Literature DB >> 22846178

Conclusions via unique predictions obtained despite unidentifiability--new definitions and a general method.

Gunnar Cedersund1.   

Abstract

It is often predicted that model-based data analysis will revolutionize biology, just as it has physics and engineering. A widely used tool within such analysis is hypothesis testing, which focuses on model rejections. However, the fact that a systems biology model is non-rejected is often a relatively weak statement, as such models usually are highly over-parametrized with respect to the available data, and both parameters and predictions may therefore be arbitrarily uncertain. For this reason, we formally define and analyse the concept of a core prediction. A core prediction is a uniquely identified property that must be fulfilled if the given model structure is to explain the data, even if the individual parameters are non-uniquely identified. It is shown that such a prediction is as strong a conclusion as a rejection. Furthermore, a new method for core prediction analysis is introduced, which is beneficial for the uncertainty of specific model properties, as the method only characterizes the space of acceptable parameters in the relevant directions. This avoids the curse of dimensionality associated with the generic characterizations used by previously proposed methods. Analysis on examples shows that the new method is comparable to profile likelihood with regard to practical identifiability, and thus generalizes profile likelihood to the more general problem of observability. If used, the concepts and methods presented herein make it possible to distinguish between a conclusion and a mere suggestion, which hopefully will contribute to a more justified confidence in systems biology analyses.
© 2012 The Author Journal compilation © 2012 FEBS.

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Year:  2012        PMID: 22846178     DOI: 10.1111/j.1742-4658.2012.08725.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  22 in total

Review 1.  Requirements for multi-level systems pharmacology models to reach end-usage: the case of type 2 diabetes.

Authors:  Elin Nyman; Yvonne J W Rozendaal; Gabriel Helmlinger; Bengt Hamrén; Maria C Kjellsson; Peter Strålfors; Natal A W van Riel; Peter Gennemark; Gunnar Cedersund
Journal:  Interface Focus       Date:  2016-04-06       Impact factor: 3.906

2.  A systems biology analysis connects insulin receptor signaling with glucose transporter translocation in rat adipocytes.

Authors:  Niclas Bergqvist; Elin Nyman; Gunnar Cedersund; Karin G Stenkula
Journal:  J Biol Chem       Date:  2017-05-11       Impact factor: 5.157

3.  A single mechanism can explain network-wide insulin resistance in adipocytes from obese patients with type 2 diabetes.

Authors:  Elin Nyman; Meenu Rohini Rajan; Siri Fagerholm; Cecilia Brännmark; Gunnar Cedersund; Peter Strålfors
Journal:  J Biol Chem       Date:  2014-10-15       Impact factor: 5.157

4.  Grey-box modeling and hypothesis testing of functional near-infrared spectroscopy-based cerebrovascular reactivity to anodal high-definition tDCS in healthy humans.

Authors:  Yashika Arora; Pushpinder Walia; Mitsuhiro Hayashibe; Makii Muthalib; Shubhajit Roy Chowdhury; Stephane Perrey; Anirban Dutta
Journal:  PLoS Comput Biol       Date:  2021-10-06       Impact factor: 4.475

5.  Insulin signaling in type 2 diabetes: experimental and modeling analyses reveal mechanisms of insulin resistance in human adipocytes.

Authors:  Cecilia Brännmark; Elin Nyman; Siri Fagerholm; Linnéa Bergenholm; Eva-Maria Ekstrand; Gunnar Cedersund; Peter Strålfors
Journal:  J Biol Chem       Date:  2013-02-11       Impact factor: 5.157

6.  Mathematical modeling of white adipocyte exocytosis predicts adiponectin secretion and quantifies the rates of vesicle exo- and endocytosis.

Authors:  Cecilia Brännmark; William Lövfors; Ali M Komai; Tom Axelsson; Mickaël F El Hachmane; Saliha Musovic; Alexandra Paul; Elin Nyman; Charlotta S Olofsson
Journal:  J Biol Chem       Date:  2017-09-25       Impact factor: 5.157

7.  Model-Based Quantification of the Systemic Interplay between Glucose and Fatty Acids in the Postprandial State.

Authors:  Fianne L P Sips; Elin Nyman; Martin Adiels; Peter A J Hilbers; Peter Strålfors; Natal A W van Riel; Gunnar Cedersund
Journal:  PLoS One       Date:  2015-09-10       Impact factor: 3.240

8.  An Updated Organ-Based Multi-Level Model for Glucose Homeostasis: Organ Distributions, Timing, and Impact of Blood Flow.

Authors:  Tilda Herrgårdh; Hao Li; Elin Nyman; Gunnar Cedersund
Journal:  Front Physiol       Date:  2021-06-01       Impact factor: 4.566

9.  Parameter trajectory analysis to identify treatment effects of pharmacological interventions.

Authors:  Christian A Tiemann; Joep Vanlier; Maaike H Oosterveer; Albert K Groen; Peter A J Hilbers; Natal A W van Riel
Journal:  PLoS Comput Biol       Date:  2013-08-01       Impact factor: 4.475

10.  Physiologically realistic and validated mathematical liver model reveals [corrected] hepatobiliary transfer rates for Gd-EOB-DTPA using human DCE-MRI data.

Authors:  Mikael Fredrik Forsgren; Olof Dahlqvist Leinhard; Nils Dahlström; Gunnar Cedersund; Peter Lundberg
Journal:  PLoS One       Date:  2014-04-18       Impact factor: 3.240

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