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Leptin gene polymorphism affects leptin level in childhood asthma

BACKGROUND: Leptin may induce inflammation in asthma by activation of Th2 cells. It has also been demonstrated that leptin expression increases upon inflammation and that asthmatic patients show increased serum leptin levels. We hypothesized that the polymorphism in leptin (LEP) and leptin receptor...

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Autores principales: Szczepankiewicz, Dawid, Sobkowiak, Paulina, Narożna, Beata, Wojsyk-Banaszak, Irena, Bręborowicz, Anna, Szczepankiewicz, Aleksandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Childrens Hospital, Zhejiang University School of Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208747/
https://www.ncbi.nlm.nih.gov/pubmed/30203371
http://dx.doi.org/10.1007/s12519-018-0182-2
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author Szczepankiewicz, Dawid
Sobkowiak, Paulina
Narożna, Beata
Wojsyk-Banaszak, Irena
Bręborowicz, Anna
Szczepankiewicz, Aleksandra
author_facet Szczepankiewicz, Dawid
Sobkowiak, Paulina
Narożna, Beata
Wojsyk-Banaszak, Irena
Bręborowicz, Anna
Szczepankiewicz, Aleksandra
author_sort Szczepankiewicz, Dawid
collection PubMed
description BACKGROUND: Leptin may induce inflammation in asthma by activation of Th2 cells. It has also been demonstrated that leptin expression increases upon inflammation and that asthmatic patients show increased serum leptin levels. We hypothesized that the polymorphism in leptin (LEP) and leptin receptor (LEPR) genes is associated with childhood asthma and may affect their serum level. To our knowledge, there are no reports analyzing LEP and LEPR polymorphisms in association with their serum levels in childhood asthma. METHODS: We analyzed 35 subjects: 25 asthmatic pediatric patients and 10 healthy children aged from 6 to 18. The diagnosis of allergic asthma was based on clinical manifestation, lung function, positive skin prick tests and increased immunoglobulin E levels. The polymorphisms were genotyped with use of polymerase chain reaction-restriction fragment length polymorphism method. Serum levels of leptin and leptin receptor were determined using BioVendor enzyme-linked immunosorbent assay kits. Statistical analysis was done with Statistica v.12. RESULTS: We observed that leptin levels were increased in asthmatic subjects as compared to healthy controls and were significantly higher during exacerbation than in the asymptomatic period (P = 0.025). We observed that LEP polymorphism (rs13228377) was associated with higher serum leptin levels in asthma and these two variables had high predictive value for asthma risk (P = 0.007, odds ratio 17.5, predictive accuracy 83.9%). LEPR polymorphisms did not show association with its serum level and asthma risk. CONCLUSION: LEP polymorphism may increase asthma risk via influence on its serum level.
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spelling pubmed-62087472018-11-09 Leptin gene polymorphism affects leptin level in childhood asthma Szczepankiewicz, Dawid Sobkowiak, Paulina Narożna, Beata Wojsyk-Banaszak, Irena Bręborowicz, Anna Szczepankiewicz, Aleksandra World J Pediatr Original Article BACKGROUND: Leptin may induce inflammation in asthma by activation of Th2 cells. It has also been demonstrated that leptin expression increases upon inflammation and that asthmatic patients show increased serum leptin levels. We hypothesized that the polymorphism in leptin (LEP) and leptin receptor (LEPR) genes is associated with childhood asthma and may affect their serum level. To our knowledge, there are no reports analyzing LEP and LEPR polymorphisms in association with their serum levels in childhood asthma. METHODS: We analyzed 35 subjects: 25 asthmatic pediatric patients and 10 healthy children aged from 6 to 18. The diagnosis of allergic asthma was based on clinical manifestation, lung function, positive skin prick tests and increased immunoglobulin E levels. The polymorphisms were genotyped with use of polymerase chain reaction-restriction fragment length polymorphism method. Serum levels of leptin and leptin receptor were determined using BioVendor enzyme-linked immunosorbent assay kits. Statistical analysis was done with Statistica v.12. RESULTS: We observed that leptin levels were increased in asthmatic subjects as compared to healthy controls and were significantly higher during exacerbation than in the asymptomatic period (P = 0.025). We observed that LEP polymorphism (rs13228377) was associated with higher serum leptin levels in asthma and these two variables had high predictive value for asthma risk (P = 0.007, odds ratio 17.5, predictive accuracy 83.9%). LEPR polymorphisms did not show association with its serum level and asthma risk. CONCLUSION: LEP polymorphism may increase asthma risk via influence on its serum level. Childrens Hospital, Zhejiang University School of Medicine 2018-09-10 2018 /pmc/articles/PMC6208747/ /pubmed/30203371 http://dx.doi.org/10.1007/s12519-018-0182-2 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Szczepankiewicz, Dawid
Sobkowiak, Paulina
Narożna, Beata
Wojsyk-Banaszak, Irena
Bręborowicz, Anna
Szczepankiewicz, Aleksandra
Leptin gene polymorphism affects leptin level in childhood asthma
title Leptin gene polymorphism affects leptin level in childhood asthma
title_full Leptin gene polymorphism affects leptin level in childhood asthma
title_fullStr Leptin gene polymorphism affects leptin level in childhood asthma
title_full_unstemmed Leptin gene polymorphism affects leptin level in childhood asthma
title_short Leptin gene polymorphism affects leptin level in childhood asthma
title_sort leptin gene polymorphism affects leptin level in childhood asthma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208747/
https://www.ncbi.nlm.nih.gov/pubmed/30203371
http://dx.doi.org/10.1007/s12519-018-0182-2
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