Genetics

Obesity (2008) doi:10.1038/oby.2008.465

Association of the FTO rs9939609 Single Nucleotide Polymorphism With C-reactive Protein Levels

Eva Fisher1, Matthias B. Schulze2, Norbert Stefan3, Hans-Ulrich Häring3, Frank Döring4, Hans-Georg Joost5, Hadi Al-Hasani5, Heiner Boeing1 and Tobias Pischon1

  1. 1Department of Epidemiology, German Institute of Human Nutrition Potsdam-Rehbrücke, Nuthetal, Germany
  2. 2Public Health Nutrition Unit, Department of Nutrition and Food Sciences, Center of Life and Food Science Weihenstephan, Technical University, Munich, Germany
  3. 3Department of Internal Medicine IV, University Hospital, Eberhard Karls University, Tübingen, Germany
  4. 4Department of Molecular Nutrition, Christian-Albrechts University, Kiel, Germany
  5. 5Department of Pharmacology, German Institute of Human Nutrition Potsdam-Rehbrücke, Nuthetal, Germany

Correspondence: Eva Fisher (fisher@dife.de)

Received 30 May 2008; Accepted 16 July 2008; Published online 23 October 2008.

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Abstract

Adipose tissue is a key factor determining C-reactive protein (CRP) plasma levels. Variation at the fat-mass and obesity-associated (FTO) gene locus has been reported to be associated with increased body fat. We investigated whether the FTO rs9939609 T>A single nucleotide polymorphism might alter CRP levels in a population-based sample of 2,415 participants from a large prospective cohort study. Genotype/phenotype relationships were studied by linear trend analysis stratified by sex. The rs9939609 A-allele was significantly associated with CRP levels in both genders (men, +21%, P = 0.002; women, +14%, P = 0.01 per A-allele). The association was attenuated, but remained statistically significant after additional adjustment for BMI, waist-to-hip ratio, and other potential confounding factors (men, +14%, P = 0.03; women, +12%, P = 0.02; per A-allele). Similar results were obtained when subjects with CRP levels higher then 10 mg/l were excluded. Our data provide preliminary evidence that the FTO rs9939609 T>A polymorphism contributes to variation in plasma CRP levels independently of obesity indices.

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