potential in pediatric asthma management.
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基于治疗反应的儿科患者哮喘个性化管理
哮喘是儿科人群中最常见的慢性疾病,其特点是在表型和治疗反应上存在很大的异质性。需要一种精确的医学方法来推进哮喘护理和改善儿童哮喘发病率。本研究综述了目前可用于儿科哮喘诊断和治疗的生物标志物。我们讨论了一组由美国国立卫生研究院哮喘结局工作组认可的核心生物标志物,包括嗜酸性粒细胞计数、IgE水平和呼出一氧化氮的比例。我们还回顾了新兴的生物标志物,包括骨膜蛋白、胸腺基质淋巴生成素和挥发性有机化合物。这些生物标志物已被证明在区分哮喘表型和预测和监测治疗反应方面是有效的,并导致了儿童哮喘改变游戏规则的生物疗法的发展。在鉴定关键生物标志物以帮助儿童哮喘的分类和管理方面取得了实质性进展。然而,为了在临床实践中常规使用生物标志物,需要进一步的研究来扩大生物标志物在其他哮喘表型中的代表性。还需要一种系统生物学方法,结合各种“组学”策略,使精准医学在儿科哮喘管理中充分发挥其潜力。
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来源期刊
CiteScore
2.30
自引率
0.00%
发文量
9
期刊介绍: Expert Review of Precision Medicine and Drug Development publishes primarily review articles covering the development and clinical application of medicine to be used in a personalized therapy setting; in addition, the journal also publishes original research and commentary-style articles. In an era where medicine is recognizing that a one-size-fits-all approach is not always appropriate, it has become necessary to identify patients responsive to treatments and treat patient populations using a tailored approach. Areas covered include: Development and application of drugs targeted to specific genotypes and populations, as well as advanced diagnostic technologies and significant biomarkers that aid in this. Clinical trials and case studies within personalized therapy and drug development. Screening, prediction and prevention of disease, prediction of adverse events, treatment monitoring, effects of metabolomics and microbiomics on treatment. Secondary population research, genome-wide association studies, disease–gene association studies, personal genome technologies. Ethical and cost–benefit issues, the impact to healthcare and business infrastructure, and regulatory issues.
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