Blood MicroRNA Biomarker Distinguishes Myocarditis from Myocardial Infarction
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By LabMedica International staff writers Posted on 08 Jun 2021 |
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Image: First biomarker in blood that distinguishes myocarditis from an acute myocardial infarction (Photo courtesy of Centro Nacional De Investigaciones Cardiovasculares)
A novel microRNA has been found that can be used to distinguish patients with myocarditis from those with myocardial infarction.
MiRNAs comprise a class of about 20 nucleotides-long RNA fragments that block gene expression by attaching to molecules of messenger RNA in a fashion that prevents them from transmitting the protein synthesizing instructions they had received from the DNA. With their capacity to fine-tune protein expression via sequence-specific interactions, miRNAs help regulate cell maintenance and differentiation. In addition to miRNAs playing an essential role in tumor development, dysregulation of certain miRNAs has been associated with many different diseases, such as dementia and cardiovascular conditions.
Myocarditis is usually diagnosed after coronary angiography or computed tomography scans have ruled out coronary artery disease, followed by confirmation of the diagnosis by magnetic resonance imaging (MRI). However, not all centers have access to MRI technology, and the current gold standard for myocarditis diagnosis is endomyocardial biopsy, an invasive procedure normally reserved for severe cases. Thus a pressing clinical need exists for the development of reliable and accessible tools for the early diagnosis of acute myocarditis.
In this regard, investigators at the Centro Nacional de Investigaciones Cardiovasculares (Madrid, Spain) and their collaborators in Spain and abroad sought to identify a novel microRNA for the diagnosis of acute myocarditis.
To identify a microRNA specific for myocarditis, they 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. They 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 revealed that the human homologue, designated hsa-miR-Chr8:96, could be 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. The microRNA retained its diagnostic value in models after adjustment for age, sex, ejection fraction, and serum troponin level.
"Our finding has great potential as a valuable clinical tool for the precise and noninvasive diagnosis of myocarditis from small drops of blood," said senior author Dr. Pilar Martín, a research professor at the Centro Nacional de Investigaciones Cardiovasculares.
The myocarditis paper was published in the May 27, 2021, online edition of The New England Journal of Medicine.
Related Links:
Centro Nacional de Investigaciones Cardiovasculares
MiRNAs comprise a class of about 20 nucleotides-long RNA fragments that block gene expression by attaching to molecules of messenger RNA in a fashion that prevents them from transmitting the protein synthesizing instructions they had received from the DNA. With their capacity to fine-tune protein expression via sequence-specific interactions, miRNAs help regulate cell maintenance and differentiation. In addition to miRNAs playing an essential role in tumor development, dysregulation of certain miRNAs has been associated with many different diseases, such as dementia and cardiovascular conditions.
Myocarditis is usually diagnosed after coronary angiography or computed tomography scans have ruled out coronary artery disease, followed by confirmation of the diagnosis by magnetic resonance imaging (MRI). However, not all centers have access to MRI technology, and the current gold standard for myocarditis diagnosis is endomyocardial biopsy, an invasive procedure normally reserved for severe cases. Thus a pressing clinical need exists for the development of reliable and accessible tools for the early diagnosis of acute myocarditis.
In this regard, investigators at the Centro Nacional de Investigaciones Cardiovasculares (Madrid, Spain) and their collaborators in Spain and abroad sought to identify a novel microRNA for the diagnosis of acute myocarditis.
To identify a microRNA specific for myocarditis, they 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. They 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 revealed that the human homologue, designated hsa-miR-Chr8:96, could be 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. The microRNA retained its diagnostic value in models after adjustment for age, sex, ejection fraction, and serum troponin level.
"Our finding has great potential as a valuable clinical tool for the precise and noninvasive diagnosis of myocarditis from small drops of blood," said senior author Dr. Pilar Martín, a research professor at the Centro Nacional de Investigaciones Cardiovasculares.
The myocarditis paper was published in the May 27, 2021, online edition of The New England Journal of Medicine.
Related Links:
Centro Nacional de Investigaciones Cardiovasculares
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