Deconvolving the Input to Random Abstract Parabolic Systems; A Population Model-Based Approach to Estimating Blood/Breath Alcohol Concentration from Transdermal Alcohol Biosensor Data

TL;DR

This paper introduces a novel population model-based method to estimate blood and breath alcohol concentrations from transdermal biosensor data by deconvolving the input signal using a diffusion equation framework with random parameters.

Contribution

It reformulates the dynamical system to treat random parameters as spatial variables, enabling direct estimation of distributions and deconvolution of alcohol signals from biosensor data.

Findings

Successfully estimated bivariate normal distributions of alcohol levels.

Deconvolved BAC/BrAC signals from TAC data in multiple subject populations.

Provided credible bands without simulation for the estimated distributions.

Abstract

The distribution of random parameters in, and the input signal to, a distributed parameter model with unbounded input and output operators for the transdermal transport of ethanol are estimated. The model takes the form of a diffusion equation with the input, which is on the boundary of the domain, being the blood or breath alcohol concentration (BAC/BrAC), and the output, also on the boundary, being the transdermal alcohol concentration (TAC). Our approach is based on the reformulation of the underlying dynamical system in such a way that the random parameters are treated as additional spatial variables. When the distribution to be estimated is assumed to be defined in terms of a joint density, estimating the distribution is equivalent to estimating a functional diffusivity in a multi-dimensional diffusion equation. The resulting system is referred to as a population model, and well-established finite dimensional approximation schemes, functional analytic based convergence arguments, optimization techniques, and computational methods can be used to fit it to population data and to analyze the resulting fit. Once the forward population model has been identified or trained based on a sample from the population, the resulting distribution can then be used to deconvolve the BAC/BrAC input signal from the biosensor observed TAC output signal formulated as either a quadratic programming or linear quadratic tracking problem. In addition, our approach allows for the direct computation of corresponding credible bands without simulation. We use our technique to estimate bivariate normal distributions and deconvolve BAC/BrAC from TAC based on data from a population that consists of multiple drinking episodes from a single subject and a population consisting of single drinking episodes from multiple subjects.