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Gene polymorphisms in APOE, NOS3, and LIPC genes may be risk factors for cardiac adverse events after primary CABG
Sandra Eifert1, Astrid Rasch, Andres Beiras-Fernandez
1Department of Cardiac Surgery, Ludwig Maximilians University Munich, Germany. seifert@med.uni-muenchen.de
Insights
Genetic predisposition influences coronary artery disease progression after coronary artery bypass grafting (CABG). A combined gene risk profile effectively stratified patient risk for adverse cardiac events, outperforming individual gene polymorphisms.
Area of Science:
- Cardiovascular Genetics
- Atherosclerosis Research
- Surgical Outcomes
Background:
- Coronary artery disease (CAD) progression post-coronary artery bypass grafting (CABG) may be influenced by genetic factors beyond traditional risk factors.
- Understanding genetic predispositions can improve long-term patient management after CABG.
Purpose of the Study:
- To investigate the association between specific gene polymorphisms and CAD progression in CABG patients.
- To evaluate the utility of a combined gene risk profile for predicting adverse cardiac events post-CABG.
Main Methods:
- 192 CABG patients were studied, with data on clinical outcomes and gene polymorphisms (ApoE, NOS3, LIPC, CETP, SERPINE-1, Prothrombin).
- Adverse cardiac events included reoperation, reintervention, and angina, with a mean follow-up of 10.1 years.
- Gene polymorphisms were analyzed individually and combined into a gene risk profile.
Main Results:
- Arterial hypertension and hypercholesterinemia were significant risk factors for CAD progression.
- Individual polymorphisms (ApoE, NOS3, LIPC) showed limited predictive value, though some associations were noted (e.g., ApoE epsilon 3 absence with reintervention).
- A gene risk profile significantly differentiated between patients with faster and slower occurrence of adverse cardiac events (p = 0.0012).
Conclusions:
- Single gene polymorphisms (APOE, LIPC, NOS3) offer limited prognostic capability for cardiac adverse events after CABG.
- A comprehensive gene risk profile provides effective risk stratification for patients undergoing CABG.
Introduction:
Coronary artery disease progression after primary coronary artery bypass grafting may, beside classical atherosclerosis risk factors, be depending on genetic predisposition.
Methods:
We investigated 192 CABG patients (18% female, age: 60.9 +/- 7.4 years). Clinically cardiac adverse events were defined as need for reoperation (n = 88; 46%), reintervention (n = 58; 30%), or angina (n = 89; 46%). Mean follow-up time measured 10.1 +/- 5.1 years. Gene polymorphisms (ApoE, NOS3, LIPC, CETP, SERPINE-1, Prothrombin) were investigated separately and combined (gene risk profile).
Results:
Among classical risk factors, arterial hypertension and hypercholesterinemia significantly influenced CAD progression. Single ApoE, NOS3 and LIPC polymorphisms provided limited information. Patients missing the most common ApoE epsilon 3 allele (5,2%), showed recurrent symptoms (p = 0,077) and had more frequently reintervention (p = 0,001). NOS3 a allele was associated with a significant increase for reintervention (p = 0,041) and recurrent symptoms (p = 0,042). Homozygous LIPC patients had a higher reoperation rate (p = 0.049). A gene risk profile enabled us to discriminate between faster and slower occurrence of cardiac adverse events (p = 0.0012).
Conclusion:
Single APOE, LIPC and NOS3 polymorphisms permitted limited prognosis of cardiac adverse events in patients after CABG. Risk profile, in contrast, allowed for risk stratification.
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