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MicroRNA Signatures in Cardiometabolic Disorders as a Next-Generation Diagnostic Approach: Current Insight
Concetta Iside1, Francesca Picone1, Paola Di Pietro1
1Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, 84081 Baronissi, Italy.
Insights
Circulating microRNAs (miRNAs) show promise as sensitive biomarkers for early detection and risk stratification of cardiometabolic diseases. Further research is needed to overcome challenges for clinical translation of these molecular signatures.
Area of Science:
- Biochemistry
- Molecular Biology
- Genetics
Background:
- Cardiometabolic diseases are a leading cause of global morbidity and mortality.
- Current diagnostic tools lack sensitivity and specificity for early risk stratification.
- There is a need for novel biomarkers to capture molecular complexity.
Purpose of the Study:
- To review the diagnostic and prognostic role of circulating microRNAs (miRNAs) in cardiometabolic disease.
- To highlight miRNAs as potential early detection biomarkers and indicators of therapeutic response.
- To discuss limitations and future directions for clinical translation of miRNAs.
Main Methods:
- Comprehensive review of current evidence on circulating miRNAs in cardiometabolic disease.
- Analysis of miRNA characteristics, including stability, specificity, and dynamic changes.
- Discussion of challenges in methodological standardization and clinical validation.
Main Results:
- Altered circulating miRNA profiles are linked to key pathological processes in cardiometabolic disease.
- miRNAs demonstrate potential for early detection, patient stratification, and monitoring therapeutic response.
- Significant variability in methodologies and normalization strategies exists.
Conclusions:
- Circulating miRNAs hold significant potential as next-generation biomarkers for precision medicine in cardiometabolic diseases.
- Standardization of methodologies and robust clinical validation are crucial for widespread adoption.
- Overcoming current limitations will enable the full harnessing of miRNA potential.
Abstract:
Cardiometabolic diseases, including cardiovascular disorders and type 2 diabetes mellitus, are the leading cause of morbidity and mortality worldwide, placing a significant burden on healthcare systems. Although advances in imaging and risk stratification have improved disease management, conventional diagnostic and prognostic tools often lack the requisite sensitivity and specificity for early and precise risk stratification. This limitation stems from their poor ability to capture the full molecular complexity of these conditions, underscoring an urgent need for innovative biomarkers to bridge these gaps. MicroRNAs, small non-coding RNAs that regulate gene expression post-transcriptionally, have emerged as promising candidates. Their characteristics offer several advantages over traditional methods, including exceptional stability in biological fluids, strong tissue and disease specificity, and the ability to reflect dynamic pathological changes. These unique features enable miRNAs to detect subtle molecular alterations that may precede clinical symptoms, thereby overcoming key limitations of current diagnostic approaches. Altered circulating miRNA profiles have been linked to pathological processes such as endothelial dysfunction, inflammation, oxidative stress, and maladaptive cardiac remodeling. This review provides a comprehensive overview of the current evidence supporting the diagnostic and prognostic role of circulating miRNAs in cardiometabolic disease. We highlight their potential as early detection biomarkers, tools for patient stratification, and indicators of therapeutic response. Furthermore, we discuss key limitations to clinical translation, including methodological variability, challenges in sample handling, differences in normalization strategies, and platform-dependent quantification inconsistencies. Overcoming these obstacles and achieving robust large-scale clinical validation will be essential to fully harness the potential of miRNAs as next-generation molecular signatures in precision medicine.
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