The ENPP1 K121Q Polymorphism Is Associated With Type 2 Diabetes in European Populations

Evidence From an Updated Meta-Analysis in 42,042 Subjects

  1. for the ENPP1 Consortium*
  1. 1Diabetes Unit and Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts
  2. 2Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts
  3. 3Research Unit of Diabetes and Endocrine Diseases, CSS Scientific Institute, San Giovanni Rotondo, Italy
  4. 4CSS-Mendel Institute, Rome, Italy
  5. 5Unit of Endocrinology, CSS Scientific Institute, San Giovanni Rotondo, Italy
  6. 6Divisions of Genetics and Endocrinology, Children's Hospital Boston, Boston, Massachusetts
  7. 7Department of Genetics, Harvard Medical School, Boston, Massachusetts
  8. 8Department of Clinical Sciences, Sapienza University of Rome, Rome, Italy
  9. 9Department of Medicine, Harvard Medical School, Boston, Massachusetts
  1. Address correspondence and reprint requests to Jose C. Florez, Simches Research Building, CPZN 5.250, Diabetes Unit/Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114. E-mail: jcflorez{at}partners.org

Abstract

OBJECTIVE—Functional studies suggest that the nonsynonymous K121Q polymorphism in the ectoenzyme nucleotide pyrophosphate phosphodiesterase 1 (ENPP1) may confer susceptibility to insulin resistance; genetic evidence on its effect on type 2 diabetes, however, has been conflicting. We therefore conducted a new meta-analysis that includes novel unpublished data from the ENPP1 Consortium and recent negative findings from large association studies to address the contribution of K121Q to type 2 diabetes.

RESEARCH DESIGN AND METHODS—After a systematic review of the literature, we evaluated the effect of ENPP1 K121Q on diabetes risk under three genetic models using a random-effects approach. Our primary analysis consisted of 30 studies comprising 15,801 case and 26,241 control subjects. Due to considerable heterogeneity and large differences in allele frequencies across populations, we limited our meta-analysis to those of self-reported European descent and, when available, included BMI as a covariate.

RESULTS—We found a modest increase in risk of type 2 diabetes for QQ homozygotes in white populations (combined odds ratio [OR] 1.38 [95% CI 1.10–1.74], P = 0.005). There was no evidence of publication bias, but we noted significant residual heterogeneity among studies (P = 0.02). On meta-regression, 16% of the effect was accounted for by the mean BMI of control subjects. This association was stronger in studies in which control subjects were leaner but disappeared after adjustment for mean control BMI (combined OR 0.93 [95% CI 0.75–1.15], P = 0.50).

CONCLUSIONS—The ENPP1 Q121 variant increases risk of type 2 diabetes under a recessive model of inheritance in whites, an effect that appears to be modulated by BMI.

Footnotes

  • Published ahead of print at http://diabetes.diabetesjournals.org on 10 December 2007. DOI: 10.2337/db07-1336.

  • Additional information for this article can be found in an online appendix at http://dx.doi.org/10.2337/db07-1336.

  • * A complete list of the investigators of the ENPP1 Consortium can be found in the appendix.

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Received September 19, 2007.
    • Accepted November 30, 2007.
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  1. Diabetes vol. 57 no. 4 1125-1130
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