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Joint analysis for multivariate longitudinal and event time data with a change point anchored at interval-censored event time

Yue Zhan, Cheng Zheng, Ying Zhang

TL;DR

A joint model for multivariate longitudinal biomarkers with a change point anchored at an interval-censored event time is developed and applied to PREDICT-HD, a multisite observational cohort study of prodromal HD individuals, to ascertain how cognitive impairment and motor dysfunction interact during disease progression.

Abstract

Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor dysfunction, psychiatric disturbances, and cognitive decline. The onset of HD is marked by severe motor impairment, which may be predicted by prior cognitive decline and, in turn, exacerbate cognitive deficits. Clinical data, however, are often collected at discrete time points, so the timing of disease onset is subject to interval censoring. To address the challenges posed by such data, we develop a joint model for multivariate longitudinal biomarkers with a change point anchored at an interval-censored event time. The model simultaneously assesses the effects of longitudinal biomarkers on the event time and the changes in biomarker trajectories following the event. We conduct a comprehensive simulation study to demonstrate the finite-sample performance of the proposed method for causal inference. Finally, we apply the method to PREDICT-HD, a multisite observational cohort study of prodromal HD individuals, to ascertain how cognitive impairment and motor dysfunction interact during disease progression.

Joint analysis for multivariate longitudinal and event time data with a change point anchored at interval-censored event time

TL;DR

A joint model for multivariate longitudinal biomarkers with a change point anchored at an interval-censored event time is developed and applied to PREDICT-HD, a multisite observational cohort study of prodromal HD individuals, to ascertain how cognitive impairment and motor dysfunction interact during disease progression.

Abstract

Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor dysfunction, psychiatric disturbances, and cognitive decline. The onset of HD is marked by severe motor impairment, which may be predicted by prior cognitive decline and, in turn, exacerbate cognitive deficits. Clinical data, however, are often collected at discrete time points, so the timing of disease onset is subject to interval censoring. To address the challenges posed by such data, we develop a joint model for multivariate longitudinal biomarkers with a change point anchored at an interval-censored event time. The model simultaneously assesses the effects of longitudinal biomarkers on the event time and the changes in biomarker trajectories following the event. We conduct a comprehensive simulation study to demonstrate the finite-sample performance of the proposed method for causal inference. Finally, we apply the method to PREDICT-HD, a multisite observational cohort study of prodromal HD individuals, to ascertain how cognitive impairment and motor dysfunction interact during disease progression.
Paper Structure (13 sections, 17 equations, 3 figures, 3 tables)

This paper contains 13 sections, 17 equations, 3 figures, 3 tables.

Figures (3)

  • Figure 1: A hypothetical model for the HD disease progression: V and U are the two adjacent diagnosed times, with V being negative and U being positive for the HD diagnosis.
  • Figure 2: Estimated B-spline cumulative hazard with interior knots=6, n=400, true $\Lambda_0(t)=(0.2t)^{1.5}$.
  • Figure 3: Estimated B-spline cumulative hazard with interior knots=6, n=800, true $\Lambda_0(t)=(0.2t)^{1.5}$.