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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Main Authors: Nollert Georg, Beiras-Fernandez Andres, Rasch Astrid, Eifert Sandra, Reichart Bruno, Lohse Peter
Format: Article
Language:English
Published: BMC 2009-08-01
Series:Journal of Cardiothoracic Surgery
Online Access:http://www.cardiothoracicsurgery.org/content/4/1/46
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spelling 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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