• 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

俄罗斯族人群中FOXC2基因附近多态性与静脉曲张风险的关联

Association of polymorphisms near the FOXC2 gene with the risk of varicose veins in ethnic Russians.

作者信息

Shadrina Alexandra S, Smetanina Mariya A, Sokolova Ekaterina A, Sevost'ianova Kseniya S, Shevela Andrey I, Demekhova Marina Y, Shonov Oleg A, Ilyukhin Evgenii A, Voronina Elena N, Zolotukhin Igor A, Kirienko Alexander I, Filipenko Maxim L

机构信息

Institute of Chemical Biology and Fundamental Medicine, Novosibirsk, Russia Novosibirsk State University, Novosibirsk, Russia

Institute of Chemical Biology and Fundamental Medicine, Novosibirsk, Russia.

出版信息

Phlebology. 2016 Oct;31(9):640-8. doi: 10.1177/0268355515607404. Epub 2015 Sep 28.

DOI:10.1177/0268355515607404
PMID:26420053
Abstract

OBJECTIVE

To investigate the association of polymorphisms located near the FOXC2 gene with the risk of varicose veins in ethnic Russians.

METHODS

Allele, genotype, and haplotype frequencies were determined in the sample of 474 patients with primary varicose veins and in the control group of 478 individuals without a history of chronic venous disease.

RESULTS

Polymorphisms rs7189489, rs4633732, and rs1035550 showed the association with the increased risk of varicose veins, but none of the observed associations remained significant after correction for multiple testing. Haplotype analysis revealed the association of haplotype rs7189489 C-rs4633732 T-rs34221221 C-rs1035550 C-rs34152738 T-rs12711457 G with the increased risk of varicose veins (OR = 2.67, P = 0.01).

CONCLUSIONS

Our results provide evidence that the studied polymorphisms do not play a major role in susceptibility to varicose veins development in the Russian population.

摘要

目的

研究俄罗斯族人群中FOXC2基因附近的多态性与静脉曲张风险的关联。

方法

在474例原发性静脉曲张患者样本以及478例无慢性静脉疾病病史个体的对照组中,测定等位基因、基因型和单倍型频率。

结果

多态性位点rs7189489、rs4633732和rs1035550显示与静脉曲张风险增加有关,但在多重检验校正后,观察到的关联均无统计学意义。单倍型分析显示单倍型rs7189489 C-rs4633732 T-rs34221221 C-rs1035550 C-rs34152738 T-rs12711457 G与静脉曲张风险增加有关(OR = 2.67,P = 0.01)。

结论

我们的结果表明,所研究的多态性在俄罗斯人群静脉曲张易感性中不起主要作用。

相似文献

1
Association of polymorphisms near the FOXC2 gene with the risk of varicose veins in ethnic Russians.俄罗斯族人群中FOXC2基因附近多态性与静脉曲张风险的关联
Phlebology. 2016 Oct;31(9):640-8. doi: 10.1177/0268355515607404. Epub 2015 Sep 28.
2
Allele rs2010963 C of the VEGFA gene is associated with the decreased risk of primary varicose veins in ethnic Russians.血管内皮生长因子A(VEGFA)基因的rs2010963 C等位基因与俄罗斯族原发性静脉曲张风险降低相关。
Phlebology. 2018 Feb;33(1):27-35. doi: 10.1177/0268355516683611. Epub 2016 Dec 8.
3
Polymorphisms in inflammation-related genes and the risk of primary varicose veins in ethnic Russians.炎症相关基因多态性与俄罗斯族原发性静脉曲张风险的关系。
Immunol Res. 2018 Feb;66(1):141-150. doi: 10.1007/s12026-017-8981-4.
4
Polymorphic Variants rs13155212 (T/C) and rs7704267 (G/C) in the AGGF1 Gene and Risk of Varicose Veins of the Lower Extremities in the Population of Ethnic Russians.俄罗斯族人群中AGGF1基因多态性变异rs13155212(T/C)和rs7704267(G/C)与下肢静脉曲张风险的关系
Bull Exp Biol Med. 2016 Sep;161(5):698-702. doi: 10.1007/s10517-016-3488-x. Epub 2016 Oct 4.
5
Polymorphisms in the MTHFR and MTR genes and the risk of varicose veins in ethnical Russians.MTHFR和MTR基因多态性与俄罗斯族人群静脉曲张风险
Biomarkers. 2016 Nov;21(7):619-24. doi: 10.3109/1354750X.2016.1171902. Epub 2016 Apr 21.
6
HFE p.C282Y gene variant is associated with varicose veins in Russian population.HFE p.C282Y基因变异与俄罗斯人群的静脉曲张有关。
Clin Exp Med. 2016 Aug;16(3):463-70. doi: 10.1007/s10238-015-0377-y. Epub 2015 Sep 28.
7
Genome-wide association study in ethnic Russians suggests an association of the MHC class III genomic region with the risk of primary varicose veins.全基因组关联研究在俄罗斯族群中提示 MHC Ⅲ类基因组区域与原发性静脉曲张风险之间存在关联。
Gene. 2018 Jun 15;659:93-99. doi: 10.1016/j.gene.2018.03.039. Epub 2018 Mar 15.
8
Functional polymorphism rs1024611 in the MCP1 gene is associated with the risk of varicose veins of lower extremities.功能性多态性 rs1024611 位于 MCP1 基因中,与下肢静脉曲张的风险相关。
J Vasc Surg Venous Lymphat Disord. 2017 Jul;5(4):561-566. doi: 10.1016/j.jvsv.2016.12.008. Epub 2017 Feb 20.
9
Forkhead box C2 promoter variant c.-512C>T is associated with increased susceptibility to chronic venous diseases.叉头框C2启动子变体c.-512C>T与慢性静脉疾病易感性增加相关。
PLoS One. 2014 Mar 7;9(3):e90682. doi: 10.1371/journal.pone.0090682. eCollection 2014.
10
Polymorphism of Matrix Metalloproteinases Genes MMP1, MMP2, MMP3, and MMP7 and the Risk of Varicose Veins of Lower Extremities.基质金属蛋白酶基因MMP1、MMP2、MMP3和MMP7的多态性与下肢静脉曲张风险
Bull Exp Biol Med. 2017 Sep;163(5):650-654. doi: 10.1007/s10517-017-3871-2. Epub 2017 Sep 25.

引用本文的文献

1
Molecular Determinants of Chronic Venous Disease: A Comprehensive Review.慢性静脉疾病的分子决定因素:全面综述。
Int J Mol Sci. 2023 Jan 18;24(3):1928. doi: 10.3390/ijms24031928.
2
Microdeletion of 16q24.1-q24.2-A unique etiology of Lymphedema-Distichiasis syndrome and neurodevelopmental disorder.16q24.1-q24.2 微缺失——淋巴水肿-并指(趾)畸形综合征和神经发育障碍的独特病因。
Am J Med Genet A. 2022 Jul;188(7):1990-1996. doi: 10.1002/ajmg.a.62730. Epub 2022 Mar 21.