Parametric and Nonparametric Nonlinear System Identification of Lung Tissue Strip Mechanics

AbstractLung parenchyma is a soft biological material composed of many interacting elements such as the interstitial cells, extracellular collagen–elastin fiber network, and proteoglycan ground substance. The mechanical behavior of this delicate structure is complex showing several mild but distinct types of nonlinearities and a fractal-like long memory stress relaxation characterized by a power-law function. To characterize tissue nonlinearity in the presence of such long memory, we investigated the robustness and predictive ability of several nonlinear system identification techniques on stress–strain data obtained from lung tissue strips with various input wave forms. We found that in general, for a mildly nonlinear system with long memory, a nonparametric nonlinear system identification in the frequency domain is preferred over time-domain techniques. More importantly, if a suitable parametric nonlinear model is available that captures the long memory of the system with only a few parameters, high predictive ability with substantially increased robustness can be achieved. The results provide evidence that the first-order kernel of the stress–strain relationship is consistent with a fractal-type long memory stress relaxation and the nonlinearity can be described as a Wiener-type nonlinear structure for displacements mimicking tidal breathing. © 1999 Biomedical Engineering Society. PAC99: 8719Rr, 8710+e

[1]  L. E. Bayliss,et al.  THE VISCO‐ELASTIC PROPERTIES OF THE LUNGS , 1939 .

[2]  E SALAZAR,et al.  AN ANALYSIS OF PRESSURE-VOLUME CHARACTERISTICS OF THE LUNGS. , 1964, Journal of applied physiology.

[3]  J. Hildebrandt Comparison of mathematical models for cat lung and viscoelastic balloon derived by Laplace transform methods from pressure-volume data. , 1969, The Bulletin of mathematical biophysics.

[4]  J. Hildebrandt Dynamic properties of air-filled excised cat lung determined by liquid plethysmograph. , 1969, Journal of applied physiology.

[5]  J. Hildebrandt,et al.  Pressure-volume data of cat lung interpreted by a plastoelastic, linear viscoelastic model. , 1970, Journal of applied physiology.

[6]  R. Shapley,et al.  A method of nonlinear analysis in the frequency domain. , 1980, Biophysical journal.

[7]  M. Schetzen The Volterra and Wiener Theories of Nonlinear Systems , 1980 .

[8]  Lennart Ljung,et al.  System Identification: Theory for the User , 1987 .

[9]  Tibor Csendes,et al.  Nonlinear Parameter Estimation by Global Optimization - Efficiency and reliability , 1989, Acta Cybern..

[10]  M. Korenberg Fast Orthogonal Algorithms for Nonlinear System Identification and Time-Series Analysis , 1989 .

[11]  B. West Physiology in Fractal Dimensions , 1990 .

[12]  J. Fredberg,et al.  Input impedance and peripheral inhomogeneity of dog lungs. , 1992, Journal of applied physiology.

[13]  D. Stamenović,et al.  Lung and chest wall impedances in the dog: effects of frequency and tidal volume. , 1992, Journal of applied physiology.

[14]  K. Lutchen,et al.  Pseudorandom signals to estimate apparent transfer and coherence functions of nonlinear systems: applications to respiratory mechanics , 1992, IEEE Transactions on Biomedical Engineering.

[15]  J. Fredberg,et al.  Tissue resistance and the contractile state of lung parenchyma. , 1993, Journal of applied physiology.

[16]  D. Stamenović,et al.  Dynamic moduli of rabbit lung tissue and pigeon ligamentum propatagiale undergoing uniaxial cyclic loading. , 1994, Journal of applied physiology.

[17]  Z. Hantos,et al.  Airway and tissue mechanics during physiological breathing and bronchoconstriction in dogs. , 1994, Journal of applied physiology.

[18]  A. Barabasi,et al.  Lung tissue viscoelasticity: a mathematical framework and its molecular basis. , 1994, Journal of applied physiology.

[19]  Kenneth R. Lutchen,et al.  Relationship between frequency and amplitude dependence in the lung: a nonlinear block-structured modeling approach. , 1995, Journal of applied physiology.

[20]  B. Suki,et al.  Dynamic properties of lung parenchyma: mechanical contributions of fiber network and interstitial cells. , 1997, Journal of applied physiology.

[21]  J. Bates,et al.  A distributed nonlinear model of lung tissue elasticity. , 1997, Journal of applied physiology.

[22]  Gerald M. Saidel,et al.  Role of O2 in Regulation of Lactate Dynamics during Hypoxia: Mathematical Model and Analysis , 2004, Annals of Biomedical Engineering.

[23]  Kenneth R. Lutchen,et al.  A Frequency Domain Approach to Nonlinear and Structure Identification for Long Memory Systems: Application to Lung Mechanics , 2004, Annals of Biomedical Engineering.

[24]  J. Bates A Micromechanical Model of Lung Tissue Rheology , 1998, Annals of Biomedical Engineering.

[25]  M. J. Korenberg,et al.  The identification of nonlinear biological systems: Wiener and Hammerstein cascade models , 1986, Biological Cybernetics.

[26]  David T. Westwick,et al.  Factors Affecting Volterra Kernel Estimation: Emphasis on Lung Tissue Viscoelasticity , 2004, Annals of Biomedical Engineering.

[27]  R. Kearney,et al.  Nonparametric Block-Structured Modeling of Lung Tissue Strip Mechanics , 1998, Annals of Biomedical Engineering.

[28]  D. Navajas,et al.  Lung tissue rheology and 1/f noise , 1994, Annals of Biomedical Engineering.

[29]  Michael J. Korenberg,et al.  Parallel cascade identification and kernel estimation for nonlinear systems , 2006, Annals of Biomedical Engineering.

[30]  J. Bates,et al.  Nonparametric block-structured modeling of rat lung mechanics , 2007, Annals of Biomedical Engineering.