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AI 根据所提供的论文材料归类:摘要明确研究因果中介路径与间接效应,变量选择服务于中介效应分析,最直接对应因果推断。

反馈分类问题

Bayesian Variable Selection for High-Dimensional Mediation Analysis: Application to Metabolomics Data in Epidemiological Studies

高维中介分析的贝叶斯变量选择:流行病学代谢组数据应用

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代码、数据与补充材料

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关注这篇论文的作者
Youngho Bae
Chanmin Kim
Fenglei Wang
Qi Sun
Kyu Ha Lee

高维中介分析的贝叶斯变量选择:流行病学代谢组数据应用

研究问题
当潜在中介数量很多且相互相关时,如何识别暴露影响健康结局的活跃中介路径,并稳定估计间接效应?
方法与思路
作者提出多元随机搜索变量选择框架,以马尔可夫随机场先验利用中介相关性,并用序贯子集伯努利先验协调选择。
材料陈述的贡献
摘要称该框架能识别活跃路径并估计间接效应,模拟显示检测功效改善,并应用于两个队列的代谢组数据。
阅读关注点
应核对中介效应的识别条件、两类先验的具体作用、相关中介下的效应定义,以及功效与误选率的比较方式。
阅读边界
所给版本为 arXiv 预印本,同行评审及接收未核实;摘要未说明因果识别假设、模拟数值及结论对先验的敏感性。

原文摘要

In epidemiological research, causal models incorporating potential mediators along a pathway are crucial for understanding how exposures influence health outcomes. This work is motivated by integrated epidemiological and blood biomarker studies, investigating the relationship between long-term adherence to a Mediterranean diet and cardiometabolic health, with plasma metabolomes as potential mediators. Analyzing causal mediation in such high-dimensional omics data presents substantial challenges, including complex dependencies among mediators and the need for advanced regularization or Bayesian techniques to ensure stable and interpretable estimation and selection of indirect effects. To this end, we propose a novel Bayesian framework for identifying active pathways and estimating indirect effects in the presence of high-dimensional multivariate mediators. Our approach adopts a multivariate stochastic search variable selection method, tailored for such complex mediation scenarios. Central to our method is the introduction of a set of priors for the selection: a Markov random field prior and sequential subsetting Bernoulli priors. The first prior's Markov property leverages the inherent correlations among mediators, thereby increasing power to detect mediated effects. The sequential subsetting aspect of the second prior encourages the simultaneous selection of relevant mediators and their corresponding indirect effects from the two model parts, providing a more coherent and efficient variable selection framework, specific to mediation analysis. Comprehensive simulation studies demonstrate that the proposed method provides superior power in detecting active mediating pathways. We further illustrate the practical utility of the method through its application to metabolome data from two cohort studies, highlighting its effectiveness in real data setting.

笔记与分组
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