首页> 外文期刊>Genetic epidemiology. >Prognostic and Predictive Values and Statistical Interactions in the Era of Targeted Treatment
【24h】

Prognostic and Predictive Values and Statistical Interactions in the Era of Targeted Treatment

机译:靶向治疗时代的预后和预测价值以及统计学相互作用

获取原文
获取原文并翻译 | 示例
           

摘要

The current era of targeted treatment has accelerated the interest in studying gene-treatment, gene-gene, and gene-environment interactions using statistical models in the health sciences. Interactions are incorporated into models as product terms of risk factors. The statistical significance of interactions is traditionally examined using a likelihood ratio test (LRT). Epidemiological and clinical studies also evaluate interactions in order to understand the prognostic and predictive values of genetic factors. However, it is not clear how different types and magnitudes of interaction effects are related to prognostic and predictive values. The contribution of interaction to prognostic values can be examined via improvements in the area under the receiver operating characteristic curve due to the inclusion of interaction terms in the model (AUC). We develop a resampling based approach to test the significance of this improvement and show that it is equivalent to LRT. Predictive values provide insights into whether carriers of genetic factors benefit from specific treatment or preventive interventions relative to noncarriers, under some definition of treatment benefit. However, there is no unique definition of the term treatment benefit. We show that AUC and relative excess risk due to interaction (RERI) measure predictive values under two specific definitions of treatment benefit. We investigate the properties of LRT, AUC, and RERI using simulations. We illustrate these approaches using published melanoma data to understand the benefits of possible intervention on sun exposure in relation to the MC1R gene. The goal is to evaluate possible interventions on sun exposure in relation to MC1R.
机译:当前的靶向治疗时代已经加速了人们对使用卫生科学中的统计模型研究基因治疗,基因-基因和基因-环境相互作用的兴趣。交互作为风险因素的乘积项并入模型。传统上,使用似然比检验(LRT)检查相互作用的统计显着性。流行病学和临床研究还评估了相互作用,以了解遗传因素的预后和预测价值。但是,尚不清楚相互作用影响的不同类型和大小如何与预后和预测值相关。由于模型中包括相互作用项,因此可以通过改善接收器工作特性曲线下的面积来检查相互作用对预后价值的贡献。我们开发了一种基于重采样的方法来测试此改进的重要性,并证明它等效于LRT。预测值提供了关于遗传因素携带者是否受益于特定治疗或相对于非携带者而言的预防性干预的见解,在某些治疗益处的定义下。但是,术语“治疗收益”没有唯一定义。我们显示,AUC和因交互作用引起的相对超额风险(RERI)在两种特定的治疗收益定义下测量预测值。我们使用模拟研究LRT,AUC和RERI的属性。我们用已发表的黑色素瘤数据说明了这些方法,以了解与MC1R基因相关的可能的日照干预措施的益处。目的是评估与MC1R相关的可能的阳光照射干预措施。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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