Discussion of "Optimal test procedures for multiple hypotheses controlling the familywise expected loss" by Willi Maurer, Frank Bretz, and Xiaolei Xun.
Discussion of "Optimal test procedures for multiple hypotheses controlling the familywise expected loss" by Willi Maurer, Frank Bretz, and Xiaolei Xun.
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Willi Maurer、Frank Bretz 和 Xiaolei Xun 讨论“控制家庭预期损失的多重假设的最优检验程序”。
DOI:
10.1111/biom.13908
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发表时间:
2023
期刊:
影响因子:
1.9
通讯作者:
Banerjee,Sudipto
中科院分区:
文献类型:
--
作者:
Banerjee,Sudipto
I congratulate the authors (Mauer, Bretz, and Xun) on an interesting article and thank the Editors for the opportunity to discuss the work. The authors pursue a classical decision-theoretic approach by defining suitable loss functions for a given decision rule. They control the familywise expected loss, rather than the more customary familywise error rate (FWER), based upon the sampling distribution of the data. Arguing that FWER may not be appropriate in certain real-world clinical decision settings and noting that the number of hypotheses is relatively small in customary clinical applications, the authors adopt a finite actions perspective and seek to minimize a measure of false negatives subject to some measure of false positives being bounded by a given threshold for any parameter configuration. Instead of offering a critical analysis of the proposed approach, my discussion will focus on some less traditional settings that are witnessing increasing use of multiple hypothesis tests and where, in my opinion, a classical decision-theoretic approach such as the one adopted by the authors’ may not render itself seamlessly. My discussion is not intended to disparage the classical decisiontheoretic approach, but to foment further explorations into fully model-based Bayesian approaches when the classical approach may be too restrictive. More specifically, I will consider applications of spatial data analysis in public health where one seeks to detect differences in effects among neighboring regions. A salient feature of such applications is that multiple tests are sought on unobserved correlated spatial random effects that need to be estimated from a spatial model. Let us consider spatial disease mapping, where regional aggregates such as counts or rates from a disease are mapped over clearly delineated administrative units such as counties or census tracts or zip codes in a state to better understand geographic variation of diseases (Koch, 2005; Lawson, 2013, 2018; Lawson et al., 2016). Let 𝑦𝑖 denote a disease outcome of interest in region 𝑖 for 𝑖= 1,…, 𝑛. We assume a typical generalized linear mixed model setting where 𝑦𝑖 follows a distribution from the exponential family with canonical link 𝑔 (E (𝑦𝑖))= 𝒙T 𝑖 𝜷+ 𝜙𝑖,(1) where 𝒙𝑖𝑑 is a 𝑝× 1 vector of explanatory variables specific within region 𝑖, 𝜷 are the slopes corresponding to the explanatory variables and 𝜙𝑖 is a spatial random effect corresponding to region 𝑖. The explanatory variables can comprise risk factors for the disease or potential confounders that need to be reckoned with. Spatial dependence is introduced in the 𝑛× 1 vector of spatial random effects, 𝝓=(𝜙1, 𝜙2,…, 𝜙𝑛) T, using stochastic models on graphs, where the nodes correspond to regions and an edge between two nodes relate them as neighbors. Examples include Markov random fields using undirected graphs (Besag, 1974; Besag et al., 1991; Kissling & Carl, 2008; Rue & Held, 2005) or directed acyclic graphical autoregression (DAGAR) models (Datta et al., 2019).