A Novel Circulating Noncoding Small RNA for the Detection of Acute Myocarditis

Rafael Blanco-Domínguez(MACOM (United States)), Raquel Sánchez‐Díaz(MACOM (United States)), Hortensia de la Fuente(MACOM (United States)), Luis Jesús Jiménez‐Borreguero(MACOM (United States)), Adela Matesanz-Marín(MACOM (United States)), Marta Relaño(MACOM (United States)), Rosa Jiménez-Alejandre(MACOM (United States)), Beatriz Linillos-Pradillo(MACOM (United States)), Katerina Tsilingiri(MACOM (United States)), Maria Luisa Martín‐Mariscal(MACOM (United States)), Laura Alonso-Herranz(MACOM (United States)), Guillermo Moreno(MACOM (United States)), Roberto Martín‐Asenjo(MACOM (United States)), Marcos García-Guimarães(MACOM (United States)), Katelyn A. Bruno(MACOM (United States)), E. Daudén(MACOM (United States)), Isidoro González‐Álvaro(MACOM (United States)), Luisa M. Villar-Guimerans(MACOM (United States)), Amaia Martínez-León(MACOM (United States)), Ane M. Salvador-Garicano(MACOM (United States)), Sam A. Michelhaugh(MACOM (United States)), Nasrien E. Ibrahim(MACOM (United States)), James L. Januzzi(MACOM (United States)), Jan Kottwitz(MACOM (United States)), Sabino Iliceto(MACOM (United States)), Mario Plebani(MACOM (United States)), Cristina Basso(MACOM (United States)), Anna Baritussio(MACOM (United States)), Mara Seguso(MACOM (United States)), R Marcolongo(MACOM (United States)), Mercedes Ricote(MACOM (United States)), DeLisa Fairweather(MACOM (United States)), Héctor Bueno(MACOM (United States)), Leticia Fernández‐Friera(MACOM (United States)), Fernándo Alfonso(MACOM (United States)), Alida L.P. Caforio(MACOM (United States)), Domingo A. Pascual‐Figal(MACOM (United States)), Bettina Heidecker(MACOM (United States)), Thomas F. Lüscher(MACOM (United States)), Saumya Das(MACOM (United States)), Valentı́n Fuster(MACOM (United States)), Borja Ibáñez(MACOM (United States)), Francisco Sánchez‐Madrid(MACOM (United States)), Pilar Martı́n(MACOM (United States))
New England Journal of Medicine
May 26, 2021
Cited by 188Open Access
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Abstract

BACKGROUND: The diagnosis of acute myocarditis typically requires either endomyocardial biopsy (which is invasive) or cardiovascular magnetic resonance imaging (which is not universally available). Additional approaches to diagnosis are desirable. We sought to identify a novel microRNA for the diagnosis of acute myocarditis. METHODS: To identify a microRNA specific for myocarditis, we performed microRNA microarray analyses and quantitative polymerase-chain-reaction (qPCR) assays in sorted CD4+ T cells and type 17 helper T (Th17) cells after inducing experimental autoimmune myocarditis or myocardial infarction in mice. We also performed qPCR in samples from coxsackievirus-induced myocarditis in mice. We then identified the human homologue for this microRNA and compared its expression in plasma obtained from patients with acute myocarditis with the expression in various controls. RESULTS: We confirmed that Th17 cells, which are characterized by the production of interleukin-17, are a characteristic feature of myocardial injury in the acute phase of myocarditis. The microRNA mmu-miR-721 was synthesized by Th17 cells and was present in the plasma of mice with acute autoimmune or viral myocarditis but not in those with acute myocardial infarction. The human homologue, designated hsa-miR-Chr8:96, was identified in four independent cohorts of patients with myocarditis. The area under the receiver-operating-characteristic curve for this novel microRNA for distinguishing patients with acute myocarditis from those with myocardial infarction was 0.927 (95% confidence interval, 0.879 to 0.975). The microRNA retained its diagnostic value in models after adjustment for age, sex, ejection fraction, and serum troponin level. CONCLUSIONS: After identifying a novel microRNA in mice and humans with myocarditis, we found that the human homologue (hsa-miR-Chr8:96) could be used to distinguish patients with myocarditis from those with myocardial infarction. (Funded by the Spanish Ministry of Science and Innovation and others.).


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