跳到正文
← 返回论文列表与筛选
阅读说明

本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

本页为预印本版本;arXiv 收录、作者填写的期刊信息以及作者既有发表经历,都不单独证明本篇已接收。作者发表记录按 OpenAlex 身份与完整姓名、本站覆盖期刊 ISSN 及正式卷期核对,只展示已核实例,档案仍可能误合并。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。

分类依据与纠错

AI 根据所提供的论文材料归类:摘要直接研究处理效应的因果中介分解与推断,属于因果推断。

反馈分类问题

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Mijeong Kim

非高斯误差线性模型的半参数因果中介分析:药物治疗与社会项目评估

研究问题
在线性中介模型存在非高斯误差及处理与中介交互时,如何更精确地估计直接和间接效应,并构造可靠区间?
方法与思路
作者结合半参数有效回归、多起点拟合算法与堆叠估计方程,处理标准及含处理与中介交互的模型,构造置信区间。
材料陈述的贡献
摘要称,模拟中该方法相对 OLS 降低均方根误差并缩短区间,在药物治疗与社会项目数据中提供更精确的效应分解。
阅读关注点
应核对因果识别条件、误差分布允许范围、有效性证明及多起点算法,并检查边界功效设计与区间覆盖率。
阅读边界
所据为 arXiv 预印本,同行评审或期刊接收未核实;摘要未说明完整识别条件,特定模拟优势不能直接推广。

原文摘要

\textbf{Background:} Mediation analysis is widely used to investigate how treatments and programs exert their effects, but standard ordinary least squares (OLS) inference can be unreliable when regression errors are non-Gaussian. In medical and public-health studies, this can affect whether indirect and direct effects are judged clinically or scientifically meaningful. \textbf{Methods:} We developed a semiparametric causal mediation framework for linear models allowing possibly non-Gaussian errors, covering both standard models and models with treatment--mediator interaction. The method combines semiparametric efficient regression estimation, a reproducible multi-start fitting algorithm for numerical stability, and stacked estimating equations for confidence-interval construction without requiring Gaussian error assumptions. \textbf{Results:} Across Gaussian, skewed, and mixture-error simulations, the semiparametric estimator reduced root mean squared error and confidence-interval length relative to OLS, with the largest gains under non-Gaussian errors. In a near-boundary power design, the OLS confidence interval achieved 18.3\% empirical power, whereas the semiparametric confidence interval identified significant effects in all replications. In the \textit{uis} drug-treatment data, it yielded sharper treatment-specific effect estimates under clear treatment--mediator interaction. In the \textit{jobs} social-program data, the semiparametric analysis produced shorter confidence intervals for mediated effects and detected nonzero mediation where OLS did not. \textbf{Conclusions:} Semiparametric mediation analysis can improve the precision and reliability of effect decomposition in studies with non-Gaussian outcomes, offering a practical alternative to OLS when indirect and direct effects may inform clinical or policy decision-making.

笔记与分组
相关领域论文