4.7 Article

CDK4 IVS4-nt40G→A and T2D-Associated Obesity in Italians Rapid Communication

Journal

JOURNAL OF CELLULAR PHYSIOLOGY
Volume 221, Issue 2, Pages 273-275

Publisher

WILEY
DOI: 10.1002/jcp.21874

Keywords

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Funding

  1. Office for the Advancement of Telehealth (OAT) [DIBTH06321-01]
  2. Health Resources and Services Administration, DHHS

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Cell cycle regulators play crucial roles in the preadipocyte proliferation and adipocyte differentiation. Cyclin-dependent kinase 4 (CDK4) mediates with D-type cyclins entry of cells into cell cycle in response to external stimuli. CDK4 plays a role in body weight, adipogenesis, and beta cell proliferation. CDK4 null mice develop type 2 diabetes (T2D). Furthermore, CDK4 variants are associated with obesity-associated tumors/cancer. We aimed at identifying a role of CDK4 IVS4-nt40G -> A variant in T2D-associated obesity (body mass index, BMI >= 30) by association tests in an Italian T2D subjects dataset. We recruited from Italy 128 unrelated T2D subjects with BMI <30 kg/m(2) and 54 unrelated T2D subjects with BMI >= 30 kg/m(2). We performed statistical power calculations in our dataset. DNA samples were directly sequenced with specific primers for CDK4 IVS4-nt40G -> A variant. We identified a significant association of the G allele with T2D-associated obesity and of the A allele with T2D-associated BMI < 30. In our study, we found that the CDK4 IVS4-nt40GG genotype is a risk variant for T2D-associated obesity and that the AA genotype is associated with BMI < 30 in T2D. Hence, CDK4 IVS4-nt40A allele is protective and G allele confers risk for obesity in T2D patients. This study should prompt further work aiming at establishing CDK4 role in contributing to human obesity and T2D-associated obesity. J. Cell. Physiol. 22 1: 273-275, 2009. (C) 2009 Wiley-Liss, Inc.

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