Immature Surfactant Protein Type-B Associates With Graft Patency in Patients Undergoing Coronary Artery Bypass
Sonia Eligini1, Erica Gianazza2, Fabrizio Veglia3
1Unit of Functional Proteomics, Metabolomics and Network Analysis, Centro Cardiologico Monzino IRCCS, Milano, Italy.
Insights
Elevated immature surfactant protein type-B (proSP-B) before coronary artery bypass graft (CABG) surgery predicts long-term graft occlusion. This biomarker improves risk prediction for graft patency after CABG surgery.
Area of Science:
- Cardiovascular Surgery
- Biomarker Discovery
- Medical Diagnostics
Background:
- Coronary artery bypass graft (CABG) surgery is a key treatment for complex multivessel coronary artery disease.
- Long-term graft occlusion after CABG remains a significant clinical challenge.
- Immature surfactant protein type-B (proSP-B) is a potential predictor of adverse cardiovascular events.
Purpose of the Study:
- To investigate the association between preoperative plasma proSP-B levels and graft occlusion 18 months post-CABG.
- To determine if elevated proSP-B can predict graft occlusion after CABG.
- To assess the added predictive value of proSP-B in a multivariable model for long-term graft patency.
Main Methods:
- Evaluated proSP-B in 40 patients with occluded grafts and 130 without occlusions.
- Assessed 18-month graft patency using coronary computed tomography angiography and/or invasive angiography.
- Employed logistic regression and receiver-operating characteristic curves for analysis.
Main Results:
- Preoperative proSP-B was significantly higher in patients with occluded grafts compared to those without (P = 0.002).
- ProSP-B independently predicted increased risk of graft occlusion, even after adjusting for clinical factors.
- Inclusion of proSP-B improved the predictive model's area under the curve from 0.7204 to 0.7733 (P = 0.02).
Conclusions:
- Elevated preoperative proSP-B is an independent predictor of 18-month graft occlusion following CABG.
- ProSP-B enhances existing predictive models for graft patency.
- ProSP-B shows promise as a novel biomarker for risk stratification in patients undergoing surgical revascularization.
Background:
Coronary artery bypass graft (CABG) surgery is performed in patients with complex multivessel coronary artery disease, but long-term graft occlusion remains a major limitation. The immature surfactant protein type-B (proSP-B) has emerged as a predictor of adverse cardiovascular outcomes.
Objectives:
The purpose of this study was to examine the relationship between preoperative plasma proSP-B and graft occlusion 18 months post-CABG. The aims were to evaluate whether elevated proSP-B could predict graft occlusion and to assess its predictive value within a multivariable model for long-term graft patency.
Methods:
We evaluated proSP-B in relation to graft occlusion in 40 patients with occluded grafts (cases) and 130 patients without occlusions (noncases), with 18-month graft patency assessed by coronary computed tomography angiography and/or invasive angiography. Logistic regression assessed the association between proSP-B and graft occlusion. Predictive performance was evaluated using receiver-operating characteristic curves and category-free net reclassification improvement.
Results:
Preoperative proSP-B was significantly elevated in cases compared to noncases (24.0 [IQR: 19.8-31.0] AU vs 19.4 [IQR: 14.0-25.0] AU; P = 0.002). In a multivariable analysis, proSP-B associated with increased risk of graft occlusion, even after adjusting for factors like D-dimer, left ventricular ejection fraction, and extracorporeal circulation time. Including proSP-B in a reference model improved the area under the curve from 0.7204 to 0.7733, significantly enhancing patient classification (net reclassification improvement = 0.43; SE = 0.18; P = 0.02).
Conclusions:
Elevated preoperative proSP-B is independently associated with 18-month graft occlusion following CABG. Including proSP-B improves existing predictive models, supporting its role as a novel biomarker for risk stratification in surgical revascularization.
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