Association of a Cyclin-Dependent Kinase 5 Regulatory Subunit-Associated Protein 1-Like 1 (CDKAL1) Polymorphism With Elevated Hemoglobin A1c Levels and the Prevalence of Metabolic Syndrome in Japanese Men: Interaction With Dietary Energy Intake

• Published in: American journal of epidemiology 2010-11, Vol.172 (9), p.985-991
• Main Authors: Miyaki, Koichi, Oo, Than, Song, Yixuan, Lwin, Htay, Tomita, Yutaka, Hoshino, Haruhiko, Suzuki, Norihiro, Muramatsu, Masaaki
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; CDKAL1 protein; Diseases of the digestive system; energy intake; Epidemiology; General aspects; Hemoglobin; hemoglobin A1c protein; human; Japan; Medical sciences; Metabolic diseases; Metabolic syndrome; metabolic syndrome X; Metabolism; Miscellaneous; Other metabolic disorders; Proteins; Public health. Hygiene; Public health. Hygiene-occupational medicine; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
• ISSN: 0002-9262; 1476-6256
• DOI: 10.1093/aje/kwq281

Genome-wide association studies have identified the cyclin-dependent kinase 5 regulatory subunit-associated protein 1-like 1 (CDKAL1) gene as a novel risk factor for type 2 diabetes mellitus. Application of this genetic marker for prevention of type 2 diabetes and metabolic syndrome (MetS) in healthy populations has not yet been evaluated. The authors examined the effects of a CDKAL1 polymorphism (rs9465871) on metabolic phenotype and of gene-lifestyle (CDKAL1-energy intake) interaction on MetS in a cohort of apparently healthy Japanese men examined in 2003. The CC genotype of the CDKAL1 variant was associated with elevated glycosylated hemoglobin A1c (HbA1c) levels. The prevalence of MetS was 25.6% for CC and 16.3% for TT + CT (odds ratio = 2.18, 95% confidence interval: 1.06, 4.48; P = 0.035). When dietary energy intake was accounted for, the variant's effect on HbA1c was observed in the highest energy-intake group (mean: CC, 5.6% (standard deviation, 1.7); TT + CT, 5.0% (standard deviation, 0.5); P = 0.025). In addition, the positive association between HbA1c and energy intake was stronger in subjects with the CC genotype than in subjects with TT + CT. These results suggest that the interaction between the CDKAL1 polymorphism and dietary energy intake influences the dysglycemic phenotype leading to MetS, possibly through impaired insulin secretion. The CDKAL1 polymorphism may be a marker for MetS in the Japanese population.