• 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

Atherosclerosis and PTPN22: a study in coronary artery disease.

作者信息

Saccucci P, Banci M, Cozzoli E, Neri A, Magrini A, Bottini E, Gloria-Bottini F

机构信息

Department of Biopathology and Imaging Diagnostics, University of Rome Tor Vergata, Rome, Italy.

出版信息

Cardiology. 2011;119(1):54-6. doi: 10.1159/000329919. Epub 2011 Aug 12.

DOI:10.1159/000329919
PMID:21846984
Abstract

OBJECTIVES

Recently, it has been shown that PTPN22 genetic polymorphism is associated with phenotypes related to the risk of atherosclerosis. In the present note, we have searched for a possible association of PTPN22 polymorphism with coronary artery disease (CAD).

METHODS

One hundred and thirty-four non-diabetic subjects admitted to hospital for CAD and 174 healthy subjects (blood donors) were studied. PTPN22 genotypes were determined by DNA analysis. Statistical analyses were performed by SPSS programs.

RESULTS

In CAD patients, the proportion of carriers of the *T allele of PTPN22 is significantly higher compared to healthy controls (OR 2.66; 95% CI 1.07-6.72).

CONCLUSIONS

The present observation confirms the association of PTPN22 phenotype with atherosclerosis and suggests a role of immune mechanism in the pathogenesis of CAD.

摘要

相似文献

1
Atherosclerosis and PTPN22: a study in coronary artery disease.
Cardiology. 2011;119(1):54-6. doi: 10.1159/000329919. Epub 2011 Aug 12.
2
Coronary artery disease: evidence of interaction between PTPN22 and p53 genetic polymorphisms.冠状动脉疾病:PTPN22与p53基因多态性之间相互作用的证据。
Cardiology. 2011;120(3):166-8. doi: 10.1159/000334808. Epub 2011 Dec 29.
3
Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma.蛋白酪氨酸磷酸酶非受体型22(PTPN22)单核苷酸多态性与类风湿性关节炎相关,但与过敏性哮喘无关。
Eur J Hum Genet. 2007 Oct;15(10):1043-8. doi: 10.1038/sj.ejhg.5201879. Epub 2007 Jun 20.
4
Gender-specific association of the PTPN22 C1858T polymorphism with achalasia.蛋白酪氨酸磷酸酶非受体型22(PTPN22)基因C1858T多态性与贲门失弛缓症的性别特异性关联。
Hum Immunol. 2007 Oct;68(10):867-70. doi: 10.1016/j.humimm.2007.07.005. Epub 2007 Aug 28.
5
Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset.波兰人群中淋巴样酪氨酸磷酸酶(PTPN22/LYP)变异与格雷夫斯病:与发病年龄的关联及基因剂量依赖性相关性
Clin Endocrinol (Oxf). 2005 Jun;62(6):679-82. doi: 10.1111/j.1365-2265.2005.02279.x.
6
Genetic variant in visfatin gene promoter is associated with decreased risk of coronary artery disease in a Chinese population.中国人群中内脂素基因启动子区遗传变异与冠心病发病风险降低相关。
Clin Chim Acta. 2010 Jan;411(1-2):26-30. doi: 10.1016/j.cca.2009.09.033. Epub 2009 Oct 3.
7
The protein tyrosine phosphatase nonreceptor 22 (PTPN22) is associated with high GAD antibody titer in latent autoimmune diabetes in adults: Non Insulin Requiring Autoimmune Diabetes (NIRAD) Study 3.蛋白酪氨酸磷酸酶非受体22(PTPN22)与成人隐匿性自身免疫性糖尿病患者的谷氨酸脱羧酶抗体高滴度相关:非胰岛素依赖型自身免疫性糖尿病(NIRAD)研究3。
Diabetes Care. 2008 Mar;31(3):534-8. doi: 10.2337/dc07-1457. Epub 2007 Dec 4.
8
The presence of apolipoprotein epsilon4 and epsilon2 alleles augments the risk of coronary artery disease in type 2 diabetic patients.载脂蛋白ε4和ε2等位基因的存在会增加2型糖尿病患者患冠状动脉疾病的风险。
Clin Biochem. 2007 Oct;40(15):1150-6. doi: 10.1016/j.clinbiochem.2007.06.010. Epub 2007 Jul 6.
9
The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population.突尼斯人群中蛋白酪氨酸磷酸酶22基因R620W多态性与自身免疫性甲状腺疾病及类风湿关节炎的关系
Ann Hum Biol. 2009 May-Jun;36(3):342-9. doi: 10.1080/03014460902817968.
10
[Association of polymorphism of protein tyrosine phosphatase nonreceptor-22 gene with AITD].蛋白酪氨酸磷酸酶非受体22基因多态性与自身免疫性甲状腺疾病的关联
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2008 Aug;24(8):804-7.

引用本文的文献

1
Peel: A Promising Source of Nutraceutical for the Mitigation of Cardiovascular Risk in Arthritic Rats Through the Gut-Joint Axis.果皮:通过肠-关节轴减轻关节炎大鼠心血管风险的营养保健品的潜在来源。
Biomolecules. 2025 Apr 16;15(4):590. doi: 10.3390/biom15040590.
2
Targeted inhibition of PTPN22 is a novel approach to alleviate osteogenic responses in aortic valve interstitial cells and aortic valve lesions in mice.靶向抑制 PTPN22 可减轻小鼠主动脉瓣间质细胞成骨反应和主动脉瓣病变。
BMC Med. 2023 Jul 13;21(1):252. doi: 10.1186/s12916-023-02888-6.
3
Gene Polymorphisms Are Associated with Susceptibility to Large Artery Atherosclerotic Stroke and Microembolic Signals.
基因多态性与大动脉粥样硬化性卒中及微栓子信号易感性相关。
Dis Markers. 2019 May 5;2019:2193835. doi: 10.1155/2019/2193835. eCollection 2019.
4
Protein tyrosine phosphatase non-receptor 22 and C-Src tyrosine kinase genes are down-regulated in patients with rheumatoid arthritis.蛋白酪氨酸磷酸酶非受体 22 和 C-Src 酪氨酸激酶基因在类风湿关节炎患者中下调。
Sci Rep. 2017 Sep 5;7(1):10525. doi: 10.1038/s41598-017-10915-9.
5
Association between phosphatase related gene variants and coronary artery disease: case-control study and meta-analysis.磷酸酶相关基因变异与冠状动脉疾病之间的关联:病例对照研究与荟萃分析。
Int J Mol Sci. 2014 Aug 13;15(8):14058-76. doi: 10.3390/ijms150814058.
6
Coherent somatic mutation in autoimmune disease.自身免疫性疾病中的一致性体细胞突变。
PLoS One. 2014 Jul 2;9(7):e101093. doi: 10.1371/journal.pone.0101093. eCollection 2014.
7
Effect of genetic factors on the association between coronary artery disease and PTPN22 polymorphism.遗传因素对冠状动脉疾病与蛋白酪氨酸磷酸酶非受体型22(PTPN22)基因多态性之间关联的影响。
World J Cardiol. 2014 Jun 26;6(6):376-80. doi: 10.4330/wjc.v6.i6.376.