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Genetic study of common variants at the Apo E,Apo AI,Apo CIII,Apo B,lipoprotein lipase (LPL) and hepatic lipase (LIPC) genes and coronary artery disease (CAD): variation in LIPC gene associates with clinical outcomes in patients with established CAD
Authors:Marco?G?Baroni  author-information"  >  author-information__contact u-icon-before"  >  mailto:marco.baroni@uniroma.it"   title="  marco.baroni@uniroma.it"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Andrea?Berni,Stefano?Romeo,Marcello?Arca,Tullio?Tesorio,Giovanni?Sorropago,Umberto?Di Mario,David?J?Galton
Affiliation:(1) Department of Clinical Sciences, Division of Endocrinology, University of Rome "La Sapienza", Italy;(2) Department of Cardiology, II Faculty of Medicine, University of Rome "La Sapienza", Rome, Italy;(3) Department of Terapia Medica, University of Rome "La Sapienza", Italy;(4) Cardiac Catheterisation Unit, Casa di Cura Montevergine di Mercogliano (Av), Italy;(5) Department of Human Genetics and Metabolism, St. Bartholomew's Hospital, London, UK
Abstract:

Background  

Current evidence demonstrates that positive family history and several alterations in lipid metabolism are all important risk factors for coronary artery disease (CAD). All lipid abnormalities themselves have genetic determinants. Thus, objective of this study was to determine whether 6 genetic variants potentially related to altered lipid metabolism were associated with CAD and with lipid abnormalities in an Italian population. These genetic variables were: apolipoprotein E (Apo E), Apo AI, Apo CIII, Apo B, lipoprotein lipase (LPL) and the hepatic lipase (LIPC) genes. Furthermore, an 8 years prospective analysis of clinical cardiovascular events was related to the various genetic markers.
Keywords:
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