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日本人群中GNB3基因与脉压及心血管疾病危险因素聚集的关联

Association of GNB3 gene with pulse pressure and clustering of risk factors for cardiovascular disease in Japanese.

作者信息

Yamamoto Miyuki, Abe Michiko, Jin Jing Ji, Wu Zhihong, Tabara Yasuharu, Mogi Masaki, Kohara Katsuhiko, Miki Tetsuro, Nakura Jun

机构信息

Department of Geriatric Medicine, School of Medicine, Ehime University, Shigenobu-cho, Onsen-gun, Ehime 791-0295, Japan.

出版信息

Biochem Biophys Res Commun. 2004 Apr 9;316(3):744-8. doi: 10.1016/j.bbrc.2004.02.113.

Abstract

Heterotrimeric guanine nucleotide-binding proteins (G proteins) mediate many pathways including the beta-adrenergic signaling pathway. The C825T polymorphism in the gene coding for the beta3 subunit of G proteins (GNB3) has been shown to be associated with several phenotypes such as hypertension, obesity, and diabetes mellitus comprising the metabolic syndrome. The GNB3 C825T polymorphism may therefore be associated with many atherosclerosis-related phenotypes. On these grounds, we studied the C825T polymorphism in relation to atherosclerosis-related phenotypes in a large Japanese population. Analyses in general linear models showed that T carriers had a significantly wider pulse pressure (P=0.0089) as well as a significantly higher systolic blood pressure (P=0.026). In contrast, analyses in logistic regression models showed that the C825T polymorphism was not significantly associated with each of the four major classical risk factors for cardiovascular and cerebrovascular disease (obesity, hypertension, hypertriglyceridemia, and diabetes mellitus). However, a significantly higher percentage of subjects had none of the four disorders in CC homozygotes than in T carriers (P=0.026). Thus, the C825T polymorphism was significantly associated with clustering of these four risk factors. Although the effect of the gene on each phenotype appears to be weak, considering the combined impact of the effects of the C825T polymorphism on risk factors, the GNB3 gene may be an important gene for human health.

摘要

异源三聚体鸟嘌呤核苷酸结合蛋白(G蛋白)介导包括β-肾上腺素能信号通路在内的多种信号通路。G蛋白β3亚基(GNB3)编码基因中的C825T多态性已被证明与包括代谢综合征在内的多种表型相关,如高血压、肥胖和糖尿病。因此,GNB3基因的C825T多态性可能与许多动脉粥样硬化相关表型有关。基于这些原因,我们在一个庞大的日本人群中研究了C825T多态性与动脉粥样硬化相关表型的关系。一般线性模型分析显示,携带T等位基因的个体脉压显著更宽(P = 0.0089),收缩压也显著更高(P = 0.026)。相比之下,逻辑回归模型分析显示,C825T多态性与心血管和脑血管疾病的四大主要经典危险因素(肥胖、高血压、高甘油三酯血症和糖尿病)中的任何一个均无显著关联。然而,CC纯合子中没有这四种疾病的受试者比例显著高于携带T等位基因的个体(P = 0.026)。因此,C825T多态性与这四种危险因素的聚集显著相关。尽管该基因对每种表型的影响似乎较弱,但考虑到C825T多态性对危险因素影响的综合作用,GNB3基因可能是影响人类健康的一个重要基因。

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