A PARTIALLY FUNCTIONAL LINEAR REGRESSION FRAMEWORK FOR INTEGRATING GENETIC, IMAGING, AND CLINICAL DATA

• 成果类型: Article
• 署名作者: Li, Ting; Yu, Yang; Marron, J. S.; Zhu, Hongtu
• 署名单位: Shanghai University of Finance & Economics; University of North Carolina; University of North Carolina Chapel Hill; University of North Carolina; University of North Carolina Chapel Hill
• 刊物名称: ANNALS OF APPLIED STATISTICS
• ISSN/ISSBN: 1932-6157
• DOI: 10.1214/23-AOAS1808
• 发表日期: 2024
• 页码: 704-728
• 关键词: genome-wide association; alzheimers-disease; hypothetical model; heritability; prediction; mri

摘要

This paper is motivated by the joint analysis of genetic, imaging, and clinical (GIC) data collected in the Alzheimer's Disease Neuroimaging Initiative (ADNI) study. We propose a partially functional linear regression (PFLR) framework to map high -dimensional GIC-related pathways for Alzheimer's disease (AD). We develop a joint model selection and estimation procedure by embedding imaging data in the reproducing kernel Hilbert space and imposing the t0 penalty for the coefficients of genetic variables. We apply the proposed method to the ADNI dataset to identify important features from tens of thousands of genetic polymorphisms (reduced from millions using a preprocessing step) and study the effects of a certain set of informative genetic variants and the baseline hippocampus surface on 13 future cognitive scores. We also explore the shared and distinct heritability patterns of these cognitive scores. Analysis results suggest that both the hippocampal and genetic data have heterogeneous effects on different scores, with the trend that the value of both hippocampi are negatively associated with the severity of cognition deficits. Polygenic effects are observed for all the thirteen cognitive scores. The well-known APOE4 genotype only explains a small part of the cognitive function. Shared genetic etiology exists; however, greater genetic heterogeneity exists within disease classifications after accounting for the baseline diagnosis status. These analyses are useful in further investigation of functional mechanisms for AD progression.