Skip to main content
Log in

Understanding and Quantifying Network Robustness to Stochastic Inputs

  • Original Article
  • Published:
Bulletin of Mathematical Biology Aims and scope Submit manuscript

Abstract

A variety of biomedical systems are modeled by networks of deterministic differential equations with stochastic inputs. In some cases, the network output is remarkably constant despite a randomly fluctuating input. In the context of biochemistry and cell biology, chemical reaction networks and multistage processes with this property are called robust. Similarly, the notion of a forgiving drug in pharmacology is a medication that maintains therapeutic effect despite lapses in patient adherence to the prescribed regimen. What makes a network robust to stochastic noise? This question is challenging due to the many network parameters (size, topology, rate constants) and many types of noisy inputs. In this paper, we propose a summary statistic to describe the robustness of a network of linear differential equations (i.e. a first-order mass-action system). This statistic is the variance of a certain random walk passage time on the network. This statistic can be quickly computed on a modern computer, even for complex networks with thousands of nodes. Furthermore, we use this statistic to prove theorems about how certain network motifs increase robustness. Importantly, our analysis provides intuition for why a network is or is not robust to noise. We illustrate our results on thousands of randomly generated networks with a variety of stochastic inputs.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Data availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

References

  • Anderson DF, Mattingly JC (2007) Propagation of fluctuations in biochemical systems, II: nonlinear chains. IET Syst Biol 1(6):313–325

    Article  Google Scholar 

  • Anderson DF, Mattingly JC, Frederik Nijhout H, Reed MC (2007) Propagation of fluctuations in biochemical systems, I: Linear SSC networks. Bull Math Biol 69(6):1791–1813

    Article  MathSciNet  Google Scholar 

  • Bao J-D, Jia Y (2004) Determination of fission rate by mean last passage time. Phys Rev C 69(2):027602

    Article  Google Scholar 

  • Bena I (2006) Dichotomous markov noise: exact results for out-of-equilibrium systems. Int J Mod Phys B 20(20):2825–2888

    Article  MathSciNet  Google Scholar 

  • Browning AP, Jenner AL, Baker RE, Maini PK (2023) Smoothing in linear multicompartment biological processes subject to stochastic input. arXiv preprint arXiv:2305.09004

  • Campbell A (2003) The future of bacteriophage biology. Nat Rev Genet 4(6):471–477

    Article  Google Scholar 

  • Cannon WB (1932) The wisdom of the body. Norton & Co., New York

    Book  Google Scholar 

  • Carr EJ, Simpson MJ (2019) New homogenization approaches for stochastic transport through heterogeneous media. J Chem Phys 150(4)

  • Clark ED, Lawley SD (2023) How drug onset rate and duration of action affect drug forgiveness. J Pharmacokin Pharmacodyn (in press)

  • Clark ED, Lawley SD (2022) Should patients skip late doses of medication? A pharmacokinetic perspective. J Pharmacokinet Pharmacodyn 49(4):429–444

    Article  Google Scholar 

  • Comtet A, Cornu F, Schehr G (2020) Last-passage time for linear diffusions and application to the emptying time of a box. J Stat Phys 181(5):1565–1602

    Article  MathSciNet  Google Scholar 

  • Counterman ED, Lawley SD (2021) What should patients do if they miss a dose of medication? A theoretical approach. J Pharmacokinet Pharmacodyn 48(6):873–892

    Article  Google Scholar 

  • Counterman ED, Lawley SD (2022) Designing drug regimens that mitigate nonadherence. Bull Math Biol 84(1):1–36

    Article  MathSciNet  Google Scholar 

  • Félix M-A, Barkoulas M (2015) Pervasive robustness in biological systems. Nat Rev Genet 16(8):483–496

    Article  Google Scholar 

  • Felmlee MA, Morris ME, Mager DE (2012) Mechanism-based pharmacodynamic modeling. In: Computational toxicology, pp 583–600. Springer

  • Fermín LJ, Lévy-Véhel J (2017) Variability and singularity arising from poor compliance in a pharmacokinetic model ii: the multi-oral case. J Math Biol 74(4):809–841

    Article  MathSciNet  Google Scholar 

  • Fill JA (2009) The passage time distribution for a birth-and-death chain: strong stationary duality gives a first stochastic proof. J Theor Probab 22(3):543–557

    Article  MathSciNet  Google Scholar 

  • Gibaldi M, Perrier D (1982) Pharmacokinetics, 2nd edn. Marcelly Dekker, New York

    Book  Google Scholar 

  • Haynes RB, McDonald HP, Garg A, Montague P (2002) Interventions for helping patients to follow prescriptions for medications. Cochrane Database Syste Rev 2

  • Huang C, Ferrell JE (1996) Ultrasensitivity in the mitogen-activated protein kinase cascade. Proc Natl Acad Sci USA 93(19):10078–10083

    Article  Google Scholar 

  • Kloeden PE, Platen E (1992) Numerical solution of stochastic differential equations, corrected edition. Springer, Berlin

    Book  Google Scholar 

  • Lévy-Véhel P-E, Lévy-Véhel J (2013) Variability and singularity arising from poor compliance in a pharmacokinetic model i: the multi-iv case. J Pharmacokinet Pharmacodyn 40(1):15–39

    Article  Google Scholar 

  • Li J, Nekka F (2007) A pharmacokinetic formalism explicitly integrating the patient drug compliance. J Pharmacokinet Pharmacodyn 34(1):115–139

    Article  Google Scholar 

  • Li J, Nekka F (2009) A probabilistic approach for the evaluation of pharmacological effect induced by patient irregular drug intake. J Pharmacokinet Pharmacodyn 36(3):221–238

    Article  Google Scholar 

  • Liu L, Liu X, Yao DD (2004) Analysis and optimization of a multistage inventory-queue system. Manag Sci 50(3):365–380

    Article  Google Scholar 

  • Louten J (2016) Virus structure and classification. In: Essential human virology, pp 19

  • McAllister N, Lawley S (2022) A pharmacokinetic and pharmacodynamic analysis of drug forgiveness. J Pharmacokinet Pharmacodyn 49:1–17

    Article  Google Scholar 

  • Meyer B, Chevalier C, Voituriez R, Bénichou O (2011) Universality classes of first-passage-time distribution in confined media. Phys Rev E 83(5):051116

    Article  Google Scholar 

  • Michael J (2007) Conceptual assessment in the biological sciences: a national science foundation-sponsored workshop

  • Morgan DO (2007) The cell cycle: principles of control. New Science Press, Beijing

    Google Scholar 

  • Norris JR (1998) Markov chains, statistical & probabilistic mathematics. Cambridge University Press, Cambridge

    Google Scholar 

  • Osterberg L, Blaschke T (2005) Adherence to medication. N Engl J Med 353(5):487–497

    Article  Google Scholar 

  • Osterberg LG, Urquhart J, Blaschke TF (2010) Understanding forgiveness: minding and mining the gaps between pharmacokinetics and therapeutics. Clin Pharmacol Therapeutics 88(4):457–459

    Article  Google Scholar 

  • Pavliotis GA (2014) Stochastic processes and applications: diffusion processes, the Fokker-Planck and Langevin equations, vol 60. Springer, Berlin

    Google Scholar 

  • Rosenbaum SE (2016) Basic pharmacokinetics and pharmacodynamics: an integrated textbook and computer simulations. Wiley, Hoboken

    Google Scholar 

  • Sabaté E, Sabaté E et al (2003) Adherence to long-term therapies: evidence for action. World Health Organization, Geneva

    Google Scholar 

  • Simpson EH (1949) Measurement of diversity. Nature 163(4148):688–688

    Article  Google Scholar 

Download references

Acknowledgements

SDL was supported by the National Science Foundation (Grant Nos. CAREER DMS-1944574, DMS-1814832, and DMS-2325258).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sean D. Lawley.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tung, HR., Lawley, S.D. Understanding and Quantifying Network Robustness to Stochastic Inputs. Bull Math Biol 86, 55 (2024). https://doi.org/10.1007/s11538-024-01283-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s11538-024-01283-3

Keywords

Navigation