Hypertension is a common disorder of multifactorial origin that constitutes a major risk factor for cardiovascular events such as stroke and myocardial infarction. The subunits of the heterotrimeric G proteins are attractive candidate gene products for susceptibility to hypertension, obesity and insulin resistance syndrome. A polymorphism (825C/T) in exon 10 of the GNB3 gene, encoding for the Gβ3 subunit, has been described. The 825T allele is associated with alternative splicing of the gene and formation of a truncated but functionally active β3 subunit. Many studies have investigated whether carriers of the 825T allele are at increased risk for hypertension, obesity, insulin-resistance and left ventricular hypertrophy with apparently conflicting results. The present review demonstrates that GNB3 825T allele is a useful genetic marker for better defining the risk profile of hypertensive patients, as it is associated with increased risk of stroke and myocardial infarction in longitudinal studies in Caucasians.
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http://dx.doi.org/10.1007/s40292-015-0093-4 | DOI Listing |
Sovrem Tekhnologii Med
March 2022
Leading Researcher, Department of Medical and Social Research, Monitoring and Supervision Ivanovo Research Institute of Motherhood and Childhood named after V.N. Gorodkov, Ministry of Health of the Russian Federation, 20 Pobeda St., Ivanovo, 153045, Russia.
Unlabelled: was to develop technologies for predicting the development of preeclampsia (PE) based on biomedical and molecular-genetic predictors and the calculation of individual risks for this pregnancy complication.
Materials And Methods: The study involved 457 pregnant women. Of them, 147 women had chronic arterial hypertension (CAH); 109 pregnant women had CAH and secondary preeclampsia (PE); 201 patients had PE.
Clin Exp Hypertens
February 2017
a Department of Cardiology , Xuanwu Hospital, Capital Medical University, Beijing , China.
Several recent studies showed that C825T polymorphism is related to cardiovascular diseases in normal population. However, studies on whether 825T allele influences the incidence of cardiovascular diseases in hypertensive patients are rare. In the current study, 729 patients (CC, n = 332; CT, n = 313; TT, n = 84) with essential hypertension were genotyped for C825T polymorphism of the GNB3 gene and followed 8 years for major adverse cardiovascular events (MACEs) which include stroke, the onset of coronary artery disease (CAD), and all-cause death.
View Article and Find Full Text PDFCell Discov
July 2016
Key Laboratory of Molecular Medicine, Ministry of Education, and Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai, China; Molecular and Cell Biology Lab, Institutes of Biomedical Sciences, Fudan University, Shanghai, China; Department of Biochemistry and Biophysics, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Population-based and case-control studies in different ethnicities have linked a polymorphism, C825T, in exon 10 of GNB3 gene to hypertension and several additional diseases. The 825T allele is associated with alternative splicing and results in a shortened Gβ3 protein, referred to as Gβ3s, which loses 41 amino acids encompassing one WD40 repeat domain. The mechanism of how Gβ3 C825T polymorphism is associated with hypertension has remained unclear, but an impairment of its canonical function in G-protein-coupled receptor signaling has been ruled out.
View Article and Find Full Text PDFBiomark Insights
May 2016
Endocrine Unit, Internal Medicine Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Background: The guanine nucleotide-binding protein beta polypeptide 3 (GNB3) 825T allele encodes a product that enhances the activation of heterotrimeric G proteins, which is associated with the occurrence of the splice variant Gβ3 s that could play a role in vascular reactivity and hyperproliferation of smooth muscle cells, that makes such proteins attractive candidate gene products for susceptibility to essential hypertension (EH).
Objective: To predict the risk for EH in individuals with C825T genetic polymorphism of G protein β3 gene.
Methods: The study consisted of 222 normotensive individuals and 216 hypertensive patients.
Meta Gene
September 2016
Department of Pharmacy, Xiangya Hospital, Central South University, Changsha 410008, Hunan, PR China.
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