Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABG
<p>Abstract</p> <p>Introduction</p> <p>Coronary artery disease progression after primary coronary artery bypass grafting may, beside classical atherosclerosis risk factors, be depending on genetic predisposition.</p> <p>Methods</p> <p>We investig...
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doaj-390164669f5541ad8fa0db40f20121de2020-11-24T20:59:25ZengBMCJournal of Cardiothoracic Surgery1749-80902009-08-01414610.1186/1749-8090-4-46Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABGNollert GeorgBeiras-Fernandez AndresRasch AstridEifert SandraReichart BrunoLohse Peter<p>Abstract</p> <p>Introduction</p> <p>Coronary artery disease progression after primary coronary artery bypass grafting may, beside classical atherosclerosis risk factors, be depending on genetic predisposition.</p> <p>Methods</p> <p>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 (<b><it>ApoE, NOS3, LIPC, CETP, SERPINE-1, Prothrombin</it></b>) were investigated separately and combined (gene risk profile).</p> <p>Results</p> <p>Among classical risk factors, arterial hypertension and hypercholesterinemia significantly influenced CAD progression. Single <b><it>ApoE, NOS3 </it></b>and <b><it>LIPC </it></b>polymorphisms provided limited information. Patients missing the most common <b><it>ApoE </it></b>ε3 allele (5,2%), showed recurrent symptoms (p = 0,077) and had more frequently reintervention (p = 0,001). <b><it>NOS3 </it></b>a allele was associated with a significant increase for reintervention (p = 0,041) and recurrent symptoms (p = 0,042).</p> <p>Homozygous <b><it>LIPC </it></b>patients had a higher reoperation rate (p = 0.049).</p> <p>A gene risk profile enabled us to discriminate between faster and slower occurrence of cardiac adverse events (p = 0.0012).</p> <p>Conclusion</p> <p>Single <b><it>APOE, LIPC </it></b>and <b><it>NOS3 </it></b>polymorphisms permitted limited prognosis of cardiac adverse events in patients after CABG. Risk profile, in contrast, allowed for risk stratification.</p> http://www.cardiothoracicsurgery.org/content/4/1/46 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nollert Georg Beiras-Fernandez Andres Rasch Astrid Eifert Sandra Reichart Bruno Lohse Peter |
spellingShingle |
Nollert Georg Beiras-Fernandez Andres Rasch Astrid Eifert Sandra Reichart Bruno Lohse Peter Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABG Journal of Cardiothoracic Surgery |
author_facet |
Nollert Georg Beiras-Fernandez Andres Rasch Astrid Eifert Sandra Reichart Bruno Lohse Peter |
author_sort |
Nollert Georg |
title |
Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABG |
title_short |
Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABG |
title_full |
Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABG |
title_fullStr |
Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABG |
title_full_unstemmed |
Gene polymorphisms in <it>APOE, NOS3</it>, and <it>LIPC </it>genes may be risk factors for cardiac adverse events after primary CABG |
title_sort |
gene polymorphisms in <it>apoe, nos3</it>, and <it>lipc </it>genes may be risk factors for cardiac adverse events after primary cabg |
publisher |
BMC |
series |
Journal of Cardiothoracic Surgery |
issn |
1749-8090 |
publishDate |
2009-08-01 |
description |
<p>Abstract</p> <p>Introduction</p> <p>Coronary artery disease progression after primary coronary artery bypass grafting may, beside classical atherosclerosis risk factors, be depending on genetic predisposition.</p> <p>Methods</p> <p>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 (<b><it>ApoE, NOS3, LIPC, CETP, SERPINE-1, Prothrombin</it></b>) were investigated separately and combined (gene risk profile).</p> <p>Results</p> <p>Among classical risk factors, arterial hypertension and hypercholesterinemia significantly influenced CAD progression. Single <b><it>ApoE, NOS3 </it></b>and <b><it>LIPC </it></b>polymorphisms provided limited information. Patients missing the most common <b><it>ApoE </it></b>ε3 allele (5,2%), showed recurrent symptoms (p = 0,077) and had more frequently reintervention (p = 0,001). <b><it>NOS3 </it></b>a allele was associated with a significant increase for reintervention (p = 0,041) and recurrent symptoms (p = 0,042).</p> <p>Homozygous <b><it>LIPC </it></b>patients had a higher reoperation rate (p = 0.049).</p> <p>A gene risk profile enabled us to discriminate between faster and slower occurrence of cardiac adverse events (p = 0.0012).</p> <p>Conclusion</p> <p>Single <b><it>APOE, LIPC </it></b>and <b><it>NOS3 </it></b>polymorphisms permitted limited prognosis of cardiac adverse events in patients after CABG. Risk profile, in contrast, allowed for risk stratification.</p> |
url |
http://www.cardiothoracicsurgery.org/content/4/1/46 |
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