Abstract
AbstractMathematical models are increasingly being developed and calibrated in tandem with data collection, empowering scientists to intervene in real time based on quantitative model predictions. Well-designed experiments can help augment the predictive power of a mathematical model but the question of when to collect data to maximize its utility for a model is non-trivial. Here we define data as model-informative if it results in a unique parametrization, assessed through the lens of practical identifiability. The framework we propose identifies an optimal experimental design (how much data to collect and when to collect it) that ensures parameter identifiability (permitting confidence in model predictions), while minimizing experimental time and costs. We demonstrate the power of the method by applying it to a modified version of a classic site-of-action pharmacokinetic/pharmacodynamic model that describes distribution of a drug into the tumor microenvironment (TME), where its efficacy is dependent on the level of target occupancy in the TME. In this context, we identify a minimal set of time points when data needs to be collected that robustly ensures practical identifiability of model parameters. The proposed methodology can be applied broadly to any mathematical model, allowing for the identification of a minimally sufficient experimental design that collects the most informative data.
Funder
National Science Foundation
Publisher
Springer Science and Business Media LLC
Reference49 articles.
1. Eisenberg, M. C. & Jain, H. V. A confidence building exercise in data and identifiability: modeling cancer chemotherapy as a case study. J. Theor. Biol. 431, 63–78 (2017).
2. Hu, S. Optimal time points sampling in pathway modelling. 26th Annu. Int. Conf. IEEE Eng. Med. Biol. Soc. 1, 671–674 (2004).
3. Kreutz, C. & Timmer, J. Systems biology: experimental design. FEBS J. 276, 923–942 (2009).
4. Rajakaruna, H. & Ganusov, V. V. Mathematical modeling to guide experimental design: T cell clustering as a case study. Bull. Math. Biol. 84, 103 (2022).
5. Cassidy, T. A continuation technique for maximum likelihood estimators in biological models. Bull. Math. Biol. 85, 90 (2023).