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| Research article summary (published 30 Oct 2009): |
CDK4 IVS4-nt40G-->A and T2D-associated obesity in Italians.
Full Abstract
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 > or = 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 > or = 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.
Author information
Author/s: Meenakshisundaram, Ramachandran (R); Gragnoli, Claudia (C);
Affiliation: Department of Medicine, Cellular & Molecular Physiology, Biostatistics, Milton S Hershey Medical Center, Hershey, PA 17033, USA.
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
Journal: Journal of cellular physiology (J Cell Physiol), published in United States. (Language: eng)
Reference: 2009-Nov; vol 221 (issue 2) : pp 273-5
Dates: Created 2009/08/27; Completed 2009/09/09;
PMID: 19634152, status: MEDLINE (last retrieval date: 9/9/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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