• 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

CYP4F2基因rs2108622多态性与高血压的关联:一项荟萃分析。

Association of the CYP4F2 rs2108622 genetic polymorphism with hypertension: a meta-analysis.

作者信息

Luo X-H, Li G-R, Li H-Y

机构信息

Department of Geriatrics, the Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Railway Vocational and Technical College of Zhengzhou, Zhengzhou, China.

出版信息

Genet Mol Res. 2015 Nov 26;14(4):15133-9. doi: 10.4238/2015.November.25.1.

DOI:10.4238/2015.November.25.1
PMID:26634476
Abstract

Previous case-control studies on the relationship between the CYP4F2 gene rs2108622 polymorphism and hypertension have produced contrasting results. In this study, we aimed to further evaluate the relationship between the CYP4F2 gene rs2108622 polymorphism and hypertension. We selected four case-control studies related to the CYP4F2 gene rs2108622 polymorphism and hypertension by searching PubMed, EMBase, the Chinese Biomedical Literature Database, and the Wanfang database. We utilized the Cochran Q-test and the I2 index to measure the heterogeneity across studies. To merge the odds ratio (OR) and the 95% confidence interval (95%CI), we utilized the fixed and random-effect models during the analyses. The present study included 1878 patients with hypertension and 1512 healthy control subjects. By meta-analysis, we did not find any association of the CYP4F2 gene rs2108622 polymorphism with hypertension in either genotype or allele distribution [AA+AG vs GG: OR = 1.18, 95%CI (0.91-1.54), P = 0.21; GG+AG vs AA: OR = 0.91, 95%CI (0.80-1.05), P = 0.20; A allele vs G allele: OR = 1.04, 95%CI (0.93-1.16), P = 0.53]. We concluded that the CYP4F2 gene rs2108622 polymorphism was not associated with hypertension.

摘要

先前关于CYP4F2基因rs2108622多态性与高血压之间关系的病例对照研究得出了相互矛盾的结果。在本研究中,我们旨在进一步评估CYP4F2基因rs2108622多态性与高血压之间的关系。我们通过检索PubMed、EMBase、中国生物医学文献数据库和万方数据库,选取了四项与CYP4F2基因rs2108622多态性和高血压相关的病例对照研究。我们使用Cochran Q检验和I2指数来衡量各研究间的异质性。为合并比值比(OR)和95%置信区间(95%CI),我们在分析过程中使用了固定效应模型和随机效应模型。本研究纳入了1878例高血压患者和1512例健康对照者。通过荟萃分析,我们发现在基因型或等位基因分布方面,CYP4F2基因rs2108622多态性与高血压均无关联[AA + AG vs GG:OR = 1.18,95%CI(0.91 - 1.54),P = 0.21;GG + AG vs AA:OR = 0.91,95%CI(0.80 - 1.05),P = 0.20;A等位基因vs G等位基因:OR = 1.04,95%CI(0.93 - 1.16),P = 0.53]。我们得出结论,CYP4F2基因rs2108622多态性与高血压无关。

相似文献

1
Association of the CYP4F2 rs2108622 genetic polymorphism with hypertension: a meta-analysis.CYP4F2基因rs2108622多态性与高血压的关联:一项荟萃分析。
Genet Mol Res. 2015 Nov 26;14(4):15133-9. doi: 10.4238/2015.November.25.1.
2
Association Between the Gene rs1558139 and rs2108622 Polymorphisms and Hypertension: A Meta-Analysis.基因rs1558139和rs2108622多态性与高血压之间的关联:一项荟萃分析。
Genet Test Mol Biomarkers. 2019 May;23(5):342-347. doi: 10.1089/gtmb.2018.0202. Epub 2019 Mar 30.
3
Cytochrome P450 family 4 subfamily F member 2 (CYP4F2) rs1558139, rs2108622 polymorphisms and susceptibility to several cardiovascular and cerebrovascular diseases.细胞色素P450家族4亚家族F成员2(CYP4F2)rs1558139、rs2108622多态性与几种心脑血管疾病的易感性
BMC Cardiovasc Disord. 2018 Feb 9;18(1):29. doi: 10.1186/s12872-018-0763-y.
4
CYP4F2 genetic polymorphisms are associated with coronary heart disease in a Chinese population.CYP4F2 基因多态性与中国人群冠心病有关。
Lipids Health Dis. 2014 May 20;13:83. doi: 10.1186/1476-511X-13-83.
5
Association of 1347 G/A cytochrome P450 4F2 (CYP4F2) gene variant with hypertension and stroke.1347 G/A 细胞色素 P450 4F2(CYP4F2)基因变异与高血压和脑卒中的相关性。
Mol Biol Rep. 2012 Feb;39(2):1677-82. doi: 10.1007/s11033-011-0907-y. Epub 2011 May 31.
6
CYP4F2 gene V433M polymorphism is associated with ischemic stroke in the male Northern Chinese Han population.CYP4F2 基因 V433M 多态性与中国北方汉族男性缺血性脑卒中的发生相关。
Prog Neuropsychopharmacol Biol Psychiatry. 2010 May 30;34(4):664-8. doi: 10.1016/j.pnpbp.2010.03.009. Epub 2010 Mar 11.
7
CYP4F2 rs2108622: a minor significant genetic factor of warfarin dose in Han Chinese patients with mechanical heart valve replacement.CYP4F2 rs2108622:汉族机械心脏瓣膜置换患者华法林剂量的次要显著遗传因素。
Br J Clin Pharmacol. 2010 Aug;70(2):234-40. doi: 10.1111/j.1365-2125.2010.03698.x.
8
A haplotype of the CYP4F2 gene is associated with cerebral infarction in Japanese men.CYP4F2基因的一种单倍型与日本男性的脑梗死有关。
Am J Hypertens. 2008 Nov;21(11):1216-23. doi: 10.1038/ajh.2008.276. Epub 2008 Sep 11.
9
Influence of CYP4F2 genotype on warfarin dose requirement-a systematic review and meta-analysis.CYP4F2 基因型对华法林剂量需求的影响:系统评价和荟萃分析。
Thromb Res. 2012 Jul;130(1):38-44. doi: 10.1016/j.thromres.2011.11.043. Epub 2011 Dec 20.
10
CYP4F2 gene single nucleotide polymorphism is associated with ischemic stroke.细胞色素P450 4F2(CYP4F2)基因单核苷酸多态性与缺血性脑卒中相关。
Genet Mol Res. 2015 Jan 30;14(1):659-64. doi: 10.4238/2015.January.30.8.

引用本文的文献

1
Bioactive lipids in hypertension.高血压中的生物活性脂质。
Adv Pharmacol. 2023;97:1-35. doi: 10.1016/bs.apha.2023.01.001. Epub 2023 May 10.
2
Suggestive evidence of CYP4F2 gene polymorphisms with HAPE susceptibility in the Chinese Han population.提示 CYP4F2 基因多态性与中国汉族人群 HAPE 易感性相关。
PLoS One. 2023 Jan 12;18(1):e0280136. doi: 10.1371/journal.pone.0280136. eCollection 2023.
3
Correlation of TNF-α and IL-10 gene polymorphisms with primary nephrotic syndrome.肿瘤坏死因子-α和白细胞介素-10基因多态性与原发性肾病综合征的相关性
Exp Ther Med. 2020 Nov;20(5):87. doi: 10.3892/etm.2020.9215. Epub 2020 Sep 11.
4
Cytochrome P450 family 4 subfamily F member 2 (CYP4F2) rs1558139, rs2108622 polymorphisms and susceptibility to several cardiovascular and cerebrovascular diseases.细胞色素P450家族4亚家族F成员2(CYP4F2)rs1558139、rs2108622多态性与几种心脑血管疾病的易感性
BMC Cardiovasc Disord. 2018 Feb 9;18(1):29. doi: 10.1186/s12872-018-0763-y.