Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodeling

Background and aims: Cardiomyocyte hypertrophy and interstitial fibrosis are key components of myocardial remodeling in Heart Failure (HF) with preserved (HFpEF) or reduced ejection fraction (HFrEF). MicroRNAs (miRNAs) are non-coding, evolutionarily conserved RNA molecules that may offer novel insig...

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Main Authors: Layde Rosane Paim, Luis Miguel da Silva, Lígia M. Antunes-Correa, Vinicius Citelli Ribeiro, Roberto Schreiber, Eduarda O.Z. Minin, Larissa C.M. Bueno, Elisangela C.P. Lopes, Renan Yamaguti, Andréa Coy-Canguçu, Sergio San Juan Dertkigil, Andrei Sposito, Jose Roberto Matos-Souza, Thiago Quinaglia, Tomas G. Neilan, Licio A. Velloso, Wilson Nadruz, Michael Jerosch-Herold, Otavio R. Coelho-Filho
Format: Article
Language:English
Published: Elsevier 2024-03-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844024032377
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author Layde Rosane Paim
Luis Miguel da Silva
Lígia M. Antunes-Correa
Vinicius Citelli Ribeiro
Roberto Schreiber
Eduarda O.Z. Minin
Larissa C.M. Bueno
Elisangela C.P. Lopes
Renan Yamaguti
Andréa Coy-Canguçu
Sergio San Juan Dertkigil
Andrei Sposito
Jose Roberto Matos-Souza
Thiago Quinaglia
Tomas G. Neilan
Licio A. Velloso
Wilson Nadruz
Michael Jerosch-Herold
Otavio R. Coelho-Filho
author_facet Layde Rosane Paim
Luis Miguel da Silva
Lígia M. Antunes-Correa
Vinicius Citelli Ribeiro
Roberto Schreiber
Eduarda O.Z. Minin
Larissa C.M. Bueno
Elisangela C.P. Lopes
Renan Yamaguti
Andréa Coy-Canguçu
Sergio San Juan Dertkigil
Andrei Sposito
Jose Roberto Matos-Souza
Thiago Quinaglia
Tomas G. Neilan
Licio A. Velloso
Wilson Nadruz
Michael Jerosch-Herold
Otavio R. Coelho-Filho
author_sort Layde Rosane Paim
collection DOAJ
description Background and aims: Cardiomyocyte hypertrophy and interstitial fibrosis are key components of myocardial remodeling in Heart Failure (HF) with preserved (HFpEF) or reduced ejection fraction (HFrEF). MicroRNAs (miRNAs) are non-coding, evolutionarily conserved RNA molecules that may offer novel insights into myocardial remodeling. This study aimed to characterize miRNA expression in HFpEF (LVEF ≥ 45%) and HFrEF (LVEF < 45%) and its association with myocardial remodeling. Methods: Prospectively enrolled symptomatic HF patients (HFpEF:n = 36; HFrEF:n = 31) and controls (n = 23) underwent cardiac magnetic resonance imaging with T1-mapping and circulating miRNA expression (OpenArray system). Results: 13 of 188 miRNAs were differentially expressed between HF groups (11 downregulated in HFpEF). Myocardial extracellular volume (ECV) was increased in both HF groups (HFpEF 30 ± 5%; HFrEF 30 ± 3%; controls 26 ± 2%, p < 0.001). miR-128a-3p, linked to cardiac hypertrophy, fibrosis, and dysfunction, correlated positively with ECV in HFpEF (r = 0.60, p = 0.01) and negatively in HFrEF (r = −0.51, p = 0.04). miR-423-5p overexpression, previously associated HF mortality, was inversely associated with LVEF (r = − 0.29, p = 0.04) and intracellular water lifetime (τic) (r = −0.45, p < 0.05) in both HF groups, and with NT-proBNP in HFpEF (r = −0.63, p < 0.01). Conclusions: miRNA expression profiles differed between HF phenotypes. The differential expression and association of miR-128a-3p with ECV may reflect the distinct vascular, interstitial, and cellular etiologies of HF phenotypes.
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spelling doaj.art-eaa9d3f818ab46b9aaa81b7cf96f79042024-04-04T05:04:27ZengElsevierHeliyon2405-84402024-03-01106e27206Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodelingLayde Rosane Paim0Luis Miguel da Silva1Lígia M. Antunes-Correa2Vinicius Citelli Ribeiro3Roberto Schreiber4Eduarda O.Z. Minin5Larissa C.M. Bueno6Elisangela C.P. Lopes7Renan Yamaguti8Andréa Coy-Canguçu9Sergio San Juan Dertkigil10Andrei Sposito11Jose Roberto Matos-Souza12Thiago Quinaglia13Tomas G. Neilan14Licio A. Velloso15Wilson Nadruz16Michael Jerosch-Herold17Otavio R. Coelho-Filho18Faculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Engenharia Elétrica e de Computação – Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Medicina – Pontifícia Universidade Católica de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, Brazil; Cardiovascular Imaging Research Center, Division of Cardiology and Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USACardiovascular Imaging Research Center, Division of Cardiology and Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USAFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, BrazilNon-Invasive Cardiovascular Imaging Program, Department of Radiology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USAFaculdade de Ciências Médicas - Universidade Estadual de Campinas, São Paulo, Brazil; Corresponding author. School of Medical Science, University of Campinas - UNICAMP, Rua Tessália Vieira de Camargo, 126 - Cidade Universitária ''Zeferino Vaz'', Campinas - SP CEP: 13083-887, Brazil.Background and aims: Cardiomyocyte hypertrophy and interstitial fibrosis are key components of myocardial remodeling in Heart Failure (HF) with preserved (HFpEF) or reduced ejection fraction (HFrEF). MicroRNAs (miRNAs) are non-coding, evolutionarily conserved RNA molecules that may offer novel insights into myocardial remodeling. This study aimed to characterize miRNA expression in HFpEF (LVEF ≥ 45%) and HFrEF (LVEF < 45%) and its association with myocardial remodeling. Methods: Prospectively enrolled symptomatic HF patients (HFpEF:n = 36; HFrEF:n = 31) and controls (n = 23) underwent cardiac magnetic resonance imaging with T1-mapping and circulating miRNA expression (OpenArray system). Results: 13 of 188 miRNAs were differentially expressed between HF groups (11 downregulated in HFpEF). Myocardial extracellular volume (ECV) was increased in both HF groups (HFpEF 30 ± 5%; HFrEF 30 ± 3%; controls 26 ± 2%, p < 0.001). miR-128a-3p, linked to cardiac hypertrophy, fibrosis, and dysfunction, correlated positively with ECV in HFpEF (r = 0.60, p = 0.01) and negatively in HFrEF (r = −0.51, p = 0.04). miR-423-5p overexpression, previously associated HF mortality, was inversely associated with LVEF (r = − 0.29, p = 0.04) and intracellular water lifetime (τic) (r = −0.45, p < 0.05) in both HF groups, and with NT-proBNP in HFpEF (r = −0.63, p < 0.01). Conclusions: miRNA expression profiles differed between HF phenotypes. The differential expression and association of miR-128a-3p with ECV may reflect the distinct vascular, interstitial, and cellular etiologies of HF phenotypes.http://www.sciencedirect.com/science/article/pii/S2405844024032377Heart failureBiomarkersMicroRNAInterstitial fibrosisMyocardial remodeling
spellingShingle Layde Rosane Paim
Luis Miguel da Silva
Lígia M. Antunes-Correa
Vinicius Citelli Ribeiro
Roberto Schreiber
Eduarda O.Z. Minin
Larissa C.M. Bueno
Elisangela C.P. Lopes
Renan Yamaguti
Andréa Coy-Canguçu
Sergio San Juan Dertkigil
Andrei Sposito
Jose Roberto Matos-Souza
Thiago Quinaglia
Tomas G. Neilan
Licio A. Velloso
Wilson Nadruz
Michael Jerosch-Herold
Otavio R. Coelho-Filho
Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodeling
Heliyon
Heart failure
Biomarkers
MicroRNA
Interstitial fibrosis
Myocardial remodeling
title Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodeling
title_full Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodeling
title_fullStr Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodeling
title_full_unstemmed Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodeling
title_short Profile of serum microRNAs in heart failure with reduced and preserved ejection fraction: Correlation with myocardial remodeling
title_sort profile of serum micrornas in heart failure with reduced and preserved ejection fraction correlation with myocardial remodeling
topic Heart failure
Biomarkers
MicroRNA
Interstitial fibrosis
Myocardial remodeling
url http://www.sciencedirect.com/science/article/pii/S2405844024032377
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