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Published on: January 28, 2020
Prospective analysis after coronary-artery bypass grafting: platelet GP IIIa polymorphism (HPA-1b/PIA2) is a risk
R B Zotz1, M Klein, H P Dauben
1Department of Haemostasis and Transfusion Medicine, Heinrich Heine University Medical Center, Düsseldorf, Germany. zotz@med.uni-duesseldorf.de
Insights
Human Platelet Antigen 1b (HPA-1b) is a hereditary risk factor for adverse outcomes after coronary artery bypass surgery. This includes bypass occlusion, myocardial infarction, or death, highlighting its clinical significance.
Area of Science:
- Cardiovascular Medicine
- Immunogenetics
- Surgical Outcomes
Background:
- Human Platelet Antigen 1b (HPA-1b) is a known risk factor for thrombogenicity and myocardial infarction in patients with coronary artery disease.
- HPA-1b is not a risk factor for coronary artery disease itself.
- The role of HPA-1b in outcomes following coronary artery bypass grafting (CABG) remains to be elucidated.
Purpose of the Study:
- To investigate the association between HPA-1b genotype and clinical outcomes in patients undergoing saphenous-vein coronary-artery bypass grafting.
- To determine if HPA-1b is an independent risk factor for postoperative complications after CABG.
Main Methods:
- Prospective determination of HPA-1 genotype in 261 consecutive patients before CABG.
- One-year follow-up to assess for bypass occlusion, myocardial infarction, or death.
- Stepwise logistic regression analysis including clinical and demographic variables.
Main Results:
- A significantly higher prevalence of HPA-1b was observed in patients with postoperative complications (60%) compared to those without (24%).
- HPA-1b was independently associated with an increased risk of bypass occlusion, myocardial infarction, or death (odds ratio 4.7, p=0.019).
- No other tested variables (age, sex, BMI, smoking, hypertension, diabetes, lipids) showed a significant independent association.
Conclusions:
- HPA-1b is a significant hereditary risk factor for adverse outcomes after coronary artery bypass surgery.
- The presence of HPA-1b is linked to increased risks of bypass occlusion, myocardial infarction, and mortality post-CABG.
- These findings suggest HPA-1b genotyping may aid in risk stratification for patients undergoing CABG.
Abstract:
Recently, we have demonstrated that human platelet antigen 1b (HPA-1b or P1A2) is a hereditary risk factor for platelet thrombogenicity leading to premature myocardial infarction in preexisting coronary artery disease. However, HPA-lb does not represent a risk factor for coronary artery disease itself. The aim of our present study was to evaluate the role of HPA-lb on the outcome in patients after coronary-artery bypass surgery. We prospectively determined the HPA-1 genotype in 261 consecutive patients prior to saphenous-vein coronary-artery bypass grafting. The patients were followed for one year. Among patients with bypass occlusion, myocardial infarction, or death more than 30 days after surgery, the prevalence of HPA-lb was significantly higher than among patients without postoperative complications (60 percent, 6/10, vs. 24 percent, 58/241, p <0.05, odds ratio 4.7). Using a stepwise logistic regression analysis with the variables HPA-1b, age, sex, body mass index, smoking (pack-years), hypertension, diabetes, cholesterol and triglyceride concentration, only HPA-lb had a significant association with bypass occlusion, myocardial infarction, or death after bypass surgery (p = 0.019, odds ratio 4.7). This study shows that HPA-1b is a hereditary risk factor for bypass occlusion, myocardial infarction, or death in patients after coronary-artery bypass surgery.
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