Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Arteriosclerosis, Thrombosis, and Vascular Biology. 2004;24:2403-2407
Published online before print October 14, 2004, doi: 10.1161/01.ATV.0000147897.57527.e4
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
24/12/2403    most recent
01.ATV.0000147897.57527.e4v1
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 arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Doney, A. S.F.
Right arrow Articles by Palmer, C. N.A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Doney, A. S.F.
Right arrow Articles by Palmer, C. N.A.
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2004;24:2403.)
© 2004 American Heart Association, Inc.


Atherosclerosis and Lipoproteins

Cardiovascular Risk in Type 2 Diabetes Is Associated With Variation at the PPARG Locus

A Go-DARTS Study

Alex S.F. Doney; Bettina Fischer; Graham Leese; Andrew D. Morris; Colin N.A. Palmer

From the Institute for Cardiovascular Research (B.F., C.N.A.P.), Biomedical Research Centre, and the Department of Medicine and Therapeutics (A.S.F.D., G.L., A.D.M.), Ninewells Hospital and Medical School, Dundee, Scotland.

Correspondence to Dr Colin N.A. Palmer, Biomedical Research Centre, Ninewells Hospital and Medical School, University of Dundee, Dundee, Scotland, DD1 9SY. E-mail nuclear-receptor{at}dundee.ac.uk

Objective— The Pro12Ala polymorphism of PPARG modulates risk of developing type 2 diabetes. The Ala allele has also been associated with a reduced risk of cardiovascular events. We have shown previously that the linked T allele of the C1431T polymorphism influences Ala12-associated diabetes risk and that the 2 polymorphisms have opposing associations with body weight. We therefore investigated the association of these 2 variants with cardiovascular events in people with type 2 diabetes.

Methods and Results— We performed a cohort study of 2016 individuals and used Cox proportional hazards to analyze risk of myocardial infarction or death by PPARG Pro12Ala and C1431T genotypes, adjusting for age, sex, and smoking status. In individuals enrolled <70 years of age, the hazard for a first nonfatal event associated with the Ala12 allele was 0.21 (CI, 0.06 to 0.69; P=0.01) and the T1431 allele 9.9 (CI, 1.90 to 51.29; P=0.007). These opposing associations remained significant after correction for other conventional risk factors. The T1431 allele was also associated with all-cause mortality.

Conclusions— This study confirms the association of the Ala12 allele with reduced risk of myocardial infarction in a type 2 diabetic population and demonstrates that the T allele independently associates with an increased risk.

Variants of PPARG may influence cardiovascular risk. The association of the linked Pro12Ala and C1431T variants with myocardial infarction was investigated in a large cohort of patients with type 2 diabetes. Ala12 was associated with a significantly decreased risk and T1431 a significantly increased risk.


Key Words: type 2 diabetes • myocardial infarction • PPARG • polymorphism




This article has been cited by other articles:


Home page
Am. J. Clin. Nutr.Home page
E. A Ruiz-Narvaez, P. Kraft, and H. Campos
Ala12 variant of the peroxisome proliferator-activated receptor-{gamma} gene (PPARG) is associated with higher polyunsaturated fat in adipose tissue and attenuates the protective effect of polyunsaturated fat intake on the risk of myocardial infarction
Am. J. Clinical Nutrition, October 1, 2007; 86(4): 1238 - 1242.
[Abstract] [Full Text] [PDF]