General Medicine Division, Massachusetts General Hospital, 50 Staniford Street, 9th floor, Boston, MA, 02114, USA.
Department of Medicine, Harvard Medical School, Boston, MA, USA.
Diabetologia. 2012 Oct;55(10):2604-2612. doi: 10.1007/s00125-012-2637-7. Epub 2012 Jul 11.
AIMS/HYPOTHESIS: 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 ≥ 30 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.
CONCLUSIONS/INTERPRETATION: 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.
目的/假设:基因型不会随时间变化,因此可以方便地确定 2 型糖尿病高危个体。我们假设基因型评分可以预测年轻成年人的 2 型糖尿病发病情况,并基于临床危险因素改善仅基于临床危险因素的糖尿病预测模型。
冠状动脉风险发展在年轻人(CARDIA)研究中,年轻人(年龄 18-30 岁,平均年龄 25 岁)连续进入中年期。我们使用 Cox 回归建立基于年轻成年人(年龄、性别、种族、父母糖尿病史、BMI、平均动脉压、空腹血糖、高密度脂蛋白胆固醇和三酰甘油)评估的 2 型糖尿病发病的嵌套预测模型,不包括和包括 38 个变异基因型评分。使用 C 统计量和连续净重新分类改善指数(NRI)比较模型。
在 2439 名参与者中,830 名(34%)为黑人,249 名(10%)基线时 BMI≥30kg/m2。在平均 23.9 年的随访中,215 名(8.8%)参与者发生 2 型糖尿病。基因型评分在所有模型中均显著预测发病糖尿病,在全模型中每个风险等位基因的 HR 为 1.08(95%CI1.04,1.13)。评分加入全模型可适度改善重新分类(连续 NRI0.285;95%CI0.126,0.433),但不改善区分度(C 统计量在有和无评分的全模型中分别为 0.824 和 0.829)。种族分层分析结果相似。
结论/解释:基因型知识可预测白人及黑人年轻成年人 25 年内 2 型糖尿病的发病情况,但可能无法改善常规临床测量的预测。