Key result
Review details molecular pathways driving post-MI fibrosis and imaging techniques to assess clinical impact.
Why the study?
Dysregulation of inflammatory or reparative processes following myocardial infarction may cause ventricular dysfunction and life-threatening arrhythmias affecting clinical outcomes.
This review summarizes the cellular processes, molecular pathways, and imaging techniques related to fibrosis and scar formation after myocardial infarction.
May guide antifibrotic target selection post-MI; leaves open prospective validation of imaging for clinical risk stratification.
The ischemic injury caused by myocardial infarction activates a complex healing process wherein a powerful inflammatory response and a reparative phase follow and balance each other. An intricate network of mediators finely orchestrate a large variety of cellular subtypes throughout molecular signaling pathways that determine the intensity and duration of each phase. At the end of this process, the necrotic tissue is replaced with a fibrotic scar whose quality strictly depends on the delicate balance resulting from the interaction between multiple actors involved in fibrogenesis. An inflammatory or reparative dysregulation, both in term of excess and deficiency, may cause ventricular dysfunction and life-threatening arrhythmias that heavily affect clinical outcome. This review discusses cellular process and molecular signaling pathways that determine fibrosis and the imaging technique that can characterize the clinical impact of this process in-vivo.
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Scalise et al. (2021) conducted a review in Myocardial Infarction. This review outlines the cellular processes and molecular signaling pathways driving post-myocardial infarction fibrosis and discusses imaging techniques for evaluating its clinical impact in vivo.
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