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Circulating microRNAs as biomarkers of Chagas cardiomyopathy.
Antonietti, Laura; Mariani, Javier; Martínez, María Jose; Santalla, Manuela; Vensentini, Natalia; Kyle, Diego Alfredo; de Abreu, Maximiliano; Tajer, Carlos; Lacunza, Ezequiel; Ferrero, Paola.
Afiliação
  • Antonietti L; Department of Cardiology, El Cruce Hospital, Florencio Varela, Buenos Aires, Argentina.
  • Mariani J; Health Sciences Institute, Arturo Jauretche National University, Florencio Varela, Buenos Aires, Argentina.
  • Martínez MJ; Department of Cardiology, El Cruce Hospital, Florencio Varela, Buenos Aires, Argentina.
  • Santalla M; Health Sciences Institute, Arturo Jauretche National University, Florencio Varela, Buenos Aires, Argentina.
  • Vensentini N; Department of Cardiology, El Cruce Hospital, Florencio Varela, Buenos Aires, Argentina.
  • Kyle DA; Cardiovascular Research Center Dr. Horacio Cingolani, Faculty of Medical Sciences, La Plata National University, La Plata, Buenos Aires, Argentina.
  • de Abreu M; Department of Cardiology, El Cruce Hospital, Florencio Varela, Buenos Aires, Argentina.
  • Tajer C; Department of Cardiology, El Cruce Hospital, Florencio Varela, Buenos Aires, Argentina.
  • Lacunza E; Department of Cardiology, El Cruce Hospital, Florencio Varela, Buenos Aires, Argentina.
  • Ferrero P; Health Sciences Institute, Arturo Jauretche National University, Florencio Varela, Buenos Aires, Argentina.
Front Cardiovasc Med ; 10: 1250029, 2023.
Article em En | MEDLINE | ID: mdl-38173812
ABSTRACT

Background:

Chagas cardiomyopathy (CHCM) is the most important clinical manifestation of Chagas disease. The analysis of cardiac miRNAs may contribute to predicting the progression to CHCM in Chagas indeterminate phase and/or to the differential diagnosis for cardiomyopathy.

Methods:

We carried out a case-control study to identify circulating miRNAs associated with CHCM. We assigned 104 participants to four groups healthy controls (HC), Chagas non-cardiomyopathy controls, CHCM cases, and ischemic cardiomyopathy controls. We performed a clinical, echocardiographic, and laboratory evaluation and profiled circulating miRNA in the serum samples.

Results:

Differences between groups were observed in clinical variables and in the analysis of miRNAs. Compared to HC, CHCM participants had 4 over-expressed and 6 under-expressed miRNAs; miR-95-3p and miR-130b-3p were upregulated in CHCM compared with controls, Chagas non-cardiomyopathy and ischemic cardiomyopathy participants, suggesting that might be a hallmark of CHCM. Analysis of gene targets associated with cardiac injury yielded results of genes involved in arrhythmia generation, cardiomegaly, and hypertrophy.

Conclusions:

Our data suggest that the expression of circulating miRNAs identified by deep sequencing in CHCM could be associated with different cardiac phenotypes in CHCM subjects, compared with Chagas non-CHCM, ischemic cardiomyopathy controls, and healthy controls.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article