首页> 美国卫生研究院文献>other >Assessing the incremental predictive performance of novel biomarkers over standard predictors
【2h】

Assessing the incremental predictive performance of novel biomarkers over standard predictors

机译:评估新型生物标志物相对于标准预测物的增量预测性能

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

It is unclear to what extent the incremental predictive performance of a novel biomarker is impacted by the method used to control for standard predictors. We investigated whether adding a biomarker to a model with a published risk score overestimates its incremental performance as compared to adding it to a multivariable model with individual predictors (or a composite risk score estimated from the sample of interest), and to a null model. We used 1000 simulated datasets (with a range of risk factor distributions and event rates) to compare these methods, using the continuous Net Reclassification Index (NRI), the Integrated Discrimination Index (IDI), and change in the C-statistic as discrimination metrics. The new biomarker was added to a: >null model; model including a >published risk score; model including a >composite risk score estimated from the sample of interest; and multivariable model with >individual predictors. We observed a gradient in the incremental performance of the biomarker, with the null model resulting in the highest predictive performance of the biomarker and the model using individual predictors resulting in the lowest (mean increases in C-statistic between models without and with the biomarker: 0.261, 0.085, 0.030, and 0.031; NRI: 0.767, 0.621, 0.513, and 0.530; IDI: 0.153, 0.093, 0.053 and 0.057, respectively). These findings were supported by Framingham Study data predicting atrial fibrillation using novel biomarkers. We recommend that authors report the effect of a new biomarker after controlling for standard predictors modeled as individual variables.
机译:目前尚不清楚新型生物标志物的增量预测性能在多大程度上受用于控制标准预测因子的方法的影响。我们调查了将生物标志物添加到具有已发布风险评分的模型中,与将其添加到具有单独预测变量的多变量模型(或从目标样本中估算出的复合风险评分)和空模型相比,是否高估了其增量性能。我们使用了1000个模拟数据集(具有一系列风险因子分布和事件发生率),使用连续的净重分类指数(NRI),综合歧视指数(IDI)和C统计量的变化作为歧视指标,来比较这些方法。 。新的生物标记已添加到:>空模型中;包含>已发布风险评分的模型;该模型包括根据感兴趣的样本估算出的>综合风险评分;和具有>单个预测变量的多变量模型。我们观察到生物标志物增量性能的梯度,其中空模型导致生物标志物的最高预测性能,而使用单独预测因子的模型导致最低(在没有生物标志物和有生物标志物的模型之间C统计量的平均值增加:分别为0.261、0.085、0.030和0.031; NRI:0.767、0.621、0.513和0.530; IDI:分别为0.153、0.093、0.053和0.057)。这些发现得到了Framingham研究数据的预测,这些数据使用新型生物标记物预测了心房颤动。我们建议作者在控制建模为单个变量的标准预测变量后报告新生物标记的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号