The Peroxisome Poliferator–Activated Receptor-γ2 Pro12Ala Variant

Author:

Douglas Julie A.1,Erdos Michael R.2,Watanabe Richard M.3,Braun Andi4,Johnston Cristy L.4,Oeth Paul4,Mohlke Karen L.2,Valle Timo T.5,Ehnholm Christian5,Buchanan Thomas A.6,Bergman Richard N.7,Collins Francis S.2,Boehnke Michael1,Tuomilehto Jaakko58

Affiliation:

1. Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan

2. Genetics and Molecular Biology Branch, National Human Genome Research Institute, Bethesda, Maryland

3. Division of Biostatistics, Department of Preventative Medicine, Keck School of Medicine, University of Southern California, Los Angeles

4. Sequenom Inc., San Diego, California

5. Department of Epidemiology and Health Promotion, Diabetes and Genetic Epidemiology Unit, and the Department of Biochemistry, National Public Health Institute, Helsinki, Finland

6. Department of Medicine and the

7. Department of Physiology and Biophysics, Keck School of Medicine, University of Southern California, Los Angeles, California

8. Department of Public Health, University of Helsinki, Helsinki, Finland

Abstract

Recent studies have identified a common proline-to-alanine substitution (Pro12Ala) in the peroxisome proliferator–activated receptor-γ2 (PPAR-γ2), a nuclear receptor that regulates adipocyte differentiation and possibly insulin sensitivity. The Pro12Ala variant has been associated in some studies with diabetes-related traits and/or protection against type 2 diabetes. We examined this variant in 935 Finnish subjects, including 522 subjects with type 2 diabetes, 193 nondiabetic spouses, and 220 elderly nondiabetic control subjects. The frequency of the Pro12Ala variant was significantly lower in diabetic subjects than in nondiabetic subjects (0.15 vs. 0.21; P = 0.001). We also compared diabetes-related traits between subjects with and without the Pro12Ala variant within subgroups. Among diabetic subjects, the variant was associated with greater weight gain after age 20 years (P = 0.023) and lower triglyceride levels (P = 0.033). Diastolic blood pressure was higher in grossly obese (BMI >40 kg/m2) diabetic subjects with the variant. In nondiabetic spouses, the variant was associated with higher fasting insulin (P = 0.033), systolic blood pressure (P = 0.021), and diastolic blood pressure (P = 0.045). These findings support a role for the PPAR-γ2 Pro12Ala variant in the etiology of type 2 diabetes and the insulin resistance syndrome.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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