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Genetic polymorphism G894T and the prognosis of heart failure outpatients
Insights
This study found no link between the G894T gene variant and heart failure outcomes in Brazilian patients. Further research is needed to understand genetic factors influencing heart failure prognosis.
Area of Science:
- Cardiology
- Genetics
- Molecular Biology
Background:
- Endothelial nitric oxide synthase (eNOS) genetic polymorphisms have been studied for their impact on heart failure prognosis.
- Previous research has not specifically investigated the G894T polymorphism in relation to heart failure within the Brazilian population.
Purpose of the Study:
- To investigate the association between the G894T polymorphism of endothelial nitric oxide synthase and the prognosis of heart failure in Brazilian outpatients.
- To determine if G894T genotype or allele frequencies correlate with clinical outcomes such as reverse remodeling, functional class improvement, mortality, and hospitalization rates.
Main Methods:
- A cohort study involving 145 Brazilian patients with systolic heart failure, followed for up to 40 months.
- Evaluation of G894T polymorphism using polymerase chain reaction and restriction fragment length polymorphism.
- Assessment of outcomes including left ventricular reverse remodeling, New York Heart Association (NYHA) functional class, mortality, and hospitalization rates.
Main Results:
- Genotypic frequencies were GG (40%), GT (48.3%), and TT (11.7%). Allele frequencies were guanine (64.1%) and thiamine (35.8%).
- No significant differences in genotype or allele frequencies were observed based on self-declared race.
- No statistically significant relationship was found between G894T genotype or allele frequencies and the evaluated heart failure outcome measures.
Conclusions:
- The G894T polymorphism (Glu298Asp) in endothelial nitric oxide synthase does not appear to be associated with the prognosis of systolic heart failure in this Brazilian cohort.
- These findings suggest that the G894T variant may not be a significant predictor of heart failure outcomes in the Brazilian population studied.
Background:
Previous studies have analyzed the role of the genetic polymorphism of endothelial nitric oxide synthase on heart failure prognosis. However, there are no studies relating the G894T and heart failure in Brazil.
Objective:
To evaluate the association between G894T GP and the prognosis of a sample of Brazilian outpatients with heart failure.
Methods:
Cohort study included 145 patients with systolic heart failure, followed for up to 40 months (mean = 22), at two university hospitals, in the State of Rio de Janeiro. We evaluated the relationship between G894T and the following outcomes: reverse remodeling, improvement in functional class (NYHA), and mortality and hospitalization rates. The diameters of the left atrium and ventricle, as well as the ejection fraction of the left ventricle, were evaluated at baseline and at 6 months to assess reverse remodeling. The improvement in functional class was evaluated after 6 months, and mortality rate and hospitalization were evaluated during follow-up. Race was self-declared. G894T polymorphism was analyzed by polymerase chain reaction and restriction fragment length polymorphism.
Results:
The genotypic frequencies were GG (40%), GT (48.3%) and TT (11.7%). The allele frequency was guanine (64.1%) and thiamine (35.8%). There were no differences between the genotype or allelic frequencies according to self-declared race, either as baseline characteristics. There was no relationship between genotype or allele frequency and the outcome measures.
Conclusion:
No association was observed between the G894T polymorphism (Glu298Asp) and prognosis in this sample of Brazilian outpatients with systolic heart failure.
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