Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic Background

Background. Neurohormonal systems play an important role in chronic heart failure (CHF). Due to interindividual heterogeneity in the benefits of therapy, it may be hypothesized that polymorphisms of neurohormonal systems may affect left ventricular (LV) remodelling and systolic function. We aimed to...

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Main Authors: Marzia Rigolli, Mariantonietta Cicoira, Corinna Bergamini, Andrea Chiampan, Andrea Rossi, Corrado Vassanelli
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:Cardiology Research and Practice
Online Access:http://dx.doi.org/10.4061/2011/798658
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author Marzia Rigolli
Mariantonietta Cicoira
Corinna Bergamini
Andrea Chiampan
Andrea Rossi
Corrado Vassanelli
author_facet Marzia Rigolli
Mariantonietta Cicoira
Corinna Bergamini
Andrea Chiampan
Andrea Rossi
Corrado Vassanelli
author_sort Marzia Rigolli
collection DOAJ
description Background. Neurohormonal systems play an important role in chronic heart failure (CHF). Due to interindividual heterogeneity in the benefits of therapy, it may be hypothesized that polymorphisms of neurohormonal systems may affect left ventricular (LV) remodelling and systolic function. We aimed to assess whether genetic background of maximally treated CHF patients predicts variations in LV systolic function and volumes. Methods and Results. We prospectively studied 131 CHF outpatients on optimal treatment for at least six months. Echocardiographic evaluations were performed at baseline and after 12 months. Genotype analysis for ACE I/D, β1adrenergic receptor (AR) Arg389Gly, β2AR Arg16Gly, and β2AR Gln27Glu polymorphisms was performed. No differences in baseline characteristics were detected among subgroups. ACE II was a significant predictor of improvement of LV end-diastolic and end-systolic volume (𝑃=.003 and 𝑃=.002, respectively) but not of LV ejection fraction (LVEF); β1AR389 GlyGly was related to improvement of LVEF (𝑃=.02) and LV end-systolic volume (𝑃=.01). The predictive value of polymorphisms remained after adjustment for other clinically significant predictors (𝑃<.05 for all). Conclusions. ACE I/D and β1AR Arg389Gly polymorphisms are independent predictors of reverse remodeling and systolic function recovery in CHF patients under optimal treatment.
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spelling doaj-art-0feb35d660254af3a9ce68968c29d5542025-02-03T05:45:10ZengWileyCardiology Research and Practice2090-05972011-01-01201110.4061/2011/798658798658Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic BackgroundMarzia Rigolli0Mariantonietta Cicoira1Corinna Bergamini2Andrea Chiampan3Andrea Rossi4Corrado Vassanelli5Division of Cardiology, Department of Biomedical and Surgical Sciences, University of Verona, 37129 Verona, ItalyDivision of Cardiology, Department of Biomedical and Surgical Sciences, University of Verona, 37129 Verona, ItalyDivision of Cardiology, Department of Biomedical and Surgical Sciences, University of Verona, 37129 Verona, ItalyDivision of Cardiology, Department of Biomedical and Surgical Sciences, University of Verona, 37129 Verona, ItalyDivision of Cardiology, Department of Biomedical and Surgical Sciences, University of Verona, 37129 Verona, ItalyDivision of Cardiology, Department of Biomedical and Surgical Sciences, University of Verona, 37129 Verona, ItalyBackground. Neurohormonal systems play an important role in chronic heart failure (CHF). Due to interindividual heterogeneity in the benefits of therapy, it may be hypothesized that polymorphisms of neurohormonal systems may affect left ventricular (LV) remodelling and systolic function. We aimed to assess whether genetic background of maximally treated CHF patients predicts variations in LV systolic function and volumes. Methods and Results. We prospectively studied 131 CHF outpatients on optimal treatment for at least six months. Echocardiographic evaluations were performed at baseline and after 12 months. Genotype analysis for ACE I/D, β1adrenergic receptor (AR) Arg389Gly, β2AR Arg16Gly, and β2AR Gln27Glu polymorphisms was performed. No differences in baseline characteristics were detected among subgroups. ACE II was a significant predictor of improvement of LV end-diastolic and end-systolic volume (𝑃=.003 and 𝑃=.002, respectively) but not of LV ejection fraction (LVEF); β1AR389 GlyGly was related to improvement of LVEF (𝑃=.02) and LV end-systolic volume (𝑃=.01). The predictive value of polymorphisms remained after adjustment for other clinically significant predictors (𝑃<.05 for all). Conclusions. ACE I/D and β1AR Arg389Gly polymorphisms are independent predictors of reverse remodeling and systolic function recovery in CHF patients under optimal treatment.http://dx.doi.org/10.4061/2011/798658
spellingShingle Marzia Rigolli
Mariantonietta Cicoira
Corinna Bergamini
Andrea Chiampan
Andrea Rossi
Corrado Vassanelli
Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic Background
Cardiology Research and Practice
title Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic Background
title_full Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic Background
title_fullStr Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic Background
title_full_unstemmed Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic Background
title_short Progression of Left Ventricular Dysfunction and Remodelling under Optimal Medical Therapy in CHF Patients: Role of Individual Genetic Background
title_sort progression of left ventricular dysfunction and remodelling under optimal medical therapy in chf patients role of individual genetic background
url http://dx.doi.org/10.4061/2011/798658
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