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Adeline Samson

Publications and source records attributed to Adeline Samson.

21 records · Page 2Linked to original sources

Estimation in the partially observed stochastic Morris-Lecar neuronal model with particle filter and stochastic approximation methods

Parameter estimation in multidimensional diffusion models with only one coordinate observed is highly relevant in many biological applications, but a statistically difficult problem. In neuroscience, the membrane potential evolution in single neurons can be measured at high frequency, but biophysical realistic models have to include the unobserved dynamics of ion channels. One such model is the stochastic Morris-Lecar model, defined by a nonlinear two-dimensional stochastic differential equation. The coordinates are coupled, that is, the unobserved coordinate is nonautonomous, the model exhibits oscillations to mimic the spiking behavior, which means it is not of gradient-type, and the measurement noise from intracellular recordings is typically negligible. Therefore, the hidden Markov model framework is degenerate, and available methods break down. The main contributions of this paper are an approach to estimate in this ill-posed situation and nonasymptotic convergence results for the method. Specifically, we propose a sequential Monte Carlo particle filter algorithm to impute the unobserved coordinate, and then estimate parameters maximizing a pseudo-likelihood through a stochastic version of the Expectation-Maximization algorithm. It turns out that even the rate scaling parameter governing the opening and closing of ion channels of the unobserved coordinate can be reasonably estimated. An experimental data set of intracellular recordings of the membrane potential of a spinal motoneuron of a red-eared turtle is analyzed, and the performance is further evaluated in a simulation study.

stat.ME

Estimation in autoregressive model with measurement error

Consider an autoregressive model with measurement error: we observe $Z_i=X_i+ε_i$, where $X_i$ is a stationary solution of the equation $X_i=f_{θ^0}(X_{i-1})+ξ_i$. The regression function $f_{θ^0}$ is known up to a finite dimensional parameter $θ^0$. The distributions of $X_0$ and $ξ_1$ are unknown whereas the distribution of $ε_1$ is completely known. We want to estimate the parameter $θ^0$ by using the observations $Z_0,..,Z_n$. We propose an estimation procedure based on a modified least square criterion involving a weight function $w$, to be suitably chosen. We give upper bounds for the risk of the estimator, which depend on the smoothness of the errors density $f_ε$ and on the smoothness properties of $w f_θ$.

math.ST

Extension of the SAEM algorithm for nonlinear mixed models with two levels of random effects

This article focuses on parameter estimation of multi-levels nonlinear mixed effects models (MNLMEMs). These models are used to analyze data presenting multiple hierarchical levels of grouping (cluster data, clinical trials with several observation periods,...). The variability of the individual parameters of the regression function is thus decomposed as a between-sub ject variability and higher levels of variability (for example within-sub ject variability). We propose maximum likelihood estimates of parameters of those MNLMEMs with two levels of random effects, using an extension of the SAEM-MCMC algorithm. The extended SAEM algorithm is split into an explicit direct EM algorithm and a stochastic EM part. Compared to the original algorithm, additional sufficient statistics have to be approximated by relying on the conditional distribution of the second level of random effects. This estimation method is evaluated on pharmacokinetic cross-over simulated trials, mimicking theophyllin concentration data. Results obtained on those datasets with either the SAEM algorithm or the FOCE algorithm (implemented in the nlme function of R software) are compared: biases and RMSEs of almost all the SAEM estimates are smaller than the FOCE ones. Finally, we apply the extended SAEM algorithm to analyze the pharmacokinetic interaction of tenofovir on atazanavir, a novel protease inhibitor, from the ANRS 107-Puzzle 2 study. A significant decrease of the area under the curve of atazanavir is found in patients receiving both treatments.

stat.ME