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Random Change-Point Non-linear Mixed Effects Model for left-censored longitudinal data: An application to HIV
Binod Manandhar1, Hongbin Zhang1
1City University of New York, Graduate School of Public Health, 55 W 125th St,New York, NY 10027.
This study introduces a new statistical model to identify unknown change points in longitudinal data. The method accurately estimates individual trends after an event, using HIV viral load data as an example.
Area of Science:
- Biostatistics
- Epidemiology
- Longitudinal Data Analysis
Background:
- Change-point models are crucial for analyzing longitudinal data to detect trend shifts.
- Identifying the exact time of change is challenging, especially with unknown change points in population data.
- Existing models often struggle with non-linear trends and left-censored observations.
Purpose of the Study:
- To develop and validate an unknown change-point model for longitudinal data.
- To accommodate both linear and non-linear mixed effects before and after a change point.
- To handle left-censored data within a random change-point non-linear mixed effects framework.
Main Methods:
- Utilized the stochastic approximation expectation maximization (SAEM) algorithm.
- Incorporated the Metropolis-Hasting sampler for parameter estimation.
- Applied the model to longitudinal viral load (VL) data from the New York City HIV surveillance registry.
Main Results:
- Successfully fitted a random change-point non-linear mixed effects model to the VL data.
- The model effectively estimated individual-specific trends and change points.
- Demonstrated the model's capability in handling left-censored observations in real-world epidemiological data.
Conclusions:
- The proposed unknown change-point model provides a robust framework for analyzing longitudinal data with trend shifts.
- The SAEM algorithm with Metropolis-Hasting sampler is effective for fitting complex mixed-effects models.
- This methodology offers valuable insights for understanding disease progression and intervention effects using HIV viral load data.
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