Ontology highlight
ABSTRACT: Study objective
This study aimed to determine if variants in NR3C2, which codes the target protein of spironolactone, or CYP11B2, which is involved in aldosterone synthesis, were associated with spironolactone response, focused on the primary end point of diastolic function (E/e'), in Aldosterone Receptor Blockade in Diastolic Heart Failure (Aldo-DHF) participants.Design
Post-hoc genetic analysis.Data source
Data and samples were derived from the multi-center, randomized, double-blind, placebo-controlled Aldo-DHF trial.Patients
Aldo-DHF participants treated with spironolactone (n = 184) or placebo (n = 178) were included.Intervention
Participants were genotyped for NR3C2 rs5522, NR3C2 rs2070951 and CYP11B2 rs1799998 via pyrosequencing.Measurement
SUBMITTER: Dumeny L
PROVIDER: S-EPMC8688239 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature