Archives of Medical Research
Volume 37, Issue 6 , Pages 736-743, August 2006

Lack of Association between the Pro12Ala Polymorphism in PPAR-γ2 Gene and Body Weight Changes, Insulin Resistance and Chronic Diabetic Complications in Obese Patients with Type 2 Diabetes

  • Adam Stefanski

      Affiliations

    • Department of Endocrinology, Hypertension and Metabolic Diseases, Pomeranian Medical University, Szczecin, Poland
    • Corresponding Author InformationAddress reprint requests to: Dr. Adam Stefanski, Department of Endocrinology, Hypertension and Metabolic Diseases, Pomeranian Medical University, ul. Arkonska 4, 71-455 Szczecin, Poland
  • ,
  • Liliana Majkowska

      Affiliations

    • Department of Endocrinology, Hypertension and Metabolic Diseases, Pomeranian Medical University, Szczecin, Poland
  • ,
  • Andrzej Ciechanowicz

      Affiliations

    • Department of Clinical Biochemistry and Laboratory Diagnostics, Pomeranian Medical University, Szczecin, Poland
  • ,
  • Miroslaw Frankow

      Affiliations

    • Department of Endocrinology, Hypertension and Metabolic Diseases, Pomeranian Medical University, Szczecin, Poland
  • ,
  • Krzysztof Safranow

      Affiliations

    • Department of Biochemistry, Pomeranian Medical University, Szczecin, Poland
  • ,
  • Milosz Parczewski

      Affiliations

    • Department of Clinical Biochemistry and Laboratory Diagnostics, Pomeranian Medical University, Szczecin, Poland
  • ,
  • Krystyna Pilarska

      Affiliations

    • Department of Endocrinology, Hypertension and Metabolic Diseases, Pomeranian Medical University, Szczecin, Poland

Received 24 July 2005; accepted 9 January 2006.

(ARCMED-D-05-00287)

Background

It is generally accepted that the Pro12Ala polymorphism in peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) is associated with an increased risk of type 2 diabetes. However, studies on an association between the polymorphism and obesity have yielded inconsistent findings. Also, a role of PPAR-γ receptors in development of chronic diabetic complications cannot be excluded. The aim of this study was to investigate an association between Pro12Ala polymorphism and body weight changes, insulin resistance, insulin secretion and incidence of diabetic complications in obese patients with long-lasting type 2 diabetes.

Methods

In 216 obese patients with at least a 10-year history of type 2 diabetes, a detailed medical history was taken and a physical examination with assessment of diabetic complications was performed as well as evaluation of insulin resistance (homeostatic model assessment−HOMA), insulin secretion and other biochemical parameters. PCR-RFLP was used to assess Pro12Ala polymorphism. Two subgroups of patients were compared: homozygotic Pro/Pro and Ala allele carriers (Ala/Ala + Ala/Pro).

Results

No differences between the analyzed groups in body weight changes, insulin resistance and insulin secretion were found, but Ala allele was significantly more frequent in males than in females. There was no difference in incidence and progression of diabetic complications with only a trend towards higher incidence of diabetic retinopathy in patients with Ala allele.

Conclusions

There is no association between Pro12Ala PPAR-γ2 polymorphism and body mass changes observed during a course of type 2 diabetes, differences in peripheral insulin resistance and incidence and progression of diabetic complications in obese patients with long-lasting type 2 diabetes.

Key Words: Type 2 diabetes, Pro12Ala polymorphism, PPAR-γ, Diabetic complications

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0188-4409(06)00092-0

doi:10.1016/j.arcmed.2006.01.009

Archives of Medical Research
Volume 37, Issue 6 , Pages 736-743, August 2006