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Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD

BACKGROUND: Asthma and COPD are complex, heterogeneous conditions comprising a wide range of phenotypes, some of which are refractory to currently available treatments. Elucidation of these phenotypes and identification of biomarkers with which to recognize them and guide appropriate treat-ment rema...

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Autores principales: Kostikas, Konstantinos, Brindicci, Caterina, Patalano, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225326/
https://www.ncbi.nlm.nih.gov/pubmed/29437007
http://dx.doi.org/10.2174/1389450119666180212120012
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author Kostikas, Konstantinos
Brindicci, Caterina
Patalano, Francesco
author_facet Kostikas, Konstantinos
Brindicci, Caterina
Patalano, Francesco
author_sort Kostikas, Konstantinos
collection PubMed
description BACKGROUND: Asthma and COPD are complex, heterogeneous conditions comprising a wide range of phenotypes, some of which are refractory to currently available treatments. Elucidation of these phenotypes and identification of biomarkers with which to recognize them and guide appropriate treat-ment remain a priority. OBJECTIVE: This review describes the utility of blood eosinophils as a surrogate biomarker of eosinophilic airway inflammation, a common feature of specific asthma and COPD phenotypes. The role of blood eosinophils in airway disease is described, as is their relevance in reflecting airway eosinophilia. Each disease is discussed separately as the manner in which blood eosinophils might be used as biomarkers differs. Focusing on patients with severe disease (persistent eosinophilic asthma and exacerbating COPD), we evaluate evidence examining eosinophils as biomarkers. RESULTS: In asthma, the rationale for using blood eosinophils to guide treatment is clearly defined, backed by prospective, well-controlled studies. Higher eosinophil counts identify patients with more se-vere disease and poorer outcomes, patients for whom biologic therapies targeting allergic and/or eosino-philic pathways are recommended. In COPD, the evidence is less robust. High blood eosinophil counts are a modest predictor of future exacerbations, and may predict a favourable response to ICS on top of LABA/LAMA, especially in patients with a history of frequent exacerbations. CONCLUSION: Before extensive application in clinical practice, further evaluation of these findings in pro-spective clinical studies, and standardization of the appropriate thresholds of clinically relevant eosino-philia are needed, together with establishing whether single or multiple measurements are required in dif-ferent clinical settings
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spelling pubmed-62253262018-12-07 Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD Kostikas, Konstantinos Brindicci, Caterina Patalano, Francesco Curr Drug Targets Article BACKGROUND: Asthma and COPD are complex, heterogeneous conditions comprising a wide range of phenotypes, some of which are refractory to currently available treatments. Elucidation of these phenotypes and identification of biomarkers with which to recognize them and guide appropriate treat-ment remain a priority. OBJECTIVE: This review describes the utility of blood eosinophils as a surrogate biomarker of eosinophilic airway inflammation, a common feature of specific asthma and COPD phenotypes. The role of blood eosinophils in airway disease is described, as is their relevance in reflecting airway eosinophilia. Each disease is discussed separately as the manner in which blood eosinophils might be used as biomarkers differs. Focusing on patients with severe disease (persistent eosinophilic asthma and exacerbating COPD), we evaluate evidence examining eosinophils as biomarkers. RESULTS: In asthma, the rationale for using blood eosinophils to guide treatment is clearly defined, backed by prospective, well-controlled studies. Higher eosinophil counts identify patients with more se-vere disease and poorer outcomes, patients for whom biologic therapies targeting allergic and/or eosino-philic pathways are recommended. In COPD, the evidence is less robust. High blood eosinophil counts are a modest predictor of future exacerbations, and may predict a favourable response to ICS on top of LABA/LAMA, especially in patients with a history of frequent exacerbations. CONCLUSION: Before extensive application in clinical practice, further evaluation of these findings in pro-spective clinical studies, and standardization of the appropriate thresholds of clinically relevant eosino-philia are needed, together with establishing whether single or multiple measurements are required in dif-ferent clinical settings Bentham Science Publishers 2018-12 2018-12 /pmc/articles/PMC6225326/ /pubmed/29437007 http://dx.doi.org/10.2174/1389450119666180212120012 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Kostikas, Konstantinos
Brindicci, Caterina
Patalano, Francesco
Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD
title Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD
title_full Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD
title_fullStr Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD
title_full_unstemmed Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD
title_short Blood Eosinophils as Biomarkers to Drive Treatment Choices in Asthma and COPD
title_sort blood eosinophils as biomarkers to drive treatment choices in asthma and copd
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225326/
https://www.ncbi.nlm.nih.gov/pubmed/29437007
http://dx.doi.org/10.2174/1389450119666180212120012
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