• 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

阿司匹林不耐受性哮喘中的腺苷脱氨酶和腺苷受体多态性

Adenosine deaminase and adenosine receptor polymorphisms in aspirin-intolerant asthma.

作者信息

Kim Sang-Heon, Kim Yoon-Keun, Park Heung-Woo, Kim Sang-Hoon, Kim Seung-Hyun, Ye Young-Min, Min Kyung-Up, Park Hae-Sim

机构信息

Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Republic of Korea.

出版信息

Respir Med. 2009 Mar;103(3):356-63. doi: 10.1016/j.rmed.2008.10.008. Epub 2008 Nov 18.

DOI:10.1016/j.rmed.2008.10.008
PMID:19019667
Abstract

In asthmatic airways, adenosine is a potent bronchoconstrictor with either pro- or anti-inflammatory effects depending on receptor interactions. While aspirin has been suggested to mediate adenosine action, the roles of adenosine and its receptors in aspirin-intolerant asthma (AIA) are not well-defined. Therefore, we evaluated associations between genetic polymorphisms of adenosine deaminase and the four adenosine receptors (A(1), A(2A), A(2B), and A(3)) with the AIA phenotype. The genes for adenosine deaminase (ADA) and the four adenosine receptors (ADORA1, ADORA2A, ADORA2B, and ADORA3) were screened by direct sequencing, and 13 single nucleotide polymorphisms (SNPs) were selected among 23 polymorphisms. Using multivariate logistic regression analysis, we compared the frequencies of SNP genotypes and haplotypes among 136 patients with AIA, 181 patients with aspirin-tolerant asthma (ATA), and 183 normal individuals. We found significant differences between normal and patients with AIA in the ADORA1 SNP genotype frequencies for 1405C>T (P=0.001) and A102A (P=0.013). No other significant associations were detected for the other SNPs. In the haplotype analysis, ht[C-T-G] (P=0.003) and ht[A-C-G] (P=0.032) in ADORA1 and ht[A-T] in ADORA2 (P=0.013) were significantly associated with AIA. Genetic polymorphisms of adenosine receptors A(1) and A(2A) were associated with AIA, suggesting that adenosine might play a crucial role in the development of AIA through interactions with the A(1) and A(2A) receptors.

摘要

在哮喘气道中,腺苷是一种强效支气管收缩剂,根据受体相互作用具有促炎或抗炎作用。虽然有人提出阿司匹林可介导腺苷作用,但腺苷及其受体在阿司匹林不耐受性哮喘(AIA)中的作用尚不清楚。因此,我们评估了腺苷脱氨酶和四种腺苷受体(A(1)、A(2A)、A(2B)和A(3))的基因多态性与AIA表型之间的关联。通过直接测序对腺苷脱氨酶(ADA)和四种腺苷受体(ADORA1、ADORA2A、ADORA2B和ADORA3)的基因进行筛选,在23个多态性位点中选择了13个单核苷酸多态性(SNP)。使用多因素逻辑回归分析,我们比较了136例AIA患者、181例阿司匹林耐受哮喘(ATA)患者和183例正常个体中SNP基因型和单倍型的频率。我们发现,在ADORA1 SNP基因型频率方面,正常人与AIA患者在1405C>T(P=0.001)和A102A(P=0.013)存在显著差异。其他SNP未检测到其他显著关联。在单倍型分析中,ADORA1中的ht[C-T-G](P=0.003)和ht[A-C-G](P=0.032)以及ADORA2中的ht[A-T](P=0.013)与AIA显著相关。腺苷受体A(1)和A(2A)的基因多态性与AIA相关,表明腺苷可能通过与A(1)和A(2A)受体相互作用在AIA的发生发展中起关键作用。

相似文献

1
Adenosine deaminase and adenosine receptor polymorphisms in aspirin-intolerant asthma.阿司匹林不耐受性哮喘中的腺苷脱氨酶和腺苷受体多态性
Respir Med. 2009 Mar;103(3):356-63. doi: 10.1016/j.rmed.2008.10.008. Epub 2008 Nov 18.
2
Cysteinyl leukotriene receptor 1 promoter polymorphism is associated with aspirin-intolerant asthma in males.半胱氨酰白三烯受体1启动子多态性与男性阿司匹林不耐受性哮喘相关。
Clin Exp Allergy. 2006 Apr;36(4):433-9. doi: 10.1111/j.1365-2222.2006.02457.x.
3
Association of three sets of high-affinity IgE receptor (FcepsilonR1) polymorphisms with aspirin-intolerant asthma.三组高亲和力IgE受体(FcepsilonR1)多态性与阿司匹林不耐受性哮喘的关联。
Respir Med. 2008 Aug;102(8):1132-9. doi: 10.1016/j.rmed.2008.03.017. Epub 2008 Jul 1.
4
Association between polymorphisms in prostanoid receptor genes and aspirin-intolerant asthma.前列腺素受体基因多态性与阿司匹林不耐受性哮喘之间的关联。
Pharmacogenet Genomics. 2007 Apr;17(4):295-304. doi: 10.1097/01.fpc.0000239977.61841.fe.
5
Association of angiotensin I-converting enzyme gene polymorphisms with aspirin intolerance in asthmatics.血管紧张素I转换酶基因多态性与哮喘患者阿司匹林不耐受的关联
Clin Exp Allergy. 2008 Nov;38(11):1727-37. doi: 10.1111/j.1365-2222.2008.03082.x. Epub 2008 Aug 24.
6
Gene-expression profiles in human nasal polyp tissues and identification of genetic susceptibility in aspirin-intolerant asthma.人类鼻息肉组织中的基因表达谱及阿司匹林不耐受性哮喘遗传易感性的鉴定
Clin Exp Allergy. 2009 Jul;39(7):972-81. doi: 10.1111/j.1365-2222.2009.03229.x. Epub 2009 Mar 27.
7
A polymorphism of MS4A2 (- 109T > C) encoding the beta-chain of the high-affinity immunoglobulin E receptor (FcepsilonR1beta) is associated with a susceptibility to aspirin-intolerant asthma.编码高亲和力免疫球蛋白E受体(FcepsilonR1β)β链的MS4A2基因多态性(-109T>C)与阿司匹林不耐受性哮喘易感性相关。
Clin Exp Allergy. 2006 Jul;36(7):877-83. doi: 10.1111/j.1365-2222.2006.02443.x.
8
Association of thromboxane A2 receptor gene polymorphism with the phenotype of acetyl salicylic acid-intolerant asthma.血栓素A2受体基因多态性与阿司匹林不耐受性哮喘表型的关联
Clin Exp Allergy. 2005 May;35(5):585-90. doi: 10.1111/j.1365-2222.2005.02220.x.
9
Polymorphisms in the prostaglandin E2 receptor subtype 2 gene confer susceptibility to aspirin-intolerant asthma: a candidate gene approach.前列腺素E2受体2型基因多态性赋予阿司匹林不耐受性哮喘易感性:一种候选基因研究方法。
Hum Mol Genet. 2004 Dec 15;13(24):3203-17. doi: 10.1093/hmg/ddh332. Epub 2004 Oct 20.
10
Association of TNF-alpha genetic polymorphism with HLA DPB1*0301.肿瘤坏死因子-α基因多态性与人类白细胞抗原DPB1*0301的关联。
Clin Exp Allergy. 2006 Oct;36(10):1247-53. doi: 10.1111/j.1365-2222.2006.02567.x.

引用本文的文献

1
In-silico identification and prioritization of therapeutic targets of asthma.计算机辅助鉴定和优先考虑哮喘的治疗靶点。
Sci Rep. 2023 Sep 21;13(1):15706. doi: 10.1038/s41598-023-42803-w.
2
ACDC: a general approach for detecting phenotype or exposure associated co-expression.ACDC:一种检测与表型或暴露相关的共表达的通用方法。
Front Med (Lausanne). 2023 May 19;10:1118824. doi: 10.3389/fmed.2023.1118824. eCollection 2023.
3
A Biomedical Knowledge Graph System to Propose Mechanistic Hypotheses for Real-World Environmental Health Observations: Cohort Study and Informatics Application.
一个用于为实际环境健康观察提出机制假设的生物医学知识图谱系统:队列研究与信息学应用
JMIR Med Inform. 2021 Jul 20;9(7):e26714. doi: 10.2196/26714.
4
Pharmacogenomics of Hypersensitivity to Non-steroidal Anti-inflammatory Drugs.非甾体抗炎药超敏反应的药物基因组学
Front Genet. 2021 Jun 25;12:647257. doi: 10.3389/fgene.2021.647257. eCollection 2021.
5
Adenosine Signaling in Mast Cells and Allergic Diseases.腺苷信号在肥大细胞和过敏性疾病中的作用。
Int J Mol Sci. 2021 May 14;22(10):5203. doi: 10.3390/ijms22105203.
6
Immune-Mediated Mechanisms in Cofactor-Dependent Food Allergy and Anaphylaxis: Effect of Cofactors in Basophils and Mast Cells.依赖共因子的食物过敏和过敏反应中的免疫介导机制:在嗜碱性粒细胞和肥大细胞中共同因子的作用。
Front Immunol. 2021 Feb 17;11:623071. doi: 10.3389/fimmu.2020.623071. eCollection 2020.
7
Analysis of association of ADORAA and ADORA polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis.分析 ADORAA 和 ADORA 多态性基因型/单倍型与甲氨蝶呤治疗类风湿关节炎患者疗效和毒性的关系。
Pharmacogenomics J. 2020 Dec;20(6):784-791. doi: 10.1038/s41397-020-0168-z. Epub 2020 May 24.
8
Single Nucleotide and Copy-Number Variants in IL4 and IL13 Are Not Associated with Asthma Susceptibility or Inflammatory Markers: A Case-Control Study in a Mexican-Mestizo Population.白细胞介素4和白细胞介素13中的单核苷酸和拷贝数变异与哮喘易感性或炎症标志物无关:墨西哥梅斯蒂索人群的病例对照研究。
Diagnostics (Basel). 2020 Apr 30;10(5):273. doi: 10.3390/diagnostics10050273.
9
The Polymorphism in Decreases Transcriptional Activity and Influences the Chronic Heart Failure Risk in the Chinese.在中国人群中, 多态性降低转录活性并影响慢性心力衰竭的风险。
Biomed Res Int. 2018 May 31;2018:4969385. doi: 10.1155/2018/4969385. eCollection 2018.
10
Association analysis of ILVBL gene polymorphisms with aspirin-exacerbated respiratory disease in asthma.白细胞介素结合蛋白基因多态性与哮喘阿司匹林加重性呼吸道疾病的相关性分析。
BMC Pulm Med. 2017 Dec 16;17(1):210. doi: 10.1186/s12890-017-0556-6.