生物标志物和严重哮喘:一个关键的评估。

Q2 Medicine
Clinical and Molecular Allergy Pub Date : 2015-10-01 eCollection Date: 2015-01-01 DOI:10.1186/s12948-015-0027-7
Alessandra Chiappori, Laura De Ferrari, Chiara Folli, Pierluigi Mauri, Anna Maria Riccio, Giorgio Walter Canonica
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引用次数: 59

摘要

严重哮喘(SA)是一种临床和病因异质性的呼吸系统疾病,约占哮喘患者的5- 10%。尽管接受了大剂量治疗,但仍有很大比例的患者没有得到完全控制,生活质量很差。在这篇综述中,我们描述了在科学文献中已知的并在临床实践中用于SA评估和管理的生物标志物:中性粒细胞、嗜酸性粒细胞、骨膜蛋白、分数呼出一氧化氮、呼出冷凝物和凝集素。此外,我们还概述了重症哮喘的临床和生物学特征,并特别关注这些特征作为可靠标志物的潜在用途。我们最后强调需要定义不同的生物标志物组来选择受严重哮喘影响的患者进行特定和个性化的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Biomarkers and severe asthma: a critical appraisal.

Biomarkers and severe asthma: a critical appraisal.

Biomarkers and severe asthma: a critical appraisal.

Severe asthma (SA) is a clinically and etiologically heterogeneous respiratory disease which affects among 5-10 % of asthmatic patients. Despite high-dose therapy, a large patients percentage is not fully controlled and has a poor quality of life. In this review, we describe the biomarkers actually known in scientific literature and used in clinical practice for SA assessment and management: neutrophils, eosinophils, periostin, fractional exhaled nitric oxide, exhaled breath condensate and galectins. Moreover, we give an overview on clinical and biological features characterizing severe asthma, paying special attention to the potential use of these ones as reliable markers. We finally underline the need to define different biomarkers panels to select patients affected by severe asthma for specific and personalized therapeutic approach.

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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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