Lu Qing, Elston Robert C
Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, Ohio 44106, USA.
Am J Hum Genet. 2008 Mar;82(3):641-51. doi: 10.1016/j.ajhg.2007.12.025.
Current extensive genetic research into common complex diseases, especially with the completion of genome-wide association studies, is bringing to light many novel genetic risk loci. These new discoveries, along with previously known genetic risk variants, offer an important opportunity for researchers to improve health care. We describe a method of quick evaluation of these new findings for potential clinical practice by designing a new predictive genetic test, estimating its classification accuracy, and determining the sample size required for the verification of this accuracy. The proposed predictive test is asymptotically more powerful than tests built on any other existing method and can be extended to scenarios where loci are linked or interact. We illustrate the approach for the case of type 2 diabetes. We incorporate recently discovered risk factors into the proposed test and find a potentially better predictive genetic test. The area under the receiver operating characteristic (ROC) curve (AUC) of the proposed test is estimated to be higher (AUC = 0.671) than for the existing test (AUC = 0.580).
当前针对常见复杂疾病的广泛基因研究,尤其是随着全基因组关联研究的完成,正揭示出许多新的基因风险位点。这些新发现,连同先前已知的基因风险变异,为研究人员改善医疗保健提供了重要契机。我们描述了一种通过设计新的预测性基因检测、估计其分类准确性以及确定验证该准确性所需的样本量,来快速评估这些新发现用于潜在临床实践的方法。所提出的预测性检测在渐近意义上比基于任何其他现有方法构建的检测更具效力,并且可以扩展到基因座连锁或相互作用的情形。我们以2型糖尿病为例阐述该方法。我们将最近发现的风险因素纳入所提出的检测中,发现了一个潜在更好的预测性基因检测。所提出检测的受试者工作特征(ROC)曲线下面积(AUC)估计高于现有检测(AUC = 0.671,现有检测AUC = 0.580)。