Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 1996;93:1339-1345

This Article
Right arrow Full Text
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wang, X.L.
Right arrow Articles by Wilcken, D.E.L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, X.L.
Right arrow Articles by Wilcken, D.E.L.

(Circulation. 1996;93:1339-1345.)
© 1996 American Heart Association, Inc.


Articles

Common DNA Polymorphisms at the Lipoprotein Lipase Gene

Association With Severity of Coronary Artery Disease and Diabetes

X.L. Wang, MB, BS, PhD; R.M. McCredie, MD, FRCP, FRACP, FRCPE; D.E.L. Wilcken, MD, FRCP, FRACP

From the Department of Cardiovascular Medicine, University of New South Wales, Prince Henry/Prince of Wales Hospitals, Sydney, Australia.

Correspondence to Professor David Wilcken, Department of Cardiovascular Medicine, Clinical Sciences Bldg, Prince Henry Hospital, Little Bay, NSW 2036, Australia.

Background DNA variants of the lipoprotein lipase gene are associated with changes in lipid metabolism similar to those in diabetes and may relate to the development of atherosclerotic lesions, particularly premature lesions.

Methods and Results To determine whether lipoprotein lipase gene variants are relevant to ongoing atherogenesis, we explored relationships between two common lipoprotein lipase gene polymorphic markers, Pvu II at intron 6 and HindIII at intron 8; the severity of coronary artery disease (CAD); and lipid variables in 475 white patients 65 years of age or younger. We assessed CAD severity as the number of significantly stenosed (>50% luminal obstruction) major coronary arteries at angiography and by the Green Lane coronary score. We found a significant association between the Pvu II polymorphism and the number of significantly diseased vessels (P=.0099) and coronary score (P=.028), with the Pvu II(-) alleles associated with less severe disease. The HindIII polymorphism was not associated with severity but had an additive effect with the Pvu II polymorphism. There was a close relationship between the Pvu II(+/+) genotype and the presence of diabetes (P=.0025), with an OR of 3.12 (95% CI, 1.30 to 7.49) compared with the Pvu II(-/-) genotype. The interaction between these polymorphisms and CAD severity (rather than occurrence) was independent of the levels of triglycerides and HDL cholesterol and of other lipid variables. There was also a dosage-dependent relationship between the Pvu II polymorphism and levels of triglyceride. The Pvu II(-) allele was associated with low levels and variances of triglycerides.

Conclusions We conclude that the lipoprotein lipase Pvu II polymorphism is significantly associated with CAD severity and with type II diabetes in CAD patients, independent of changes in circulating lipid levels. These findings may be relevant to mechanisms mediating atherogenesis.


Key Words: lipoproteins • coronary disease • diabetes mellitus • cholesterol




This article has been cited by other articles:


Home page
Am J EpidemiolHome page
G. S. Sagoo, I. Tatt, G. Salanti, A. S. Butterworth, N. Sarwar, M. van Maarle, J. W. Jukema, B. Wiman, J. J. P. Kastelein, A. M. Bennet, et al.
Seven Lipoprotein Lipase Gene Polymorphisms, Lipid Fractions, and Coronary Disease: A HuGE Association Review and Meta-Analysis
Am. J. Epidemiol., December 1, 2008; 168(11): 1233 - 1246.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
N. Tiffin, E. Adie, F. Turner, H. G. Brunner, M. A. van Driel, M. Oti, N. Lopez-Bigas, C. Ouzounis, C. Perez-Iratxeta, M. A. Andrade-Navarro, et al.
Computational disease gene identification: a concert of methods prioritizes type 2 diabetes and obesity candidate genes
Nucleic Acids Res., June 6, 2006; 34(10): 3067 - 3081.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
K P Burdon, C D Langefeld, S R Beck, L E Wagenknecht, J J Carr, B I Freedman, D Herrington, and D W Bowden
Association of genes of lipid metabolism with measures of subclinical cardiovascular disease in the Diabetes Heart Study
J. Med. Genet., September 1, 2005; 42(9): 720 - 724.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
Y. Shimo-Nakanishi, T. Urabe, N. Hattori, Y. Watanabe, T. Nagao, M. Yokochi, M. Hamamoto, and Y. Mizuno
Polymorphism of the Lipoprotein Lipase Gene and Risk of Atherothrombotic Cerebral Infarction in the Japanese
Stroke, July 1, 2001; 32(7): 1481 - 1486.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
S. R Holmer, C. Hengstenberg, B. Mayer, A. Doring, H. Lowel, S. Engel, H.-W. Hense, M. Wolf, G. Klein, G. A.J Riegger, et al.
Lipoprotein lipase gene polymorphism, cholesterol subfractions and myocardial infarction in large samples of the general population
Cardiovasc Res, September 1, 2000; 47(4): 806 - 812.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
I. Larson, M. M. Hoffmann, J. M. Ordovas, E. J. Schaefer, W. Marz, and J. Kreuzer
The Lipoprotein Lipase HindIII Polymorphism: Association with Total Cholesterol and LDL-Cholesterol, but not with HDL and Triglycerides in 342 Females
Clin. Chem., July 1, 1999; 45(7): 963 - 968.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
J. L. Anderson, G. J. King, T. L. Bair, S. P. Elmer, J. B. Muhlestein, J. Habashi, L. Mixson, and J. F. Carlquist
Association of lipoprotein lipase gene polymorphisms with coronary artery disease
J. Am. Coll. Cardiol., March 15, 1999; 33(4): 1013 - 1020.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
Y. Hong, T. Rice, J. Gagnon, J.-P. Després, A. Nadeau, L. Pérusse, C. Bouchard, A. S. Leon, J. S. Skinner, J. H. Wilmore, et al.
Familial Clustering of Insulin and Abdominal Visceral Fat: The HERITAGE Family Study
J. Clin. Endocrinol. Metab., December 1, 1998; 83(12): 4239 - 4245.
[Abstract] [Full Text]


Home page
CirculationHome page
B. E. Groenemeijer, M. D. Hallman, P. W.A. Reymer, E. Gagne, J. A. Kuivenhoven, T. Bruin, H. Jansen, K. I. Lie, A. V.G. Bruschke, E. Boerwinkle, et al.
Genetic Variant Showing a Positive Interaction With ß-Blocking Agents With a Beneficial Influence on Lipoprotein Lipase Activity, HDL Cholesterol, and Triglyceride Levels in Coronary Artery Disease Patients: The Ser447-Stop Substitution in the Lipoprotein Lipase Gene
Circulation, June 17, 1997; 95(12): 2628 - 2635.
[Abstract] [Full Text]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
X.L. Wang, J. Wang, R.M. McCredie, and D.E.L. Wilcken
Polymorphisms of Factor V, Factor VII, and Fibrinogen Genes: Relevance to Severity of Coronary Artery Disease
Arterioscler Thromb Vasc Biol, February 1, 1997; 17(2): 246 - 251.
[Abstract] [Full Text]