Polymorphism of some JAK-STAT pathway genes and its regulators in patients with systemic lupus erythematosus and lupus nephritis in Repubic of Belarus

IF 0.1 Q4 MULTIDISCIPLINARY SCIENCES DOKLADY NATSIONALNOI AKADEMII NAUK BELARUSI Pub Date : 2023-07-06 DOI:10.29235/1561-8323-2023-67-3-222-230
N. Nikitchenko, H. Yatskiu, E. Siniauskaya, H. Bialkevich, I. Kazyra, N. Dostanko, V. Yagur, R. Goncharova
{"title":"Polymorphism of some JAK-STAT pathway genes and its regulators in patients with systemic lupus erythematosus and lupus nephritis in Repubic of Belarus","authors":"N. Nikitchenko, H. Yatskiu, E. Siniauskaya, H. Bialkevich, I. Kazyra, N. Dostanko, V. Yagur, R. Goncharova","doi":"10.29235/1561-8323-2023-67-3-222-230","DOIUrl":null,"url":null,"abstract":"Genes of interest – STAT4, PTPN2 and PTPN22 – are components of the JAK-STAT signaling pathway, one of the important regulators of the immune system. The JAK-STAT pathway plays a key role in the development of both systemic lupus erythematosus (SLE) and its manifestation, lupus nephritis (LN) by mediating interferon levels and promoting IFN-induced gene expression. We investigated the allele and genotypes frequencies at the polymorphic loci of the STAT4 (rs7574865, rs3821236), PTPN2 (rs2542151, rs7234029) and PTPN22 (rs2476601) genes in groups of children (n = 37) and adults (n = 63) with SLE and LN. The control group included children (n = 420) and adults (n = 345) without autoimmune diseases. The analysis of the combined group of pediatric and adult patients revealed that the rs7574865 polymorphic locus of the STAT4 gene is associated with the risk of developing SLE (Т: OR 1,99 [1,42–2,79], р = 0,0001; TT: OR 3,36 [1,64–6,87], р = 0,0018) and LN (Т: OR 1,91 [1,32–2,78], р = 0,0008; TT: OR 4,25 [2,02–8,95], р = 0,0004). These associations also persisted when analyzing the pediatric and adult groups of patients with SLE and LN separately. Moreover, the rs7574865 polymorphic locus of the STAT4 gene appears to be a common genetic risk factor for autoimmune diseases development. The association of the polymorphic locus rs2542151 of the PTPN2 gene with the SLE (G: OR 1,66 [1,12–2,47], p = 0,014; GT: OR 1,74 [1,10–2,77], р = 0,021) and LN (G: OR 1,87 [1,21–2,88], р = 0,006; GT: OR 1,90 [1,13–3,18], р = 0,017) susceptibility was also found in a combined group of patients. The polymorphic loci rs7234029 in the PTPN2 gene and rs2476601 in the PTPN22 gene were not associated with SLE or LN regardless of the age of the patients.","PeriodicalId":41825,"journal":{"name":"DOKLADY NATSIONALNOI AKADEMII NAUK BELARUSI","volume":" ","pages":""},"PeriodicalIF":0.1000,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"DOKLADY NATSIONALNOI AKADEMII NAUK BELARUSI","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29235/1561-8323-2023-67-3-222-230","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Genes of interest – STAT4, PTPN2 and PTPN22 – are components of the JAK-STAT signaling pathway, one of the important regulators of the immune system. The JAK-STAT pathway plays a key role in the development of both systemic lupus erythematosus (SLE) and its manifestation, lupus nephritis (LN) by mediating interferon levels and promoting IFN-induced gene expression. We investigated the allele and genotypes frequencies at the polymorphic loci of the STAT4 (rs7574865, rs3821236), PTPN2 (rs2542151, rs7234029) and PTPN22 (rs2476601) genes in groups of children (n = 37) and adults (n = 63) with SLE and LN. The control group included children (n = 420) and adults (n = 345) without autoimmune diseases. The analysis of the combined group of pediatric and adult patients revealed that the rs7574865 polymorphic locus of the STAT4 gene is associated with the risk of developing SLE (Т: OR 1,99 [1,42–2,79], р = 0,0001; TT: OR 3,36 [1,64–6,87], р = 0,0018) and LN (Т: OR 1,91 [1,32–2,78], р = 0,0008; TT: OR 4,25 [2,02–8,95], р = 0,0004). These associations also persisted when analyzing the pediatric and adult groups of patients with SLE and LN separately. Moreover, the rs7574865 polymorphic locus of the STAT4 gene appears to be a common genetic risk factor for autoimmune diseases development. The association of the polymorphic locus rs2542151 of the PTPN2 gene with the SLE (G: OR 1,66 [1,12–2,47], p = 0,014; GT: OR 1,74 [1,10–2,77], р = 0,021) and LN (G: OR 1,87 [1,21–2,88], р = 0,006; GT: OR 1,90 [1,13–3,18], р = 0,017) susceptibility was also found in a combined group of patients. The polymorphic loci rs7234029 in the PTPN2 gene and rs2476601 in the PTPN22 gene were not associated with SLE or LN regardless of the age of the patients.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
白俄罗斯共和国系统性红斑狼疮和狼疮性肾炎患者部分JAK-STAT通路基因及其调控因子多态性
感兴趣的基因——STAT4、PTPN2和PTPN22——是免疫系统的重要调节因子之一JAK-STAT信号通路的组成部分。JAK-STAT通路通过介导干扰素水平和促进干扰素诱导的基因表达,在系统性红斑狼疮(SLE)及其表现狼疮肾炎(LN)的发展中发挥着关键作用。我们研究了儿童(n=37)和成人(n=63)SLE和LN患者STAT4(rs7574865,rs3821236)、PTPN2(rs2542151,rs7234029)和PTPN22(rs2476601)基因多态性位点的等位基因和基因型频率。对照组包括没有自身免疫性疾病的儿童(n=420)和成人(n=345)。对儿童和成人患者联合组的分析显示,STAT4基因的rs7574865多态性位点与SLE(Т:OR 1,99[1,42~2,79],р=0.0001;TT:OR 3,36[1,64~6,87],р=000018)和LN(Т:OR1,91[1,32~2,78],р=00008;TT:OR4,25[2,02~8,95],р=00004)的发病风险相关。当分别分析SLE和LN的儿童和成人组患者时,这些相关性也持续存在。此外,STAT4基因的rs7574865多态位点似乎是自身免疫性疾病发展的常见遗传风险因素。PTPN2基因多态性位点rs2542151与SLE(G:OR 1,66[1,12–2,47],p=0.014;GT:OR 1,74[1,10–2,77],р=0.021)和LN(G:OR1,87[1,21–2,88],р=0006;GT:OR1,90[1,13–3,18],р=0.017)易感性的相关性也在一组合并患者中发现。PTPN2基因的rs7234029和PTPN22基因的rs2476601多态位点与SLE或LN无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
DOKLADY NATSIONALNOI AKADEMII NAUK BELARUSI
DOKLADY NATSIONALNOI AKADEMII NAUK BELARUSI MULTIDISCIPLINARY SCIENCES-
自引率
0.00%
发文量
69
期刊最新文献
Tolerance of several construction materials and polycrystalline SiC to blistering and flecking due to ion implantation and annealing Quantum-chemical study of the stability of solvents with respect to strong organic bases Hardening mechanism of waste polyolefin mixtures in the presence of modified bentonite clay Predictive model for identifying new CYP19A1 ligands on the KNIME analytical platform Role of CD68+ and CD206+ cells in the progression of toxic liver fibrosis in rats
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1