Key result
The concomitant presence of Met235Thr (AGT) and Glu298Asp (NOS3) polymorphisms significantly increased the risk of hypertension (p=0.001), with 95% of double mutant homozygotes being hypertensive.
Why the study?
Do AGT and NOS3 gene polymorphisms and their interaction with conventional risk factors increase the predisposition to hypertension?
Case-Control (n=192)
Do AGT and NOS3 gene polymorphisms and their interaction with conventional risk factors increase the predisposition to hypertension?
p-value: p=0.001
The interaction of AGT and NOS3 gene polymorphisms with conventional risk factors such as smoking, sedentariness, age, and total cholesterol significantly increases the predisposition to hypertension.
Supports AGT-NOS3 interaction in hypertension predisposition; hypothesis-generating and should not yet change clinical risk assessment.
Renin-angiotensin and kallikrein-kinin systems are interconnected, regulating blood pressure homeostasis. We have demonstrated the interactions among polymorphisms of the angiotensinogen (AGT) and endothelial nitric oxide synthase (NOS3) genes and conventional risk factors affecting the hypertension occurrence. Individuals were recruited (n=192) and classified into hypertensive (HG; n=140) and normotensive (NG; n=52) groups. The genotypic distribution of the Met235Thr (AGT) and Glu298Asp (NOS3) polymorphisms demonstrated that both are independent risk factors of hypertension (p=0.02 and p=0.008, respectively). The concomitant presence of these polymorphisms in the HG group was significantly different (p=0.001) from the NG. Both gene polymorphisms presented an additive effect for the unfavourable alleles T and A, respectively, and 95% of the double mutant homozygotes were classified into the HG. Specific interactions among certain conventional factors and the presence of at least one unfavourable allele presented significant odds towards hypertension. Blood pressure homeostasis was affected by genetic polymorphisms conditioned by the T and A alleles of the AGT and NOS3 genes, respectively, which acted independently. However, their interaction with smoking, sedentariness, age and total cholesterol may have increased the predisposition to hypertension, which may explain most of the hypertension cases.
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Gatti et al. (2012) conducted a case-control in Hypertension (n=192). Met235Thr (AGT) and Glu298Asp (NOS3) gene polymorphisms vs. Absence of unfavourable alleles was evaluated on Hypertension occurrence (p=0.001). The concomitant presence of Met235Thr (AGT) and Glu298Asp (NOS3) polymorphisms significantly increased the risk of hypertension (p=0.001), with 95% of double mutant homozygotes being hypertensive.
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