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Updated: Feb 20, 2026

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
Characterization of serum miRNAs as molecular biomarkers for acute Stanford type A aortic dissection diagnosis
Zhenjun Xu1, Qiang Wang1, Jun Pan1
1Department of Thoracic and Cardiovascular Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing, 210008, China.
Abstract:
Early and convenient diagnosis is urgently needed for acute Stanford type A aortic dissection (AAAD) patients due to its high mortality within the first 48 hours. Circulating microRNAs (miRNAs) are promising biomarkers of cardiovascular diseases, however, little is known about circulating miRNAs involved in AAAD. Here, the blood serum was sampled from 104 AAAD+ patients and 103 age-matched donors. Initial screening was conducted using the TaqMan Low Density Array followed by RT-qPCR confirmation. According to the two-phase selection and validation process, we found that miR-25, miR-29a and miR-155 were significantly elevated, while miR-26b was markedly decreased in AAAD+ serum samples compared with AAAD- individuals. Most importantly, for individuals with hypertension, which is a major contributor to AAAD, the 4-miRNA panel also showed high accuracy in predicting those who are more likely to develop AAAD. In the blind trial set, the panel correctly classified 93.33% AAAD+ patients and 86.67% controls from the hypertension cohort. Finally, the serum miRNA-based biomarker for early AAAD detection was supported by a retrospective analysis. Taken together, we identify a distinct profile of 4-miRNA that can serve as a noninvasive biomarker for AAAD diagnosis, especially for those with hypertension.
Insights
A novel panel of four circulating microRNAs (miRNAs) shows promise for early, noninvasive diagnosis of acute Stanford type A aortic dissection (AAAD), particularly in hypertensive patients. This discovery aids in timely intervention for this critical cardiovascular condition.
Area of Science:
- Cardiovascular Research
- Molecular Diagnostics
- Biomarker Discovery
Background:
- Acute Stanford type A aortic dissection (AAAD) presents a high mortality risk within 48 hours, necessitating urgent and convenient diagnostic methods.
- Circulating microRNAs (miRNAs) are emerging as potential biomarkers for cardiovascular diseases, but their role in AAAD remains largely unexplored.
Purpose of the Study:
- To identify circulating miRNAs as noninvasive biomarkers for the early diagnosis of acute Stanford type A aortic dissection (AAAD).
- To evaluate the diagnostic accuracy of a specific miRNA panel, especially in individuals with hypertension, a key risk factor for AAAD.
Main Methods:
- Serum samples were collected from 104 AAAD+ patients and 103 healthy controls.
- Initial miRNA screening utilized TaqMan Low Density Array, followed by RT-qPCR for confirmation.
- A two-phase selection and validation process identified significant miRNA alterations.
Main Results:
- A distinct profile of four miRNAs (miR-25, miR-29a, miR-155 elevated; miR-26b decreased) was identified in AAAD+ serum.
- The 4-miRNA panel demonstrated high accuracy in a hypertensive cohort, classifying 93.33% of AAAD+ patients and 86.67% of controls in a blind trial.
- Retrospective analysis supported the utility of this serum miRNA panel for early AAAD detection.
Conclusions:
- A specific 4-miRNA signature in serum serves as a potential noninvasive biomarker for early AAAD diagnosis.
- This miRNA panel is particularly effective for identifying individuals at higher risk within the hypertensive population.
- The findings support the development of novel diagnostic tools for acute aortic dissection.
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