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G蛋白β3亚基C825T变异与原发性高血压患者的动态血压

G-Protein beta3 subunit C825T variant and ambulatory blood pressure in essential hypertension.

作者信息

Beige J, Hohenbleicher H, Distler A, Sharma A M

机构信息

Department of Internal Medicine, Division of Endocrinology and Nephrology, Universitätsklinikum Benjamin Franklin, Free University of Berlin, Germany.

出版信息

Hypertension. 1999 Apr;33(4):1049-51. doi: 10.1161/01.hyp.33.4.1049.

Abstract

Recent studies have identified a novel polymorphism (C825T) of the gene encoding the beta3 subunit of heterotrimeric G proteins (Gbeta3) associated with enhanced activation of G proteins, which appears to be more common in hypertensive patients. In the present study we examine the relationship between this genetic variant and hypertension in 479 white patients with established essential hypertension recruited from the hypertension clinic of the Universitätsklinikum Benjamin Franklin in Berlin, Germany, and 1000 normotensive gender- and age-matched controls. All patients were screened for the presence of secondary hypertension and were further characterized by ambulatory blood pressure measurements performed in 295 treated and 184 untreated patients. Genotype distribution for the Gbeta3-C825T genotype in patients (CC=204, CT=224, TT=51) was significantly different from that in controls (CC=514, CT=412, TT=74; chi2=11.5, P<0.01), and the T allele was associated with an odds ratio of 1.5 (95% CI, 1.1 to 2.2) versus non-T carriers for the presence of hypertension. However, in both the whole group and the untreated subgroup, blood pressure levels between the genotypic groups were virtually identical. Furthermore, age of onset of hypertension and number of antihypertensive medications (in treated patients) were similar between the genotypic groups. Thus, while our data confirm the association between the Gbeta3-C825T variant and essential hypertension, they do not support the hypothesis that this marker is associated with more severe blood pressure in patients with already established hypertension.

摘要

最近的研究发现了一种新的多态性(C825T),它存在于编码异三聚体G蛋白(Gβ3)β3亚基的基因中,与G蛋白的激活增强有关,这种多态性在高血压患者中似乎更为常见。在本研究中,我们调查了479例从德国柏林本杰明·富兰克林大学医院高血压门诊招募的确诊原发性高血压白人患者以及1000例年龄和性别匹配的血压正常对照者中,这种基因变异与高血压之间的关系。所有患者均接受继发性高血压筛查,并对295例接受治疗和184例未接受治疗的患者进行动态血压测量以进一步明确特征。患者(CC = 204,CT = 224,TT = 51)中Gβ3 - C825T基因型的分布与对照者(CC = 514,CT = 412,TT = 74;χ2 = 11.5,P < 0.01)显著不同,T等位基因与高血压存在相关的比值比为1.5(95%可信区间,1.1至2.2),相对于非T携带者。然而,在整个组和未治疗亚组中,各基因型组之间的血压水平实际上是相同的。此外,各基因型组之间高血压的发病年龄和(接受治疗患者的)抗高血压药物数量相似。因此,虽然我们的数据证实了Gβ3 - C825T变异与原发性高血压之间的关联,但并不支持该标志物与已确诊高血压患者更严重血压相关的假说。

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