• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一个非同义的FCER1B单核苷酸多态性与变应性鼻炎的发病风险及免疫球蛋白E水平相关。

A Nonsynonymous FCER1B SNP is Associated with Risk of Developing Allergic Rhinitis and with IgE Levels.

作者信息

Amo Gemma, García-Menaya Jesús, Campo Paloma, Cordobés Concepción, Plaza Serón M Carmen, Ayuso Pedro, Esguevillas Gara, Blanca Miguel, Agúndez Jose A G, García-Martín Elena

机构信息

Department of Pharmacology, Universidad de Extremadura, Cáceres, Spain.

Allergy Service, University Hospital Infanta Cristina, Badajoz, Spain.

出版信息

Sci Rep. 2016 Jan 21;6:19724. doi: 10.1038/srep19724.

DOI:10.1038/srep19724
PMID:26792385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4726269/
Abstract

Allergic rhinitis is associated with elevated serum IgE levels. IgE response is mediated by the high-affinity IgE receptor (FcεRI), which is polymorphic. Studies analyzing the association between allergic rhinitis and FcεRI variants have been conducted with controversial results. The objective of this study is to analyze, in 1,041 individuals, the putative clinical association of allergic rhinitis with common polymorphisms in FcεRI subunits genes. These SNPs included FECR1A rs2494262, rs2427837 and rs2251746; FECR1B rs1441586, rs569108 and rs512555; FCER1G rs11587213, rs2070901 and rs11421. Statistically significant differences were observed for the FCER1B rs569108 and rs512555 polymorphisms frequencies when comparing patients with allergic rhinitis without asthma and controls. The OR (95% CI) value for the 237Gly allele (rs569108) is equal to 0.26 (0.08-0.86, P = 0.017) and for the G allele (rs512555) it is equal to 0.27 (0.08-0.88, P = 0.020). These two SNPs are linked (D' = 1.0, LOD = 56.05). Also observed was a statistically significant trend towards lower IgE values among allergic rhinitis patients with variant alleles for both SNPs. In conclusion, in patients with allergic rhinitis without asthma, the FCER1B rs569108 and rs512555 polymorphisms are associated with increased risk of developing allergic rhinitis and with lower IgE levels.

摘要

变应性鼻炎与血清IgE水平升高有关。IgE反应由高亲和力IgE受体(FcεRI)介导,该受体具有多态性。分析变应性鼻炎与FcεRI变体之间关联的研究结果存在争议。本研究的目的是在1041名个体中分析变应性鼻炎与FcεRI亚基基因常见多态性之间的假定临床关联。这些单核苷酸多态性(SNP)包括FECR1A rs2494262、rs2427837和rs2251746;FECR1B rs1441586、rs569108和rs512555;FCER1G rs11587213、rs2070901和rs11421。在比较无哮喘的变应性鼻炎患者和对照组时,观察到FCER1B rs569108和rs512555多态性频率存在统计学显著差异。237Gly等位基因(rs569108)的比值比(OR,95%可信区间)为0.26(0.08 - 0.86,P = 0.017),G等位基因(rs512555)的比值比为0.27(0.08 - 0.88,P = 0.020)。这两个SNP处于连锁状态(D' = 1.0,LOD = 56.05)。还观察到,对于这两个SNP具有变异等位基因的变应性鼻炎患者中,IgE值有统计学显著降低趋势。总之,在无哮喘的变应性鼻炎患者中,FCER1B rs569108和rs512555多态性与变应性鼻炎发病风险增加及较低的IgE水平相关。

相似文献

1
A Nonsynonymous FCER1B SNP is Associated with Risk of Developing Allergic Rhinitis and with IgE Levels.一个非同义的FCER1B单核苷酸多态性与变应性鼻炎的发病风险及免疫球蛋白E水平相关。
Sci Rep. 2016 Jan 21;6:19724. doi: 10.1038/srep19724.
2
Functional variants of 17q12-21 are associated with allergic asthma but not allergic rhinitis.17q12-21 上的功能变体与过敏性哮喘有关,但与过敏性鼻炎无关。
J Allergy Clin Immunol. 2016 Mar;137(3):758-66.e3. doi: 10.1016/j.jaci.2015.08.038. Epub 2015 Oct 23.
3
Increased total serum IgE levels in patients with asthma and promoter polymorphisms at CTLA4 and FCER1B.哮喘患者血清总IgE水平升高以及CTLA4和FCER1B基因启动子多态性
J Allergy Clin Immunol. 2001 Jul;108(1):74-9. doi: 10.1067/mai.2001.116119.
4
FCERI and Histamine Metabolism Gene Variability in Selective Responders to NSAIDS.非甾体抗炎药选择性反应者中的高亲和力IgE受体I和组胺代谢基因变异性
Front Pharmacol. 2016 Sep 29;7:353. doi: 10.3389/fphar.2016.00353. eCollection 2016.
5
The alpha-chain of high-affinity receptor for IgE (FcepsilonRIalpha) gene polymorphisms and serum IgE levels.免疫球蛋白E高亲和力受体α链(FcepsilonRIα)基因多态性与血清免疫球蛋白E水平
Allergy. 2006 Oct;61(10):1230-3. doi: 10.1111/j.1398-9995.2006.01195.x.
6
A multi-centre study of candidate genes for wheeze and allergy: the International Study of Asthma and Allergies in Childhood Phase 2.多中心候选基因研究喘息和过敏:儿童哮喘和过敏国际研究第二阶段。
Clin Exp Allergy. 2009 Dec;39(12):1875-88. doi: 10.1111/j.1365-2222.2009.03364.x.
7
Association between two polymorphisms of histamine-metabolising enzymes and the severity of allergic rhinitis in a group of Mexican children.一组墨西哥儿童中组胺代谢酶的两种多态性与过敏性鼻炎严重程度之间的关联
Allergol Immunopathol (Madr). 2016 Sep-Oct;44(5):433-8. doi: 10.1016/j.aller.2016.01.002. Epub 2016 May 30.
8
Analysis of the high affinity IgE receptor genes reveals epistatic effects of FCER1A variants on eczema risk.分析高亲和力 IgE 受体基因揭示了 FCER1A 变体对湿疹风险的上位效应。
Allergy. 2010 Jul;65(7):875-82. doi: 10.1111/j.1398-9995.2009.02297.x. Epub 2009 Dec 21.
9
The β2-adrenoreceptor gene promoter polymorphisms may modulate β2-agonist- and glucocorticoid-induced IgE synthesis.β2-肾上腺素能受体基因启动子多态性可能调节β2-激动剂和糖皮质激素诱导的IgE合成。
Allergol Immunopathol (Madr). 2014 Nov-Dec;42(6):586-93. doi: 10.1016/j.aller.2013.07.002. Epub 2013 Oct 30.
10
Variation in the TEK gene is not associated with asthma but with allergic conjunctivitis.TEK基因的变异与哮喘无关,而与过敏性结膜炎有关。
Int J Immunogenet. 2018 Jun;45(3):102-108. doi: 10.1111/iji.12365. Epub 2018 Apr 18.

引用本文的文献

1
MS4A superfamily molecules in tumors, Alzheimer's and autoimmune diseases.肿瘤、阿尔茨海默病和自身免疫性疾病中的MS4A超家族分子。
Front Immunol. 2024 Dec 9;15:1481494. doi: 10.3389/fimmu.2024.1481494. eCollection 2024.
2
Transcriptome immune-regulatory differences between leprosy patients and type 1 reaction patients, before onset of symptoms.麻风病患者与1型反应患者在症状出现前的转录组免疫调节差异。
PLoS Negl Trop Dis. 2024 Dec 16;18(12):e0011866. doi: 10.1371/journal.pntd.0011866. eCollection 2024 Dec.
3
The relationship between Fc epsilon receptor-1α and β ( and ) gene polymorphisms in patients with chronic urticaria using omalizumab.使用奥马珠单抗治疗的慢性荨麻疹患者中Fcε受体-1α和β(及)基因多态性之间的关系
Postepy Dermatol Alergol. 2024 Aug;41(4):357-363. doi: 10.5114/ada.2024.142285. Epub 2024 Aug 14.
4
SingleNucleotide Polymorphisms as Biomarkers of Mepolizumab and Benralizumab Treatment Response in Severe Eosinophilic Asthma.单核苷酸多态性作为美泊利珠单抗和贝那利珠单抗治疗重度嗜酸性粒细胞性哮喘应答的生物标志物。
Int J Mol Sci. 2024 Jul 26;25(15):8139. doi: 10.3390/ijms25158139.
5
Influence of Genetics on the Response to Omalizumab in Patients with Severe Uncontrolled Asthma with an Allergic Phenotype.遗传学对过敏性表型的重度未控制哮喘患者奥马珠单抗应答的影响。
Int J Mol Sci. 2023 Apr 10;24(8):7029. doi: 10.3390/ijms24087029.
6
Pathogenesis of allergic diseases and implications for therapeutic interventions.过敏性疾病的发病机制及治疗干预的意义。
Signal Transduct Target Ther. 2023 Mar 24;8(1):138. doi: 10.1038/s41392-023-01344-4.
7
Comments on 'Association of FcϵRIβ polymorphisms with risk of asthma and allergic rhinitis: evidence based on 29 case-control studies'.关于“FcϵRIβ 多态性与哮喘和过敏性鼻炎风险的关联:基于 29 项病例对照研究的证据”的评论。
Biosci Rep. 2020 Jul 31;40(7). doi: 10.1042/BSR20193424.
8
GATA2 and PU.1 Collaborate To Activate the Expression of the Mouse Gene, Encoding FcεRIβ, through Distinct Mechanisms.GATA2 和 PU.1 通过不同的机制协同激活编码 FcεRIβ 的小鼠基因的表达。
Mol Cell Biol. 2019 Oct 28;39(22). doi: 10.1128/MCB.00314-19. Print 2019 Nov 15.
9
Identification of Novel Biomarkers for Drug Hypersensitivity After Sequencing of the Promoter Area in 16 Genes of the Vitamin D Pathway and the High-Affinity IgE Receptor.对维生素D途径和高亲和力IgE受体的16个基因启动子区域进行测序后,鉴定药物超敏反应的新型生物标志物。
Front Genet. 2019 Jun 25;10:582. doi: 10.3389/fgene.2019.00582. eCollection 2019.
10
Association of FcεRIβ polymorphisms with risk of asthma and allergic rhinitis: evidence based on 29 case-control studies.FcεRIβ 多态性与哮喘和过敏性鼻炎风险的关联:基于 29 项病例对照研究的证据。
Biosci Rep. 2018 Jul 31;38(4). doi: 10.1042/BSR20180177. Print 2018 Aug 31.

本文引用的文献

1
Genetic determinants of metamizole metabolism modify the risk of developing anaphylaxis.安乃近代谢的遗传决定因素会改变发生过敏反应的风险。
Pharmacogenet Genomics. 2015 Sep;25(9):462-4. doi: 10.1097/FPC.0000000000000157.
2
Human FcR polymorphism and disease.人类FcR多态性与疾病。
Curr Top Microbiol Immunol. 2014;382:275-302. doi: 10.1007/978-3-319-07911-0_13.
3
Association of the MS4A2 gene promoter C-109T or the 7th exon E237G polymorphisms with asthma risk: a meta-analysis.MS4A2基因启动子C-109T或第7外显子E237G多态性与哮喘风险的关联:一项荟萃分析。
Clin Biochem. 2014 May;47(7-8):605-11. doi: 10.1016/j.clinbiochem.2014.01.022. Epub 2014 Feb 1.
4
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.全基因组关联研究的荟萃分析确定了 10 个影响过敏敏化的位点。
Nat Genet. 2013 Aug;45(8):902-906. doi: 10.1038/ng.2694. Epub 2013 Jun 30.
5
Investigating highly replicated asthma genes as candidate genes for allergic rhinitis.研究高度复制的哮喘基因作为变应性鼻炎的候选基因。
BMC Med Genet. 2013 May 10;14:51. doi: 10.1186/1471-2350-14-51.
6
Poor reproducibility of allergic rhinitis SNP associations.变应性鼻炎 SNP 关联的可重复性差。
PLoS One. 2013;8(1):e53975. doi: 10.1371/journal.pone.0053975. Epub 2013 Jan 30.
7
Replication of genome-wide association study loci for allergic rhinitis and house dust mite sensitization in an Asian population of ethnic Chinese in Singapore.新加坡华裔亚洲人群中过敏性鼻炎和屋尘螨致敏的全基因组关联研究位点的重复研究
J Allergy Clin Immunol. 2013 May;131(5):1431-3.e8. doi: 10.1016/j.jaci.2012.11.001. Epub 2012 Dec 8.
8
Current concepts of IgE regulation and impact of genetic determinants.当前 IgE 调节的概念和遗传决定因素的影响。
Clin Exp Allergy. 2012 Jun;42(6):852-71. doi: 10.1111/j.1365-2222.2011.03953.x.
9
Deciphering the structure and function of FcεRI/mast cell axis in the regulation of allergy and anaphylaxis: a functional genomics paradigm.解析 FcεRI/肥大细胞轴在过敏和过敏反应调控中的结构和功能:一种功能基因组学范例。
Cell Mol Life Sci. 2012 Jun;69(12):1917-29. doi: 10.1007/s00018-011-0886-0. Epub 2011 Dec 7.
10
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.一项与过敏性鼻炎和草致敏相关遗传变异及其与出生顺序相互作用的全基因组荟萃分析
J Allergy Clin Immunol. 2011 Nov;128(5):996-1005. doi: 10.1016/j.jaci.2011.08.030.