T-786C Polymorphism of the NOS3 Gene and Its Role in the Development of Renal Dysfunction in Patients of the Uzbek Population with Chronic Heart Failure.

Impaired renal function is significantly linked to the T-786C NOS3 polymorphism, indicating a genetic risk factor.
The genetic variant C at the T-786C location correlates with chronic heart failure in the Uzbek population.

Is the genetic variant C of the T-786C NOS3 polymorphism associated with impaired renal function in patients with chronic heart failure?

Population

Patients of the Uzbek population with Chronic Heart Failure (CHF)

Intervention

Genetic variant C of the T-786C NOS3 polymorphism

Outcome

Impaired renal function / development of renal dysfunctionsurrogate

The C variant of the T-786C NOS3 polymorphism may serve as a genetic marker for renal dysfunction in Uzbek patients with chronic heart failure.

The genetic variant C of the T-786C NOS3 polymorphism is associated with impaired renal function in patients with CHF.

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Cite This Study

Zakirova et al. (Mon,) studied this question.

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