A genotype risk score predicts type 2 diabetes from young adulthood: the CARDIA study

被引:47
作者
Vassy, J. L. [1 ,2 ]
Durant, N. H. [3 ]
Kabagambe, E. K. [4 ]
Carnethon, M. R. [5 ]
Rasmussen-Torvik, L. J. [5 ]
Fornage, M. [6 ]
Lewis, C. E. [7 ]
Siscovick, D. S. [8 ,9 ]
Meigs, J. B. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Gen Med Serv, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Univ Alabama Birmingham, Med Sch Birmingham, Dept Pediat, Div Pediat & Adolescent Med, Birmingham, AL USA
[4] Univ Alabama Birmingham, Dept Epidemiol, Birmingham Sch Publ Hlth, Birmingham, AL USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL 60611 USA
[6] Univ Texas Hlth Sci Ctr, Inst Mol Med Res, Ctr Human Genet, Houston, TX USA
[7] Univ Alabama Birmingham, Dept Med, Div Prevent Med, Birmingham, AL 35294 USA
[8] Univ Washington, Dept Med, Cardiovasc Hlth Res Unit, Seattle, WA USA
[9] Univ Washington, Dept Epidemiol, Cardiovasc Hlth Res Unit, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
Genetic susceptibility; Risk prediction; Type; 2; diabetes; Young adults; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; POLYMORPHISMS; MELLITUS; RECLASSIFICATION; DISCRIMINATION; CONCORDANCE;
D O I
10.1007/s00125-012-2637-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genotype does not change over the life course and may thus facilitate earlier identification of individuals at high risk for type 2 diabetes. We hypothesised that a genotype score predicts incident type 2 diabetes from young adulthood and improves diabetes prediction models based on clinical risk factors alone. The Coronary Artery Risk Development in Young Adults (CARDIA) study followed young adults (aged 18-30 years, mean age 25) serially into middle adulthood. We used Cox regression to build nested prediction models for incident type 2 diabetes based on clinical risk factors assessed in young adulthood (age, sex, race, parental history of diabetes, BMI, mean arterial pressure, fasting glucose, HDL-cholesterol and triacylglyercol), without and with a 38-variant genotype score. Models were compared with C statistics and continuous net reclassification improvement indices (NRI). Of 2,439 participants, 830 (34%) were black and 249 (10%) had a BMI a parts per thousand yen30 kg/m(2) at baseline. Over a mean 23.9 years of follow-up, 215 (8.8%) participants developed type 2 diabetes. The genotype score significantly predicted incident diabetes in all models, with an HR of 1.08 per risk allele (95% CI 1.04, 1.13) in the full model. The addition of the score to the full model modestly improved reclassification (continuous NRI 0.285; 95% CI 0.126, 0.433) but not discrimination (C statistics 0.824 and 0.829 in full models with and without score). Race-stratified analyses were similar. Knowledge of genotype predicts type 2 diabetes over 25 years in white and black young adults but may not improve prediction over routine clinical measurements.
引用
收藏
页码:2604 / 2612
页数:9
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