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Published on: November 24, 2014
D-dimer is associated with arterial and venous coronary artery bypass graft occlusion
Alessandro Parolari1, Laura Cavallotti2, Daniele Andreini3
1Università degli Studi di Milano, Dipartimento di Scienze Biomediche per la Salute, Milan, Italy; IRCCS Policlinico San Donato, U.O. Cardiochirurgia e Ricerca traslazionale, San Donato Milanese, Italy.
Insights
Lower D-dimer levels are linked to graft occlusion after coronary artery bypass grafting. This finding may help identify patients at risk for graft failure and develop new prevention strategies.
Area of Science:
- Cardiovascular Surgery
- Biomarkers
- Graft Patency
Background:
- Coronary artery bypass grafting (CABG) is a common procedure to treat coronary artery disease.
- Graft occlusion remains a significant cause of graft failure and adverse cardiac events post-CABG.
- Identifying reliable biomarkers for predicting graft occlusion is crucial for improving long-term outcomes.
Purpose of the Study:
- To investigate the association between clinical variables and circulating biomarkers with graft occlusion at 18 months post-CABG.
- To identify a predictive signature for graft occlusion in patients undergoing coronary artery bypass grafting.
- To explore D-dimer as a potential biomarker for graft failure.
Main Methods:
- Prospective observational study including 330 patients undergoing primary elective CABG.
- Blood samples collected pre-surgery and at discharge for biomarker analysis.
- Coronary computed tomography angiography performed at 18 months follow-up in 179 patients to assess graft patency.
Main Results:
- Overall graft occlusion rate was 9.1% (46/503 grafts), with 24% of patients experiencing at least one occluded graft.
- Lower baseline D-dimer levels (OR, 2.58) and higher discharge total protein (OR, 1.09) were associated with overall graft occlusion.
- D-dimer levels were significantly associated with both venous (OR, 2.67) and arterial (OR, 2.5) graft occlusion at follow-up.
Conclusions:
- D-dimer is identified as a significant biomarker associated with both arterial and venous graft occlusion after CABG.
- These findings suggest D-dimer can aid in stratifying patients at risk of graft failure.
- The study highlights potential molecular targets for developing novel strategies to prevent graft occlusion.
Objective:
In this observational prospective study, we assessed the role of clinical variables and circulating biomarkers in graft occlusion at 18 months to identify a signature for graft occlusion.
Methods:
A total of 330 patients undergoing primary elective coronary artery bypass grafting were enrolled. Blood collection for biomarker assessment was performed before surgery and discharge. Patients were then scheduled to undergo coronary computed tomography angiography at 18 months follow-up, and 179 patients underwent coronary computed tomography angiography 18 ± 2 months postoperatively.
Results:
There were 46 of 503 (9.1%) occluded grafts; of these, 29 (63%) were venous and 17 (37%) were arterial grafts; overall, 43 of 179 patients (24%) had at least 1 occluded graft. Logistic mixed effects model assessing independent factors associated with graft occlusion identified that lower D-dimer levels at baseline (odds ratio [OR], 2.58; 95% confidence interval [CI], 1.36-4.89; P = .00) and total protein content at discharge (OR, 1.09; 95% CI, 1.01-1.19; P = .028) were related to overall graft occlusion at follow-up, along with an arterial graft other than the left internal thoracic artery (OR, 2.92; 95% CI, 1.24-6.9; P = .078); moreover, a venous graft emerged was possibly associated with graft occlusion (OR, 1.51; 95% CI, 0.95-2.39; P = .078). By separately analyzing saphenous vein and arterial grafts, D-dimer levels (OR, 2.67; 95% CI, 1.15-6.2; P = .022 and OR, 2.5; 95% CI, 1.01-7.0; P = .05 for venous and arterial graft, respectively) were still associated with arterial and venous graft occlusion at follow-up.
Conclusions:
We identified D-dimer as a biomarker associated with arterial and venous grafts occlusion. This may help stratify patients at risk of graft failure and identify new molecular targets to prevent this complication.
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