A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy
(1) Background: Left ventricular hypertrophy, myocardial disarray and interstitial fibrosis are the hallmarks of hypertrophic cardiomyopathy (HCM). Access to the myocardium for diagnostic purposes is limited. Circulating biomolecules reflecting the myocardial disease processes could improve the earl...
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2021
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oai:doaj.org-article:14ab195569af493da3d53124a54132a92021-11-25T16:54:16ZA Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy10.3390/biom111117182218-273Xhttps://doaj.org/article/14ab195569af493da3d53124a54132a92021-11-01T00:00:00Zhttps://www.mdpi.com/2218-273X/11/11/1718https://doaj.org/toc/2218-273X(1) Background: Left ventricular hypertrophy, myocardial disarray and interstitial fibrosis are the hallmarks of hypertrophic cardiomyopathy (HCM). Access to the myocardium for diagnostic purposes is limited. Circulating biomolecules reflecting the myocardial disease processes could improve the early detection of HCM. Circulating miRNAs have been found to reflect disease processes in several cardiovascular diseases. (2) Methods: We quantified circulating miRNA molecules in the plasma of 24 HCM and 11 healthy controls using the Human v3 miRNA Expression Assay Kit Code set (Nanostring Tech., Seattle, WA, USA) and validated differentially expressed miRNAs using RT-PCR. (3) Results: In comparison to healthy controls, the levels of six miRNAs (miR-1, miR-3144, miR-4454, miR-495-3p, miR-499a-5p and miR-627-3p) were higher in the plasma of HCM patients than healthy individuals (<i>p</i> < 0.05). Of these, higher levels of miR-1, miR-495 and miR-4454 could be validated by real-time PCR. In addition, elevated miR-4454 levels were significantly correlated with cardiac fibrosis, detected by magnetic resonance imaging in HCM patients. (4) Conclusions: Circulating miR-1, miR-495-3p and miR-4454 levels are elevated in the plasma of HCM patients. To the best of our knowledge, this is the first report showing a correlation between miR-4454 levels and cardiac fibrosis in HCM. This suggests miR-4454 as a potential biomarker for fibrosis in these patients.Tilo ThottakaraNatalie LundElisabeth KrämerPaulus KirchhofLucie CarrierMonica PattenMDPI AGarticlecirculating miRNAbiomarkerventricular hypertrophyhypertrophic cardiomyopathycardiac fibrosisMicrobiologyQR1-502ENBiomolecules, Vol 11, Iss 1718, p 1718 (2021) |
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circulating miRNA biomarker ventricular hypertrophy hypertrophic cardiomyopathy cardiac fibrosis Microbiology QR1-502 |
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circulating miRNA biomarker ventricular hypertrophy hypertrophic cardiomyopathy cardiac fibrosis Microbiology QR1-502 Tilo Thottakara Natalie Lund Elisabeth Krämer Paulus Kirchhof Lucie Carrier Monica Patten A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy |
description |
(1) Background: Left ventricular hypertrophy, myocardial disarray and interstitial fibrosis are the hallmarks of hypertrophic cardiomyopathy (HCM). Access to the myocardium for diagnostic purposes is limited. Circulating biomolecules reflecting the myocardial disease processes could improve the early detection of HCM. Circulating miRNAs have been found to reflect disease processes in several cardiovascular diseases. (2) Methods: We quantified circulating miRNA molecules in the plasma of 24 HCM and 11 healthy controls using the Human v3 miRNA Expression Assay Kit Code set (Nanostring Tech., Seattle, WA, USA) and validated differentially expressed miRNAs using RT-PCR. (3) Results: In comparison to healthy controls, the levels of six miRNAs (miR-1, miR-3144, miR-4454, miR-495-3p, miR-499a-5p and miR-627-3p) were higher in the plasma of HCM patients than healthy individuals (<i>p</i> < 0.05). Of these, higher levels of miR-1, miR-495 and miR-4454 could be validated by real-time PCR. In addition, elevated miR-4454 levels were significantly correlated with cardiac fibrosis, detected by magnetic resonance imaging in HCM patients. (4) Conclusions: Circulating miR-1, miR-495-3p and miR-4454 levels are elevated in the plasma of HCM patients. To the best of our knowledge, this is the first report showing a correlation between miR-4454 levels and cardiac fibrosis in HCM. This suggests miR-4454 as a potential biomarker for fibrosis in these patients. |
format |
article |
author |
Tilo Thottakara Natalie Lund Elisabeth Krämer Paulus Kirchhof Lucie Carrier Monica Patten |
author_facet |
Tilo Thottakara Natalie Lund Elisabeth Krämer Paulus Kirchhof Lucie Carrier Monica Patten |
author_sort |
Tilo Thottakara |
title |
A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy |
title_short |
A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy |
title_full |
A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy |
title_fullStr |
A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy |
title_full_unstemmed |
A Novel miRNA Screen Identifies miRNA-4454 as a Candidate Biomarker for Ventricular Fibrosis in Patients with Hypertrophic Cardiomyopathy |
title_sort |
novel mirna screen identifies mirna-4454 as a candidate biomarker for ventricular fibrosis in patients with hypertrophic cardiomyopathy |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/14ab195569af493da3d53124a54132a9 |
work_keys_str_mv |
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