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2000
Volume 9, Issue 2
  • ISSN: 2211-5366
  • E-ISSN: 2211-5374

Abstract

Introduction: Alcoholic Cardiomyopathy (ACM) is a disease with a difficult diagnosis. The real mechanisms related to its pathophysiology are not fully understood. Objective: The aims of this study were to investigate whether miR-133b and miR-138 could be associated with ACM. Methods: Forty-four patients were included comprising 24 with ACM and 20 with cardiomyopathies of different etiologies (control group). Real-time PCR was performed to verify the relative expression among the studied groups. In the statistical analysis, the quantitative variables t-student Mann- Whitney and correlation of Pearson tests were carried out, while the qualitative variable comprised the chi-square test, with p<0.05 being considered statistically significant. Results: There was no association between clinical and sociodemographic characteristics of the groups. The patients with ACM presented downregulation of miR-133b in comparison with control patients (p=0.004). On the other hand, for the miR-138, there was no association when the ACM group was compared with the control group. The presence of miR-133b among cases and controls was not correlated with any of the echocardiographic parameters. However, the increase in the expression of miR-138 was correlated with an increase in the ejection fraction (r=0.28, p=0.01) and the diameter of the left atrium (r=0.23, p=0.04) in patients with ACM. Conclusion: The downregulation of miR-133b might be a marker for ACM and, in addition, miR- 138 could be used to correlate the increase in ejection fraction with and normalization of the diameter of the left atrium diameter in patients with this disease.

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/content/journals/mirna/10.2174/2211536608666190716151900
2020-04-01
2025-10-04
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/content/journals/mirna/10.2174/2211536608666190716151900
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  • Article Type:
    Research Article
Keyword(s): Alcoholic cardiomyopathy; biomarkers; cardiomegaly; echocardiography; fibrosis; microRNA
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