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蛋白酪氨酸激酶2β作为高血压的候选基因。

Protein tyrosine kinase 2beta as a candidate gene for hypertension.

作者信息

Kamide Kei, Kokubo Yoshihiro, Fukuhara Shigetomo, Hanada Hironori, Yang Jin, Kada Akiko, Nagura Junko, Takiuchi Shin, Horio Takeshi, Kawano Yuhei, Okayama Akira, Tomoike Hitonobu, Miyata Toshiyuki

机构信息

Divisions of Hypertension, National Cardiovascular Center, Suita, Osaka, Japan.

出版信息

Pharmacogenet Genomics. 2007 Nov;17(11):931-9. doi: 10.1097/FPC.0b013e3282ef640e.

Abstract

Protein tyrosine kinase 2beta (PTK2B) is a member of the focal adhesion kinase family and is activated by angiotensin II through Ca2+-dependent pathways. An evidence exists that PTK2B is involved in cell growth, vascular contraction, inflammatory responses, and salt and water retention through activation of the angiotensin II type 1 receptor. To examine the contribution of PTK2B, we sequenced the PTK2B gene using 48 patients with hypertension, identified 62 genetic polymorphisms, and genotyped six representative single nucleotide polymorphisms in population-based case-control samples from 3655 Japanese individuals (1520 patients with hypertension and 2135 controls). Multivariate logistic regression analysis after adjustments for age, body mass index, present illness (hyperlipidemia and diabetes mellitus), and lifestyle (smoking and drinking) showed -22A>G to have an association with hypertension in men (AA vs. AG+GG: odds ratio=1.27; 95% confidence interval: 1.02-1.57; P=0.030). Another polymorphism, 53484A>C (K838T), in linkage disequilibrium with -22A>G showed a marginal association with hypertension in men (AA vs. AC+CC: odds ratio=1.25; 95% confidence interval: 0.99-1.57; P=0.059). Diastolic blood pressure was 1.6 mmHg higher in men with the AC+CC genotype of 53484A>C than those with the AA genotype (P=0.003), after adjustments for the same factors. These polymorphisms are in linkage disequilibrium with others in a range of 113 kb in PTK2B. The intracellular distribution of the recombinant PTK2B protein and that of the mutant protein with T838 were indistinguishable even after angiotensin II stimulation, both proteins localizing at a focal point in the peripheral area in the cells. Thus, a haplotype in PTK2B may play a role in essential hypertension in Japanese.

摘要

蛋白酪氨酸激酶2β(PTK2B)是粘着斑激酶家族的成员,可通过Ca2+依赖途径被血管紧张素II激活。有证据表明,PTK2B通过激活血管紧张素II 1型受体参与细胞生长、血管收缩、炎症反应以及盐和水潴留。为了研究PTK2B的作用,我们对48例高血压患者的PTK2B基因进行了测序,鉴定出62个基因多态性,并在来自3655名日本人(1520例高血压患者和2135名对照)的基于人群的病例对照样本中对6个代表性单核苷酸多态性进行了基因分型。在对年龄、体重指数、现患疾病(高脂血症和糖尿病)以及生活方式(吸烟和饮酒)进行调整后的多因素逻辑回归分析显示,-22A>G与男性高血压有关(AA与AG+GG:比值比=1.27;95%置信区间:1.02-1.57;P=0.030)。另一个与-22A>G处于连锁不平衡的多态性53484A>C(K838T)在男性中与高血压存在边缘关联(AA与AC+CC:比值比=1.25;95%置信区间:0.99-1.57;P=0.059)。在对相同因素进行调整后,53484A>C的AC+CC基因型男性的舒张压比AA基因型男性高1.6 mmHg(P=0.0

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