Mohammadreza Ganji, Anas El Fathi Ph. D., Chiara Fabris Ph. D., Dayu Lv Ph. D., Boris Kovatchev Ph. D., Marc Breton Ph. D
{"title":"Distribution-Based Sub-Population Selection (DSPS): A Method for in-Silico Reproduction of Clinical Trials Outcomes","authors":"Mohammadreza Ganji, Anas El Fathi Ph. D., Chiara Fabris Ph. D., Dayu Lv Ph. D., Boris Kovatchev Ph. D., Marc Breton Ph. D","doi":"arxiv-2409.00232","DOIUrl":null,"url":null,"abstract":"Background and Objective: Diabetes presents a significant challenge to\nhealthcare due to the negative impact of poor blood sugar control on health and\nassociated complications. Computer simulation platforms, notably exemplified by\nthe UVA/Padova Type 1 Diabetes simulator, has emerged as a promising tool for\nadvancing diabetes treatments by simulating patient responses in a virtual\nenvironment. The UVA Virtual Lab (UVLab) is a new simulation platform to mimic\nthe metabolic behavior of people with Type 2 diabetes (T2D) with a large\npopulation of 6062 virtual subjects. Methods: The work introduces the\nDistribution-Based Population Selection (DSPS) method, a systematic approach to\nidentifying virtual subsets that mimic the clinical behavior observed in real\ntrials. The method transforms the sub-population selection task into a Linear\nPrograming problem, enabling the identification of the largest representative\nvirtual cohort. This selection process centers on key clinical outcomes in\ndiabetes research, such as HbA1c and Fasting plasma Glucose (FPG), ensuring\nthat the statistical properties (moments) of the selected virtual\nsub-population closely resemble those observed in real-word clinical trial.\nResults: DSPS method was applied to the insulin degludec (IDeg) arm of a phase\n3 clinical trial. This method was used to select a sub-population of virtual\nsubjects that closely mirrored the clinical trial data across multiple key\nmetrics, including glycemic efficacy, insulin dosages, and cumulative\nhypoglycemia events over a 26-week period. Conclusion: The DSPS algorithm is\nable to select virtual sub-population within UVLab to reproduce and predict the\noutcomes of a clinical trial. This statistical method can bridge the gap\nbetween large population simulation platforms and previously conducted clinical\ntrials.","PeriodicalId":501172,"journal":{"name":"arXiv - STAT - Applications","volume":"160 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - STAT - Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.00232","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background and Objective: Diabetes presents a significant challenge to
healthcare due to the negative impact of poor blood sugar control on health and
associated complications. Computer simulation platforms, notably exemplified by
the UVA/Padova Type 1 Diabetes simulator, has emerged as a promising tool for
advancing diabetes treatments by simulating patient responses in a virtual
environment. The UVA Virtual Lab (UVLab) is a new simulation platform to mimic
the metabolic behavior of people with Type 2 diabetes (T2D) with a large
population of 6062 virtual subjects. Methods: The work introduces the
Distribution-Based Population Selection (DSPS) method, a systematic approach to
identifying virtual subsets that mimic the clinical behavior observed in real
trials. The method transforms the sub-population selection task into a Linear
Programing problem, enabling the identification of the largest representative
virtual cohort. This selection process centers on key clinical outcomes in
diabetes research, such as HbA1c and Fasting plasma Glucose (FPG), ensuring
that the statistical properties (moments) of the selected virtual
sub-population closely resemble those observed in real-word clinical trial.
Results: DSPS method was applied to the insulin degludec (IDeg) arm of a phase
3 clinical trial. This method was used to select a sub-population of virtual
subjects that closely mirrored the clinical trial data across multiple key
metrics, including glycemic efficacy, insulin dosages, and cumulative
hypoglycemia events over a 26-week period. Conclusion: The DSPS algorithm is
able to select virtual sub-population within UVLab to reproduce and predict the
outcomes of a clinical trial. This statistical method can bridge the gap
between large population simulation platforms and previously conducted clinical
trials.