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TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans

BACKGROUND: Atopic march (AM) is the progression from atopic dermatitis (AD) to allergic rhinitis and asthma. The development of AD is as high as 20% in children worldwide and continues to increase. AD seems to be caused by both genetic and environmental factors. Recently, polymorphisms of the thymi...

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Autores principales: Heo, Won Il, Park, Kui Young, Lee, Mi-Kyung, Moon, Nam Ju, Seo, Seong Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992469/
https://www.ncbi.nlm.nih.gov/pubmed/33911474
http://dx.doi.org/10.5021/ad.2018.30.5.529
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author Heo, Won Il
Park, Kui Young
Lee, Mi-Kyung
Moon, Nam Ju
Seo, Seong Jun
author_facet Heo, Won Il
Park, Kui Young
Lee, Mi-Kyung
Moon, Nam Ju
Seo, Seong Jun
author_sort Heo, Won Il
collection PubMed
description BACKGROUND: Atopic march (AM) is the progression from atopic dermatitis (AD) to allergic rhinitis and asthma. The development of AD is as high as 20% in children worldwide and continues to increase. AD seems to be caused by both genetic and environmental factors. Recently, polymorphisms of the thymic stromal lymphopoietin (TSLP) gene associated with allergic disorders were reported in ethnic groups from various countries. OBJECTIVE: Identification of TSLP polymorphisms in Koreans with AD or AM. METHODS: Whole-exome sequencing was performed in 20 AD and 20 AM patients. RESULTS: Nine single nucleotide polymorphisms (SNPs) of TSLP were detected (rs191607411, rs3806933, rs2289276, rs2289277, rs2289278, rs139817258, rs11466749, rs11466750, rs10073816). These SNPs have been correlated with susceptibility to allergic diseases in ethnic groups from China, Japan, Turkey, and Costa Rica in previous studies. Remarkably, one of 20 patients in the AD group lacked all SNPs, compared to six of 20 patients in the AM group. Odds ratios showed that Korean patients without the nine TSLP variants had an 8.14 times higher risk of moving from AD to AM. Two haplotype blocks were validated in 60 AD and 59 AM patients using Sanger sequencing. The haplotype blocks (rs3806933 and rs2289276) and (rs11466749 and rs11466750) were in high linkage disequilibrium, respectively (D′=0.97, D′=1). CONCLUSION: The increase of major allele frequency of respective nine TSLP variants may enhance the risk of AM. These data will contribute to improved genetic surveillance system in the early diagnosis technology of allergic disease.
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spelling pubmed-79924692021-04-27 TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans Heo, Won Il Park, Kui Young Lee, Mi-Kyung Moon, Nam Ju Seo, Seong Jun Ann Dermatol Original Article BACKGROUND: Atopic march (AM) is the progression from atopic dermatitis (AD) to allergic rhinitis and asthma. The development of AD is as high as 20% in children worldwide and continues to increase. AD seems to be caused by both genetic and environmental factors. Recently, polymorphisms of the thymic stromal lymphopoietin (TSLP) gene associated with allergic disorders were reported in ethnic groups from various countries. OBJECTIVE: Identification of TSLP polymorphisms in Koreans with AD or AM. METHODS: Whole-exome sequencing was performed in 20 AD and 20 AM patients. RESULTS: Nine single nucleotide polymorphisms (SNPs) of TSLP were detected (rs191607411, rs3806933, rs2289276, rs2289277, rs2289278, rs139817258, rs11466749, rs11466750, rs10073816). These SNPs have been correlated with susceptibility to allergic diseases in ethnic groups from China, Japan, Turkey, and Costa Rica in previous studies. Remarkably, one of 20 patients in the AD group lacked all SNPs, compared to six of 20 patients in the AM group. Odds ratios showed that Korean patients without the nine TSLP variants had an 8.14 times higher risk of moving from AD to AM. Two haplotype blocks were validated in 60 AD and 59 AM patients using Sanger sequencing. The haplotype blocks (rs3806933 and rs2289276) and (rs11466749 and rs11466750) were in high linkage disequilibrium, respectively (D′=0.97, D′=1). CONCLUSION: The increase of major allele frequency of respective nine TSLP variants may enhance the risk of AM. These data will contribute to improved genetic surveillance system in the early diagnosis technology of allergic disease. The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2018-10 2018-08-28 /pmc/articles/PMC7992469/ /pubmed/33911474 http://dx.doi.org/10.5021/ad.2018.30.5.529 Text en Copyright © 2018 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Heo, Won Il
Park, Kui Young
Lee, Mi-Kyung
Moon, Nam Ju
Seo, Seong Jun
TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans
title TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans
title_full TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans
title_fullStr TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans
title_full_unstemmed TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans
title_short TSLP Polymorphisms in Atopic Dermatitis and Atopic March in Koreans
title_sort tslp polymorphisms in atopic dermatitis and atopic march in koreans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992469/
https://www.ncbi.nlm.nih.gov/pubmed/33911474
http://dx.doi.org/10.5021/ad.2018.30.5.529
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