学术文献库

Longitudinal biomarker data and cross-sectional outcomes are routinely collected in modern epidemiology studies, often with the goal of informing tailored early intervention decisions. For example, hormones such as estradiol and follicle-stimulating hormone may predict changes in womens' health during the midlife. Most existing methods focus on constructing predictors from mean marker trajectories. However, subject-level biomarker variability may also provide critical information about disease risks and health outcomes. In this paper, we develop a joint model that estimates subject-level means and variances of longitudinal biomarkers to predict a cross-sectional health outcome. Simulations demonstrate excellent recovery of true model parameters. The proposed method provides less biased and more efficient estimates, relative to alternative approaches that either ignore subject-level differences in variances or perform two-stage estimation where estimated marker variances are treated as observed. Analyses of women's health data reveal larger variability of E2 or larger variability of FSH were associated with higher levels of fat mass change and higher levels of lean mass change across the menopausal transition.