| Literature DB >> 32717100 |
Lili Zhao1, Susan Murray1, Laura H Mariani2, Wenjun Ju3.
Abstract
Longitudinal biomarker data are often collected in studies, providing important information regarding the probability of an outcome of interest occurring at a future time. With many new and evolving technologies for biomarker discovery, the number of biomarker measurements available for analysis of disease progression has increased dramatically. A large amount of data provides a more complete picture of a patient's disease progression, potentially allowing us to make more accurate and reliable predictions, but the magnitude of available data introduces challenges to most statistical analysts. Existing approaches suffer immensely from the curse of dimensionality. In this article, we propose methods for making dynamic risk predictions using repeatedly measured biomarkers of a large dimension, including cases when the number of biomarkers is close to the sample size. The proposed methods are computationally simple, yet sufficiently flexible to capture complex relationships between longitudinal biomarkers and potentially censored events times. The proposed approaches are evaluated by extensive simulation studies and are further illustrated by an application to a data set from the Nephrotic Syndrome Study Network.Entities:
Keywords: Joint modeling; dynamic prediction; pseudo observations; random forests; risk prediction
Mesh:
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Year: 2020 PMID: 32717100 PMCID: PMC8011834 DOI: 10.1002/sim.8687
Source DB: PubMed Journal: Stat Med ISSN: 0277-6715 Impact factor: 2.373