Associations of angiotensinogen gene mutations with hypertension and myocardial infarction in a gulf population |
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Authors: | Philippe M Frossard Susan H Hill Yassin I Elshahat Eniyoma N Obineche Awais M Bokhari Gilles G Lestringant Anne John Abdishakur M Abdulle |
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Affiliation: | Department of Pathology, Faculty of Medicine and Health Sciences, Al Ain,;Nephrology Unit, Central Hospital, Abu Dhabi,;;Department of Internal Medicine, Faculty of Medicine and Health Sciences, Al Ain,;Department of Internal Medicine, Tawam Hospital, Al Ain, United Arab Emirates |
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Abstract: | To date, the human angiotensinogen ( AGT ) gene and some of its variants represent the best examples of genetic influences that are involved in the determination of essential hypertension (EH) and associated cardiovascular diseases (CVDs). To assess the value of genotyping AGT in a genetically homogeneous population, we carried out a retrospective, case–control study of variants M235T and T174M for putative correlations with CVDs among nationals from the United Arab Emirates (Emirati) – an ethnic group characterized by no alcohol intake and no cigarette smoking.We investigated a sample population of 229 Emirati (119 males and 110 females), comprising groups of controls and patients with clinical diagnoses of EH, left ventricular hypertrophy (LVH), ischaemic heart disease (IHD) and myocardial infarction (MI). M235T and T174M alleles were determined via assays based on the polymerase chain reaction. T174M showed no correlation with any of the four clinical entities included in this study. T235 alleles, however, occurred more frequently in the EH group and less frequently in the group of MI survivors. We also found that T235 allele frequencies decreased with age, indicating that in the Emirati population, T235 alleles are associated with a reduced life span and that this effect could occur through independent mechanisms underlying genetic susceptibilities to both EH and MI. |
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Keywords: | angiotensinogen cardiovascular diseases genetics hypertension left ventricular hypertrophy myocardial infarction polymerase chain reaction |
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