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Updated: Mar 18, 2026

Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Plasma proteomic analysis of stable coronary artery disease indicates impairment of reverse cholesterol pathway
Trayambak Basak1,2, Vinay Singh Tanwar1, Gourav Bhardwaj1
1Genomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Insights
Quantitative plasma proteomics identified four key proteins—albumin, Apo A1, Apo C1, and Apo AIV—associated with coronary artery disease (CAD). These proteins, involved in reverse cholesterol transport, significantly improve CAD prediction when combined with traditional risk factors.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Proteomics
Background:
- Coronary artery disease (CAD) is a leading global cause of mortality.
- Traditional risk factors for CAD have limited predictive accuracy.
- Quantitative plasma proteomics offers potential for novel biomarker discovery.
Purpose of the Study:
- To identify differentially expressed proteins in stable CAD patients using a multi-phase approach.
- To discover novel plasma protein biomarkers for improved CAD risk stratification.
- To investigate the role of the reverse cholesterol pathway in CAD pathogenesis.
Main Methods:
- Three-phase study involving discovery, verification, and validation cohorts.
- iTRAQ-based quantitative proteomic analysis of plasma samples.
- Multivariate logistic regression and ROC analysis for biomarker association and predictive accuracy.
Main Results:
- Four proteins—Apolipoprotein A1 (Apo A1), Apolipoprotein A4 (ApoA4), Apolipoprotein C1 (Apo C1), and albumin—were significantly associated with CAD.
- These proteins, along with diabetes and hypertension, accounted for approximately 88% of CAD cases by ROC analysis.
- Albumin (OR 6.70) and Apo AI (OR 5.07) showed the strongest association with CAD.
Conclusions:
- Down-regulation of specific apolipoproteins and albumin suggests impaired reverse cholesterol transport in CAD.
- The identified proteins represent promising novel biomarkers for CAD.
- Proteomic approaches can enhance the understanding and prediction of cardiovascular diseases.
Abstract:
Coronary artery disease (CAD) is one of the largest causes of death worldwide yet the traditional risk factors, although useful in identifying people at high risk, lack the desired predictive accuracy. Techniques like quantitative plasma proteomics holds immense potential to identify newer markers and this study (conducted in three phases) was aimed to identify differentially expressed proteins in stable CAD patients. In the first (discovery) phase, plasma from CAD cases (angiographically proven) and controls were subjected to iTRAQ based proteomic analysis. Proteins found to be differentially expressed were then validated in the second and third (verification and validation) phases in larger number of (n = 546) samples. After multivariate logistic regression adjusting for confounding factors (age, diet, etc.), four proteins involved in the reverse cholesterol pathway (Apo A1, ApoA4, Apo C1 and albumin) along with diabetes and hypertension were found to be significantly associated with CAD and could account for approximately 88% of the cases as revealed by ROC analysis. The maximum odds ratio was found to be 6.70 for albumin (p < 0.0001), followed by Apo AI (5.07, p < 0.0001), Apo CI (4.03, p = 0.001), and Apo AIV (2.63, p = 0.003). Down-regulation of apolipoproteins and albumin implicates the impairment of reverse cholesterol pathway in CAD.
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