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Updated: Apr 13, 2026

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease
Hai Gao1, Raviteja Reddy Guddeti2, Yasushi Matsuzawa2
1Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China; Beijing Institute of Heart, Lung and Blood Vessel Disease, Beijing, China.
Background And Objective:
MicroRNAs (miRNAs) have been shown to be associated with various physiological and pathological conditions, including inflammation and cardiovascular disease, but little is known about their relationship with the presence of coronary artery disease (CAD) and disease severity.
Methods:
A total of 195 consecutive subjects who underwent coronary angiography for chest pain evaluation were enrolled in this study. In CAD patients severity of coronary lesions was assessed by the number of diseased vessels and the Synergy between PCI with Taxus and Cardiac surgery score (SYNTAX score). Plasma levels of miRNA-145 were quantified by real-time quantitative polymerase chain reaction test, and logarithmic transformation of miRNA-145 levels (Ln_miRNA-145) was used for analyses due to its skewed distribution.
Results:
Of the 195 total subjects 167 patients were diagnosed as having CAD. Ln_miRNA-145 was significantly lower in CAD patients compared with the non-CAD group (-6.11 ± 0.92 vs. -5.06 ± 1.25; p < 0.001). In multivariable linear regression analyses CAD was significantly associated with lower Ln_miRNA-145 (Estimate, -0.50; standard error (SE), 0.11; p < 0.0001). Furthermore, among CAD patients, three-vessel disease, higher SYNTAX scores and STEMI were significantly associated with lower Ln_miRNA-145 ([Estimate, -0.40; SE, 0.07; p < 0.0001]; [Estimate, -0.02, SE, 0.10; p = 0.005] and [Estimate, -0.35, SE, 0.10; p < 0.001] respectively).
Conclusions:
Lower plasma levels of miRNA-145 were significantly associated with the presence as well as severity of CAD. As a potential biomarker for CAD, plasma miRNA-145 may be useful in predicting CAD and its severity in patients presenting with chest pain.
Insights
Lower plasma levels of microRNA-145 (miRNA-145) are linked to the presence and severity of coronary artery disease (CAD). This finding suggests miRNA-145 may serve as a biomarker for predicting CAD in patients with chest pain.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Molecular Biology
Background:
- MicroRNAs (miRNAs) are implicated in various physiological and pathological processes, including inflammation and cardiovascular disease.
- The specific relationship between miRNA levels, coronary artery disease (CAD) presence, and disease severity remains largely unexplored.
Purpose of the Study:
- To investigate the association between plasma levels of miRNA-145 and the presence and severity of coronary artery disease (CAD).
Main Methods:
- 195 subjects undergoing coronary angiography for chest pain evaluation were analyzed.
- Coronary artery disease (CAD) severity was assessed using the number of diseased vessels and the SYNTAX score.
- Plasma miRNA-145 levels were quantified using real-time quantitative polymerase chain reaction and logarithmically transformed (Ln_miRNA-145).
Main Results:
- Lower Ln_miRNA-145 levels were observed in patients with CAD compared to those without (p < 0.001).
- Multivariable analysis confirmed that CAD was significantly associated with lower Ln_miRNA-145 (p < 0.0001).
- Among CAD patients, three-vessel disease, higher SYNTAX scores, and STEMI were significantly correlated with reduced Ln_miRNA-145 levels (p < 0.0001, p = 0.005, and p < 0.001, respectively).
Conclusions:
- Plasma miRNA-145 levels are significantly lower in patients with coronary artery disease (CAD).
- Decreased miRNA-145 levels correlate with increased CAD severity.
- Plasma miRNA-145 shows potential as a biomarker for predicting CAD presence and severity in patients presenting with chest pain.
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Coronary Artery Disease I: Introduction
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Coronary Artery Disease II: Pathophysiology
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