• 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

台湾人群中MD-1基因单核苷酸多态性与儿童及成人哮喘的关联。

Association of single nucleotide polymorphisms of MD-1 gene with pediatric and adult asthma in the Taiwanese population.

作者信息

Lee Shih-Wei, Wang Jiu-Yao, Hsieh Yuan-Chun, Wu Ying-Jye, Ting Hsien-Wei, Wu Lawrence Shih-Hsin

机构信息

Chest Medicine Department of Internal Medicine, Taoyuan General Hospital, Taoyuan, Taiwan.

出版信息

J Microbiol Immunol Infect. 2008 Dec;41(6):445-9.

PMID:19255686
Abstract

BACKGROUND AND PURPOSE

MD-1 (myeloid differentiation 1; also known as Ly86, lymphocyte antigen 86), interacting with radioprotective 105, plays an important role in the Toll-like receptor 4 signaling pathway. It has been suggested that MD-1 is involved in the development of inflammation and atopic diseases. The purpose of this study was to investigate the genetic association of single nucleotide polymorphisms (SNPs) of MD-1 and asthma in the Taiwanese population.

METHODS

Genotyping 34 SNPs in the MD-1 gene region was performed in a case-control study involving 281 children with asthma and 237 controls. A further 309 children and adults were genotyped for the SNP rs7740529 only, for validation of an identified association.

RESULTS

In intron 1, we identified an SNP, rs7740529, which is associated with asthma in Taiwanese children (p=0.0358). Inclusion of a further 309 subjects increased the significance of the association (p=0.0093), and also demonstrated that rs7740529 is associated with adult asthma. The TT genotype confers risk of both pediatric and adult asthma.

CONCLUSION

These results suggest that MD-1 could be a susceptible gene for asthma in the Taiwanese population.

摘要

背景与目的

髓样分化蛋白1(MD-1;也称为Ly86,淋巴细胞抗原86)与辐射防护蛋白105相互作用,在Toll样受体4信号通路中发挥重要作用。有研究表明,MD-1参与炎症和特应性疾病的发生发展。本研究旨在探讨台湾人群中MD-1单核苷酸多态性(SNP)与哮喘的遗传关联。

方法

在一项病例对照研究中,对281例哮喘儿童和237例对照进行了MD-1基因区域34个SNP的基因分型。另外309名儿童和成人仅对SNP rs7740529进行基因分型,以验证已确定的关联。

结果

在内含子1中,我们鉴定出一个SNP,rs7740529,它与台湾儿童哮喘相关(p=0.0358)。纳入另外309名受试者增加了关联的显著性(p=0.0093),并且还表明rs7740529与成人哮喘相关。TT基因型赋予儿童和成人哮喘风险。

结论

这些结果表明,MD-1可能是台湾人群中哮喘的易感基因。

相似文献

1
Association of single nucleotide polymorphisms of MD-1 gene with pediatric and adult asthma in the Taiwanese population.台湾人群中MD-1基因单核苷酸多态性与儿童及成人哮喘的关联。
J Microbiol Immunol Infect. 2008 Dec;41(6):445-9.
2
Single nucleotide polymorphisms and haplotype of MD-1 gene associated with high serum IgE phenotype with mite-sensitive allergy in Taiwanese children.台湾儿童中与螨敏感型过敏高血清IgE表型相关的MD-1基因单核苷酸多态性及单倍型
Int J Immunogenet. 2007 Dec;34(6):407-12. doi: 10.1111/j.1744-313X.2007.00711.x.
3
The polymorphisms of interleukin 17A (IL17A) gene and its association with pediatric asthma in Taiwanese population.台湾人群中白细胞介素17A(IL17A)基因多态性及其与小儿哮喘的关联。
Allergy. 2009 Jul;64(7):1056-60. doi: 10.1111/j.1398-9995.2009.01950.x. Epub 2009 Feb 5.
4
Tumor necrosis factor-alpha is a common genetic risk factor for asthma, juvenile rheumatoid arthritis, and systemic lupus erythematosus in a Mexican pediatric population.肿瘤坏死因子-α是墨西哥儿科人群中哮喘、青少年类风湿性关节炎和系统性红斑狼疮的常见遗传风险因素。
Hum Immunol. 2009 Apr;70(4):251-6. doi: 10.1016/j.humimm.2009.01.027. Epub 2009 Feb 4.
5
TBX21 gene variants increase childhood asthma risk in combination with HLX1 variants.TBX21基因变异与HLX1变异共同作用会增加儿童患哮喘的风险。
J Allergy Clin Immunol. 2009 May;123(5):1062-8, 1068.e1-8. doi: 10.1016/j.jaci.2009.02.025. Epub 2009 Apr 10.
6
[Association of single nucleotide polymorphisms of MD-1 gene with asthma in adults of Han Nationality in Southern China].[中国南方汉族成年人中MD-1基因单核苷酸多态性与哮喘的关联]
Zhonghua Jie He He Hu Xi Za Zhi. 2011 Feb;34(2):104-8.
7
Toll-like receptor heterodimer variants protect from childhood asthma.Toll样受体异二聚体变体可预防儿童哮喘。
J Allergy Clin Immunol. 2008 Jul;122(1):86-92, 92.e1-8. doi: 10.1016/j.jaci.2008.04.039. Epub 2008 Jun 10.
8
The role of polymorphisms in ADAM33, a disintegrin and metalloprotease 33, in childhood asthma and lung function in two German populations.解整合素金属蛋白酶33(ADAM33)基因多态性在两个德国人群儿童哮喘及肺功能中的作用
Respir Res. 2006 Jun 19;7(1):91. doi: 10.1186/1465-9921-7-91.
9
Association of prostaglandin-endoperoxide synthase 2 gene polymorphisms with asthma and atopy in Chinese children.中国儿童中前列腺素-内过氧化物合酶2基因多态性与哮喘及特应性的关联
Allergy. 2007 Jul;62(7):802-9. doi: 10.1111/j.1398-9995.2007.01400.x.
10
HLX1 gene variants influence the development of childhood asthma.HLX1基因变异影响儿童哮喘的发展。
J Allergy Clin Immunol. 2009 Jan;123(1):82-88.e6. doi: 10.1016/j.jaci.2008.09.047. Epub 2008 Nov 28.

引用本文的文献

1
Meta-analysis of exome array data identifies six novel genetic loci for lung function.外显子组芯片数据的荟萃分析确定了六个影响肺功能的新基因位点。
Wellcome Open Res. 2018 Jan 12;3:4. doi: 10.12688/wellcomeopenres.12583.3. eCollection 2018.
2
Association of Single Nucleotide Polymorphisms in Toll-like Receptor Genes With Asthma Risk: A Systematic Review and Meta-analysis.Toll样受体基因单核苷酸多态性与哮喘风险的关联:一项系统评价和Meta分析。
Allergy Asthma Immunol Res. 2015 Mar;7(2):130-40. doi: 10.4168/aair.2015.7.2.130. Epub 2014 Nov 5.