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It is demonstrated that rs699 polymorphism of AGT gene is significantly associated with the susceptibility to hypertension.
BACKGROUND The prevalence of rs5186 (AGTR1 A1166C) in the Mekong Delta remains largely unexplored. This study aimed to determine the prevalence of rs5186 in patients with primary hypertension at Xuyen A Vinh Long hospital and to investigate its association with some risk factors for hypertension. METHODS A case-control...
Objective: In this study, the relationship between CYP11B2 gene polymorphisms and the risk of cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM), illnesses whose incidence is rising quickly in North Indian populations, is examined. Methods: Physiometric, biochemical, and anthropometric characteristics wer...
Objective: To investigate the association between the TCF7L2 rs7903146 polymorphism and type 2 diabetes mellitus susceptibility in a southern Iraqi population Study Design: Case-control studyPlace and Duration of Study: This study was conducted at the Al-Fayhaa Teaching Hospital, Basrah, Iraq, from 1st November 2025 to...
Type 2 diabetes mellitus (T2DM) is a complex, multifactorial metabolic disease that involves a number of interactions between genetic and environmental factors. There are gene variants that are involved in insulin secretion control including KCNJ11 which have been found to contribute to the susceptibility of T2DM in di...
Introduction. The study of modifiable cardiometabolic risk factors (CMRFs) influencing the clinical phenotype of hypertrophic cardiomyopathy (HCM) is currently relevant. It is known that modifier genes can affect the course and progression of symptoms in HCM. At the same time, the analysis of associations between si...
The data revealed a relationship between the genetic variant in the HSB1 gene and the risk of developing CHD, supporting further research on the potential value of this emerging marker in predicting cardiovascular disease.
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