The Leu72Met polymorphism of the ghrelin gene is associated with a decreased risk for type 2 diabetes
pmid: 18848536
The Leu72Met polymorphism of the ghrelin gene is associated with a decreased risk for type 2 diabetes
Ghrelin is involved in several metabolic and cardiovascular processes. The Leu72Met polymorphism of its gene was associated with an increased risk of type 2 diabetes (DM2) in some, but not all studies. Its association with atherosclerosis is not known.We investigated 420 Caucasian subjects with DM2 and 430 controls without diabetes (56.6% male, age 62+/-10 years).The Leu72Leu genotype frequencies were 89.76/84.65%, the Leu72Met 9.52/15.12% and the Met72Met 0.71/0.23% (P=0.029) in the DM2 and controls groups, respectively. In subjects with Met72+ genotypes the risk of DM2 was significantly decreased (univariate OR 0.63, 95% CI 0.42-0.95, P=0.026). In a logistic regression model, body mass index, hypertension and a positive family history for diabetes were predictors of diabetes while the polymorphism remained negatively associated with the disease (OR 0.62, 95% CI 0.40-0.97, P=0.036). After adjusting for known risk factors for atherosclerosis, the Met72+ variant was not associated with atherosclerotic disease (OR 1.41, 95% CI 0.78-2.54, P=0.25). Ghrelin concentrations were not associated with the polymorphism, DM2 or atherosclerotic disease.The Leu72Met polymorphism of the ghrelin gene is associated with a decreased risk for DM2. There is no association between the variant and atherosclerotic disease or ghrelin concentrations.
- University of Bonn Germany
- University of Cologne Germany
- Harvard University United States
- Beth Israel Deaconess Medical Center United States
Male, Polymorphism, Genetic, Genotype, Middle Aged, Atherosclerosis, Ghrelin, White People, Methionine, Diabetes Mellitus, Type 2, Leucine, Reference Values, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Aged
Male, Polymorphism, Genetic, Genotype, Middle Aged, Atherosclerosis, Ghrelin, White People, Methionine, Diabetes Mellitus, Type 2, Leucine, Reference Values, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Aged
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