MethodsX (Jan 2022)

Burst-pause criterion derivation for drinkometer measurements of ingestive behavior

  • Michele Serra,
  • Bálint File,
  • Daniela Alceste,
  • Ivana Raguz,
  • Daniel Gero,
  • Andreas Thalheimer,
  • Jeannette Widmer,
  • Aiman Ismaeil,
  • Robert E. Steinert,
  • Alan C. Spector,
  • Marco Bueter

Journal volume & issue
Vol. 9
p. 101726

Abstract

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The drinkometer is a promising device for the study of ingestive behavior of liquid meals in humans. It can be used to investigate behavior in different target populations. However, ingestive behavior has a great variability across study participants. Therefore, a new analytical approach is required for the extraction and analysis of drinkometer-derived data that could account for this variability. We developed an optimized protocol to predict an optimal burst-pause criterion (PC) for the extraction of PC-dependent microstructural parameters of ingestive behavior. These describe the microstructure of bursts, while PC-independent parameters describe the microstructure of sucks. Therefore, a PC is required to analyze separately two physiologically different parts of behavior. To accomplish this burst-pause criterion derivation (BPCD), a Gaussian Mixture Model (GMM) was built for estimation of two probability density functions (PDFs). These model the distribution of inter-suck intervals (ISIs) and inter-burst intervals (IBIs), respectively. The PC is defined at the intersection point of the two density functions. A Kaplan-Meier (KM) survival analysis was performed for post-hoc verification of the fit of the predicted optimal PC to the ISI distribution. In this protocol paper, we present a walkthrough of the data analysis of drinkometer-derived data for the measurement of microstructure of ingestive behavior based on previous results published by our group [1]. • Standardization of the burst-pause criterion derivation for drinkometer measurements of ingestive behavior. • All codes are publicly available in a repository. • The method can be easily adapted to studies with larger sample size or more than one study stimulus.

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