Variational Autoencoders for Data Augmentation in Clinical Studies

被引:16
|
作者
Papadopoulos, Dimitris [1 ]
Karalis, Vangelis D. [1 ,2 ]
机构
[1] Natl & Kapodistrian Univ Athens, Sch Hlth Sci, Dept Pharm, Athens 15784, Greece
[2] Fdn Res & Technol Hellas FORTH, Inst Appl & Computat Math, Iraklion 70013, Greece
来源
APPLIED SCIENCES-BASEL | 2023年 / 13卷 / 15期
关键词
variational autoencoders; clinical trials; data augmentation; sample size; TRIALS;
D O I
10.3390/app13158793
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Featured Application Variational autoencoders, which are a type of neural network, are introduced in this study as a means to virtually increase the sample size of clinical studies and reduce costs, time, dropouts, and ethical concerns. The efficiency of variational autoencoders in data augmentation is proven through simulations of several scenarios. Sample size estimation is critical in clinical trials. A sample of adequate size can provide insights into a given population, but the collection of substantial amounts of data is costly and time-intensive. The aim of this study was to introduce a novel data augmentation approach in the field of clinical trials by employing variational autoencoders (VAEs). Several forms of VAEs were developed and used for the generation of virtual subjects. Various types of VAEs were explored and employed in the production of virtual individuals, and several different scenarios were investigated. The VAE-generated data exhibited similar performance to the original data, even in cases where a small proportion of them (e.g., 30-40%) was used for the reconstruction of the generated data. Additionally, the generated data showed even higher statistical power than the original data in cases of high variability. This represents an additional advantage for the use of VAEs in situations of high variability, as they can act as noise reduction. The application of VAEs in clinical trials can be a useful tool for decreasing the required sample size and, consequently, reducing the costs and time involved. Furthermore, it aligns with ethical concerns surrounding human participation in trials.
引用
收藏
页数:20
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