Vascular Tissue Specific miRNA Profiles Reveal Novel Correlations with Risk Factors in Coronary Artery Disease

Cardiovascular disease (CVD) is the leading cause of morbidity and mortality worldwide. Non-coding RNAs have already been linked to CVD development and progression. While microRNAs (miRs) have been well studied in blood samples, there is little data on tissue-specific miRs in cardiovascular relevant...

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Published inBiomolecules (Basel, Switzerland) Vol. 11; no. 11; p. 1683
Main Authors Neiburga, Katrīna D, Vilne, Baiba, Bauer, Sabine, Bongiovanni, Dario, Ziegler, Tilman, Lachmann, Mark, Wengert, Simon, Hawe, Johann S, Güldener, Ulrich, Westerlund, Annie M, Li, Ling, Pang, Shichao, Yang, Chuhua, Saar, Kathrin, Huebner, Norbert, Maegdefessel, Lars, DigiMed Bayern Consortium, Lange, Rüdiger, Krane, Markus, Schunkert, Heribert, von Scheidt, Moritz
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 12.11.2021
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Summary:Cardiovascular disease (CVD) is the leading cause of morbidity and mortality worldwide. Non-coding RNAs have already been linked to CVD development and progression. While microRNAs (miRs) have been well studied in blood samples, there is little data on tissue-specific miRs in cardiovascular relevant tissues and their relation to cardiovascular risk factors. Tissue-specific miRs derived from (IMA) from 192 coronary artery disease (CAD) patients undergoing coronary artery bypass grafting (CABG) were analyzed. The aims of the study were 1) to establish a reference atlas which can be utilized for identification of novel diagnostic biomarkers and potential therapeutic targets, and 2) to relate these miRs to cardiovascular risk factors. Overall, 393 individual miRs showed sufficient expression levels and passed quality control for further analysis. We identified 17 miRs-miR-10b-3p, miR-10-5p, miR-17-3p, miR-21-5p, miR-151a-5p, miR-181a-5p, miR-185-5p, miR-194-5p, miR-199a-3p, miR-199b-3p, miR-212-3p, miR-363-3p, miR-548d-5p, miR-744-5p, miR-3117-3p, miR-5683 and miR-5701-significantly correlated with cardiovascular risk factors (correlation coefficient >0.2 in both directions, -value ( < 0.006, false discovery rate (FDR) <0.05). Of particular interest, miR-5701 was positively correlated with hypertension, hypercholesterolemia, and diabetes. In addition, we found that miR-629-5p and miR-98-5p were significantly correlated with acute myocardial infarction. We provide a first atlas of miR profiles in IMA samples from CAD patients. In perspective, these miRs might play an important role in improved risk assessment, mechanistic disease understanding and local therapy of CAD.
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Contributed equally.
Membership of the DigiMed Bayern Consortium is provided in the supplementary materials.
ISSN:2218-273X
2218-273X
DOI:10.3390/biom11111683