A Novel Circulating MicroRNA for the Detection of Acute Myocarditis

被引:144
作者
Blanco-Dominguez, Rafael [1 ]
Sanchez-Diaz, Raquel [1 ,12 ]
de la Fuente, Hortensia [3 ,12 ]
Jimenez-Borreguero, Luis J. [4 ,12 ]
Matesanz-Marin, Adela [1 ]
Relano, Marta [1 ]
Jimenez-Alejandre, Rosa [1 ]
Linillos-Pradillo, Beatriz [1 ]
Tsilingiri, Katerina [1 ]
Martin-Mariscal, Maria L. [7 ]
Alonso-Herranz, Laura [2 ]
Moreno, Guillermo [8 ,9 ]
Martin-Asenjo, Roberto [8 ,9 ]
Garcia-Guimaraes, Marcos M. [4 ]
Bruno, Katelyn A. [15 ]
Dauden, Esteban [5 ]
Gonzalez-Alvaro, Isidoro [6 ]
Villar-Guimerans, Luisa M. [10 ]
Martinez-Leon, Amaia [13 ]
Salvador-Garicano, Ane M. [16 ,17 ,18 ]
Michelhaugh, Sam A. [16 ,17 ,18 ]
Ibrahim, Nasrien E. [16 ,17 ,18 ]
Januzzi, James L. [16 ,17 ,18 ]
Kottwitz, Jan [19 ]
Iliceto, Sabino [20 ]
Plebani, Mario [22 ]
Basso, Cristina [21 ]
Baritussio, Anna [20 ]
Seguso, Mara [22 ]
Marcolongo, Renzo [23 ]
Ricote, Mercedes [2 ]
Fairweather, DeLisa [15 ]
Bueno, Hector [2 ,8 ,9 ]
Fernandez-Friera, Leticia [2 ,11 ]
Alfonso, Fernando [4 ,12 ]
Caforio, Alida L. P. [20 ]
Pascual-Figal, Domingo A. [1 ,12 ,14 ]
Heidecker, Bettina [24 ]
Luscher, Thomas F. [25 ,26 ]
Das, Saumya [16 ,17 ,18 ]
Fuster, Valentin [1 ,27 ]
Ibanez, Borja [2 ,7 ,12 ]
Sanchez-Madrid, Francisco [1 ,3 ,12 ]
Martin, Pilar [1 ,12 ]
机构
[1] Ctr Nacl Invest Cardiovasc CNIC, Vasc Pathophysiol Area, Madrid, Spain
[2] Ctr Nacl Invest Cardiovasc CNIC, Myocardial Pathophysiol Area, Madrid, Spain
[3] Hosp Univ Princesa, Inst Invest Sanit, Dept Immunol, Madrid, Spain
[4] Hosp Univ Princesa, Inst Invest Sanitaria, Dept Cardiol, Madrid, Spain
[5] Hosp Univ Princesa, Inst Invest Sanit, Dept Dermatol, Madrid, Spain
[6] Hosp Univ Princesa, Inst Invest Sanit, Dept Rheumatol, Madrid, Spain
[7] Fdn Jimenez Diaz, Madrid, Spain
[8] Hosp Univ 12 Octubre, Cardiol Dept, Madrid, Spain
[9] Inst Invest Sanit Hosp 12 Octubre, Madrid, Spain
[10] Hosp Ramon & Cajal, Dept Immunol, Madrid, Spain
[11] HM Hosp, Ctr Integral Enfermedades Cardiovasc, Madrid, Spain
[12] CIBER Enfermedades Cardiovasc, Madrid, Spain
[13] Hosp Univ Cent Asturias, Oviedo, Spain
[14] Hosp Univ Virgen Arrixaca, Cardiol Dept, Murcia, Spain
[15] Mayo Clin, Dept Cardiovasc Med, Jacksonville, FL 32224 USA
[16] Massachusetts Gen Hosp, Cardiovasc Div, Boston, MA 02114 USA
[17] Massachusetts Gen Hosp, Corrigan Minehan Heart Ctr, Boston, MA 02114 USA
[18] Harvard Med Sch, Boston, MA 02115 USA
[19] Kanntonsspital St Gallen, Klin Anesthesiol & Intens Med, St Gallen, Switzerland
[20] Univ Padua, Dept Cardiac Thorac Vasc Sci & Publ Hlth, Cardiol, Padua, Italy
[21] Univ Padua, Dept Cardiac Thorac Vasc Sci & Publ Hlth, Cardiovasc Pathol Unit, Padua, Italy
[22] Univ Padua, Dept Lab Med, Padua, Italy
[23] Univ Padua, Dept Med Hematol & Clin Immunol, Padua, Italy
[24] Charite Univ Med Berlin, Campus Benjamin Franklin, Berlin, Germany
[25] Imperial Coll, London, England
[26] Royal Brompton & Harefield Hosp, London, England
[27] Icahn Sch Med Mt Sinai, Cardiovasc Inst, New York, NY 10029 USA
关键词
CARDIOVASCULAR MAGNETIC-RESONANCE; EUROPEAN-SOCIETY; MANAGEMENT; DIAGNOSIS; THERAPY;
D O I
10.1056/NEJMoa2003608
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.) A Novel MicroRNA in Acute Myocarditis Using microRNA microarray analysis of Th17 cells in mice with myocarditis or myocardial infarction, investigators found that the microRNA mmu-miR-721 was specific for myocarditis. The human homologue, designated hsa-miR-Chr8:96, was identified in patients with myocarditis and found to distinguish myocarditis from myocardial infarction.
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收藏
页码:2014 / 2027
页数:14
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