Williamson Brian D, Huang Ying
Biostatistics Division, Kaiser Permanente Washington Health Research Institute, Seattle, USA.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, USA.
Int J Biostat. 2024 Feb 13;20(2):347-359. doi: 10.1515/ijb-2023-0059. eCollection 2024 Nov 1.
In many applications, it is of interest to identify a parsimonious set of features, or panel, from multiple candidates that achieves a desired level of performance in predicting a response. This task is often complicated in practice by missing data arising from the sampling design or other random mechanisms. Most recent work on variable selection in missing data contexts relies in some part on a finite-dimensional statistical model, e.g., a generalized or penalized linear model. In cases where this model is misspecified, the selected variables may not all be truly scientifically relevant and can result in panels with suboptimal classification performance. To address this limitation, we propose a nonparametric variable selection algorithm combined with multiple imputation to develop flexible panels in the presence of missing-at-random data. We outline strategies based on the proposed algorithm that achieve control of commonly used error rates. Through simulations, we show that our proposal has good operating characteristics and results in panels with higher classification and variable selection performance compared to several existing penalized regression approaches in cases where a generalized linear model is misspecified. Finally, we use the proposed method to develop biomarker panels for separating pancreatic cysts with differing malignancy potential in a setting where complicated missingness in the biomarkers arose due to limited specimen volumes.
在许多应用中,从多个候选特征中识别出一组简洁的特征(即特征组)以在预测响应时达到期望的性能水平是很有意义的。在实践中,由于抽样设计或其他随机机制导致的数据缺失,这项任务通常会变得复杂。最近在缺失数据情况下进行变量选择的工作在某种程度上依赖于有限维统计模型,例如广义线性模型或惩罚线性模型。在该模型设定错误的情况下,所选变量可能并非全部在科学上真正相关,并且可能导致特征组的分类性能次优。为了解决这一局限性,我们提出一种非参数变量选择算法,并结合多重填补法,以便在存在随机缺失数据的情况下开发灵活的特征组。我们概述了基于所提出算法的策略,这些策略能够控制常用的错误率。通过模拟,我们表明,在广义线性模型设定错误的情况下,与几种现有的惩罚回归方法相比,我们的方法具有良好的操作特性,并能得到具有更高分类和变量选择性能的特征组。最后,在生物标志物因样本量有限而出现复杂缺失的情况下,我们使用所提出的方法开发生物标志物特征组,以区分具有不同恶性潜能的胰腺囊肿。