Abstract | BACKGROUND: OBJECTIVE: To evaluate the association between the K121Q polymorphism of the ENPP1 gene and IHD in white patients with type 2 diabetes mellitus (DM). METHODS: A cross-sectional study was performed in type 2 DM patients (n = 573, 50.6% males, age 59.5+/-10.4 years). IHD was defined by the presence of angina or myocardial infarction according to the Worth Health Organization cardiovascular questionnaire and/or compatible electrocardiographic (Minnesota Code), or perfusional abnormalities in myocardial scintigraphy. The K121Q polymorphism of ENPP1 gene was genotyped using PCR-based methods and restriction enzyme digestion. RESULTS: IHD was present in 209 (36.5%) patients. The distribution of KK, KQ and QQ genotypes among patients with IHD was 60.8%, 34.4% and 4.8%, not different from the genotype distribution in the group without IHD (64%, 32.7% and 3.3%, P=0.574). No difference was found in the clinical and laboratory characteristics between the three genotypes, neither regarding the prevalence of Metabolic Syndrome. CONCLUSION: No association was found between polymorphism K121A of ENPP1 gene and the presence of IHD.
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Authors | Milene Moehlecke, Caroline K Kramer, Cristiane B Leitão, Ana Luiza Krahe, Ivaldir Balbosco, Mirela Jobim de Azevedo, Jorge L Gross, Luis Henrique Canani |
Journal | Arquivos brasileiros de cardiologia
(Arq Bras Cardiol)
Vol. 94
Issue 2
Pg. 157-61, 168-73, 159-63
(Feb 2010)
ISSN: 1678-4170 [Electronic] Brazil |
PMID | 20428609
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Phosphoric Diester Hydrolases
- ectonucleotide pyrophosphatase phosphodiesterase 1
- Pyrophosphatases
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Topics |
- Diabetes Mellitus, Type 2
(complications)
- Epidemiologic Methods
- Female
- Humans
- Male
- Metabolic Syndrome
(genetics)
- Middle Aged
- Myocardial Ischemia
(genetics)
- Phosphoric Diester Hydrolases
(genetics)
- Polymorphism, Genetic
(genetics)
- Pyrophosphatases
(genetics)
- White People
(genetics)
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