Modelling methodology in physiopathology

被引:10
作者
Boissel, Jean-Pierre [1 ,2 ,3 ]
Ribba, Benjamin [1 ,4 ]
Grenier, Emmanuel [1 ,5 ]
Chapuisat, Guillemette [1 ,6 ]
Dronne, Marie-Aimee [1 ,2 ]
机构
[1] Univ Lyon 1, Inst Theoret Med, RTH Laennec Sch Med, UMR5558, F-69008 Lyon, France
[2] CNRS, UMR5558, Lyon, France
[3] Leon Berard Anticanc Ctr, Lyon, France
[4] Lyon Sud Sch Med, EA, Lyon, France
[5] Ecole Normale Super Lyon, UMPA, UMR5669, F-69364 Lyon, France
[6] Pres UniverSud, CNRS, ENS Cachan, CMLA, F-94235 Cachan, France
关键词
systems physiopathology; modelling; methodology; strategy;
D O I
10.1016/j.pbiomolbio.2007.10.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diseases are complex systems. Modelling them, i.e. systems physiopathology, is a quite demanding, complicated, multidimensional, multiscale process. As such, in order to achieve the goal of the model and further to optimise a rather-time and resource-consuming process, a relevant and easy to practice methodology is required. It includes guidance for validation. Also, the model development should be managed as a complicated process, along a strategy which has been elaborated in the beginning. It should be flexible enough to meet every case. A model is a representation of the available knowledge. All available knowledge does not have the same level of evidence and, further, there is a large variability of the values of all parameters (e.g. affinity constant or ionic current) across the literature. In addition, in a complex biological system there are always values lacking for a few or sometimes many parameters. All these three aspects are sources of uncertainty on the range of validity of the models and raise unsolved problems for designing a relevant model. Tools and techniques for integrating the parameter range of experimental values, level of evidence and missing data are needed. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:28 / 39
页数:12
相关论文
共 18 条
[1]  
Brenner S, 1998, CIBA F SYMP, V213, P106
[2]   A global phenomenological model of ischemic stroke with stress on spreading depressions [J].
Chapuisat, G. ;
Dronne, M. A. ;
Grenier, E. ;
Hommel, M. ;
Gilquin, H. ;
Boissel, J. P. .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2008, 97 (01) :4-27
[3]   Numerical simulation of a stroke: Computational problems and methodology [J].
Descombes, Stephane ;
Dumont, Thierry .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2008, 97 (01) :40-53
[4]   Mathematical modelling of an ischemic stroke: An integrative approach [J].
Dronne, MA ;
Boissel, JP ;
Grenier, E ;
Gilquin, H ;
Cucherat, M ;
Hommel, M ;
Barbier, E ;
Bricca, G .
ACTA BIOTHEORETICA, 2004, 52 (04) :255-272
[5]   A modelling approach to explore some hypotheses of the failure of neuroprotective trials in ischemic stroke patients [J].
Dronne, Marie-Aimee ;
Grenier, Emmanuel ;
Chapuisat, Guillemette ;
Hommel, Marc ;
Boissel, Jean-Pierre .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2008, 97 (01) :60-78
[6]   Role of astrocytes in grey matter during stroke: A modelling approach [J].
Dronne, Marie-Aimee ;
Grenier, Emmanuel ;
Dumont, Thierry ;
Hommel, Marc ;
Boissel, Jean-Pierre .
BRAIN RESEARCH, 2007, 1138 :231-242
[7]   A mathematical model of ion movements in grey matter during a stroke [J].
Dronne, Marie-Aimee ;
Boissel, Jean-Pierre ;
Grenier, Emmanuel .
JOURNAL OF THEORETICAL BIOLOGY, 2006, 240 (04) :599-615
[8]   Repositioning of cells by mechanotaxis on surfaces with micropatterned Young's modulus [J].
Gray, DS ;
Tien, J ;
Chen, CS .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 66A (03) :605-614
[9]   A numerical study of the blocking of migraine by Rolando sulcus [J].
Grenier, E. ;
Dronne, M. A. ;
Descombes, S. ;
Gilquin, H. ;
Jaillard, A. ;
Hommel, M. ;
Boissel, J. -P. .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2008, 97 (01) :54-59
[10]   A QUANTITATIVE DESCRIPTION OF MEMBRANE CURRENT AND ITS APPLICATION TO CONDUCTION AND EXCITATION IN NERVE [J].
HODGKIN, AL ;
HUXLEY, AF .
JOURNAL OF PHYSIOLOGY-LONDON, 1952, 117 (04) :500-544