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Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene

Multiple lines of evidence have shown that systemic lupus erythematosus (SLE) is attributable to both genetic and environmental factors. The product of GRB2 is a key factor in the activation of B cells and has been reported to be significantly associated with SLE in European populations. In the stud...

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Autores principales: Xu, Meifeng, Liu, Yan, Li, Xiaoli, Cheng, Chuantao, Liu, Yale, Dong, Wei, Du, Shaoyi, Xiao, Shengxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637148/
https://www.ncbi.nlm.nih.gov/pubmed/31316132
http://dx.doi.org/10.1038/s41598-019-46827-z
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author Xu, Meifeng
Liu, Yan
Li, Xiaoli
Cheng, Chuantao
Liu, Yale
Dong, Wei
Du, Shaoyi
Xiao, Shengxiang
author_facet Xu, Meifeng
Liu, Yan
Li, Xiaoli
Cheng, Chuantao
Liu, Yale
Dong, Wei
Du, Shaoyi
Xiao, Shengxiang
author_sort Xu, Meifeng
collection PubMed
description Multiple lines of evidence have shown that systemic lupus erythematosus (SLE) is attributable to both genetic and environmental factors. The product of GRB2 is a key factor in the activation of B cells and has been reported to be significantly associated with SLE in European populations. In the study, we aimed to investigate the relationship between GRB2 and SLE. A total of 1,710 Han Chinese women comprising 567 SLE patients and 1,143 controls were recruited to genotype 20 selected tagging SNPs. We tested the potential association between 13 clinical variables of SLE and the significant polymorphisms related to SLE. The eQTL data were extracted from the GTEx database to examine the functional consequences of the targeted SNPs. A significant association signal was identified between rs36023980 and SLE in both genotypic and allelic analyses (OR = 0.61, P = 0.0003). Complement inhibition was shown to be significantly associated with the genotypes of SNP rs36023980 in SLE patients (P(genotype) = 0.003). Further stratification analyses showed that the genetic association signal of SNP rs36023980 on SLE could only be identified in cases with complement inhibition. SNP rs36023980 was also identified to be significantly associated with the expression of GRB2 in whole blood and sun-exposed skin. In conclusion, our findings confirm the results from the previous GWAS and are the first to report the association of GRB2 with SLE in Han Chinese population.
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spelling pubmed-66371482019-07-25 Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene Xu, Meifeng Liu, Yan Li, Xiaoli Cheng, Chuantao Liu, Yale Dong, Wei Du, Shaoyi Xiao, Shengxiang Sci Rep Article Multiple lines of evidence have shown that systemic lupus erythematosus (SLE) is attributable to both genetic and environmental factors. The product of GRB2 is a key factor in the activation of B cells and has been reported to be significantly associated with SLE in European populations. In the study, we aimed to investigate the relationship between GRB2 and SLE. A total of 1,710 Han Chinese women comprising 567 SLE patients and 1,143 controls were recruited to genotype 20 selected tagging SNPs. We tested the potential association between 13 clinical variables of SLE and the significant polymorphisms related to SLE. The eQTL data were extracted from the GTEx database to examine the functional consequences of the targeted SNPs. A significant association signal was identified between rs36023980 and SLE in both genotypic and allelic analyses (OR = 0.61, P = 0.0003). Complement inhibition was shown to be significantly associated with the genotypes of SNP rs36023980 in SLE patients (P(genotype) = 0.003). Further stratification analyses showed that the genetic association signal of SNP rs36023980 on SLE could only be identified in cases with complement inhibition. SNP rs36023980 was also identified to be significantly associated with the expression of GRB2 in whole blood and sun-exposed skin. In conclusion, our findings confirm the results from the previous GWAS and are the first to report the association of GRB2 with SLE in Han Chinese population. Nature Publishing Group UK 2019-07-17 /pmc/articles/PMC6637148/ /pubmed/31316132 http://dx.doi.org/10.1038/s41598-019-46827-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xu, Meifeng
Liu, Yan
Li, Xiaoli
Cheng, Chuantao
Liu, Yale
Dong, Wei
Du, Shaoyi
Xiao, Shengxiang
Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene
title Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene
title_full Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene
title_fullStr Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene
title_full_unstemmed Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene
title_short Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene
title_sort evaluation of genetic susceptibility between systemic lupus erythematosus and grb2 gene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637148/
https://www.ncbi.nlm.nih.gov/pubmed/31316132
http://dx.doi.org/10.1038/s41598-019-46827-z
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