期刊文献+

中国东北汉族人群WNK4基因多态性与原发性高血压的关联性 被引量:1

The Relationships between the Polymorphism of WNK4 Gene and Essential Hypertension in North-Eastern Han Population
下载PDF
导出
摘要 目的探讨东北汉族人群WNK4基因多态性与原发性高血压的关系。方法259例原发性高血压患者和235例健康正常对照人群血样应用PCR-RFLP方法检测A589S多态,结果经测序验证,同时检测所有人群的血糖、血脂等生化指标。结果(1)两组研究对象基因型频率间差别无显著性意义(P>0.05),但等位基因频率间差别有显著性意义(P<0.05);(2)GT和TT基因型与收缩压及舒张压升高密切相关(P=0.041,0.032)。结论WNK4基因A589S多态可能与高血压密切相关。 Objective To elucidate the association of WNK4 gene A589S polymorphism with essential hypertension in north - eastern han isolated population. Methods Genotyping was performed using polymerase chain reaction - restriction fragment length polymorphism (PCR- RFLP) and confirmed by direct sequencing. 259 unrelated patients with essential hypertension and 235 unrelated normal controls were recruited. All the subjects had routine laboratory tests. Results ( 1 ) The frequency of WNK4 genotype GG, GT and TT were 0. 63, 0. 33, 0. 04 in controls respectively, and 0. 53, 0. 43, 0. 04 in hypertensive respectively. There was no significant differences in genotypes between hypertensive group and normal controls. ( P 〉 0. 05 ). The frequencies of G and T were 0. 80, 0. 20 in normal controls and 0. 74, 0. 26 in hypertensives respectively. And the frequencies of T allele in hypertension group is significantly higher than that in controls (25.9% versus 20. 2%, P 〈 0. 05 ). (2) The GT and TT genotypes were closely associated with raised systolic and diastolic blood pressure ( P =0. 041,0. 032). Conclusion The WNK4 gene A589S polymorphism is associated with essential hypertension in north -eastern han population.
出处 《中国全科医学》 CAS CSCD 2006年第9期706-707,711,共3页 Chinese General Practice
基金 国家自然科学基金资助项目(30300204)
关键词 WNK4基因 多态性 高血压 WNK4 gene Polymorphism Hypertension
  • 相关文献

参考文献2

二级参考文献16

  • 1全国血压抽样调查协作组.中国人群高血压患病率及其变化趋势[J].高血压杂志,1995,3(A01):7-13. 被引量:508
  • 2吴锡桂,武阳丰,周北凡,陶寿淇,沈丽卿,王淑玉,朱树雄,徐祥林,杨瑞祥,杜福昌,王益琏,何厚琦,夏舜英,阮连生.我国十组人群高血压发病率及其影响因素[J].中华医学杂志,1996,76(1):24-29. 被引量:147
  • 3栾荣生.心血管疾病流行病学[A].李立明主编.流行病学 第4版[C].北京:人民卫生出版社,1999.234-248.
  • 4梁祖光.广西壮族部分农民高血压病普查[J].中华预防医学杂志,1987,21:233-233.
  • 5Frederieh HW, Sandra DN, Keith AC, et d. Human hypertension caused by mutations in WNK kinases. Science,2001, 293(10):1107-1112.
  • 6Sambrook J, Fritsch EF, Maniatis T. In: Molecular Cloning A Laboratory Manual. Cold Spring Harbor Laboratory Press,1989.
  • 7Bing-e X, Jessie M, Julie L, et al. WNK1, a novel mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain Ⅱ. J Bid Chem, 2000,275(22):.16795-16801.
  • 8Fatima V, Peter J. WNK kinases, a novel protein kinase subfamily in muhi-cellular organisms. Oncogen, 2001,20:5562-5569.
  • 9Daniel L, Anita LD, Martin GL, et al. Evidence for a gene influencing blood pressure on chromosome 17. Hypertension,2000, 36:477-483.
  • 10Jader B, Michael N, Faina S, et al. Evidence for linkage between essential hypertension and a putative locus on human chromosome 17. Hypertension, 1999, 34:4-7.

共引文献63

同被引文献17

  • 1温绍君,王佐广,陈光慧,刘雅,刘洁琳,罗毅,汤健.HSG基因单核苷酸多态性与原发性高血压的相关性研究[J].中华预防医学杂志,2005,39(1):15-18. 被引量:19
  • 2苗丽娟,杨秋,徐应军.中国汉族人血管紧张素Ⅱ1型受体基因A1166C多态性与原发性高血压关系的系统分析[J].中国综合临床,2005,21(6):490-493. 被引量:8
  • 3Vonend O, Ahenhenne C, Buchner NJ, et al. A German family with glueoeortieoid-remediable aldosteronism. Nephrol Dial Transplant, 2007,22 : 1123-1130.
  • 4Knight KK, Olson DR, Snyder PM, et al. Liddle' s syndrome mutations increase Na^+ transport through dual effects on epithelial Na^+ channel suface expression and proteolytic clearage. PNAS,2006,103:2805-2808.
  • 5Deaton SL, Sengupta S, Cobb MH. WNK kinases and blood pressure control. Curr Hypertens Rep, 2009,11 :421-426.
  • 6Velez DR, Guruju M, Vinukonda G, et al. Angiotensinogen promoter sequence variants in essential hypertension. Am J Hypertens, 2006,19 : 1278-1285.
  • 7Cheng X, Xu G. Association between aldosterone synthase CYPllB2 polymorphism and essential hypertension in Chinese: a meta-analysis. Kidney Blood Press Res, 2009,32 : 128- 140.
  • 8Freitas SR, Pereira AC, Floriano MS, et al. Insertion/deletion polymorphism of the bradykinin type 2 receptor gene influence diastolic blood pressure. J Hum Hypertens, 2009, 23: 553-555.
  • 9Katori M, Majima M. A missing link between a high intake and blood pressure increase. J Pharmacol Sei, 2006,100:370- 390.
  • 10Lu X, Zhao W, Huang J, et al. Common variation in KLKB1 and essential hypertension riak:tagging-SNP haplotype analysis in a ease-control study. Hum Genet,2007,121:327-335.

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部