Key result
Elevated serum miR-499a is linked to acute MI with high diagnostic accuracy.
Why the study?
Circulating microRNAs and their functional genetic variants may serve as markers and influence susceptibility to cardiovascular disease, but their roles in acute MI and CVD in Egyptian patients were unclear.
Is circulating miR-499a expression and its genetic variant rs3746444 associated with acute myocardial infarction in an Egyptian population?
Case-Control (n=414)
Is circulating miR-499a expression and its genetic variant rs3746444 associated with acute myocardial infarction in an Egyptian population?
Effect estimate: > 105-fold
p-value: p=< .001
Circulating miR-499a levels and its variant rs3746444 A/G are significantly associated with acute MI and CAD in the Egyptian population, suggesting potential utility as a diagnostic biomarker.
miR-499a shows promise as acute MI biomarker; leaves open prospective validation before clinical use.
BACKGROUND: Circulating microRNAs could be powerful markers of acute myocardial infarction (MI) and its functional genetic variants could increase susceptibility to cardiovascular disease (CVD). The current study aimed to quantify the microRNA (miR)-499a levels in serum of MI patients compared to hypertensive and healthy subjects and to investigate the association of its A/G variant rs3746444 with CVD in a sample of an Egyptian population. METHODS: Serum miR-499a relative expressions were measured in 110 acute MI patients, 76 hypertensive patients, and 121 healthy controls by Real-time quantitative polymerase chain reaction. MIR-499a genotyping was performed for an additional 107 coronary artery disease patients by Real-time allele discrimination assay. RESULTS: Acute MI patients showed high relative expression of miR-499a (> 105-fold, p < .001), and it was nearly undetectable in healthy controls and hypertensive patients. It showed an area under the curve of 0.953, with a sensitivity of 97.2% and a specificity of 75.0%. ST-elevation MI (STEMI) patients had higher miR-499a serum levels than patients with Non-STEMI. There was a significant association of MIR-499a variant with acute MI but not with hypertension under all genetic models tested. As a new finding, in overall and stratified analysis, the miR-499a variant was not correlated with its expression profile. CONCLUSIONS: Circulating miR-499a levels could be a useful biomarker, discriminating acute MI within 12 hours from healthy subjects. Its variant rs3746444 A/G is associated with increased susceptibility to acute MI and CAD in Egyptian population.
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Fawzy et al. (2017) conducted a case-control in Acute myocardial infarction and cardiovascular disease (n=414). miR-499a expression and rs3746444 variant vs. Healthy controls and hypertensive patients was evaluated on Serum miR-499a relative expression (> 105-fold, p=< .001). Serum miR-499a expression was >105-fold higher in acute MI patients compared to controls (p < 0.001), yielding an AUC of 0.953 for discriminating acute MI.
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