Exp Clin Endocrinol Diabetes 2002; 110(5): 230-234
DOI: 10.1055/s-2002-33072
Articles

© Johann Ambrosius Barth

The Pro115Gln polymorphism within the PPAR γ2 gene has no epidemiological impact on morbid obesity

O. W. Hamer1 , D. Forstner1 , I. Ottinger1 , M. Ristow2 , L. C. Bollheimer1 , J. Schölmerich1 , K. D. Palitzsch1
  • 1 Department of Internal Medicine I, University of Regensburg, Germany
  • 2 German Institute for Nutrition, DIFE, KLE, C2, Bergholz-Potsdam, Germany
Further Information

Publication History

received 27 February 2001 first decision 26 April 2001

accepted 13 February 2002

Publication Date:
30 July 2002 (online)

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Summary

The peroxisome-proliferator-activated receptor γ2 (PPAR γ2) is a transcriptional key regulator of adipocyte differentiation. PPARγ2 can be inactivated by phosphorylation of a serine residue at position 114. A point mutation leading to an amino acid exchange at position 115 (Pro115Gln) was shown to preclude serine phosphorylation and to consecutively accelerate adipocyte differentiation emphasizing the pathophysiological relevance of this mutation.

So far, four markedly obese heterozygote carriers of the Pro115Gln mutation (body mass index 37.9-47.3 kg×m-2) have been identified in a circumscribed study population. In order to evaluate the epidemiological relevance of the Pro115Gln mutation in morbid obesity we screened the DNA of all subjects with a body mass index greater than 35 kg×m-2 who had participated in a nationwide German epidemiological field survey. There was no homozygote or heterozygote carrier of the Pro115Gln polymorphism among them. We conclude that the Pro115Gln polymorphism within the PPAR γ2 gene has no relevant epidemiological impact on morbid obesity in Germany. It needs further investigation whether this polymorphism might play a role in related metabolic disorders.

References

Dr. O. Hamer

Klinik und Poliklinik für Innere Medizin I

Universitätsklinik Regensburg

93042 Regensburg

Germany

Phone: +49- 941-944 7001

Fax: +49- 941-944 7002

Email: okka.hamer@klinik.uni-regensburg.de