TY - JOUR
T1 - Stochastic differential mixed-effects models
AU - Picchini, Umberto
AU - De Gaetano, Andrea
AU - Ditlevsen, Susanne
N1 - A post-publication correction to some editorial typos is available as "Corrigendum" with DOI: 10.1111/j.1467-9469.2010.00692.x
PY - 2010
Y1 - 2010
N2 - Stochastic differential equations have been shown useful in describing random continuous time processes. Biomedical experiments often imply repeated measurements on a series of experimental units and differences between units can be represented by incorporating random effects into the model. When both system noise and random effects are considered, stochastic differential mixed-effects models ensue. This class of models enables the simultaneous representation of randomness in the dynamics of the phenomena being considered and variability between experimental units, thus providing a powerful modelling tool with immediate applications in biomedicine and pharmacokinetic/pharmacodynamic studies. In most cases the likelihood function is not available, and thus maximum likelihood estimation of the unknown parameters is not possible. Here we propose a computationally fast approximated maximum likelihood procedure for the estimation of the non-random parameters and the random effects. The method is evaluated on simulations from some famous diffusion processes and on real data sets
AB - Stochastic differential equations have been shown useful in describing random continuous time processes. Biomedical experiments often imply repeated measurements on a series of experimental units and differences between units can be represented by incorporating random effects into the model. When both system noise and random effects are considered, stochastic differential mixed-effects models ensue. This class of models enables the simultaneous representation of randomness in the dynamics of the phenomena being considered and variability between experimental units, thus providing a powerful modelling tool with immediate applications in biomedicine and pharmacokinetic/pharmacodynamic studies. In most cases the likelihood function is not available, and thus maximum likelihood estimation of the unknown parameters is not possible. Here we propose a computationally fast approximated maximum likelihood procedure for the estimation of the non-random parameters and the random effects. The method is evaluated on simulations from some famous diffusion processes and on real data sets
KW - biomedical applications
KW - Brownian motion with drift
KW - CIR process
KW - closed-form transition density expansion
KW - Gaussian quadrature
KW - geometric Brownian motion
KW - maximum likelihood estimation
KW - Ornstein–Uhlenbeck process
KW - random parameters
KW - stochastic differential equations
UR - https://www.scopus.com/pages/publications/77949528435
U2 - 10.1111/j.1467-9469.2009.00665.x
DO - 10.1111/j.1467-9469.2009.00665.x
M3 - Article
SN - 1467-9469
VL - 37
SP - 67
EP - 90
JO - Scandinavian Journal of Statistics
JF - Scandinavian Journal of Statistics
IS - 1
ER -