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April 16, 2026Genes0 citationsOpen Access

Association Analyses Between the NPPB:rs198389 Gene Polymorphism, NT-proBNP Serum Concentrations and Phenotypic Features in Patients with Heart Failure

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AGAnna GorącyJRJakub RosikKLKlaudyna Lewandowska

Key Result

The NPPB:rs198389 polymorphism showed no significant association with NT-proBNP serum concentrations or clinical phenotypes in Polish patients with heart failure.

Key Points

  • To explore the relationship between the NPPB:rs198389 polymorphism, NT-proBNP levels, and phenotypic characteristics in heart failure patients.
  • 250 patients with heart failure were analyzed.
  • Genomic DNA was extracted from blood samples.
  • Genotyping was performed using PCR-RFLP methodology.
  • No significant genotype or allele distribution differences between HF females and males.
  • Significant differences in age, left-ventricular-mass index, and other health markers among NT-proBNP terciles.
  • Lower tercile patients had higher preserved ejection fraction compared to middle and upper tercile patients.

Study Design

Type

Observational (n=250)

Structured PICO

Does the NPPB:rs198389 polymorphism associate with NT-proBNP concentrations and phenotypic features in Polish patients with heart failure?

P
Population
250 Polish patients with heart failure
I
Intervention
NPPB:rs198389 (c.-381T > C) promoter polymorphism
C
Comparator
Different genotypes/alleles of NPPB:rs198389
O
Outcome
Associations among the NPPB:rs198389 polymorphism, NT-proBNP concentrations, and phenotypic featuressurrogate

The NPPB:rs198389 polymorphism does not appear to be associated with NT-proBNP serum concentrations or clinical phenotypes in Polish patients with heart failure.

Abstract

Background: Heart failure (HF) is a complex disease and one of the major causes of morbidity and mortality in the world. Increased B-type natriuretic peptide (BNP) levels have been associated with HF. The NPPB:rs198389 (c.-381T > C) promoter polymorphism has been found to modulate BNP levels. Aim: To investigate possible associations among the NPPB:rs198389 polymorphism, N-terminal pro-BNP (NT-proBNP) concentrations, and phenotypic features in Polish patients with HF. Methods: The study group comprised 250 patients with HF. Genomic DNA was extracted from blood, and genotyping was performed using PCR-RFLP. Results: There were no significant differences in the distributions of NPPB genotypes or alleles between HF females and HF males. Except for body height, there were no significant differences in phenotypic features among HF patients regarding NPPB:rs198389 genotypes. There were also no significant differences in the distributions of either NPPB:rs198389 genotypes or alleles across NT-proBNP concentration terciles. However, age, left-ventricular-mass index, C-reactive-protein levels, serum-creatinine concentrations, and the incidence of myocardial infarction, left ventricular hypertrophy, or reduced ejection fraction (EF) were significantly lower in patients from the lower tercile (LT) than in patients from the middle and/or upper terciles. EF and the frequency of preserved EF in LT patients were significantly higher than those from other terciles. Conclusions: Our results did not confirm associations between NPPB:rs198389 and NT-proBNP serum concentrations or clinical phenotypes in Polish patients with HF.

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Cite This Study

Gorący et al. (2026) conducted an observational in Heart failure (n=250). NPPB:rs198389 polymorphism was evaluated on Associations between NPPB:rs198389 genotypes, NT-proBNP concentrations, and phenotypic features. The NPPB:rs198389 polymorphism showed no significant association with NT-proBNP serum concentrations or clinical phenotypes in Polish patients with heart failure.

synapsesocial.com/papers/69e07e242f7e8953b7cbf12ehttps://doi.org/10.3390/genes17040454
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