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AI 根据所提供的论文材料归类:摘要研究临床汇总数据的多元元回归,未提供所列经济学细分方向的直接依据。

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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
Hui Yao
Sungduk Kim
Ming-Hui Chen
Joseph G. Ibrahim
Arvind K. Shah
Jianxin Lin

研究内样本协方差矩阵部分缺失时的多元元回归贝叶斯推断

研究问题
在研究层面的多元汇总数据中,若各结局的标准差已知但研究内相关系数缺失,如何实施多元元回归的贝叶斯推断?
方法与思路
作者采用多元随机效应模型,给定总体协方差时令样本协方差服从 Wishart 分布,并用偏相关变换在 MCMC 中抽取缺失元素。
材料陈述的贡献
摘要提出处理部分观测协方差矩阵的推断方法及多种协方差结构,以跨治疗组和试验共享信息,并报告模拟与临床数据评估。
阅读关注点
阅读时应核对协方差结构与先验、偏相关变换如何保证矩阵有效,以及缺失相关系数的处理、MCMC 收敛和结构敏感性。
阅读边界
仅据版本未注明的 OpenAlex 索引摘要;先验、缺失机制及具体结果未完整提供,不能据此判断推断稳健性或推断刊本变化。

原文摘要

Multivariate meta-regression models are commonly used in settings where the response variable is naturally multidimensional. Such settings are common in cardiovascular and diabetes studies where the goal is to study cholesterol levels once a certain medication is given. In this setting, the natural multivariate endpoint is low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), and triglycerides (TG) (LDL-C, HDL-C, TG). In this article, we examine study level (aggregate) multivariate meta-data from 26 Merck sponsored double-blind, randomized, active, or placebo-controlled clinical trials on adult patients with primary hypercholesterolemia. Our goal is to develop a methodology for carrying out Bayesian inference for multivariate meta-regression models with study level data when the within-study sample covariance matrix S for the multivariate response data is partially observed. Specifically, the proposed methodology is based on postulating a multivariate random effects regression model with an unknown within-study covariance matrix Σ in which we treat the within-study sample correlations as missing data, the standard deviations of the within-study sample covariance matrix S are assumed observed, and given Σ, S follows a Wishart distribution. Thus, we treat the off-diagonal elements of S as missing data, and these missing elements are sampled from the appropriate full conditional distribution in a Markov chain Monte Carlo (MCMC) sampling scheme via a novel transformation based on partial correlations. We further propose several structures (models) for Σ, which allow for borrowing strength across different treatment arms and trials. The proposed methodology is assessed using simulated as well as real data, and the results are shown to be quite promising. Supplementary materials for this article are available online.

笔记与分组