Key result
Despite the emergence of multiple candidate cardiac biomarkers for reversible myocardial damage, sufficient evidence is lacking to recommend their adoption into clinical practice.
Current evidence is insufficient to recommend the adoption of new cardiac biomarkers for reversible myocardial damage into clinical practice.
New biomarkers for reversible myocardial damage warrant clinical caution; leaves open the need for rigorous prospective validation.
Today, the increase of the blood concentration of cardiac troponins is designated as surrogate for cardiac necrosis and myocardial infarction, when an appropriate clinical and/or instrumental situation is present. As cardiac troponins reflect myocyte death, biomarkers of reversible myocardial damage in the absence of necrosis are, however, still needed to detect the presence of damage even before the irreversible injury is induced and identify "vulnerable" patients before major events occur, permitting adequate treatment. Markers of plaque destabilization and/or markers of myocardial ischemia could be enormously valuable in the emergency department setting if shown to contribute additional independent diagnostic information. However, a new cardiac biomarker is of definitive clinical value only if adequate assays for its measurement are available, its predictive value is defined in the right clinical context, optimal cut-off and release kinetics are known, demonstration of the marker incremental value is clear, there is consistency of marker performance across different settings, and, more importantly, there are data on the effect on patient management and outcome and on cost-effectiveness. Despite the emergence of multiple candidates, sufficient evidence for any of these has yet been demonstrated to recommend their adoption into clinical practice.
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Mauro Panteghini (2010) conducted a review in Myocardial damage and infarction. New cardiac biomarkers was evaluated. Despite the emergence of multiple candidate cardiac biomarkers for reversible myocardial damage, sufficient evidence is lacking to recommend their adoption into clinical practice.
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