| Literature DB >> 28239239 |
Jared C Foster1, Danping Liu1, Paul S Albert1, Aiyi Liu1.
Abstract
Longitudinal monitoring of biomarkers is often helpful for predicting disease or a poor clinical outcome. In this paper, We consider the prediction of both large and small-for-gestational-age births using longitudinal ultrasound measurements, and attempt to identify subgroups of women for whom prediction is more (or less) accurate, should they exist. We propose a tree-based approach to identifying such subgroups, and a pruning algorithm which explicitly incorporates a desired type-I error rate, allowing us to control the risk of false discovery of subgroups. The proposed methods are applied to data from the Scandinavian Fetal Growth Study, and are evaluated via simulations.Entities:
Keywords: Fetal Growth; Personalized Medicine; Prediction; Recursive Partitioning; Shared Random Effects Models
Year: 2016 PMID: 28239239 PMCID: PMC5321661 DOI: 10.1111/rssa.12182
Source DB: PubMed Journal: J R Stat Soc Ser A Stat Soc ISSN: 0964-1998 Impact factor: 2.483