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Updated: Mar 1, 2026

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
Association between circulating microRNA-208a and severity of coronary heart disease
Yao Zhang1, Hai-Hong Li1, Rui Yang1
1a Department of Intensive Medicine , Hongqi Hospital, Mudanjiang Medical University , Mudanjiang , China.
Insights
Circulating microRNA-208a levels are elevated in coronary heart disease (CHD) patients and correlate with disease severity. This cardiac-specific biomarker shows potential for diagnosing CHD and assessing coronary atherosclerosis progression.
Area of Science:
- Cardiovascular Biology
- Molecular Diagnostics
- Biomarker Discovery
Background:
- MicroRNA-208a (miR-208a) is a cardiac-specific microRNA involved in cardiac development.
- Elevated plasma miR-208a levels have been observed in coronary heart disease (CHD) patients.
- The association between miR-208a and CHD severity remained unexplored.
Purpose of the Study:
- To investigate the relationship between circulating miR-208a levels and the presence of CHD.
- To determine if miR-208a levels correlate with the severity of coronary atherosclerosis.
Main Methods:
- Quantitative real-time PCR was used to measure circulating miR-208a expression in 290 CHD patients and 110 controls.
- The Gensini score was employed to quantify the severity of coronary stenotic lesions.
- Receiver operating characteristic (ROC) analysis was performed to assess the diagnostic potential of miR-208a.
Main Results:
- CHD patients exhibited significantly higher miR-208a expression compared to controls (p < .001).
- miR-208a levels demonstrated a significant positive correlation with the Gensini score (r = 0.8525, p < .001), indicating increased expression with greater disease severity.
- ROC analysis revealed an area under the curve (AUC) of 0.919 for miR-208a, with 75.5% sensitivity and 93.6% specificity.
Conclusions:
- Circulating miR-208a levels are significantly associated with the presence and severity of coronary heart disease.
- miR-208a shows promising potential as a biomarker for diagnosing CHD and evaluating coronary atherosclerosis.
- These findings suggest miR-208a may play a role in atherogenesis.
Abstract:
Circulating microRNA (miR)-208a is specifically expressed in the heart muscle, which is involved in the regulation of myosin during cardiac development. Previous studies reported that cardiac-specific miR-208a level is significantly higher in plasma of coronary heart disease (CHD) patients. However, whether it correlates with severity of CHD, has never been elucidated before. The aim of this study was to explore the association between miR-208a and the presence and severity of CHD. Samples were collected from 290 CHD patients and 110 subjects with angiographic exclusion of CHD. Circulating miRNA-208a expression was detected using quantitative real-time PCR. The Gensini score was used to evaluate the severity of coronary stenotic lesions. Expression of miRNA-208a was identified on the basis of the quartiles of the Gensini score, and association between the miRNA-208a levels and CHD was analyzed. Diagnostic potential of miR-208a of CHD was performed by ROC analysis. CHD patients had higher miRNA-208a expression (1.61, 0.45-3.86 vs. 0.66, 0.11-1.42, p < .001), and the biomarker level significantly increased following an increasing the Gensini score (p < .001). Gensini score was significantly associated with miRNA-208a expression (r = 0.8525, p < .001). The optimal cut-off value of the relative level of miR-208a was with a specificity of 93.6% and a sensitivity of 75.5%. The AUC of miR-208a was 0.919 (95% CI, 0.893-0.945; p < .001). These preliminary results suggest that the expression of miR-208a may be associated with atherogenesis. The level of circulating miR-208a in predicting the severity of coronary atherosclerosis may have a relatively certain value.
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