• 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

肿瘤坏死因子超家族成员4(TNFSF4)基因多态性(rs3850641和rs17568)与冠心病和中风的关联性缺失:一项系统综述和荟萃分析

Lack of association of tumor necrosis factor superfamily member 4 (TNFSF4) gene polymorphisms (rs3850641 and rs17568) with coronary heart disease and stroke: A systematic review and meta-analysis.

作者信息

Lu Jin Sen, Wang Hong, Yuan Fei Fei, Wu Le Le, Wang Bin, Ye Dong Qing

机构信息

Anhui Province Key Laboratory of Major Autoimmune Diseases; Anhui- P. R. China.

出版信息

Anatol J Cardiol. 2018 Feb;19(2):86-93. doi: 10.14744/AnatolJCardiol.2017.8069.

DOI:10.14744/AnatolJCardiol.2017.8069
PMID:29424751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5864823/
Abstract

OBJECTIVE

To evaluate the association between the tumor necrosis factor superfamily member 4 (TNFSF4) gene polymorphisms and common cardiovascular and cerebrovascular diseases.

METHODS

A literature-based search was conducted through databases including PubMed, EMBASE, Cochrane Library, CNKI, and WanFang data. Crude odds ratios (ORs) and 95% confidence intervals (CI) were calculated to estimate the strength of the association between TNFSF4 polymorphisms (rs3850641 and rs17568) and the risk of coronary heart disease (CHD) and stroke.

RESULTS

Overall, 11 eligible studies were included in this meta-analysis. G allele was showed not to be associated with CHD and stroke, compared with A allele (rs3850641: OR=1.02, 95% CI=0.89-1.17; rs17568: OR=1.09, 95% CI=0.89-1.33). Genotypic analysis demonstrated that there was no significant association between the risk of CHD and stroke and rs3850641 [homozygous comparison (GG vs. AA): OR=1.05, 95% CI=0.74-1.50; heterozygous comparison (GA vs. AA): OR=1.00, 95% CI=0.88-1.13; recessive model (GG vs. GA+AA): OR=1.04, 95% CI=0.76-1.43; dominant model (GG+GA vs. AA): OR=1.01, 95% CI=0.88-1.17]. Similarly, no susceptibility between CHD and stroke and rs17568 polymorphism was uncovered (GG vs. AA: OR=1.04, 95% CI=0.74-1.46; GA vs. AA: OR=1.07, 95% CI=0.62-1.83; GG+GA vs. AA: OR=1.13, 95% CI=0.82-1.56; GG vs. GA+AA: OR=1.01, 95% CI=0.74-1.39).

CONCLUSION

The present study demonstrated that there is no significant relationship between TNFSF4 gene polymorphism and cerebrovascular and cardiovascular diseases.

摘要

目的

评估肿瘤坏死因子超家族成员4(TNFSF4)基因多态性与常见心脑血管疾病之间的关联。

方法

通过PubMed、EMBASE、Cochrane图书馆、中国知网和万方数据等数据库进行基于文献的检索。计算粗比值比(OR)和95%置信区间(CI),以估计TNFSF4多态性(rs3850641和rs17568)与冠心病(CHD)和中风风险之间关联的强度。

结果

总体而言,本荟萃分析纳入了11项符合条件的研究。与A等位基因相比,G等位基因与冠心病和中风无关(rs3850641:OR = 1.02,95% CI = 0.89 - 1.17;rs17568:OR = 1.09,95% CI = 0.89 - 1.33)。基因型分析表明,冠心病和中风风险与rs3850641之间无显著关联[纯合子比较(GG vs. AA):OR = 1.05,95% CI = 0.74 - 1.50;杂合子比较(GA vs. AA):OR = 1.00,95% CI = 0.88 - 1.1;隐性模型(GG vs. GA + AA):OR = 1.04,95% CI = 0.76 - 1.43;显性模型(GG + GA vs. AA):OR = 1.01,95% CI = 0.88 - 1.17]。同样,未发现冠心病和中风与rs17568多态性之间存在易感性(GG vs. AA:OR = 1.04,95% CI = 0.74 - 1.46;GA vs. AA:OR = 1.07,95% CI = 0.62 - 1.83;GG + GA vs. AA:OR = 1.13,95% CI = 0.82 - 1.56;GG vs. GA + AA:OR = 1.01,95% CI = 0.74 - 1.39)。

结论

本研究表明,TNFSF4基因多态性与脑血管和心血管疾病之间无显著关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/2eeef15c4e0a/AJC-19-86-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/5ff4ac0721e4/AJC-19-86-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/5f81ec3a824b/AJC-19-86-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/c00050f4d187/AJC-19-86-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/54da67570bde/AJC-19-86-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/2183d5445fc5/AJC-19-86-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/f31b5a263d5f/AJC-19-86-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/368c17351079/AJC-19-86-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/2eeef15c4e0a/AJC-19-86-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/5ff4ac0721e4/AJC-19-86-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/5f81ec3a824b/AJC-19-86-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/c00050f4d187/AJC-19-86-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/54da67570bde/AJC-19-86-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/2183d5445fc5/AJC-19-86-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/f31b5a263d5f/AJC-19-86-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/368c17351079/AJC-19-86-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/5864823/2eeef15c4e0a/AJC-19-86-g008.jpg

相似文献

1
Lack of association of tumor necrosis factor superfamily member 4 (TNFSF4) gene polymorphisms (rs3850641 and rs17568) with coronary heart disease and stroke: A systematic review and meta-analysis.肿瘤坏死因子超家族成员4(TNFSF4)基因多态性(rs3850641和rs17568)与冠心病和中风的关联性缺失:一项系统综述和荟萃分析
Anatol J Cardiol. 2018 Feb;19(2):86-93. doi: 10.14744/AnatolJCardiol.2017.8069.
2
Association of TNFSF4 (rs3850641) gene polymorphisms and coronary heart disease: an evidence-based meta-analysis.TNFSF4(rs3850641)基因多态性与冠心病的关联:一项基于证据的荟萃分析。
Int J Clin Pharmacol Ther. 2016 May;54(5):354-61. doi: 10.5414/CP202571.
3
The effect of single nucleotide polymorphisms on depression in combination with coronary diseases: a systematic review and meta-analysis.单核苷酸多态性对合并冠心病的抑郁症的影响:系统评价和荟萃分析。
Front Endocrinol (Lausanne). 2024 Apr 30;15:1369676. doi: 10.3389/fendo.2024.1369676. eCollection 2024.
4
The rs3850641 polymorphism of the TNFSF4 gene increases the risk of myocardial infarction in a Chinese Han population.rs3850641 基因座的 TNFSF4 多态性增加了汉族人群心肌梗死的发病风险。
Biosci Rep. 2018 Jul 12;38(4). doi: 10.1042/BSR20180526. Print 2018 Aug 31.
5
rs1234313 and rs45454293 are risk factors of cerebral arterial thrombosis, large artery atherosclerosis, and carotid plaque in the Han Chinese population: a case-control study.rs1234313 和 rs45454293 是汉族人群脑动脉血栓形成、大动脉粥样硬化和颈动脉斑块的危险因素:一项病例对照研究。
BMC Neurol. 2019 Feb 23;19(1):31. doi: 10.1186/s12883-019-1259-9.
6
Association of TNFSF4 Gene Polymorphisms and Plasma TNFSF4 Level with Risk of Systemic Lupus Erythematosus in a Chinese Population.中国人群中 TNFSF4 基因多态性与血浆 TNFSF4 水平与系统性红斑狼疮风险的关联。
Immunol Invest. 2022 Feb;51(2):316-330. doi: 10.1080/08820139.2020.1828912. Epub 2020 Nov 9.
7
Association between ATM rs1801516 polymorphism and cancer susceptibility: a meta-analysis involving 12,879 cases and 18,054 controls.ATM rs1801516 多态性与癌症易感性的关联:一项包含 12879 例病例和 18054 例对照的荟萃分析。
BMC Cancer. 2018 Nov 1;18(1):1060. doi: 10.1186/s12885-018-4941-1.
8
C-reactive Protein -717A>G and -286C>T>A Gene Polymorphism and Ischemic Stroke.C反应蛋白-717A>G和-286C>T>A基因多态性与缺血性脑卒中
Chin Med J (Engl). 2015 Jun 20;128(12):1666-70. doi: 10.4103/0366-6999.158371.
9
Association of transferrin G258A and transferrin receptor A82G polymorphisms with the risk of Parkinson disease in certain area.转铁蛋白G258A和转铁蛋白受体A82G基因多态性与某地区帕金森病风险的关联
Medicine (Baltimore). 2020 Nov 25;99(48):e23432. doi: 10.1097/MD.0000000000023432.
10
TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese population.TNFSF4 基因多态性 rs3861950 但不是 rs3850641 与中国人群脑梗死的风险相关。
J Thromb Thrombolysis. 2013 Oct;36(3):307-13. doi: 10.1007/s11239-012-0849-9.

本文引用的文献

1
Epidemiology of coronary heart disease and acute coronary syndrome.冠心病和急性冠脉综合征的流行病学。
Ann Transl Med. 2016 Jul;4(13):256. doi: 10.21037/atm.2016.06.33.
2
Association of six CpG-SNPs in the inflammation-related genes with coronary heart disease.炎症相关基因中六个CpG单核苷酸多态性与冠心病的关联
Hum Genomics. 2016 Jul 25;10 Suppl 2(Suppl 2):21. doi: 10.1186/s40246-016-0067-1.
3
Association of TNFSF4 (rs3850641) gene polymorphisms and coronary heart disease: an evidence-based meta-analysis.TNFSF4(rs3850641)基因多态性与冠心病的关联:一项基于证据的荟萃分析。
Int J Clin Pharmacol Ther. 2016 May;54(5):354-61. doi: 10.5414/CP202571.
4
[Association between tumor necrosis factor superfamily member 4 gene polymorphism and risk of asymptomatic carotid vulnerable plaque in a Chinese population].[肿瘤坏死因子超家族成员4基因多态性与中国人群无症状性颈动脉易损斑块风险的关联]
Zhonghua Liu Xing Bing Xue Za Zhi. 2015 Sep;36(9):998-1001.
5
Executive Summary: Heart Disease and Stroke Statistics--2016 Update: A Report From the American Heart Association.执行摘要:《2016年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2016 Jan 26;133(4):447-54. doi: 10.1161/CIR.0000000000000366.
6
Lack of Association Between rs17568 Polymorphism in OX40 Gene and Myocardial Infarction, Southern of Iran.伊朗南部OX40基因rs17568多态性与心肌梗死之间不存在关联。
Glob J Health Sci. 2015 Sep 28;8(6):41-6. doi: 10.5539/gjhs.v8n6p41.
7
Predictors of coronary heart disease in Japanese patients with type 2 diabetes: Screening for coronary artery stenosis using multidetector computed tomography.日本 2 型糖尿病患者冠心病的预测因素:多排螺旋 CT 筛查冠状动脉狭窄
J Diabetes Investig. 2010 Apr 22;1(1-2):50-5. doi: 10.1111/j.2040-1124.2009.00003.x.
8
Absence of association between atherosclerotic cerebral infarction and TNFSF4/TNFRSF4 single nucleotide polymorphisms rs1234313, rs1234314 and rs17568 in a Chinese population.中国人群中动脉粥样硬化性脑梗死与TNFSF4/TNFRSF4单核苷酸多态性rs1234313、rs1234314和rs17568之间无关联。
J Int Med Res. 2014 Apr;42(2):436-43. doi: 10.1177/0300060514521154. Epub 2014 Mar 4.
9
Effect of rosuvastatin on OX40L and PPAR-γ expression in human umbilical vein endothelial cells and atherosclerotic cerebral infarction patients.瑞舒伐他汀对人脐静脉内皮细胞及动脉粥样硬化性脑梗死患者OX40L和PPAR-γ表达的影响
J Mol Neurosci. 2014 Feb;52(2):261-8. doi: 10.1007/s12031-013-0134-1. Epub 2013 Oct 27.
10
TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese population.TNFSF4 基因多态性 rs3861950 但不是 rs3850641 与中国人群脑梗死的风险相关。
J Thromb Thrombolysis. 2013 Oct;36(3):307-13. doi: 10.1007/s11239-012-0849-9.