Why the study?
Does the T allele of the GNB3 C825T polymorphism increase the risk of essential hypertension in the Egyptian population?
Does the T allele of the GNB3 C825T polymorphism increase the risk of essential hypertension in the Egyptian population?
The T allele of the GNB3 C825T polymorphism is associated with a 1.5-fold increased risk of essential hypertension in the Egyptian population.
Hypothesis-generating for hypertension genetics in Egyptians; should not yet change clinical practice.
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. Individuals were genotyped for C825T genetic polymorphism of G protein β3 gene rs5443 by using restriction fragment length polymorphism. RESULTS: Frequencies of C and T alleles were 58.1% and 41.9%, respectively, in the control group compared with 47.7% and 52.3%, respectively, in the hypertensive group. The carriers of rs5443 (T) allele exhibited a significant greater risk for EH compared with the carriers of rs5443 (C) allele (odds ratio = 1.5, 95% confidence interval = 1.2-2.0). CONCLUSION: T allele is a risk factor for EH in the Egyptian population, which may be used as a prognostic and a therapeutic target of prophylaxis.
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Hemimi et al. (2016) studied this question.
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