TABLE 1.
Plasma | Myocardial tissue | |||||||||
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HCM (our study) | CAD | HF | AF | AMI | other pathologies | HCM (our study) | other pathologies | References_DOI | References_full citation | |
miR‐19a | UP | UP | UP (chronic Chagas disease) | NDE | UP (chronic Chagas disease) |
Nonaka, C.K.V. et al, Circulating miRNAs as Potential Biomarkers Associated with Cardiac Remodeling and Fibrosis in Chagas Disease Cardiomyopathy. International journal of molecular sciences, 20. |
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Mansouri, F. and Seyed Mohammadzad, M.H. Molecular miR‐19a in Acute Myocardial Infarction: Novel Potential Indicators of Prognosis and Early Diagnosis. Asian Pacific journal of cancer prevention: APJCP, 21, 975–982. |
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Zhong, J. et al, Circulating microRNA‐19a as a potential novel biomarker for diagnosis of acute myocardial infarction. International journal of molecular sciences, 15, 20355–20364. |
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Gao, F. et al, Therapeutic role of miR‐19a/19b in cardiac regeneration and protection from myocardial infarction. Nature communications, 10, 1802. |
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miR‐20b | UP | DOWN (T2DM) | NDE |
Wander, P.L. et al, Short Report: Circulating microRNAs are associated with incident diabetes over 10 years in Japanese Americans. Scientific reports, 10, 6509. |
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Zampetaki, A. et al, Plasma microRNA profiling reveals loss of endothelial miR‐126 and other microRNAs in type 2 diabetes. Circulation research, 107, 810–817. |
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Zhou, J.et al, microRNA expression profiling of heart tissue during fetal development. International journal of molecular medicine, 33, 1250–1260. |
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miR‐29b | UP | UP | UP (chronic Chagas disease) | NDE | UP (chronic Chagas disease, arrythmogenic right ventricle cardiomyopathy) |
Nonaka, C.K.V. et al, Circulating miRNAs as Potential Biomarkers Associated with Cardiac Remodeling and Fibrosis in Chagas Disease Cardiomyopathy. International journal of molecular sciences, 20. |
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Yang, Q. et al, Aberrant expression of miR‐29b‐3p influences heart development and cardiomyocyte proliferation by targeting NOTCH2. Cell proliferation, 53, e12764. |
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miR‐126 | UP | DOWN | UP | UP | UP | DOWN (T2DM, chronic renal disease) | NDE |
Wang, X. et al, Expression of miR‐126 and its potential function in coronary artery disease. African health sciences, 17, 474–480. |
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Li, H.Y. et al, Plasma MicroRNA‐126‐5p is Associated with the Complexity and Severity of Coronary Artery Disease in Patients with Stable Angina Pectoris. Cellular physiology and biochemistry: international journal of experimental cellular physiology, biochemistry, and pharmacology, 39, 837–846. |
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Fourdinier, O. et al, Serum levels of miR‐126 and miR‐223 and outcomes in chronic kidney disease patients. Scientific reports, 9, 4477. |
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miR‐144 | UP | UP | UP | UP (arrythmogenic right ventricle cardiomyopathy) | DOWN | UP (arrythmogenic right ventricle cardiomyopathy) |
de Gonzalo‐Calvo, D. et al, Epigenetic Biomarkers and Cardiovascular Disease: Circulating MicroRNAs. Revista espanola de cardiologia (English ed.), 70, 763–769. |
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Bye, A. et al, Circulating microRNAs predict future fatal myocardial infarction in healthy individuals ‐ The HUNT study. Journal of molecular and cellular cardiology, 97, 162–168. |
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Abu‐Halima, M. et al, Micro‐RNA signatures in monozygotic twins discordant for congenital heart defects. PloS one, 14, e0226164. |
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Song, L. et al, MiR‐451 is decreased in hypertrophic cardiomyopathy and regulates autophagy by targeting TSC1. Journal of cellular and molecular medicine, 18, 2266–2274. |
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miR‐182 | DOWN | UP | UP | UP (arrythmogenic right ventricle cardiomyopathy) | NDE | DOWN (arrythmogenic right ventricle cardiomyopathy) |
Taurino, C. et al, Gene expression profiling in whole blood of patients with coronary artery disease. Clinical science (London, England : 1979), 119, 335–343. |
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Cakmak, H.A. et al, The prognostic value of circulating microRNAs in heart failure: preliminary results from a genome‐wide expression study. Journal of cardiovascular medicine (Hagerstown, Md.), 16, 431–437. |
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https://doi.org/10.1038/srep21228 |
Li, N. et al, miR‐182 Modulates Myocardial Hypertrophic Response Induced by Angiogenesis in Heart. Scientific reports, 6, 21228. |
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miR‐223 | NDE | DOWN |
Barsanti, C. et al, Differential regulation of microRNAs in end‐stage failing hearts is associated with left ventricular assist device unloading. BioMed research international, 2015, 592512. |
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miR‐223 (Cont.) |
Chuang, T.Y. et al, MicroRNA‐223 Expression is Upregulated in Insulin Resistant Human Adipose Tissue. Journal of diabetes research, 2015, 943659. |
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Lu, H., Buchan, R.J. and Cook, S.A., MicroRNA‐223 regulates Glut4 expression and cardiomyocyte glucose metabolism. Cardiovascular research, 86, 410–420. |
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miR‐374b | NDE | DOWN | UP (STEMI vs. NSTEMI) | UP | DOWN (calcific aortic stenosis: valves) |
Ward, J.A. et al, Circulating Cell and Plasma microRNA Profiles Differ between Non‐ST‐Segment and ST‐Segment‐Elevation Myocardial Infarction. Family medicine & medical science research, 2, 108. |
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Xu, H.X. et al, Differential Expression of MicroRNAs in Calcific Aortic Stenosis. Clinical laboratory, 63, 1163–1170. |
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miR‐451a | NDE | NDE | DOWN | https://doi.org/10.1111/jcmm.12380 | Song, L. et al, MiR‐451 is decreased in hypertrophic cardiomyopathy and regulates autophagy by targeting TSC1. Journal of cellular and molecular medicine, 18, 2266–2274. | |||||
miR‐454 | DOWN | UP (DCM in children) *** | NDE | https://doi.org/10.3109/1354750x.2015.1118533 | Enes Coşkun, M. et al, Plasma microRNA profiling of children with idiopathic dilated cardiomyopathy. Biomarkers: biochemical indicators of exposure, response, and susceptibility to chemicals, 21, 56–61. | |||||
miR‐4485 | NDE | UP | / | / | ||||||
miR‐4732 | UP | UP (congenital heart defetcs) | NA | https://doi.org/10.1371/journal.pone.0226164 | Abu‐Halima, M .et al, Micro‐RNA signatures in monozygotic twins discordant for congenital heart defects. PloS one, 14, e0226164. |
LEGEND: NDE, not differentially expressed vs. ctrl; UP, up‐regulated; DOWN, down‐regulated; NA, undetermined by RT‐qPCR.