AI Article Synopsis

  • * Recent studies have shown that microRNAs, especially miR-146, can serve as promising diagnostic biomarkers and therapeutic targets for CVD, highlighting their regulatory effects on disease mechanisms.
  • * This paper reviews current research on miR-146, particularly regarding its involvement in conditions like coronary artery disease, cardiomyopathy, and myocardial infarction, and emphasizes its potential use in improving treatment outcomes for CVD patients.

Article Abstract

Cardiovascular diseases (CVDs) are the prime cause of morbidity and mortality worldwide. Although noticeable progress has been made in the diagnosis, prognosis, and treatment, there is still a critical demand for new diagnostic biomarkers and novel therapeutic interventions to reduce this disease incidence. Many investigations have been conducted on the regulatory effects of microRNAs in cardiovascular diseases. miRNA circulating serum level changes are correlated with several CVDs. In addition, there is growing evidence representing the potential role of miRNAs as diagnostic biomarkers or potential therapeutic targets for CVD. Preliminary studies identified the prominent role of miR-146 in host defense, innate immunity, and different immunological diseases by regulating cytokine production and innate immunity modification in bacterial infections. However, more recently, it was also associated with CVD development. miR-146 has received much attention, with positive results in most studies. Research demonstrated the crucial role of this molecule in the pathogenesis of cardiac disease and related mechanisms. As a result, many potential applications of miR-146 are expected. In this paper, we provide an overview of recent studies highlighting the role of miR-146 in CVD, focusing on CAD (coronary artery disease), cardiomyopathy, and MI (myocardial infarction) in particular and discussing its current scientific state, and use a prognostic biomarker as a therapeutic agent for cardiovascular diseases.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11401689PMC
http://dx.doi.org/10.1155/2022/7767598DOI Listing

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