Association of GNB3 gene with pulse pressure and clustering of risk factors for cardiovascular disease in Japanese
| Autor: | Katsuhiko Kohara, Jun Nakura, Yasuharu Tabara, Tetsuro Miki, Masaki Mogi, Michiko Abe, Miyuki Yamamoto, Zhihong Wu, Jing Ji Jin |
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| Rok vydání: | 2004 |
| Předmět: |
Male
medicine.medical_specialty Genotype Arteriosclerosis Biophysics Blood Pressure Disease Biology Biochemistry Japan Risk Factors Internal medicine Diabetes mellitus medicine Cluster Analysis Humans Molecular Biology Polymorphism Genetic Homozygote Hypertriglyceridemia DNA Cell Biology Middle Aged medicine.disease Heterotrimeric GTP-Binding Proteins Obesity Logistic Models Phenotype Blood pressure Endocrinology Cardiovascular Diseases Female Metabolic syndrome Signal Transduction GNB3 |
| Zdroj: | Biochemical and Biophysical Research Communications. 316:744-748 |
| ISSN: | 0006-291X |
| DOI: | 10.1016/j.bbrc.2004.02.113 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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