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Testing calibration of risk models at extremes of disease risk

机译:在极端疾病风险下测试风险模型的校准

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Risk-prediction models need careful calibration to ensure they produce unbiased estimates of risk for subjects in the underlying population given their risk-factor profiles. As subjects with extreme high or low risk may be the most affected by knowledge of their risk estimates, checking the adequacy of risk models at the extremes of risk is very important for clinical applications. We propose a new approach to test model calibration targeted toward extremes of disease risk distribution where standard goodness-of-fit tests may lack power due to sparseness of data. We construct a test statistic based on model residuals summed over only those individuals who pass high and/or low risk thresholds and then maximize the test statistic over different risk thresholds. We derive an asymptotic distribution for the max-test statistic based on analytic derivation of the variance-covariance function of the underlying Gaussian process. The method is applied to a large case-control study of breast cancer to examine joint effects of common single nucleotide polymorphisms (SNPs) discovered through recent genome-wide association studies. The analysis clearly indicates a non-additive effect of the SNPs on the scale of absolute risk, but an excellent fit for the linear-logistic model even at the extremes of risks.
机译:风险预测模型需要进行仔细的校准,以确保给定其潜在风险因素概况,从而对基础人群中的受试者产生无偏风险估计。由于具有极高或极低风险的受试者可能会受其风险估算知识的影响最大,因此在临床风险应用中检查处于极端风险的风险模型的充分性非常重要。我们提出了一种针对极端疾病风险分布的测试模型校准的新方法,在这种情况下,标准拟合优度测试可能由于数据稀疏而缺乏功能。我们基于模型残差构建检验统计量,仅对那些通过高和/或低风险阈值的个体求和,然后在不同风险阈值上最大化检验统计量。基于基础高斯过程的方差-协方差函数的解析推导,我们得出了最大检验统计量的渐近分布。该方法用于乳腺癌的大型病例对照研究,以检查通过最近的全基因组关联研究发现的常见单核苷酸多态性(SNP)的联合作用。该分析清楚地表明,SNP对绝对风险的规模无累加作用,但即使在极端风险下,也非常适合线性物流模型。

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