Suppr超能文献

无赖氨酸激酶1和丝氨酸/苏氨酸激酶39基因多态性及单倍型与藏族原发性高血压的关联

Association of with-no-lysine kinase 1 and Serine/Threonine kinase 39 gene polymorphisms and haplotypes with essential hypertension in Tibetans.

作者信息

Shi Rufeng, Li Jiangbo, He Jiyun, Meng Qingtao, Qian Zhiping, Shi Di, Liu Qi, Cai Yali, Li Xinran, Chen Xiaoping

机构信息

Department of Cardiology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610000, PRC.

Ganzi Tibetan Autonomous Prefecture People's Hospital, Kangding 626000, Tibetan Autonomous Prefecture, PRC.

出版信息

Environ Mol Mutagen. 2018 Mar;59(2):151-160. doi: 10.1002/em.22140. Epub 2017 Sep 25.

Abstract

Tibetans have a higher essential hypertension prevalence compared with other ethnics in China. The reason might be due to their unique environmental influence, as well as genetic factor. However, limited studies focus on Tibetan genetics and its association with hypertension. The aim of this study was to investigate the association between With-No-Lysine (K) Kinase 1 (WNK1), Serine/Threonine kinase 39(STK39) genes variants and hypertension in the Tibetan population. 204 Tibetan hypertensive patients and 305 normotensive controls were recruited in an epidemiological survey conducted at 2 sites in the Ganzi Tibetan autonomous region. Patients were genotyped for nineteen WNK1 candidate tag single nucleotide polymorphisms (SNPs) and three STK39 SNPs, and haplotype analysis was performed. Results showed that the allele A in rs1468326 was overrepresented in hypertensive patients versus control (53.4% vs 42.9%, P < 0.05). The multivariable-adjusted odds ratio (OR) for hypertension among CA + AA genotypes carriers was 1.60 (95% CI: 1.02-2.62, P < 0.05), and they also had a higher systolic blood pressure (136.5 ± 28.6 vs 131.7 ± 24.8 mmHg, P < 0.05). However, the TT genotype ratio in rs6749447 was lower in hypertensives (5.4% vs 10.8%, P < 0.05), and the hypertension risk for the TT genotype carriers in rs6749447 decreased after adjustment (OR 0.49, 95% CI 0.19-0.95, P < 0.05). Subjects with haplotype AGACAGGAATCGT showed 1.57 times higher risk of hypertension (95% CI 1.02-2.41, P < 0.05). In conclusion, SNP rs1468326 of WNK1, rs6749447 of STK39, and WNK1 haplotype AGACAGGAATCGT were associated with hypertension in Tibetan individuals. Environ. Mol. Mutagen. 59:151-160, 2018. © 2017 Wiley Periodicals, Inc.

摘要

与中国其他民族相比,藏族原发性高血压患病率更高。原因可能是其独特的环境影响以及遗传因素。然而,针对藏族遗传学及其与高血压关联的研究有限。本研究旨在调查无赖氨酸(K)激酶1(WNK1)、丝氨酸/苏氨酸激酶39(STK39)基因变异与藏族人群高血压之间的关联。在甘孜藏族自治州的两个地点进行的一项流行病学调查中,招募了204名藏族高血压患者和305名血压正常的对照者。对患者进行了19个WNK1候选标签单核苷酸多态性(SNP)和3个STK39 SNP的基因分型,并进行了单倍型分析。结果显示,与对照组相比,高血压患者中rs1468326的等位基因A比例过高(53.4%对42.9%,P<0.05)。CA+AA基因型携带者患高血压的多变量调整优势比(OR)为1.60(95%可信区间:1.02-2.62,P<0.05),他们的收缩压也更高(136.5±28.6对131.7±24.8 mmHg,P<0.05)。然而,rs6749447的TT基因型比例在高血压患者中较低(5.4%对10.8%,P<0.05),调整后rs6749447的TT基因型携带者的高血压风险降低(OR 0.49,95%可信区间0.19-0.95,P<0.05)。单倍型AGACAGGAATCGT的受试者患高血压的风险高1.57倍(95%可信区间1.02-2.41,P<0.05)。总之,WNK1的SNP rs1468326、STK39的rs6749447以及WNK1单倍型AGACAGGAATCGT与藏族个体的高血压有关。《环境与分子突变》59:151-160,2018年。©2017威利期刊公司

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