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Anna Choi and Weng Kee Wong’s Contribution to the Discussion of ‘Assumption-Lean Inference for Generalised Linear Model Parameters’ by Vansteelandt and Dukes

Choi 与 Wong 对《广义线性模型参数的弱假设推断》的讨论

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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
Anna Choi
Weng Kee Wong

Choi 与 Wong 对《广义线性模型参数的弱假设推断》的讨论

研究问题
这篇讨论关注被讨论论文的出生证明实例是否适合展示弱假设推断,以及纵向建模、因果分析与模型验证应如何考虑。
方法与思路
讨论者质疑实例的数据结构与分析适配性,建议考虑广义线性混合模型,并援引其他文献中的因果分析和统计学习方法。
材料陈述的贡献
讨论文本肯定主论文的方法进展,同时对经验实例的选择提出疑问,补充纵向分析与模型验证方面的阅读视角。
阅读关注点
应核对主论文数据是否确为纵向观测、讨论者建议是否匹配目标参数,并区分本文评论、被引方法与主论文定理的归属。
阅读边界
材料是讨论文章的索引摘要,版本未注明;不能将其当作主论文摘要,也不能把讨论者对数据结构的判断视为已核实事实。

原文摘要

We congratulate the authors for major advances in the methodology of estimands, in particular assumption-lean reference for the estimands in possibly misspecified generalised linear models. Whereas the simulation studies in Section 6 indeed support the ‘assumption-lean’ claim and the authors’ software in Practice of Epidemiology187 (pp. 1079–1084, 2018) facilitates such inference, the empirical example in Section 7 seems problematic to illustrate applications of the methodology. The example focuses on ‘data obtained from birth certificates from 2500 children born in King County, Washington in 2001’ in the First Steps program that was ‘set up in 1989’ in King County. These are longitudinal data, and the program is still ongoing. The methodology for longitudinal studies developed by Laird and Ware (1982) and applied to the Six Cities Study (Ryan, 2015, section 3) using generalised linear mixed models seems more appropriate for the re-analysis of the longitudinal data from the First Steps program of King County. Although Laird and Ware's methodology does not involve causal inference, Laird mentions how such inference can be added to the analysis in Ryan (2015, section 9 on statistical genetics). Chen et al. (2018, sections 3.6.3, 4.5, 5.4, 6.3, 6.4, 6.5, 7.4, 7.5) describe how causal inference/conclusions can be derived via multi-criteria statistical decision theory, exposure-adjusted incidence rates and multiple testing with familywise error or false discovery rate control for clinical trials data, control for confounding using inverse probability weighting, propensity scores, instrumental variables and research designs for unmeasured confounders, structural causal models and symbolic causal calculus for post-marketing safety data, empirical Bayes and Bayesian approaches to signal detection from adverse event databases. In addition, Sections 2.1.3 and 2.1.4 of that book describe recent advances in statistical learning methods which involve nonlinear basis functions such as neural networks and classification/regression trees and in validation of the prediction/regression model, in contrast to the linear (or partial linear) basis functions used in the present paper and complementary to the sample splitting asymptotic theory in its Theorem 2.

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