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Effect of Evolocumab on Grafts Post-Coronary Artery Bypass Surgery: Post-Hoc Analysis of Newton-CABG CardioLink-5
G B John Mancini1, Craig Kamimura1, Michael Szarek2
1Cardiovascular Imaging Core Laboratory, Centre for Cardiovascular Innovation, Dilawri Cardiovascular Institute, Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Insights
Evolocumab did not prevent early graft failure after coronary artery bypass grafting. However, it showed potential in reducing moderate stenoses and unfavorable plaque features in saphenous vein grafts.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Pharmacology
Background:
- Graft failure is a significant clinical challenge in coronary artery bypass grafting (CABG).
- Saphenous vein grafts (SVGs), internal mammary artery (IMA), and radial artery grafts are commonly used conduits.
Purpose of the Study:
- To evaluate the effect of evolocumab on graft failure, stenosis severity, stenosis types, and plaque burden.
- Assess outcomes in SVGs, IMA, and radial artery grafts using coronary computed tomography angiography (CCTA).
Main Methods:
- Analysis of the randomized NEWTON-CABG CardioLink-5 trial data at 24 months post-surgery.
- Graft stenosis graded as normal (<20%), moderate (20% to <50%), or graft failure (50% to 100%).
- Stenoses ≥20% classified by positive remodeling, low-attenuation plaque (LAP), or spotty calcification; plaque burden measured.
Main Results:
- No significant difference in graft failure rates between treatment groups across all graft types.
- Evolocumab showed a reduction in moderate lesions in SVGs (11.5% vs 19.3%) and a similar trend in IMA grafts.
- Fewer focal stenoses ≥20% with unfavorable features (positive remodeling, LAP, spotty calcification) were observed with evolocumab.
- SVGs accumulated more plaque burden than IMA grafts, but with a higher percentage of calcified and mixed plaque and less LAP.
Conclusions:
- Evolocumab did not improve early graft failure rates in CABG.
- Exploratory findings suggest evolocumab may reduce moderate stenoses and unfavorable plaque characteristics in SVGs.
- Differences in plaque accumulation and composition between SVGs and IMA grafts may relate to early arterialization processes.
Background:
Graft failure remains a significant clinical problem.
Objectives:
This study aimed to evaluate effects of evolocumab on graft failure, stenosis severity, stenosis types, and plaque burden in saphenous vein grafts (SVGs), internal mammary artery (IMA), and radial artery grafts using coronary computed tomography angiography (CCTA).
Methods:
Analysis of the randomized NEWTON-CABG CardioLink-5 trial was undertaken in evaluable grafts 24 months postsurgery. Graft stenosis was graded normal: <20%, moderate: 20% to <50%, or graft failure: 50% to 100%. Stenoses ≥20% were classified: positive remodeling, >25% low-attenuation plaque (LAP), or spotty calcification. Plaque burden (calcified, mixed, or LAP) was measured.
Results:
We studied 1,275 SVGs, 514 IMA grafts, and 39 radial artery grafts. There were no differences between treatment groups for graft failure in any graft type. Evolocumab had a lower percentage of moderate lesions among SVGs (11.5% vs 19.3%, P < 0.001), a similar nonsignificant trend in IMA grafts (3.5% vs 5.9%), and fewer focal stenoses ≥20% showing positive remodeling, >25% LAP, or spotty calcification. SVGs accumulated more plaque burden but with greater percentage calcified (P < 0.002) and mixed plaque (P < 0.001) and less percentage LAP (P < 0.001) than IMA grafts.
Conclusions:
Evolocumab did not improve early graft failure, but exploratory results suggest that it may diminish moderate stenoses in SVGs and stenoses with unfavorable features. SVGs accumulated more plaque burden than IMA grafts but with less percentage LAP, possibly due to the early arterialization process involving smooth muscle cell proliferation, neointimal hyperplasia, and extracellular matrix expansion affecting only the SVGs.
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