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Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population

BACKGROUND: Vitamin D receptor (VDR) is involved in multiple immune-mediated disorders including oral lichen planus (OLP). This study investigated the association between VDR gene polymorphisms and the risk of OLP. METHODS: In total, 177 OLP patients and 207 healthy participants were recruited from...

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Autores principales: Shen, Hong, Liu, Qinglan, Huang, Peng, Fan, Haozhi, Zang, Feng, Liu, Mei, Zhuo, Lingyun, Wu, Jingjing, Wu, Guoying, Yu, Rongbin, Yang, Jianrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993400/
https://www.ncbi.nlm.nih.gov/pubmed/32000758
http://dx.doi.org/10.1186/s12903-020-1002-3
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author Shen, Hong
Liu, Qinglan
Huang, Peng
Fan, Haozhi
Zang, Feng
Liu, Mei
Zhuo, Lingyun
Wu, Jingjing
Wu, Guoying
Yu, Rongbin
Yang, Jianrong
author_facet Shen, Hong
Liu, Qinglan
Huang, Peng
Fan, Haozhi
Zang, Feng
Liu, Mei
Zhuo, Lingyun
Wu, Jingjing
Wu, Guoying
Yu, Rongbin
Yang, Jianrong
author_sort Shen, Hong
collection PubMed
description BACKGROUND: Vitamin D receptor (VDR) is involved in multiple immune-mediated disorders including oral lichen planus (OLP). This study investigated the association between VDR gene polymorphisms and the risk of OLP. METHODS: In total, 177 OLP patients and 207 healthy participants were recruited from the Affiliated Hospital of Stomatology, Nanjing Medical University. Eight single nucleotide polymorphisms (SNPs: rs731236, rs739837, rs757343, rs2107301, rs2239185, rs7975232, rs11574129 and rs11568820) in the VDR gene were selected and genotyped. RESULTS: The results showed that OLP risk was increased in subjects with the rs2239185 TT genotype (Recessive model: adjusted Odd ratio(OR) = 2.68, 95% Confidence interval(CI) = 1.28–5.62, P = 0.009) and rs7975232 CC genotype (Recessive model: adjusted OR = 2.25, 95% CI = 1.10–4.58, P = 0.026). Moreover, rs2239185 and rs7975232 (P < 0.01) showed significant cumulative effects on OLP risk.Haplotype analysis showed that the CC haplotype (rs2239185-rs7975232) was associated with an increased risk of OLP (OR = 3.11, 95% CI = 1.42–6.83, P = 0.005), compared with the AC haplotype. Conclusion: The rs2239185 and rs7975232 variants of VDR may influence OLP susceptibility, and VDR gene polymorphisms may be candidate susceptibility regions for OLP in a Chinese Han population.
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spelling pubmed-69934002020-02-04 Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population Shen, Hong Liu, Qinglan Huang, Peng Fan, Haozhi Zang, Feng Liu, Mei Zhuo, Lingyun Wu, Jingjing Wu, Guoying Yu, Rongbin Yang, Jianrong BMC Oral Health Research Article BACKGROUND: Vitamin D receptor (VDR) is involved in multiple immune-mediated disorders including oral lichen planus (OLP). This study investigated the association between VDR gene polymorphisms and the risk of OLP. METHODS: In total, 177 OLP patients and 207 healthy participants were recruited from the Affiliated Hospital of Stomatology, Nanjing Medical University. Eight single nucleotide polymorphisms (SNPs: rs731236, rs739837, rs757343, rs2107301, rs2239185, rs7975232, rs11574129 and rs11568820) in the VDR gene were selected and genotyped. RESULTS: The results showed that OLP risk was increased in subjects with the rs2239185 TT genotype (Recessive model: adjusted Odd ratio(OR) = 2.68, 95% Confidence interval(CI) = 1.28–5.62, P = 0.009) and rs7975232 CC genotype (Recessive model: adjusted OR = 2.25, 95% CI = 1.10–4.58, P = 0.026). Moreover, rs2239185 and rs7975232 (P < 0.01) showed significant cumulative effects on OLP risk.Haplotype analysis showed that the CC haplotype (rs2239185-rs7975232) was associated with an increased risk of OLP (OR = 3.11, 95% CI = 1.42–6.83, P = 0.005), compared with the AC haplotype. Conclusion: The rs2239185 and rs7975232 variants of VDR may influence OLP susceptibility, and VDR gene polymorphisms may be candidate susceptibility regions for OLP in a Chinese Han population. BioMed Central 2020-01-30 /pmc/articles/PMC6993400/ /pubmed/32000758 http://dx.doi.org/10.1186/s12903-020-1002-3 Text en © The Author(s). 2020 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Shen, Hong
Liu, Qinglan
Huang, Peng
Fan, Haozhi
Zang, Feng
Liu, Mei
Zhuo, Lingyun
Wu, Jingjing
Wu, Guoying
Yu, Rongbin
Yang, Jianrong
Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population
title Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population
title_full Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population
title_fullStr Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population
title_full_unstemmed Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population
title_short Vitamin D receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a Chinese Han population
title_sort vitamin d receptor genetic polymorphisms are associated with oral lichen planus susceptibility in a chinese han population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993400/
https://www.ncbi.nlm.nih.gov/pubmed/32000758
http://dx.doi.org/10.1186/s12903-020-1002-3
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