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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Apolipoprotein C3 and necrotic core volume are correlated but also associated with future cardiovascular events
Takayuki Ohwada1, Takayuki Sakamoto2, Satoshi Suzuki3
1Department of Cardiology, Fukushima Red Cross Hospital, Fukushima, Japan. ikyoku18@fukushima-med-jrc.jp.
Insights
High levels of apolipoprotein C3 (apo-C3) are linked to more necrotic plaque and increased risk of major adverse cardiovascular events (MACEs) in stable coronary disease patients post-percutaneous coronary intervention (PCI). Apo-C3 may predict future MACEs.
Area of Science:
- Cardiovascular Medicine
- Biochemistry
- Medical Imaging
Background:
- Stable coronary disease (SCD) management involves understanding plaque vulnerability.
- Apolipoprotein C3 (apo-C3) role in plaque composition and cardiovascular events needs further clarification.
- Percutaneous coronary intervention (PCI) is a common treatment for SCD.
Purpose of the Study:
- To determine the association between apo-C3 levels and coronary plaque characteristics.
- To investigate the relationship between apo-C3 and major adverse cardiovascular events (MACEs) within 4 years post-PCI.
- To evaluate apo-C3 as a potential predictor of MACEs in SCD patients.
Main Methods:
- Analysis of 98 SCD patients undergoing PCI.
- Laboratory assessment of apo-C3 levels.
- Virtual histology-intravascular ultrasound (VH-IVUS) for plaque composition analysis (necrotic core volume - %NC).
- Kaplan-Meier and multivariate Cox hazard analyses for MACE prediction.
Main Results:
- Higher apo-C3 levels correlated with increased necrotic core volume (%NC) in culprit lesions.
- High apo-C3 group showed significantly higher %NC compared to the low apo-C3 group.
- High apo-C3 and high %NC were independent predictors of 4-year MACEs.
- Patients with high apo-C3 or high %NC had a greater risk of MACEs.
Conclusions:
- Apolipoprotein C3 is associated with vulnerable plaque characteristics (higher %NC) in SCD patients.
- Elevated apo-C3 levels are predictive of future MACEs in patients with SCD after PCI.
- Apo-C3 may serve as a valuable biomarker for assessing MACE risk in this population.
Abstract:
We aimed to clarify the relationship between apolipoprotein C3 (apo-C3) and the vascular composition of lesion plaque in stable coronary disease (SCD) before percutaneous coronary intervention (PCI), and to investigate major adverse cardiovascular events (MACEs) within 4 years. Data of 98 consecutive patients with SCD who underwent PCI between November 1, 2012, and March 10, 2015, were analyzed. Laboratory and virtual histology-intravascular ultrasound (VH-IVUS) examinations of culprit lesions were conducted before PCI. Patients were divided according to median apo-C3 into low apo-C3 (≤ 8.5 mg/dL) and high apo-C3 (> 8.5 mg/dL) groups. VH-IVUS data indicated that the percentage of necrotic core volume (%NC) was significantly higher in the high apo-C3 group than in the low apo-C3 group. Moreover, the %NC significantly correlated with the apo-C3 level (R = 0.2109, P = 0.037). Kaplan-Meier curve analysis revealed that freedom from MACEs exhibited a greater decrease in the high apo-C3 group than in the low apo-C3 group, and in the high %NC group than in the low %NC group. Multivariate Cox hazards analysis showed that the %NC and high apo-C3 were independent predictors of 4 year MACEs. Apo-C3 may be a useful marker of future MACEs in patients with SCD after PCI and contribute to %NC growth.
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