• 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

与肥胖汉族人群高血压相关的 CYP7A1 基因型和单倍型。

CYP7A1 genotypes and haplotypes associated with hypertension in an obese Han Chinese population.

机构信息

Department of Clinical Epidemiology, The First Affiliated Hospital, China Medical University, Shenyang, China.

出版信息

Hypertens Res. 2011 Jun;34(6):722-7. doi: 10.1038/hr.2011.18. Epub 2011 Feb 24.

DOI:10.1038/hr.2011.18
PMID:21346769
Abstract

This study investigated the association between single-nucleotide polymorphisms (SNPs; rs3808607 and rs1125226) within the CYP7A1 promoter and hypertension susceptibility in a Han Chinese population. From 2003 through 2006, a population-based case-control study was performed in a cohort of 1187 randomly selected Han Chinese subjects. A sib-pair study for a transmission disequilibrium test analysis was carried out in 76 hypertensive (HT) families (n=312) from northeastern Liaoning province. SNPs were detected using real-time PCR. No significant differences were found in the genotype or allele frequencies of either SNP (P>0.05), with no excessive allele sharing. For rs3808607, the frequency of the AA genotype in obese hypertensive patients was 31.91%, significantly higher than in normotensive (NT) subjects (12.73%; odds ratio (OR)=3.21, 95% confidence interval (CI)=1.35-7.66). For rs3808607, the AA genotype frequency was significantly higher in obese male HT subjects (27.87%) than in matched NTs (7.41%; OR=4.83, 95% CI=1.03-22.65). After adjustment for environmental risk factors in obese participants, the AA genotype was associated with hypertension (OR=3.395, 95% CI=1.412-8.162). Among subjects with body mass index 28 kg m(-2), the HT and NT groups had significantly different frequencies of Hap I (C/C) and Hap IV (A/A). The frequencies of rs3808607 alleles in the CYP7A1 gene differed significantly between obese HT and NT men. Haplotypes I and IV were associated with hypertension in obese participants.

摘要

本研究旨在探讨 CYP7A1 启动子中单核苷酸多态性(SNP;rs3808607 和 rs1125226)与汉族人群高血压易感性之间的关联。2003 年至 2006 年,在东北辽宁省的一个汉族人群中进行了一项基于人群的病例对照研究,共纳入 1187 名随机选择的汉族受试者。对 76 个高血压(HT)家系(n=312)进行了传递不平衡测试分析的同胞对研究。采用实时 PCR 检测 SNP。两种 SNP 的基因型或等位基因频率均无显著差异(P>0.05),且无过度等位基因共享。对于 rs3808607,肥胖高血压患者 AA 基因型的频率为 31.91%,明显高于血压正常(NT)受试者(12.73%;优势比(OR)=3.21,95%置信区间(CI)=1.35-7.66)。对于 rs3808607,肥胖男性 HT 患者 AA 基因型的频率(27.87%)明显高于匹配的 NT 患者(7.41%;OR=4.83,95% CI=1.03-22.65)。在校正肥胖患者的环境危险因素后,AA 基因型与高血压相关(OR=3.395,95% CI=1.412-8.162)。在体重指数 28 kg/m2 的受试者中,HT 组和 NT 组的 Hap I(C/C)和 Hap IV(A/A)的频率有显著差异。CYP7A1 基因中 rs3808607 等位基因在肥胖 HT 和 NT 男性之间存在显著差异。Haplotypes I 和 IV 与肥胖参与者的高血压有关。

相似文献

1
CYP7A1 genotypes and haplotypes associated with hypertension in an obese Han Chinese population.与肥胖汉族人群高血压相关的 CYP7A1 基因型和单倍型。
Hypertens Res. 2011 Jun;34(6):722-7. doi: 10.1038/hr.2011.18. Epub 2011 Feb 24.
2
CYP7A1 (-204 A>C; rs3808607 and -469 T>C; rs3824260) promoter polymorphisms and risk of gallbladder cancer in North Indian population.CYP7A1 启动子多态性(-204 A>C;rs3808607 和-469 T>C;rs3824260)与印度北部人群胆囊癌风险的关系。
Metabolism. 2010 Jun;59(6):767-73. doi: 10.1016/j.metabol.2009.09.021. Epub 2009 Dec 16.
3
The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population.CYP7A1基因rs3808607变异与摩洛哥人群的结核病易感性相关。
Pan Afr Med J. 2014 May 1;18:1. doi: 10.11604/pamj.2014.18.1.3397. eCollection 2014.
4
Association of cholesterol 7α-hydroxylase (CYP7A1) promoter polymorphism (rs3808607) and cholesterol 24S-hydroxylase (CYP46A1) intron 2 polymorphism (rs754203) with serum lipids, vitamin D levels, and multiple sclerosis risk in the Turkish population.胆固醇 7α-羟化酶(CYP7A1)启动子多态性(rs3808607)和胆固醇 24S-羟化酶(CYP46A1)内含子 2 多态性(rs754203)与土耳其人群血清脂质、维生素 D 水平和多发性硬化风险的关联。
Neurol Sci. 2022 Apr;43(4):2611-2620. doi: 10.1007/s10072-021-05597-1. Epub 2021 Sep 21.
5
[Preliminary study on the association of chemokine RANTES gene polymorphisms with HIV-1 infection in Chinese Han population].趋化因子RANTES基因多态性与中国汉族人群HIV-1感染相关性的初步研究
Zhonghua Liu Xing Bing Xue Za Zhi. 2003 Nov;24(11):971-5.
6
Variations in the calpain-10 gene are associated with the risk of type 2 diabetes and hypertension in northern Han Chinese population.钙蛋白酶-10基因的变异与中国北方汉族人群患2型糖尿病和高血压的风险相关。
Chin Med J (Engl). 2007 Dec 20;120(24):2218-23.
7
Cholesterol 7alpha-hydrolase (CYP7A1) c.-278A>C promoter polymorphism in gallstone disease patients.胆结石病患者中胆固醇7α-羟化酶(CYP7A1)基因启动子区c.-278A>C多态性
Genet Test. 2008 Mar;12(1):97-100. doi: 10.1089/gte.2007.0067.
8
The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China.中国新疆汉族和维吾尔族人群中胆固醇吸收基因Numb多态性与冠状动脉疾病的关联
Lipids Health Dis. 2015 Sep 29;14:120. doi: 10.1186/s12944-015-0102-6.
9
A functional intronic variant in the tyrosine hydroxylase (TH) gene confers risk of essential hypertension in the Northern Chinese Han population.酪氨酸羟化酶(TH)基因中的一个功能性内含子变异赋予中国北方汉族人群原发性高血压风险。
Clin Sci (Lond). 2008 Sep;115(5):151-8. doi: 10.1042/CS20070335.
10
Polymorphisms in lipid metabolism related miRNA binding sites and risk of metabolic syndrome.脂质代谢相关 miRNA 结合位点多态性与代谢综合征风险。
Gene. 2013 Oct 10;528(2):132-8. doi: 10.1016/j.gene.2013.07.036. Epub 2013 Jul 31.

引用本文的文献

1
RNA-seq transcriptome profiling of pigs' liver in response to diet with different sources of fatty acids.不同脂肪酸来源日粮对猪肝脏的RNA测序转录组分析。
Front Genet. 2023 Jan 25;14:1053021. doi: 10.3389/fgene.2023.1053021. eCollection 2023.
2
Interactions Between Regulatory Variants in CYP7A1 (Cholesterol 7α-Hydroxylase) Promoter and Enhancer Regions Regulate CYP7A1 Expression.调控因子在 CYP7A1(胆固醇 7α-羟化酶)启动子和增强子区域的相互作用调节 CYP7A1 的表达。
Circ Genom Precis Med. 2018 Oct;11(10):e002082. doi: 10.1161/CIRCGEN.118.002082.
3
The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population.
CYP7A1基因rs3808607变异与摩洛哥人群的结核病易感性相关。
Pan Afr Med J. 2014 May 1;18:1. doi: 10.11604/pamj.2014.18.1.3397. eCollection 2014.