Sphingosine-1-Phosphate: Biomarker, Contributor, or Target for Asthma?
Asthma is a complex and heterogeneous airway disease, since environmental and genetic factors have an effect on both susceptibility and severity of the disease. Due to the inherent complexity of the disease, defining asthma phenotypes, as well as endotypes that combine clinical phenotypes with a dis...
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Published in | Allergy, asthma & immunology research Vol. 11; no. 3; pp. 299 - 301 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Korea (South)
Korean Academy of Asthma, Allergy and Clinical Immunology
01.05.2019
The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 대한천식알레르기학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2092-7355 2092-7363 |
DOI | 10.4168/aair.2019.11.3.299 |
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Summary: | Asthma is a complex and heterogeneous airway disease, since environmental and genetic factors have an effect on both susceptibility and severity of the disease. Due to the inherent complexity of the disease, defining asthma phenotypes, as well as endotypes that combine clinical phenotypes with a distinct pathological mechanism, is necessary to elucidate the pathogenic mechanism of asthma and to develop targeted therapeutic strategies based on their mechanisms." Systematic analysis of metabolites (metabolomics) has been used to classify the heterogeneous phenotypes and endotypes of asthma because metabolic alterations may reflect pathophysiologic changes encompassing gene-to-environment interactions/ Metabolic changes in asthmatic patients may be examined to detect bioactive metabolites as pathogenic mediators as well as biomarkers of asthma." Sphingolipid metabolic changes represent target molecules as pathogenic and genetic susceptibility factors. |
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Bibliography: | SourceType-Scholarly Journals-1 ObjectType-Editorial Cartoon/Comic-1 content type line 14 content type line 23 ObjectType-Editorial-2 ObjectType-Commentary-1 |
ISSN: | 2092-7355 2092-7363 |
DOI: | 10.4168/aair.2019.11.3.299 |