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miRNAs emerge as circulating biomarkers of post-myocardial infarction heart failure
Marina Sampaio Cruz1, Ananília Medeiros Gomes da Silva1, Karla Simone Costa de Souza1
1Department of Clinical and Toxicology Analysis, Federal University of Rio Grande do Norte, Natal, RN, Brazil.
Insights
Circulating microRNAs (miRNAs) show promise as non-invasive biomarkers for heart failure (HF) following myocardial infarction (MI). This review identifies key miRNAs in blood samples for potential early diagnosis and monitoring of ischemic HF.
Area of Science:
- Cardiology and Molecular Biology
- Biomarker Discovery
- Genomics and RNA Biology
Background:
- Heart failure (HF) is a major clinical syndrome often resulting from myocardial infarction (MI), the leading cause of cardiovascular disease.
- Current diagnostic methods for ischemic HF rely on clinical evaluation, as existing biomarkers are costly, lack specificity, and are unsuitable for early detection.
- Late diagnosis of HF is common, with only about 25% of symptoms appearing post-MI, highlighting the need for improved diagnostic tools.
Purpose of the Study:
- To identify circulating microRNAs (miRNAs) found in plasma, serum, and whole blood of patients with post-myocardial infarction heart failure.
- To explore the potential of these circulating miRNAs as non-invasive biomarkers for the development, monitoring, and prognosis of ischemic HF.
- To propose potential therapeutic targets and future applications of miRNAs in HF diagnostics.
Main Methods:
- A comprehensive review of 19 experimental human studies was conducted.
- The studies investigated the association between circulating miRNAs and the pathophysiology, progression, or outcomes of ischemic heart failure.
- Data synthesis focused on identifying miRNAs relevant to post-MI HF patients.
Main Results:
- Circulating miRNAs are implicated in the regulation of pathophysiological processes underlying heart failure after myocardial infarction.
- Specific miRNAs detected in blood samples (plasma, serum, whole blood) are associated with post-MI HF.
- These findings suggest a role for miRNAs in the development, monitoring, and prognosis of ischemic heart failure.
Conclusions:
- Circulating miRNAs represent promising non-invasive biomarkers for early diagnosis and management of heart failure.
- Further research into specific miRNAs could lead to novel therapeutic strategies and improved patient outcomes for ischemic heart failure.
- miRNAs offer a potential advancement over current diagnostic methods for heart failure.
Abstract:
Heart failure (HF) is a clinical syndrome that involves structural changes in the heart, leading to a decrease in cardiac output, mainly caused by myocardial infarction (MI), which is the most common form of cardiovascular disease worldwide. Clinical evaluation remains the most accurate diagnostic method for ischemic HF, since the known biomarkers have high cost, are difficult to use for early diagnosis, and have low specificity. This often leads to late diagnosis since only ~ 25% symptoms of HF appear after MI. Studies suggest that small non-coding RNAs (miRNAs) play an important role in the regulation of this pathophysiological process and are, therefore, important targets in the discovery of non-invasive biomarkers for HF. Thus, the aim of this review was to identify circulating miRNAs (plasma, serum, and whole blood) described for post-MI HF patients. This review covered 19 experimental studies on humans, which investigated the relationship between circulating miRNAs and the development, monitoring, or prognosis of ischemic HF. This analysis was aimed at proposing potential targets for HF and the future application of miRNAs as HF biomarkers.
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