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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Dermatological Association; The Korean Society for Investigative Dermatology
2018
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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. |
format | Online Article Text |
id | pubmed-7992469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Dermatological Association; The Korean Society for Investigative Dermatology |
record_format | MEDLINE/PubMed |
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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