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The Construction of Risk Prediction Models Using GWAS Data and Its Application to a Type 2 Diabetes Prospective Cohort

机译:利用GWAS数据构建风险预测模型及其在2型糖尿病前瞻人群中的应用

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摘要

Recent genome-wide association studies (GWAS) have identified several novel single nucleotide polymorphisms (SNPs) associated with type 2 diabetes (T2D). Various models using clinical and/or genetic risk factors have been developed for T2D risk prediction. However, analysis considering algorithms for genetic risk factor detection and regression methods for model construction in combination with interactions of risk factors has not been investigated. Here, using genotype data of 7,360 Japanese individuals, we investigated risk prediction models, considering the algorithms, regression methods and interactions. The best model identified was based on a Bayes factor approach and the lasso method. Using nine SNPs and clinical factors, this method achieved an area under a receiver operating characteristic curve (AUC) of 0.8057 on an independent test set. With the addition of a pair of interaction factors, the model was further improved (p-value 0.0011, AUC 0.8085). Application of our model to prospective cohort data showed significantly better outcome in disease-free survival, according to the log-rank trend test comparing Kaplan-Meier survival curves (). While the major contribution was from clinical factors rather than the genetic factors, consideration of genetic risk factors contributed to an observable, though small, increase in predictive ability. This is the first report to apply risk prediction models constructed from GWAS data to a T2D prospective cohort. Our study shows our model to be effective in prospective prediction and has the potential to contribute to practical clinical use in T2D.
机译:最近的全基因组关联研究(GWAS)已发现与2型糖尿病(T2D)相关的几种新颖的单核苷酸多态性(SNP)。已经开发出使用临床和/或遗传风险因素的各种模型来进行T2D风险预测。然而,尚未研究考虑遗传风险因素检测算法的分析和结合风险因素相互作用的模型构建回归方法。在这里,我们使用7360名日本人的基因型数据,研究了风险预测模型,并考虑了算法,回归方法和相互作用。确定的最佳模型基于贝叶斯因子方法和套索方法。在使用9个SNP和临床因素的情况下,该方法在独立的测试装置上获得的接收器工作特性曲线(AUC)为0.8057以下。通过添加一对相互作用因子,进一步改善了模型(p值0.0011,AUC 0.8085)。根据比较Kaplan-Meier生存曲线的对数秩趋势检验,将我们的模型应用于前瞻性队列数据显示出无病生存的显着更好的结果。尽管主要的贡献来自临床因素而不是遗传因素,但考虑遗传风险因素有助于预测能力的提高(尽管很小)。这是第一份将根据GWAS数据构建的风险预测模型应用于T2D前瞻性队列的报告。我们的研究表明我们的模型可以有效地进行前瞻性预测,并有可能为T2D的实际临床应用做出贡献。

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